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A comparison between anorganic bone and collagen-preserving bone xenografts for alveolar ridge preservation: systematic review and future perspectives
Maxillofacial Plastic and Reconstructive Surgery volume 44, Article number: 24 (2022)
Abstract
After tooth extraction, dimensional changes affect the alveolar socket, leading to loss in alveolar bone height and width. Histological modifications also occur, with initial formation of a blood clot that is replaced with granulation tissue and subsequently with a provisional connective tissue matrix. Spontaneous healing ends with socket filling with woven bone, which is gradually replaced with lamellar bone and bone marrow. Adequate alveolar ridge dimensions and bone quality are required to assure optimal stability and osseointegration following dental implant placement. When a tooth is extracted, alveolar ridge preservation (ARP) procedures are an effective method to prevent collapse of the post-extraction socket. Heterologous bone is widely chosen by clinicians for ARP, and anorganic bone xenografts (ABXs) made bioinert by heat treatment represents the most used biomaterial in clinical applications. Collagen-preserving bone xenografts (CBXs) made of porcine or equine bone are fabricated by less invasive chemical or enzymatic treatments to remove xenogenic antigens, and these are also effective in preserving post-extraction sites. Clinical differences between anorganic bone substitutes and collagen-preserving materials are not well documented in the literature but understanding these differences could clarify how processing protocols influence biomaterial behavior in situ. This systematic review of the literature compares the dimensional changes and histological features of ABXs versus CBXs in ridge preservation procedures to promote awareness of different bone xenograft efficacies in stimulating the healing of post-extraction sockets.
Introduction
Bone grafts and substitutes are increasingly used in dental implantology due to the growing need for replacing insufficient alveolar bone before implant placement [1]. One of the primary reasons for bone deficiency is tooth loss due to periodontal disease, tooth fracture/trauma, periapical lesions, or other pathological conditions [2]. Experimental evidence collected through animal [3, 4] and human [5, 6] studies demonstrated that after tooth extraction, the alveolar bone undergoes a remodeling process with consequent resorption of the vestibular cortical bone and gradual loosening of the marrow component of the alveolus. Bone reduction is mainly due to the lack of intraosseous stimulation normally provided by periodontal ligament fibers [1], and it is probably correlated with disruption of the blood supply and osteoclastic activity that occur after tooth extraction [7, 8]. The greatest amount of alveolar socket resorption occurs in the first 3 months after extraction, with a 30% reduction of the alveolar ridge (3.87 mm in width and 1.67 mm in height) [9,10,11]. Dimensional changes take place up to 1 year thereafter, with about 50% total reduction (5–7 mm in width) of the alveolar ridge within 12 months post-extraction [8, 12, 13]. Interestingly, alveolar ridge resorption is more severe on the buccal side than on the lingual side [3, 11].
Bone dimensional changes at the post-extraction site influence the subsequent implant treatment plan; this important clinical issue is currently treated by alveolar ridge preservation (ARP) techniques. Also known as “socket preservation”, ARP includes methods of counteracting alveolar bone resorption after tooth extraction by (1) maintaining the soft and hard ridge components, (2) sustaining bone regeneration within the socket, and (3) facilitating prosthetically driven implant placement [10, 14,15,16]. Recent systematic reviews with meta-analyses demonstrated that in comparison with unassisted socket healing, ARP procedures reduce alveolar bone dimensional changes and can promote bone regeneration at the post-extraction site [17,18,19,20]. Furthermore, dental implants inserted into ARP-treated sites exhibited a high survival rate [20]. ARP is most commonly achieved by filling the alveolar socket with a bone grafting material immediately after tooth extraction [13]. The ideal properties of bone substitute materials include osteogenic, osteoinductive, and osteoconductive capacities similar to the native bone, as well as high biocompatibility and low immunogenicity [21]. Materials currently being investigated for ARP use include autologous bone, demineralized or mineralized freeze-dried bone allografts, xenogenic bone, alloplastic polymers, bioactive glasses, and composite ceramic substitutes [22, 23]. Among these options, xenografts seem to avoid comorbidity issues, ensuring larger availability from animal rather than human bone and avoiding tissue-banking costs. Furthermore, xenogenic bone shows better resorption and integration capacity with the host tissue than synthetic materials.
Amongst heterologous materials, the use of anorganic bone xenografts (ABXs) for ARP procedures is well supported by scientific literature, with successful outcomes obtained in both animal preclinical studies and human randomized clinical trials [24,25,26]. ABXs are produced by exposure to heat and chemical extraction processes to remove immunogenic and organic components and are then prepared as porous grains (0.25–2 mm) [25, 27]. Regardless of the species of origin (i.e., bovine or porcine), ABXs exhibit structures and properties similar to their human counterparts, with clinical evidence demonstrating comparable outcomes among xenografts from different sources [28]. Besides demonstrating good osteoconductive properties, heat-treated ABXs also have poor resorption rates [29,30,31].
Another xenogenic biomaterial successfully used for ARP procedures is non-heat treated cortico-cancellous porcine bone (CPB), which is subjected to a collagen-preserving chemical process for immunogenic component removal and is then prepared as micro-porous particles (diameter 0.6–1 mm) [32]. These collagen-containing porcine bone grafts possess excellent osteoconductive properties and do not cause inflammatory infiltration [33, 34]. These biomaterials also show clear signs of resorption/remodeling after socket grafting, with the formation of scalloped lacunae [35, 36].
Successful ARP outcomes were recently achieved by grafting the post-extraction socket with enzyme-deantigenic equine bone (EDEB), which also consists of a mixture of cancellous and cortical bone granules (diameter 0.25–1 mm) made non-antigenic with digestive enzymes [37, 38]. In addition to ARP procedures, EDEB was used with satisfactory results in peri-apical cyst-removal management [39], horizontal/vertical ridge and sinus augmentation [40,41,42], and orthopedic applications [43,44,45].
Unlike ABXs, CPB and EDEB are collagen-preserving bone xenografts (CBXs) manufactured by chemical (CPB) or enzymatic (EDEB) treatment that maintains type I bone collagen in its native state. This may offer important advantages in terms of stimulation of the regenerative process, integration with the host tissue, and graft resorption rate [38, 46, 47].
There is scant evidence in the literature about which of these two classes of xenogenic bone substitutes—ABXs or CBXs—is better for preserving post-extraction sockets. To the best of our knowledge, only three clinical trials have compared the dimensional and histomorphometric outcomes of ABXs and CBXs, with one suggesting that CBX might produce a better healing pattern, and one demonstrating that collagen-preserving material obtained by enzymatic treatment ensures better bone regeneration and graft resorption [31, 36, 38]. This systematic review was performed to (1) compare bone dimensional changes after tooth extraction and ARP by ABXs or CBXs and (2) analyze and compare histologic and histomorphometric outcomes for post-extraction sites grafted with the two types of bone substitutes.
Materials and methods
The present review was designed and conducted according to PRISMA (Preferred Reporting Items Systematic review and Meta-Analyses) guidelines [48, 49].
Focused questions
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1)
Bone dimensional changes: which bone xenograft between ABXs and CBXs best preserves the horizontal and vertical ridge dimensions after ARP?
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2)
Bone regeneration: which bone xenograft between ABXs and CBXs achieves the best percentage of new bone formation after ARP?
Eligibility criteria
The inclusion criteria of studies for this systematic review were organized according to the PICOT format [50].
Patients (P): Adult patients (age between 18 and 85 years) undergoing ARP procedures after tooth extraction.
Intervention (I): ARP strategies based on the use of anorganic bone or CBXs to fill the alveolar socket.
Comparison (C): All grafting procedures were considered for comparison, including different xenograft or allograft/synthetic materials, the use of a barrier membrane alone or in combination with the graft, and the non-intervention strategy (i.e., spontaneous healing).
Outcomes (O): The primary outcomes included: (1) bone dimensional changes evaluated by horizontal and vertical measurement of the alveolar ridge; (2) bone regeneration evaluated by histomorphometric analyses of bone biopsies to assess the percentage of newly formed/vital bone, as well as the amounts of connective tissue and residual grafting material. The secondary outcomes included: (1) change in buccal plate thickness; (2) bone volume alteration following extraction; (3) complications; (4) histological healing characteristics; (5) site eligibility for placement of an adequate size dental implant with or without further augmentation; (6) patient-reported outcomes.
Time (T): Follow-up after the surgical intervention at least 3 months.
Studies were filtered by considering only clinical trials investigating ABXs or CBXs for alveolar ridge preservation after tooth extraction. The exclusion criteria were the following: (1) cross-sectional studies, case series, case reports, pre-clinical studies, in vitro investigations; (2) studies reporting different primary outcome measures (i.e., soft tissue changes, implant stability after ARP); (3) clinical studies not clearly meeting the inclusion criteria.
Search strategy
Electronic databases (MEDLINE (PubMed), EMBASE, Cochrane Central Register of Controlled Trials, and Scopus) were methodically searched for eligible articles by using the following combinations of keywords and MeSH terms: “alveolar ridge preservation”, “alveolar preservation”, “ridge preservation”, “socket preservation”, “post-extractive socket”, “bone xenograft”, “bovine bone xenograft”, “deproteinized bovine bone”, “deproteinized bovine bone matrix”, “deproteinized porcine bone”, “porcine bone xenograft”, “equine bone xenograft”, “animal bone graft”, “animal bone substitute”, “heterologous bone graft”, “heterologous bone substitute”. Only studies in English language were included, whereas no time restrictions were set to filter articles.
Study selection
Titles and abstracts obtained by the electronic search were initially screened by the five authors. The full paper was considered for studies that had a missing or insufficient abstract to determine eligibility. Full-text versions of all the eligible articles were then obtained and carefully investigated by the five authors for final inclusion. The five authors performed parallel independent assessment and selection of the manuscripts and they had to agree on the inclusion/exclusion criteria and the finally included papers. Any disagreements among reviewers were resolved through discussion and consensus with the supervision by the corresponding author. At the end of the selection process, a total of 39 studies was included in the systematic review.
Data collection
Included studies were analyzed by recording the following primary outcome measures:
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1)
Horizontal dimensional changes of the alveolar socket (in mm), measured clinically or radiographically at the level of the crest, or at different vertical distances from the crest or landmarks (i.e., adjacent teeth or implants).
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2)
Vertical dimensional changes of the alveolar socket (in mm) measured clinically or radiographically either at the level of the crest or at the buccal and palatal/lingual aspect.
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3)
Histomorphometric evaluation of the percentage of newly formed bone (NFB), soft tissues, residual graft particles.
Dimensional outcomes were calculated as differences between baseline (i.e., soon after tooth extraction) and the clinical/radiological situation at follow-up. Measures could be either positive or negative, with negative and positive values indicating a loss/reduction and gain/increase of ridge dimensions, respectively.
Collected data were summarized by preparing schematic tables regarding (1) main study characteristics (i.e., first author, year of publication, study design, patient characteristics, surgical interventions, type of bone xenograft, reported outcomes), (2) dimensional outcomes of ARP procedures using ABXs, (3) dimensional outcomes of ARP procedures using CBXs, (4) histomorphometric outcomes of ARP procedures using ABXs, and (5) histomorphometric outcomes of ARP procedures using CBXs.
Due to high variability of data and heterogeneity of the selected clinical trials, no meta-analysis could be performed to statistically compare the clinical outcomes of bone xenografts in ARP procedures.
Risk of bias assessment
Quality evaluation on the selected studies was performed according to the Cochrane Handbook for Systematic Reviews of Interventions [51]. The following quality criteria were verified: random generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, incomplete outcome data, and other sources of bias.
Results
Study selection
The results of the literature search are shown in the PRISMA flow diagram (Fig. 1). The initial search yielded 542 total records. After removal of duplicates, 251 articles underwent title and abstract screening, which led to the exclusion of 145 records. Thus, 106 articles remained for full-text assessment (Fig. 1). There were 30 papers evaluating ARP techniques based on the use of ABXs [23, 26, 28, 52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78] and 9 papers evaluating ARP techniques based on the use of CBXs [31, 34, 36, 38, 79,80,81,82,83] that were eligible for inclusion (Table 1). Among these, 27 records about ABXs [23, 28, 53, 54, 56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78] and 7 records about CBXs [31, 34, 36, 79,80,81, 83] were eligible for inclusion in the analysis of horizontal and vertical changes of the alveolar ridge (Tables 2 and 3). In parallel, 19 records about ABXs [26, 28, 52,53,54,55,56,57,58, 60, 63, 66,67,68, 70, 73, 75,76,77] and 4 [31, 38, 79, 82] records about CBXs were eligible for inclusion in the analysis of histomorphometric outcomes (Tables 4 and 5). The most common reasons for exclusion were (1) not considering a xenograft material for ARP; (2) reporting of changes related to alveolar ridge volume, basal/superior surfaces, and shape; (3) reporting of implant primary and secondary stability as outcome variables; and (4) presenting case reports or case series with limited number of patients (n < 10).
Study characteristics
An overview of the main characteristics of eligible papers is provided by Table 1. Most studies (n = 30) resulted to be randomized controlled trials (RCT), with either prospective (n = 7) and retrospective (n = 2) clinical trials being selected during the literature search. Almost all the studies considered tooth extraction, ARP procedures and delayed implant placement as surgical interventions. Besides the primary outcome variables, site eligibility, histological healing characteristics, and complication were the most frequently reported secondary outcomes.
Risk of bias assessment
Considering the quality criteria listed in Paragraph "Risk of bias assessment" of the Materials and Methods section, each study was classified into one of the following groups: “low risk of bias”, when all quality criteria were considered to be “present”, “moderate risk of bias”, when one or more key domains were “unclear”, and “high risk of bias”, when one or more quality criteria were “absent”. Results of risk of bias assessment are described in Fig. 2. Overall, the analysis revealed good quality of the selected studies, with major concerns regarded Blinding of Participants and Personnel and blinding of outcome assessment, which were unclearly reported or missing in some trials.
ABXs versus CBXs: dimensional changes
Bone xenografts vs. spontaneous healing
Most reviewed clinical trials that compared spontaneously healed alveoli and the filling of post-extraction sockets with anorganic bone-based grafts reported significantly less horizontal and vertical bone resorption with the ARP procedure (Table 2) [23, 59, 61, 62, 64, 72, 73, 75, 84]. Conversely, other trials identified no significant differences among grafted and non-grafted sites [58, 69], while stating clinical relevance of ABX-based ARP in esthetically demanding cases [69] or suggesting no significant benefits of the treatment in post-extraction sites with good alveolar bone wall integrity and adequate buccal bone wall thickness [58].
Regarding collagen-preserving materials, a positive trend was recognized about the preservation of bone dimensions of post-extraction sites by clinical trials which compared spontaneously healed sockets with the grafting of CBXs associated with a collagen membrane [34, 79] or soft cortical lamina [80] (Table 3). Specifically, the ridge-preservation treatment showed to significantly reduce the resorption of horizontal ridge width and vertical ridge height at mid-buccal and mid-lingual aspects in comparison with extraction alone [79, 80]. Moreover, even when no significant differences between CBXs-treated and untreated groups were detected, less resorption of hard tissue ridge (both horizontal and vertical dimensions) was measured in grafted sites [34].
Modified bone xenografts
Association of ABXs with additional conditions/treatments has been investigated in the effort to enhance the preservation of ridge dimensions in post-extraction sockets. For instance, a composite xenograft consisting of 90% anorganic bovine bone embedded in a 10% biodegradable collagen matrix of porcine origin has been widely investigated in comparison or in substitution of ABXs alone to minimize bone dimensional changes after tooth extraction [23, 58, 59, 61, 61, 63,64,65,66, 68, 71,72,73,74, 78]. In this composite, collagen facilitates graft handling and ameliorates graft adaptation and stabilization to the defect, with pre-clinical data establishing that collagenated anorganic bone serves as a scaffold for bone formation rather than promoting tissue regeneration [85]. However, existing clinical evidence revealed non-inferiority of ABXs compared to collagenated ABXs, except for significantly less reduction in ridge width at the 5-mm level reported by some trials [58, 63, 78, 86]. As demonstrated for porcine collagen addition, the coating of ABXs with synthetic oligopeptide from the collagen-binding domain of osteopontin also showed not to ameliorate ARP outcomes [56] (Table 2).
On the other hand, trials investigating CBXs for ARP procedures never considered to implement them with collagen-derived additives, probably due to the fact that these grafting materials contain a more preserved collagenic component.
Bone xenografts associated with barrier membranes
As an aid for alveolar ridge preservation, the use of barrier membranes in combination with bone grafts during ARP procedures was demonstrated to prevent epithelial downgrowth into the alveolar socket, whereas the graft material avoids membrane collapse and promotes bone formation through osteoconduction and/or osteoinduction processes [87]. Resorbable collagen matrices are the membranes of choice to cover ABXs-grafted sockets, with conflicting outcomes reported by clinical trials which demonstrated both (a) the effective reduction of horizontal ridge changes, with significant preservation of vertical height at mid crest [73] and (b) failure to limit the loss of horizontal/vertical ridge dimensions in comparison with the application of collagen membrane without ABXs [74]. Moreover, the addition of an enamel matrix derivative (EMD) to collagenated ABXs covered with a collagen membrane did not showed significant improvement of ridge preservation compared to the EMD-lacking group, although horizontal width changes were significantly greater in the non-grafted sockets compared with both types of grafted sites [23].
Concerning CBXs, all selected trials evaluating ridge dimension outcomes described the graft covering with collagen membranes [31, 34, 36, 79, 81, 83, 88] or with a cortical bone-derived lamina [80], not even considering the CBXs alone (Table 3). Interestingly, Barone and colleagues [81] investigated the clinical effects on coupling CBXs grafts covered by a collagen matrix with a full flap procedure to cover the membrane, or a flapless procedure leaving the membrane exposed. More successful preservation of horizontal ridge dimension was assured by the flapless procedure, with additional advantages given by the positive increase in keratinized gingiva.
Besides collagen membranes, both natural and synthetic materials were tested to cover the ABX. For instance, autogenous soft tissue punches from the palate were used to cover ABXs or collagenated ABXs particles in post-extractive sockets, assuring for significantly less resorption of vertical and horizontal ridges with respect to spontaneous healing, but not to the use of collagen matrix (Table 2) [59, 69]. Interestingly, the application of a synthetic polyethylene glycol (PEG) barrier both alone or in association to ABX was reported to be effective in preventing vertical bone loss at the buccal/lingual aspects and even promoting vertical bone gain at the central aspect (Table 2) [76].
Bone xenografts vs. allogenic or autologous grafts
Considering clinical outcomes achieved by ABXs versus allograft materials, conflicting results are currently found in the literature. On the one hand, collagenated ABXs were reported to preserve the horizontal alveolar ridge dimension significantly better than allogenic materials, providing more bony width at the grafted site [65]. Conversely, no statistically significant differences in horizontal and vertical bone changes were found by a more recent RCT comparing collagenated ABXs with allogenic material [71]. Additionally, some clinical evidence even attested the superiority of bone allografts over ABXs to prevent horizontal [76] or vertical [53] bone loss after tooth extraction.
Regarding the comparison with autologous grafts, autogenous demineralized dentin matrix was demonstrated to be as effective as ABXs for augmenting vertical bone dimensions after tooth extraction [67].
Considering CBXs, no clinical comparisons with allogenic/autologous graft materials were investigated so far, this representing a significant gap of knowledge about the efficacy of these bone xenografts for ARP procedures.
Bone xenografts vs. synthetic grafts
Clinical trials investigating the effects of ABXs versus synthetic materials on ridge preservation described equivalent clinical efficacy in controlling horizontal/vertical resorption when comparing the bone xenograft and nanocrystalline hydroxyapatite (HA) [57] or HA-collagen composites [66, 77]. On the contrary, better outcomes were exhibited by the synthetic counterpart when anorganic bone was compared with biphasic calcium sulphate/hydroxyapatite (BCS/HA) [75], HA treated with recombinant human bone morphogenetic protein-2 (rhBMP-2/HA) [70] and a biphasic ceramic bone substitute made of HA and β-tricalcium phosphate (β-TCP) (i.e., Straumann Bone Ceramics-SBC) [54]. Unlike aforementioned studies, clinical evidence was reported about the significant superiority of collagenated ABXs over β-TCP particles with polylactide coating in limiting ridge height and width changes after tooth extraction (Table 2) [59].
As previously described for the comparison with allogenic/autologous grafts, no clinical trials evaluated the dimensional outcomes of CBXs vs. synthetic material grafting during ARP procedures.
Comparison among different heterologous graft materials
Some clinical trials compared anorganic bone from different species, demonstrating that alternative sources of ABXs can be used with comparable outcomes. Overall, anorganic bovine and porcine bone grafts were found to be equally effective in reducing horizontal ridge changes in post-extraction sockets, with anorganic porcine material showing significantly lower efficacy in vertical ridge preservation [68] and more frequent failure of implant stability [28]. Following this trend, two deproteinized bovine bone minerals were demonstrated to be comparable in preserving horizontal ridge width, affording a more favorable implant position [60].
Recently, CBXs and ABXs in combination with a collagen membrane were compared for alveolar ridge preservation, along with natural healing of the post-extraction sockets [31, 36] (Table 3). A significantly lower reduction of buccal-lingual width and vertical bone dimensions was registered at the grafted sockets compared to non-grafted sites, with ABXs being significantly more effective than CBXs in preserving vertical bone level at the lingual–palatal aspect [31]. On the contrary, the trial by Marconcini and collaborators [36] detected no significant differences between the two grafting materials regarding peri-implant crestal bone loss, which was significantly greater in the non-grafted sockets at each follow-up period (1, 2, and 4 years). Ridge preservation was also significantly more effective than spontaneous healing in peri-implant soft tissue recovery, with ABXs showing better aesthetic outcomes than CBXs [36].
Finally, CBXs were also shown to be significantly more effective than collagen sponges to preserve alveolar ridge width measured soon after tooth extraction and 2–3 months post-grafting with the two biomaterials. Specifically, changes in alveolar width were not significant in premolar sites, but significant differences were observed between the two graft procedures at molar sites [83].
ABXs versus CBXs: histomorphometric evaluation
Overall, histological investigations of extraction sockets grafted with ABXs or CBXs showed no signs of adverse reaction or severe inflammatory response towards the heterologous bone substitute suggesting that anorganic bone [55] and CBXs of both porcine [31, 79, 82], and equine [38] origin are safe and biocompatible ARP biomaterials.
Bone xenografts vs. spontaneous healing
Compared with alveolar sockets left to heal spontaneously, ABXs [26, 73] and CBXs [31, 79] exhibited comparable [26, 31, 73] or even improved [79] histomorphometric outcomes at the grafted site regarding new bone formation or soft tissue amount (Tables 4 and 5). Conversely, Heberer and collaborators [55] provided evidence of a significantly lower rate of new bone formation in the anorganic bone-filled sockets in comparison with non-grafted sites. Bone apposition was observed in the proximity of ABXs particles, but resorptive processes were absent. Additionally, a significantly higher amount of NFB was detected in the apical rather than the coronal region of the extraction site, regardless of the grafting procedure, suggesting that bone formation could be initiated from the apical/lateral region of the alveolar socket and was not enhanced from the coronal direction [55, 89]. These results are in line with evidence previously reported by Carmagnola and colleagues [52], who demonstrated that anorganic bone grafting led to less new bone formation and more residual connective tissue compared with cases where graft materials were not used, although no statistical analysis was performed to prove significant differences.
Modified bone xenografts
Concordant with clinical data regarding bone dimensional changes in post-extraction sockets, histomorphometric evaluations demonstrated that collagenated ABXs did not enhance newly formed bone (NFB) in comparison with ABXs [63] (Table 4). In general, ABXs particles were found to be surrounded more by new vital bone rather than connective tissue, but no signs of particle resorption were observed. These results support animal studies reporting that ABXs elimination might be very slow or even remain unaltered in the osseous tissue [85]. Unlike addition of the collagen carrier, coating the ABXs with collagen-binding peptide significantly affected the percentage of NFB in the extraction socket compared to uncoated ABXs [56] (Table 4). Histological and histomorphometric investigations highlighted new bone formation both at the periphery and in the central/coronal regions with direct bone apposition over the graft surface, indicating high osteoconductive and osteoinductive effects, with improved biocompatibility of the peptide-modified ABXs proven by the significantly higher bone-to-graft contact in comparison with unmodified ABXs [56].
Bone xenografts associated with barrier membranes
In ARP procedures, biological/synthetic resorbable membranes are used to accelerate bone formation by preventing the ingrowth of connective or epithelial tissue [90]. Histomorphometric analysis of post-extraction sockets grafted with collagenated ABXs with or without the addition of collagen membrane did not show significantly increased formation of new bone or better biomaterial resorption when the graft particles were covered with the barrier matrix [73] (Table 4). However, in the presence of the collagen membrane, the mean percentages of NFB and residual graft material were higher and lower, respectively [68]. On the other hand, improved histomorphometric outcomes were observed following the application of a PEG membrane to cover ungrafted sockets, with the formation of a significantly higher amount of new bone in comparison with anorganic bone grafts associated with the same device [76] (Table 4).
Similar to clinical evidence collected about ABXs plus collagen matrix, a clinical trial evaluating CBXs covered with collagen membrane and associated to flapless versus flap elevation techniques highlighted no significant histological or histomorphometrical differences between the two procedures [82] (Table 5).
Bone xenografts vs. allogenic or autologous grafts
Most clinical trials comparing ABXs (± heterologous collagen) and bone allografts highlighted that both materials performed well histologically and resulted in comparable amounts of new bone formation in the grafted sockets [65, 71, 76]. Significantly higher amounts of collagenated ABXs rather than allograft remnants were observed in the grafted sites, confirming a previous hypothesis on the poor resorption rate of the xenograft material. Little or no signs of osteoclastic resorption and graft remodeling were observed, whereas bone allografts histologically exhibited a more active state of turnover and replacement within the grafted socket [65]. Unlike the above cited studies, only one trial reported clear superiority of bone allograft mixed with an experimental putty carrier compared to ABXs in producing significantly more vital bone filling the extraction socket [53] (Table 4).
Finally, statistically significant differences in histomorphometric outcomes were not observed when ABXs were compared to autogenous demineralized dentin matrix for ridge preservation. The graft biomaterials displayed adequate tissue integrity, with both substitutes surrounded by and in direct contact with NFB to confirm their osteoconductive properties [62].
Bone xenografts vs. synthetic grafts
Similar to clinical measurements of ridge dimensions, histomorphometric studies showed comparable [54, 57] or inferior [70] performance of ABXs versus synthetic material grafting in the post-extraction socket. In particular, equivalent histological characteristics of biopsies ABXs from - and SBC-treated sockets were found, with NFB mainly localized in the apical region and in direct contact with the graft particles [54]. Similarly, no statistical differences were reported by histomorphometric analyses comparing ABXs and nanocrystalline hydroxyapatite (NCHA) socket grafting [57]. On the other hand, rhBMP-2/HA was found to achieve significantly greater new bone formation than ABXs in treated sockets, whereas comparable outcomes for the two biomaterials were registered for soft tissue and residual graft particles (Table 4). As reported by other histomorphometric studies [54, 55], a stronger tendency to produce new bone in the apical region compared with the coronal portion was evidenced in both treatment conditions [77]. Finally, when collagenated ABXs were compared with HA-collagen composites, a significantly lower percentage of NFB [66] and significantly higher amounts of residual biomaterial particles [77] were histomorphometrically detected within the treated alveolar sockets.
Comparison among different heterologous graft materials
Histologically, similar efficacies of anorganic bone from different species were demonstrated. No statistically significant differences were detected among extraction sites treated with bovine and porcine anorganic bone [28] or different deproteinized bovine bone xenografts [60] with regard to the mean percentage of vital bone formation, residual graft material, and connective tissue (Table 4). Both bovine and porcine ABXs showed high porosity that allowed for new bone formation and ingrowth [28].
Three clinical trials reported comparisons between CBXs and ABXs for ARP with conflicting results. On the one hand, no significant differences were detected in terms of NFB, connective tissue prevalence, and residual graft particles in the alveolar socket. Nevertheless, a higher percentage of NFB and lower amount of residual bone substitute were found in the CBXs-treated group, likely indicating different resorption rates for the two biomaterials and possibly a more promising healing pattern for CBXs compared to ABXs [31]. More intriguing histological evidence was recently reported by Di Stefano and colleagues [38]. Besides demonstrating the presence of native type I bone collagen in CBXs, but not in ABXs, this study detected a significantly greater quantity of NFB and fewer residual biomaterial particles after socket grafting with collagen-preserving material rather than anorganic heterologous bone. These findings are the first clinical demonstration that the manufacturing process can greatly affect xenograft behavior, underscoring the importance of preserving bone collagen in its native form to enhance the biomaterial’s regenerative effect (Table 5).
ABXs versus CBXs: secondary outcome variables
High heterogeneity was found regarding secondary outcome variables reported by the selected clinical trials. A frequently evaluated variable was site elegibility for implant placement after ARP and eventual need for bone augmentation regardless the grafting procedure. Concerning ABXs, several trials reported that both grafted and ungrafted sites healed uneventfully, showing adequate alveolar ridge preservation to receive an implant without any additional grafting or bone augmentation procedure [26, 52, 53, 56, 60, 62, 64, 67, 71, 78]. Conversely, other authors highlighted the need to perform additional augmentation along with dental implant placement due to insufficient ridge volume [28, 63, 65, 69, 74] or to the presence of fenestration or small dehiscence at the grafted site [57, 58, 69]. Remarkably, Cha and collaborators [72] provided evidence supporting more frequent bone augmentation for ungrafted rather than grafted sockets. Similar trends were observed for CBXs, with some trials describing implant placement without the need for bone augmentation in both untreated and treated sockets [79, 82] and other studies reporting better volume conditions for implant loading in grafted sites [34, 36].
Postoperative histological analyses of the healed sockets mostly demonstrated newly formed keratinized mucosa and no signs of inflammation for both ABXs- [26, 28, 54, 55, 70, 77] and CBXs- [38, 79, 82] grafted sites, confirming the biocompatibility of both materials. Also, supporting graft bio-safety, no post-operative complications (i.e., rejection or wound infections around the grafting region) were generally recorded at any surgical site by both ABXs [28, 55, 59,60,61,62, 64, 66, 67, 71, 74, 77, 78] and CBXs [36, 38, 79,80,81] trials.
Among dimensional outcomes, buccal plate thickness was poorly considered by selected clinical studies, although it was proven to affect the amount of horizontal and vertical crest resorption in human sockets [61]. Overall, ABXs trials detected non-significant changes in buccal plate thickness among naturally healed sites and grafted sockets [28, 61, 74, 75], finding a negative correlation between the initial thickness of the buccal bone and ridge width reduction in non-grafted but not in treated alveoli [61, 66]. Different results were reported for CBXs, which was found to lead to buccal cortical plate loss in the long term (10-year follow-up) [83].
Only one trial performed bone volume measures on the post-extraction sockets, demonstrating significantly lower bone resorption in ABXs-treated versus naturally healed sites [62].
Finally, very few studies reported on patient-related outcomes following socket preservation. The severity of pain, discomfort and swelling was assessed in ABXs trials by using the visual analog scale (VAS) score [75, 77] or self-report questionnaires [23, 77], revealing low to moderate pain level following surgery [75] and no significant score differences between grafted and ungrafted patients [23].
Discussion
The effects of ridge preservation with the use of different biomaterials have been thoroughly investigated, and filling of post-extraction sites with bone xenografts was clinically demonstrated to significantly reduce ridge changes in comparison with spontaneously healed sockets [91]. Ridge preservation treatment also reduced the need for further bone augmentation at the time of implant placement, ameliorating the aesthetic outcome of implant rehabilitation [34, 81]. Xenogenic material currently used for ridge preservation is predominantly anorganic bovine/porcine bone made from the inorganic portion of animal bone tissue. The manufacturing process to produce ABXs is based on high-temperature treatment (> 300 °C), which removes cells and xenogenic antigens to avoid potential immunologic reactions. This method also eliminates all organic components and proteins, while HA with enhanced crystallinity is maintained as the main graft constituent [60, 92, 93]. Deproteinized xenografts were demonstrated to have good physico-chemical and osteoconductive properties in ridge preservation strategies. Nevertheless, suboptimal biointegration and bioabsorption characteristics of heat-treated materials suggest that the processing protocol for xenograft bone substitutes may greatly affect the biomaterial behavior in situ regarding the regenerative potential and quality of NFB [93]. To overcome these limitations, bone xenografts fabricated with less aggressive treatment to remove xenogenic antigens were proposed to preserve the collagen component of the animal bone, ultimately improve the bioactive properties of the final product [38, 94]. The preservation of type I collagen in bone substitutes can improve socket healing in ARP procedures by a series of processes, including (1) enhanced stimulation by endogenous growth factors; (2) longer duration of regenerative stimuli; (3) physiological modulation of bone metabolism and remodeling; and (4) increased osteoblast adhesion, proliferation, and differentiation [95,96,97,98]. Indeed, this might have contributed to the successful clinical outcomes with CBXs use reported for different oral surgery procedures including sinus lift bone grafting [42, 99,100,101,102], ridge augmentation [103,104,105], and peri-implant-guided bone regeneration [106,107,108]. However, direct clinical comparisons between anorganic and CBXs for socket preservation were only reported in three clinical trials [31, 38, 82], so the superiority of one biomaterial over another has not been established yet. In this work, clinical research testing ABXs or CBXs for ridge preservation was systematically reviewed to perform a preliminary comparison in terms of the biomaterials’ dimensional and histomorphometric outcomes. Table 6 summarizes the collected results, presenting minimum and maximum average values and standard deviations recorded for horizontal/vertical ridge resorption, as well as the percentage of NFB, connective tissue, and residual graft particles at the grafted sites.
Clinical outcomes for alveolar ridge dimensional changes showed successful socket preservation when using both ABXs and CBXs in comparison with spontaneous healing, with ABXs yielding better results than untreated control and largely similar to bone allografts and synthetic materials. Horizontal ridge resorption was calculated to range from 0.065 to 2.8 mm for ABXs and from 0.93 to 3.5 mm for CBXs, with standard deviations ranging from 0.14 to 3.34 mm and from 0.55 to 1.3 mm, respectively. Thus, lower minimum and maximum values of horizontal bone loss were observed for ABXs, but the standard deviations showed a broader value range compared with CBXs (Table 6).
Vertical ridge reduction was found to be between 0.1 and 2.92 mm for ABXs and between 0.2 and 1.1 mm for CBXs, with standard deviations ranging from 0.2 to 3.6 mm and from 0.5 to 1.54 mm, respectively. In this case, ABXs showed a lower minimum change but higher maximum alteration of vertical ridge dimensions with respect to CBXs, but the value range for standard deviation was still broader for the heat-treated bone substitute (Table 6).
Histomorphometric evaluations after ARP of the post-extraction sockets produced less obvious results for the superiority of both anorganic bone substitutes and CBXs over spontaneous healing or other treatments, since significant differences in terms of new bone formation were less frequently reported by clinicians. However, high biocompatibility and capacity to promote bone regeneration were observed for both xenografts. Remarkably, Di Stefano and co-workers [38] provided the first evidence of significantly better histological performance for CBXs rather than ABXs, supporting the hypothesis that maintaining type I collagen in its native conformation may improve the biological effects of the graft and promote faster remodeling of the heterologous material [109].
In summary, despite the much larger number of clinical trials for ABXs rather than CBXs, the two types of xenografts seem to provide overlapping dimensional/histological outcomes with large measurement dispersion, underscoring the need of comparative clinical studies that may demonstrate the superiority of one material over the other at a statistically significant level.
Regarding histomorphometrical measurements, NFB was between 5.3 and 37.68% for ABXs and between 22.5 and 45.12% for CBXs, with standard deviations ranging from 4.32 to 26.51% and from 3.9 to 20.6%, respectively. Based on that, higher amount of NFB and lower variability were registered for CBXs versus ABXs. This trend was also confirmed for data concerning residual graft particles, which overall exhibited better results for CBXs (lower range values, 10.92–29.2%) compared to ABXs (higher range values, 8.89–52.03%), with less variability for the collagen-preserving biomaterials (10.91–29.2% for CBXs and 8.89–52.03% for ABXs) (Table 6). As shown in Table 6, the amount of NFB was on average higher for CBXs rather than ABXs, with the minimum value being much greater (> 17.2%) for CBXs with respect to ABXs. On the other hand, the average amount of residual graft particles was lower for CBXs, which had a clearly inferior maximum value and standard deviation range with respect to ABXs. Regarding connective tissue evaluation, lower measurement dispersion was observed for CBXs in comparison with ABXs. Although these trends need to be verified in controlled clinical studies, they are in line with evidence collected by recent trials that compared ABXs and CBXs and demonstrated better histomorphometric outcomes for CBXs in both ARP [38] and sinus augmentation [42] procedures.
Concerning dimensional outcomes, some possible trends might be hypothesized based on collected data regarding horizontal ridge resorption, which seems to be more limited by anorganic bone grafting, albeit with a larger measurement dispersion (maximum standard deviation for ABXs is about three times higher than for CBXs). Conversely, vertical ridge preservation seems to be well achieved by CBXs, with maximum resorption measures more than halved compared to ABXs (Table 6).
One topic meriting discussion is data variability, which appears high for all the endpoints of interest, both among different studies and within each study included in this review. Variability among studies may be explained by the different surgical techniques and various methods to measure the same endpoints. Endpoints describing dimensions varied: vertical or horizontal width, buccal versus lingual plates, measurements performed at the crestal level or at different vertical levels apically from the crest. In addition, no standard methods for histomorphometric measurements were considered, which also contributed to histological outcome variability.
Data variability was also present at the single-study level, highlighting how bone regeneration and dimensional resorption are multifactorial processes. That is, histomorphometric and dimensional outcomes are expected to be influenced by a number of variables that might act as confounders when investigating if the two types of xenografts have any differential effects when used for ARP.
Among such confounders, the time from surgery when dimensional and histomorphometric assessment are performed might play a pivotal role. In fact, differences in the bone-formation rate might be more evident and statistically significant if clinical evaluations are performed at earlier rather than later timepoints. This hypothesis is supported by the retrospective clinical study by Di Stefano and collaborators [100], demonstrating that when CBX was used for sinus augmentation, no significant differences in NFB and residual graft material were detected between samples evaluated at different times from grafting (i.e., 3–5 months, 6–8 months, 9–12 months). These data suggest that new bone formation with CBXs occurred soon after the grafting surgery. Remarkably, early bone deposition is consistent with the significant difference detected in the amount of NFB provided by CBXs rather than ABXs in studies of ARP and sinus augmentation [38, 42]. In this regard, the clinical trials included in this systematic review also showed certain variability for the time of analysis, suggesting that the influence of this confounding factor on detecting significant differences among experimental groups remains to be clarified with appropriate studies.
Concerning the amounts of NFB that might be achieved with the two types of xenografts, one might speculate that there is an upper limit. Indeed, recent evidence showed that post-natal intramembranous bone regeneration mirrors the intramembranous ossification that occurs during embryonic bone development, with several molecular and cellular actors involved in both scenarios [110]. Because of this, the upper limit to NFB might be equal to the physiological amount of bone that patient has at the position of the arch where regeneration will occur. This might be a reasonable assumption, at least when osteoconductive grafts are used and one does not use recombinant growth factors or other drugs capable of altering bone metabolism in a relevant way. If this is the case, another factor affecting the dimensional and histomorphometric outcomes of ARP might be the position within the two arches. Indeed, a recent retrospective assessment of 6060 bone density measurements performed in 2048 patients across the two arches showed that bone density (i.e., the amount of bone by volume unit) at each position within the upper or the lower jaw exhibits significant interindividual variation, and the same patient may display significantly different densities at various positions [111]. Thus, the amount of bone growth expected should vary according to the location of the grafted site.
Finally, within the limits of the present systematic review, it is worth pointing out that the addition of a collagen carrier to ABXs did not improve dimensional and histomorphometric results compared to ABXs alone, remaining merely a technical option that allows easier biomaterial handling and application.
Thus, although the trends described in the present study suggest that ABXs and CBXs may provide different dimensional and histomorphometric outcomes when used for ARP, whether they actually do remain an open question. Answering it will require appropriate RCTs with adequate sample sizes and an experimental design carefully conceived to eliminate or at least limit the effects of several confounding factors. Possibly, studies should focus on more homogeneous patient subgroups as far as bone density is concerned (as opposed to the general population who might be subjected to ARP). Researchers should also compare xenografts grafted in symmetric or adjacent positions within the same jaw; biopsies for histomorphometric assessment should be taken soon after procedures to detect if bone formation kinetics vary between the two types of xenografts. Furthermore, the effect of carriers should be carefully investigated. While collagen added to ABXs does not seem to provide any advantage, except for better handling, it (and other carriers) might still act as a confounder, so in our opinion, studies should first compare xenografts (i.e., bone granules) with no carrier added. Finally, should any difference in histomorphometric outcomes ever be observed between ABXs and CBXs when used in ARP, future studies should investigate if this correlates with dimensional preservation of the ridge, as this point still seems unclear. Well-designed studies comparing ABXs and CBXs for ARP procedures may also allow to minimize data variability and study heterogeneity; those of data collected and discussed in the present review were indeed too high to perform any meaningful statistical analysis. This is an important limitation of the present work.
Overall conclusions and future perspectives
The comparison between anorganic bone substitutes and CBXs for ARP procedures may provide useful information to help guide the selection of socket grafting material, but clinical data remain scant and inconclusive. Reviewed trials on ABXs and CBXs showed considerable data variation for both dimensional and histomorphometric measures of ridge preservation, which may be explained by either the intrinsic biological variability in human healing or the presence of extrinsic factors that influence the regenerative process. Overall, this systematic review supports the clinical efficacy of ARP procedures based on ABXs and CBXs, but we were unable to reach conclusions about the superiority of one xenograft over the other based on currently available data about ridge dimensional changes and histomorphometric measures. Appropriately designed clinical studies need to be carried out to directly compare anorganic bone substitutes and CBXs to assess which biomaterial provides better ridge preservation. Additionally, there is a lack of specific studies into the possible correlation between dimensional ridge preservation and histological outcomes in terms of new bone formation; such work would provide novel insights about the clinical efficacy of ARP procedures. Better characterization of these bone xenografts will be useful to guide clinical decision-making for post-extraction socket treatment and provide new perspectives on the use of different xenogenic bone substitutes.
Availability of data and materials
Not applicable.
Abbreviations
- ARP:
-
Alveolar ridge preservation
- ABXs:
-
Anorganic bone xenografts
- CBXs:
-
Collagen-preserving bone xenografts
- CPB:
-
Cancellous porcine bone
- EDEB:
-
Enzyme-deantigenic equine bone
- ABX:
-
Anorganic bone xenograft
- PICOT:
-
Patient, intervention, comparison, outcome, time
- RCTs:
-
Randomized controlled trials
- NFB:
-
Newly formed bone
- CaS:
-
Calcium sulphate
- DFDBA:
-
Demineralized freeze-dried cortical bone allograft
- d-PTFE:
-
Dense polytetrafluoroethylene
- EMD:
-
Enamel matrix derivative
- HA:
-
Hydroxyapatite
- ITT:
-
Intention-to-treat
- Mg/HA:
-
Magnesium enriched-hydroxyapatite
- NCHA:
-
Nanocrystalline hydroxyapatite
- PEG:
-
Polyethylene glycol
- PP:
-
Per protocol
- SBC:
-
Straumann bone ceramics®
- rhBMP-2/hydroxyapatite:
-
Morphogenetic protein-2/HA
- BCS/HA:
-
Biphasic calcium sulphate/hydroxyapatite
- β-TCP:
-
β-Tricalcium phosphate
- NFB:
-
Newly formed bone
References
Zhao R, Yang R, Cooper PR, Khurshid Z, Shavandi A, Ratnayake J (2021) Bone grafts and substitutes in dentistry: a review of current trends and developments. Molecules 26:3007. https://doi.org/10.3390/molecules26103007
Willenbacher M, Al-Nawas B, Berres M, Kämmerer PW, Schiegnitz E (2016) The effects of alveolar ridge preservation: a meta-analysis. Clin Implant Dent Relat Res 18:1248–1268. https://doi.org/10.1111/cid.12364
Araújo MG, Lindhe J (2005) Dimensional ridge alterations following tooth extraction. an experimental study in the dog. J Clin Periodontol 32:212–228. https://doi.org/10.1111/j.1600-051X.2005.00642.x
Scala A, Lang NP, Schweikert MT, de Oliveira JA, Rangel-Garcia I Jr, Botticelli D (2014) Sequential healing of open extraction sockets. an experimental study in monkeys. Clin Oral Implants Res 25:288–295. https://doi.org/10.1111/clr.12148
Chappuis V, Engel O, Reyes M, Shahim K, Nolte LP, Buser D (2013) Ridge alterations post-extraction in the esthetic zone: a 3D analysis with CBCT. J Dent Res 92:195S-201S. https://doi.org/10.1177/0022034513506713
Canellas JVDS, Medeiros PJD, Figueredo CMDS, Fischer RG, Ritto FG (2019) Which is the best choice after tooth extraction, immediate implant placement or delayed placement with alveolar ridge preservation? a systematic review and meta-analysis. J Craniomaxillofac Surg 47:1793–1802. https://doi.org/10.1016/j.jcms.2019.08.004
Cardaropoli G, Araújo M, Lindhe J (2003) Dynamics of bone tissue formation in tooth extraction sites. an experimental study in dogs. J Clin Periodontol 30:809–818. https://doi.org/10.1034/j.1600-051x.2003.00366.x
Balli G, Ioannou A, Powell CA, Angelov N, Romanos GE, Soldatos N (2018) Ridge preservation procedures after tooth extractions: a systematic review. Int J Dent 3:8546568. https://doi.org/10.1155/2018/8546568
Van der Weijden F, Dell’Acqua F, Slot DE (2009) Alveolar bone dimensional changes of post-extraction sockets in humans: a systematic review. J Clin Periodontol 36:1048–1058. https://doi.org/10.1111/j.1600-051X.2009.01482.x
Mardas N, Trullenque-Eriksson A, MacBeth N, Petrie A, Donos N (2015) Does ridge preservation following tooth extraction improve implant treatment outcomes: a systematic review: Group 4: Therapeutic concepts & methods. Clin Oral Implants Res 26:180–201. https://doi.org/10.1111/clr.12639
Lin HK, Pan YH, Salamanca E, Lin YT, Chang WJ (2019) Prevention of bone resorption by HA/β-TCP + collagen composite after tooth extraction: a case series. Int J Environ Res Public Health 16:4616. https://doi.org/10.3390/ijerph16234616
Schropp L, Kostopoulos L, Wenzel A (2003) Bone healing following immediate versus delayed placement of titanium implants into extraction sockets: a prospective clinical study. Int J Oral Maxillofac Implants 18:189–199
Iocca O, Farcomeni A, Pardiñas Lopez S, Talib HS (2017) Alveolar ridge preservation after tooth extraction: a Bayesian Network meta-analysis of grafting materials efficacy on prevention of bone height and width reduction. J Clin Periodontol 44:104–114. https://doi.org/10.1111/jcpe.12633
Horváth A, Mardas N, Mezzomo LA, Needleman IG, Donos N (2013) Alveolar ridge preservation. A systematic review Clin Oral Investig 17:341–363. https://doi.org/10.1007/s00784-012-0758-5
Garagiola U, Maiorana C, Ghiglione V, Marzo G, Santoro F, Szabò G (2007) Osseointegration and guided bone regeneration in Ectodermal Dysplasia patients. J Craniofac Surg 18:1296–1304. https://doi.org/10.1097/01.scs.0000246497.62065.5a
Kalsi AS, Kalsi JS, Bassi S (2019) Alveolar ridge preservation: why, when and how. Br Dent J 227:264–274. https://doi.org/10.1038/s41415-019-0647-2
Troiano G, Zhurakivska K, Lo Muzio L, Laino L, Cicciù M, Lo Russo L (2018) Combination of bone graft and resorbable membrane for alveolar ridge preservation: a systematic review, meta-analysis, and trial sequential analysis. J Periodontol 89:46–57. https://doi.org/10.1902/jop.2017.170241
Bassir SH, Alhareky M, Wangsrimongkol B, Jia Y, Karimbux N (2018) Systematic review and meta-analysis of hard tissue outcomes of alveolar ridge preservation. Int J Oral Maxillofac Implants 33:979–994. https://doi.org/10.11607/jomi.6399
Avila-Ortiz G, Chambrone L, Vignoletti F (2020) Effect of alveolar ridge preservation interventions following tooth extraction: a systematic review and meta-analysis. J Clin Periodontol 46:195–223. https://doi.org/10.1111/jcpe.13057.Erratum.In:JClinPeriodontol47:129
Apostolopoulos P, Darby I (2017) Retrospective success and survival rates of dental implants placed after a ridge preservation procedure. Clin Oral Implants Res 28:461–468. https://doi.org/10.1111/clr.12820
Siaili M, Chatzopoulou D, Gillam DG (2018) An overview of periodontal regenerative procedures for the general dental practitioner. Saudi Dent J 30:26–37. https://doi.org/10.1016/j.sdentj.2017.11.001
MacBeth N, Trullenque-Eriksson A, Donos N, Mardas N (2017) Hard and soft tissue changes following alveolar ridge preservation: a systematic review. Clin Oral Implants Res 28:982–1004. https://doi.org/10.1111/clr.12911
Lee JH, Jeong SN (2020) Effect of enamel matrix derivative on alveolar ridge preservation in the posterior maxilla: a randomized controlled clinical trial. Clin Implant Dent Relat Res 22:622–630. https://doi.org/10.1111/cid.12940
Araújo MG, Linder E, Lindhe J (2011) Bio-Oss collagen in the buccal gap at immediate implants: a 6-month study in the dog. Clin Oral Implants Res 22:1–8. https://doi.org/10.1111/j.1600-0501.2010.01920.x
Baldini N, De Sanctis M, Ferrari M (2011) Deproteinized bovine bone in periodontal and implant surgery. Dent Mater 27:61–70. https://doi.org/10.1016/j.dental.2010.10.017
Milani S, Dal Pozzo L, Rasperini G, Sforza C, Dellavia C (2016) Deproteinized bovine bone remodeling pattern in alveolar socket: a clinical immunohistological evaluation. Clin Oral Implants Res 27:295–302. https://doi.org/10.1111/clr.12535
Gross JS (1997) Bone grafting materials for dental applications: a practical guide. Compend Contin Educ Dent 18(1013–1018):1020–1022
Lai VJ, Michalek JE, Liu Q, Mealey BL (2020) Ridge preservation following tooth extraction using bovine xenograft compared with porcine xenograft: a randomized controlled clinical trial. J Periodontol 91:361–368. https://doi.org/10.1002/JPER.19-0211
Iezzi G, Degidi M, Scarano A, Petrone G, Piattelli A (2007) Anorganic bone matrix retrieved 14 years after a sinus augmentation procedure: a histologic and histomorphometric evaluation. J Periodontol 78:2057–2061. https://doi.org/10.1902/jop.2007.070062
Slotte C, Asklöw B, Lundgren D (2007) Surgical guided tissue regeneration treatment of advanced periodontal defects: a 5-year follow-up study. J Clin Periodontol 34:977–984. https://doi.org/10.1111/j.1600-051X.2007.01138.x
Barone A, Toti P, Quaranta A, Alfonsi F, Cucchi A, Negri B et al (2017) Clinical and histological changes after ridge preservation with two xenografts: preliminary results from a multicentre randomized controlled clinical trial. J Clin Periodontol 44:204–214. https://doi.org/10.1111/jcpe.12655
Barone A, Ricci M, Covani U, Nannmark U, Azarmehr I, Calvo-Guirado JL (2012) Maxillary sinus augmentation using prehydrated corticocancellous porcine bone: hystomorphometric evaluation after 6 months. Clin Implant Dent Relat Res 14:373–379. https://doi.org/10.1111/j.1708-8208.2010.00274.x
Szabó G, Huys L, Coulthard P, Maiorana C, Garagiola U, Barabás J, Németh Z, Hrabák K, Suba Z (2005) A prospective multicenter randomized clinical trial of autogenous bone versus beta-tricalcium phosphate graft alone for bilateral sinus elevation: histologic and histomorphometric evaluation. Int J Oral Maxillofac Implants 20:371–381
Barone A, Ricci M, Tonelli P, Santini S, Covani U (2013) Tissue changes of extraction sockets in humans: a comparison of spontaneous healing vs. ridge preservation with secondary soft tissue healing. Clin Oral Implants Res 24:1231–1237. https://doi.org/10.1111/j.1600-0501.2012.02535.x
Pagliani L, Andersson P, Lanza M, Nappo A, Verrocchi D, Volpe S et al (2012) A collagenated porcine bone substitute for augmentation at Neoss implant sites: a prospective 1-year multicenter case series study with histology. Clin Implant Dent Relat Res 14:746–758. https://doi.org/10.1111/j.1708-8208.2010.00314.x
Marconcini S, Giammarinaro E, Derchi G, Alfonsi F, Covani U, Barone A (2018) Clinical outcomes of implants placed in ridge-preserved versus nonpreserved sites: a 4-year randomized clinical trial. Clin Implant Dent Relat Res 20:906–914. https://doi.org/10.1111/cid.12682
Leonida A, Todeschini G, Lomartire G, Cinci L, Pieri L (2016) Socket preservation using enzyme-treated equine bone granules and an equine collagen matrix: a case report with histological and histomorphometrical assessment. J Contemp Dent Pract 17:890–896. https://doi.org/10.5005/jp-journals-10024-1949
Di Stefano DA, Zaniol T, Cinci L, Pieri L (2019) Chemical, clinical and histomorphometric comparison between equine bone manufactured through enzymatic antigen-elimination and bovine bone made non-antigenic using a high-temperature process in post-extractive socket grafting. a comparative retrospective clinical study. Dent J (Basel) 7(3):70. https://doi.org/10.3390/dj7030070
Di Stefano DA, Andreasi Bassi M, Cinci L, Pieri L, Ammirabile G (2012) Treatment of a bone defect consequent to the removal of a periapical cyst with equine bone and equine membranes: clinical and histological outcome. Minerva Stomatol 61:477–490
Artese L, Piattelli A, Di Stefano DA, Piccirilli M, Pagnutti S, D’Alimonte E, Perrotti V (2011) Sinus lift with autologous bone alone or in addition to equine bone: an immunohistochemical study in man. Implant Dent 20:383–388. https://doi.org/10.1097/ID.0b013e3182310b3d
Ludovichetti M, Di Stefano DA, Pagnutti S, Vaccari E, Ludovichetti FS, Celletti R (2011) Vertical ridge augmentation using a flexible heterologous cortical bone sheet: three-year follow-up. Int J Periodontics Restorative Dent 31:401–407
Di Stefano DA, Gastaldi G, Vinci R, Cinci L, Pieri L, Gherlone E (2015) Histomorphometric comparison of enzyme-deantigenic equine bone and anorganic bovine bone in sinus augmentation: a randomized clinical trial with 3-year follow-up. Int J Oral Maxillofac Implants 30:1161–1167. https://doi.org/10.11607/jomi.4057
Santini S, Barbera P, Modena M, Schiavon R, Bonato M (2011) Equine-derived bone substitutes in orthopedics and traumatology: authors’ experience. Minerva Chir 66:63–72
Piolanti N, Del Chiaro A, Matassi F, Nistri L, Graceffa A, Marcucci M (2020) Bone integration in acetabular revision hip arthroplasty using equine-derived bone grafts: a retrospective study. Eur J Orthop Surg Traumatol 30:575–581. https://doi.org/10.1007/s00590-019-02613-1
Sonmez MM, Armagan R, Ugurlar M, Eren T (2017) Allografts versus equine xenografts in calcaneal fracture repair. J Foot Ankle Surg 56:510–513. https://doi.org/10.1053/j.jfas.2017.01.015
Regazzoni C, Winterhalter KH, Rohrer L (2001) Type I collagen induces expression of bone morphogenetic protein receptor type II. Biochem Biophys Res Commun 283:316–322. https://doi.org/10.1006/bbrc.2001.4813
Perrotti V, Nicholls BM, Horton MA, Piattelli A (2009) Human osteoclast formation and activity on a xenogenous bone mineral. J Biomed Mater Res A 90:238–246. https://doi.org/10.1002/jbm.a.32079
Moher D, Liberati A, Tetzlaff J, Altman DG; PRISMA Group (2009) Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med 6:e1000097. https://doi.org/10.1371/journal.pmed.1000097
Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, Shamseer L, Tetzlaff JM, Akl EA, Brennan SE, Chou R, Glanville J, Grimshaw JM, Hróbjartsson A, Lalu MM, Li T, Loder EW, Mayo-Wilson E, McDonald S, McGuinness LA, Stewart LA, Thomas J, Tricco AC, Welch VA, Whiting P, Moher D (2021) The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 372:n71
Stone PW (2002) Popping the (PICO) question in research and evidence-based practice. Appl Nurs Res 15:197–198. https://doi.org/10.1053/apnr.2002.34181
Higgins JPT, Green S (eds) (2011) Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0. London: The Cochrane Collaboration, available at www.cochrane-handbook.org
Carmagnola D, Adriaens P, Berglundh T (2003) Healing of human extraction sockets filled with Bio-Oss. Clin Oral Implants Res 4:137–143. https://doi.org/10.1034/j.1600-0501.2003.140201.x
Vance GS, Greenwell H, Miller RL, Hill M, Johnston H, Scheetz JP (2004) Comparison of an allograft in an experimental putty carrier and a bovine-derived xenograft used in ridge preservation: a clinical and histologic study in humans. Int J Oral Maxillofac Implants 19:491–497
Mardas N, Chadha V, Donos N (2010) Alveolar ridge preservation with guided bone regeneration and a synthetic bone substitute or a bovine-derived xenograft: a randomized, controlled clinical trial. Clin Oral Implants Res 21:688–698. https://doi.org/10.1111/j.1600-0501.2010.01918.x
Heberer S, Al-Chawaf B, Jablonski C, Nelson JJ, Lage H, Nelson K (2011) Healing of ungrafted and grafted extraction sockets after 12 weeks: a prospective clinical study. Int J Oral Maxillofac Implants 26:385–392
Nam HW, Park JB, Lee JY, Rhee SH, Lee SC, Koo KT et al (2011) Enhanced ridge preservation by bone mineral bound with collagen-binding synthetic oligopeptide: a clinical and histologic study in humans. J Periodontol 82:471–480. https://doi.org/10.1902/jop.2010.100193
Gholami GA, Najafi B, Mashhadiabbas F, Goetz W, Najafi S (2012) Clinical, histologic and histomorphometric evaluation of socket preservation using a synthetic nanocrystalline hydroxyapatite in comparison with a bovine xenograft: a randomized clinical trial. Clin Oral Implants Res 23:1198–1204. https://doi.org/10.1111/j.1600-0501.2011.02288.x
Cook DC, Mealey BL (2013) Histologic comparison of healing following tooth extraction with ridge preservation using two different xenograft protocols. J Periodontol 84:585–594. https://doi.org/10.1902/jop.2012.120219
Jung RE, Philipp A, Annen BM, Signorelli L, Thoma DS, Hämmerle CH (2013) Radiographic evaluation of different techniques for ridge preservation after tooth extraction: a randomized controlled clinical trial. J Clin Periodontol 40:90–98. https://doi.org/10.1111/jcpe.12027
Calasans-Maia M, Resende R, Fernandes G, Calasans-Maia J, Alves AT, Granjeiro JM (2014) A randomized controlled clinical trial to evaluate a new xenograft for alveolar socket preservation. Clin Oral Implants Res 25:1125–1130. https://doi.org/10.1111/clr.12237
Cardaropoli D, Tamagnone L, Roffredo A, Gaveglio L (2014) Relationship between the buccal bone plate thickness and the healing of postextraction sockets with/without ridge preservation. Int J Periodontics Restorative Dent 34:211–217. https://doi.org/10.11607/prd.1885
Pang C, Ding Y, Zhou H, Qin R, Hou R, Zhang G, Hu K (2014) Alveolar ridge preservation with deproteinized bovine bone graft and collagen membrane and delayed implants. J Craniofac Surg 25:1698–1702. https://doi.org/10.1097/SCS.0000000000000887
Scheyer ET, Heard R, Janakievski J, Mandelaris G, Nevins ML, Pickering SR et al (2016) A randomized, controlled, multicentre clinical trial of post-extraction alveolar ridge preservation. J Clin Periodontol 43:1188–1199. https://doi.org/10.1111/jcpe.12623
Iorio-Siciliano V, Blasi A, Nicolò M, Iorio-Siciliano A, Riccitiello F, Ramaglia L (2017) Clinical outcomes of socket preservation using bovine-derived xenograft collagen and collagen membrane post-tooth extraction: a 6-month randomized controlled clinical trial. Int J Periodontics Restorative Dent 37:e290–e296. https://doi.org/10.11607/prd.2474
Lim HC, Jung UW, You H, Lee JS (2017) Randomized clinical trial of ridge preservation using porcine bone/cross-linked collagen vs. bovine bone/non-cross-linked collagen: cone beam computed tomographic analysis. Clin Oral Implants Res 28:1492–1500. https://doi.org/10.1111/clr.13017
Nart J, Barallat L, Jimenez D, Mestres J, Gómez A, Carrasco MA, Violant D, Ruíz-Magaz V (2017) Radiographic and histological evaluation of deproteinized bovine bone mineral vs. deproteinized bovine bone mineral with 10% collagen in ridge preservation. a randomized controlled clinical trial. Clin Oral Implants Res 28:840–848. https://doi.org/10.1111/clr.12889
Pang KM, Um IW, Kim YK, Woo JM, Kim SM, Lee JH (2017) Autogenous demineralized dentin matrix from extracted tooth for the augmentation of alveolar bone defect: a prospective randomized clinical trial in comparison with anorganic bovine bone. Clin Oral Implants Res 28:809–815. https://doi.org/10.1111/clr.12885
Serrano Méndez CA, Lang NP, Caneva M, Ramírez Lemus G, Mora Solano G, Botticelli D (2017) Comparison of allografts and xenografts used for alveolar ridge preservation. a clinical and histomorphometric RCT in humans. Clin Implant Dent Relat Res 19:608–615. https://doi.org/10.1111/cid.12490
Fischer KR, Mühlemann S, Jung RE, Friedmann A, Fickl S (2018) Dimensional evaluation of different ridge preservation techniques with a bovine xenograft: a randomized controlled clinical trial. Int J Periodontics Restorative Dent 38:549–556. https://doi.org/10.11607/prd.3636
Shim JY, Lee Y, Lim JH, Jin MU, Lee JM, Suh JY, Kim YG (2018) Comparative Evaluation of recombinant human bone morphogenetic protein-2/hydroxyapatite and bovine bone for new bone formation in alveolar ridge preservation. Implant Dent 27:623–629. https://doi.org/10.1097/ID.0000000000000814
Tomasi C, Donati M, Cecchinato D, Szathvary I, Corrà E, Lindhe J (2018) Effect of socket grafting with deproteinized bone mineral: an RCT on dimensional alterations after 6 months. Clin Oral Implants Res 29:435–442. https://doi.org/10.1111/clr.13141
Cha JK, Song YW, Park SH, Jung RE, Jung UW, Thoma DS (2019) Alveolar ridge preservation in the posterior maxilla reduces vertical dimensional change: a randomized controlled clinical trial. Clin Oral Implants Res 30:515–523. https://doi.org/10.1111/clr.13436
Lim HC, Shin HS, Cho IW, Koo KT, Park JC (2019) Ridge preservation in molar extraction sites with an open-healing approach: a randomized controlled clinical trial. J Clin Periodontol 46:1144–1154. https://doi.org/10.1111/jcpe.13184
Llanos AH, Sapata VM, Jung RE, Hämmerle CH, Thoma DS, César Neto JB et al (2019) Comparison between two bone substitutes for alveolar ridge preservation after tooth extraction: cone-beam computed tomography results of a non-inferiority randomized controlled trial. J Clin Periodontol 46:373–381. https://doi.org/10.1111/jcpe.13079
Machtei EE, Mayer Y, Horwitz J, Zigdon-Giladi H (2019) Prospective randomized controlled clinical trial to compare hard tissue changes following socket preservation using alloplasts, xenografts vs no grafting: clinical and histological findings. Clin Implant Dent Relat Res 21:14–20. https://doi.org/10.1111/cid.12707
Santana R, Gyurko R, Kanasi E, Xu WP, Dibart S (2019) Synthetic polymeric barrier membrane associated with blood coagulum, human allograft, or bovine bone substitute for ridge preservation: a randomized, controlled, clinical and histological trial. Int J Oral Maxillofac Surg 48:675–683. https://doi.org/10.1016/j.ijom.2018.02.012
Taschieri S, Del Fabbro M, Panda S, Goker F, Babina KS, Tampieri A, Mortellaro C (2019) prospective clinical and histologic evaluation of alveolar socket healing following ridge preservation using a combination of hydroxyapatite and collagen biomimetic xenograft versus demineralized bovine bone. J Craniofac Surg 30:1089–1094. https://doi.org/10.1097/SCS.0000000000005416
Iorio-Siciliano V, Ramaglia L, Blasi A, Bucci P, Nuzzolo P, Riccitiello F et al (2020) Dimensional changes following alveolar ridge preservation in the posterior area using bovine-derived xenografts and collagen membrane compared to spontaneous healing: a 6-month randomized controlled clinical trial. Clin Oral Investig 24:1013–1023. https://doi.org/10.1007/s00784-019-02979-w
Barone A, Aldini NN, Fini M, Giardino R, Calvo Guirado JL, Covani U (2008) Xenograft versus extraction alone for ridge preservation after tooth removal: a clinical and histomorphometric study. J Periodontol 79:1370–1377. https://doi.org/10.1902/jop.2008.070628
Festa VM, Addabbo F, Laino L, Femiano F, Rullo R (2013) Porcine-derived xenograft combined with a soft cortical membrane versus extraction alone for implant site development: a clinical study in humans. Clin Implant Dent Relat Res 15:707–713. https://doi.org/10.1111/j.1708-8208.2011.00398.x
Barone A, Toti P, Piattelli A, Iezzi G, Derchi G, Covani U (2014) Extraction socket healing in humans after ridge preservation techniques: comparison between flapless and flapped procedures in a randomized clinical trial. J Periodontol 85:14–23
Barone A, Borgia V, Covani U, Ricci M, Piattelli A, Iezzi G (2015) Flap versus flapless procedure for ridge preservation in alveolar extraction sockets: a histological evaluation in a randomized clinical trial. Clin Oral Implants Res 26:806–813. https://doi.org/10.1111/clr.12358
Roberto C, Paolo T, Giovanni C, Ugo C, Bruno B, Giovanni-Battista MF (2021) Bone remodeling around implants placed after socket preservation: a 10-year retrospective radiological study. Int J Implant Dent 7:74. https://doi.org/10.1186/s40729-021-00354-7
Choi DS, Garagiola U, Kim SG (2019) Current status of the surgery-first approach (part I): concepts and orthodontic protocols. Maxillofac Plast Reconstr Surg 41:10. https://doi.org/10.1186/s40902-019-0194-4
Araújo MG, Lindhe J (2009) Ridge preservation with the use of Bio-Oss collagen: a 6-month study in the dog. Clin Oral Implants Res 20:433–440. https://doi.org/10.1111/j.1600-0501.2009.01705.x
Moro A, Gasperini G, Foresta E, Saponaro G, Falchi M, Cardarellin L, De Angelis P, Forcione M, Garagiola U, D’Amato G (2017) Alveolar ridge split technique using piezosurgery with specially designed tips. Research International 2017:1–8. https://doi.org/10.1155/2017/4530378
Galli M, Yao Y, Giannobile WV, Wang HL (2021) Current and future trends in periodontal tissue engineering and bone regeneration. Plast Aesthet Res 8:3. https://doi.org/10.20517/2347-9264.2020.176
Tan WL, Wong TL, Wong MC, Lang NP (2012) A systematic review of post-extractional alveolar hard and soft tissue dimensional changes in humans. Clin Oral Implants Res 23:1–21
Kang YJ, Jo YY, Kweon HY, Chae WS, Yang WG, Garagiola U, Rotaru H, Kim SG (2020) Comparison of the physical properties and in vivo bioactivities of flatwise-spun silk mats and cocoon-derived silk mats for guided bone regeneration. Macromol Res 28:159–164. https://doi.org/10.1007/s13233-020-8026-z
Poulias E, Greenwell H, Hill M, Morton D, Vidal R, Shumway B, Peterson TL (2013) Ridge preservation comparing socket allograft alone to socket allograft plus facial overlay xenograft: a clinical and histologic study in humans. J Periodontol 84:1567–1575. https://doi.org/10.1902/jop.2013.120585
Majzoub J, Ravida A, Starch-Jensen T, Tattan M, Suárez-López Del Amo F (2019) The influence of different grafting materials on alveolar ridge preservation: a systematic review. J Oral Maxillofac Res 10:e6. https://doi.org/10.5037/jomr.2019.10306
Ramírez Fernández MP, Gehrke SA, Pérez Albacete Martinez C, Calvo Guirado JL, de Aza PN (2017) SEM-EDX study of the degradation process of two xenograft materials used in sinus lift procedures. Materials (Basel) 10:542. https://doi.org/10.3390/ma10050542.DOI:10.1097/ID.0000000000000893
Amid R, Kheiri A, Kheiri L, Kadkhodazadeh M, Ekhlasmandkermani M (2020) Structural and chemical features of xenograft bone substitutes: a systematic review of in vitro studies. Biotechnol Appl Biochem. https://doi.org/10.1002/bab.2065
Perrotti V, Nicholls BM, Piattelli A (2009) Human osteoclast formation and activity on an equine spongy bone substitute. Clin Oral Implants Res 20:17–23. https://doi.org/10.1111/j.1600-0501.2008.01608.x
Rico-Llanos GA, Borrego-González S, Moncayo-Donoso M, Becerra J, Visser R (2021) Collagen Type I biomaterials as scaffolds for bone tissue engineering. Polymers (Basel) 13:599. https://doi.org/10.3390/polym13040599
Kim DW, Jo YY, Garagiola U, Choi JY, Kang YJ, Oh JH, Kim SG (2020) Increased level of vascular endothelial growth factors by 4-hexylresorcinol is mediated by transforming growth factor-β1 and accelerates capillary regeneration in the burns in diabetic animals. Int J Mol Sci 21:3473. https://doi.org/10.3390/ijms21103473
Kim J-Y, Kim D-W, Lee SK, Choi J-Y, Che X, Kim S-G, Garagiola U (2021) Increased expression of TGF-β1 by 4-hexylresorcinol is mediated by endoplasmic reticulum and mitochondrial stress in human umbilical endothelial vein cells. Appl Sci 11:9128. https://doi.org/10.3390/app11199128
Jo YY, Kweon H, Kim DW, Baek K, Chae WS, Kang YJ, Oh JH, Kim SG, Garagiola U (2021) Silk sericin application increases bone morphogenic protein-2/4 expression via a toll-like receptor-mediated pathway. Int J Biol Macromol 190:607–617. https://doi.org/10.1016/j.ijbiomac.2021.09.021
Di Stefano DA, Cazzaniga A, Andreasi Bassi M, Ludovichetti M, Ammirabile G, Celletti R (2013) The use of cortical heterologous sheets for sinus lift bone grafting: a modification of Tulasne’s technique with 7-year follow-up. Int J Immunopathol Pharmacol 26:549–356. https://doi.org/10.1177/039463201302600231
Di Stefano DA, Gastaldi G, Vinci R, Polizzi EM, Cinci L, Pieri L, Gherlone E (2016) Bone formation following sinus augmentation with an equine-derived bone graft: a retrospective histologic and histomorphometric study with 36-month follow-up. Int J Oral Maxillofac Implants 31:406–412. https://doi.org/10.11607/jomi.4373
La Monaca G, Iezzi G, Cristalli MP, Pranno N, Sfasciotti GL, Vozza I (2018) Comparative histological and histomorphometric results of six biomaterials used in two-stage maxillary sinus augmentation model after 6-month healing. Biomed Res Int 2018:9430989. https://doi.org/10.1155/2018/9430989
Di Stefano DA, Vinci R, Capparè P, Gherlone EF (2021) A retrospective preliminary histomorphometric and clinical investigation on sinus augmentation using enzyme-deantigenic, collagen-preserving equine bone granules and plasma rich in growth factors. Int J Implant Dent 7:60. https://doi.org/10.1186/s40729-021-00336-9
Di Stefano DA, Artese L, Iezzi G, Piattelli A, Pagnutti S, Piccirilli M, Perrotti V (2009) Alveolar ridge regeneration with equine spongy bone: a clinical, histological, and immunohistochemical case series. Clin Implant Dent Relat Res 11:90–100. https://doi.org/10.1111/j.1708-8208.2008.00104.x
De Angelis N, Scivetti M (2011) Lateral ridge augmentation using an equine flex bone block infused with recombinant human platelet-derived growth factor BB: a clinical and histologic study. Int J Periodontics Restorative Dent 31:383–388
Di Stefano DA, Greco GB, Riboli F (2016) Guided bone regeneration of an atrophic mandible with a heterologous bone block. Craniomaxillofac Trauma Reconstr 9:88–93. https://doi.org/10.1055/s-0035-1551544
Di Stefano DA, Piattelli A, Zaniol T, Iezzi G (2020) Implant and prosthetic success following peri-implant guided bone regeneration in the esthetic zone using an equine cortical bone membrane and an equine enzyme-treated bone graft: a retrospective study with 9-year follow-up. Int J Oral Maxillofac Implants 35:824–832. https://doi.org/10.11607/jomi.7906
Di Stefano D, Garagiola U, Bassi MA (2017) Preserving the bone profile in anterior maxilla using an equine cortical bone membrane and an equine enzyme-treated bone graft: a case report with 5-year follow-up. J Contemp Dent Pract 18:614–621. https://doi.org/10.5005/jp-journals-10024-2094
Suba Z, Hrabák K, Huys L, Coulthard P, Maiorana C, Garagiola U, Szabó G (2004) Histologic and histomorphometric study of bone regeneration induced by beta tricalciumphosphate (multicenter study). Orv Hetil 145:1431–1437 (Hungarian)
Di Stefano DA, Orlando F (2020) Ridge preservation using a novel enzyme-treated xenograft. a Preliminary Retrospective Histomorphometric Investigation. Applied Sciences 10:4256. https://doi.org/10.3390/app10124256
Ko FC, Sumner DR (2021) How faithfully does intramembranous bone regeneration recapitulate embryonic skeletal development? Dev Dyn 250:377–392. https://doi.org/10.1002/dvdy.240
Di Stefano DA, Arosio P, Pagnutti S, Vinci R, Gherlone EF (2019) Distribution of trabecular bone density in the maxilla and mandible. Implant Dent 28:340–348. https://doi.org/10.1097/ID.0000000000000893
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Di Stefano, D.A., Orlando, F., Ottobelli, M. et al. A comparison between anorganic bone and collagen-preserving bone xenografts for alveolar ridge preservation: systematic review and future perspectives. Maxillofac Plast Reconstr Surg 44, 24 (2022). https://doi.org/10.1186/s40902-022-00349-3
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DOI: https://doi.org/10.1186/s40902-022-00349-3