Giannobile William V, Somerman Martha J
Department of Periodontics/Prevention/Geriatrics, Center for Craniofacial Regeneration, School of Dentistry, University of Michigan, Ann Arbor, Michigan, USA.
Ann Periodontol. 2003 Dec;8(1):193-204. doi: 10.1902/annals.2003.8.1.193.
Regeneration of tooth-supporting structures destroyed by periodontitis is a major goal of periodontal therapy. Periodontal tissue engineering utilizing growth and amelogenin-like factors (GAFs) applies advances in materials science and biology to regenerate alveolar bone, periodontal ligament, and cementum. Amelogenin-like factors (e.g., enamel matrix derivative [EMD]) and growth factors (e.g., platelet-derived growth factor [PDGF] and bone morphogenetic proteins [BMPs, also considered morphogens]) have demonstrated pleotrophic effects on the stimulation of several key events required for tissue regeneration including DNA synthesis, chemotaxis, differentiation, and matrix synthesis.
GAFs have been used for the treatment of periodontal disease as shown in preclinical and clinical studies. This systematic review evaluates the evidence to support the utilization of EMD and growth factors (GFs) for periodontal repair and regeneration associated with natural teeth.
In patients with periodontal osseous defects, what is the effect of GAFs compared with controls on clinical, radiographic, histologic, adverse, and patient-centered outcomes?
Two investigators searched MEDLINE, pre-MEDLINE, and the Cochrane Oral Health Group trials register for clinical and preclinical studies published in English. Hand searches were performed on the International Journal of Periodontics and Restorative Dentistry, Journal of Clinical Periodontology, Journal of Dental Research, Journal of Periodontology, and Journal of Periodontal Research. Searches were performed for articles published through April 2002. In addition, investigators contacted manufacturers of GAF products for related unpublished data and studies in progress.
Randomized controlled clinical trials (RCTs), cohort studies, case-control studies, case reports, and preclinical (animal) randomized controlled investigations that included a cohort population diagnosed with periodontal disease and presenting data on intrabony/interproximal defects and/or furcation defects were screened.
In vitro studies or those that did not include quantifiable data with respect to clinical or bone measures were not included.
Meta-analyses were performed for studies that fulfilled the eligibility criteria for the following continuous variables: clinical attachment level (CAL), probing depth (PD), or bone level (radiographic, re-entry, or histologic). Heterogeneity was assessed to determine whether the differences among therapies were due to systematic confounding factors (as noted in study quality assessments).
REVIEWERS' CONCLUSIONS: 1. There is evidence supporting the use of EMD for periodontal osseous defects to improve CAL and reduce PD, although long-term benefits have not been established. 2. EMD has demonstrated notable consistency among the studies investigated in terms of superiority to controls (in general compared to open flap debridement [OFD]). 3. EMD appears to be safe for single and multiple administrations in terms of lack of elicitation of antibody responses or other local/systemic inflammatory events. 4. Preclinical and initial clinical data for growth factors appear promising but are insufficient to draw definitive conclusions at this time.
牙周炎破坏的牙齿支持结构的再生是牙周治疗的主要目标。利用生长因子和类釉原蛋白因子(GAFs)的牙周组织工程将材料科学和生物学的进展应用于牙槽骨、牙周韧带和牙骨质的再生。类釉原蛋白因子(如釉基质衍生物[EMD])和生长因子(如血小板衍生生长因子[PDGF]和骨形态发生蛋白[BMPs,也被视为形态发生素])已证明对刺激组织再生所需的几个关键事件具有多效性作用,包括DNA合成、趋化性、分化和基质合成。
如临床前和临床研究所示,GAFs已被用于治疗牙周疾病。本系统评价评估支持使用EMD和生长因子(GFs)进行与天然牙相关的牙周修复和再生的证据。
在患有牙周骨缺损的患者中,与对照组相比,GAFs对临床、影像学、组织学、不良事件和以患者为中心的结局有何影响?
两名研究者检索了MEDLINE、Pre-MEDLINE以及Cochrane口腔健康组试验注册库,以查找用英文发表的临床和临床前研究。对手检《国际牙周病与修复牙科学杂志》《临床牙周病学杂志》《牙科研究杂志》《牙周病学杂志》和《牙周病研究杂志》。检索截至2002年4月发表的文章。此外,研究者联系了GAF产品制造商以获取相关未发表数据和正在进行的研究。
筛选随机对照临床试验(RCTs)、队列研究、病例对照研究、病例报告以及临床前(动物)随机对照研究,这些研究纳入了被诊断患有牙周疾病的队列人群,并提供了关于骨内/邻间缺损和/或根分叉缺损的数据。
不包括体外研究或那些未包括关于临床或骨测量的可量化数据的研究。
对符合以下连续变量资格标准的研究进行荟萃分析:临床附着水平(CAL)、探诊深度(PD)或骨水平(影像学、再次切开或组织学)。评估异质性以确定治疗之间的差异是否归因于系统性混杂因素(如研究质量评估中所指出的)。