Department of Periodontology, School of Dentistry, National and Kapodistrian University of Athens, Athens, Greece.
Centre for Oral Clinical Research, Institute of Dentistry, Barts & The London School of Medicine and Dentistry, Queen Mary University of London (QMUL), London, UK.
Clin Oral Implants Res. 2022 Feb;33(2):131-141. doi: 10.1111/clr.13882. Epub 2021 Dec 9.
The aim of this systematic review was to evaluate the association between specific genetic polymorphisms and dental implant-related biological complications in patients having a follow-up period of at least 12-months post-loading.
A sensitive search strategy was developed to identify implant-related genetic-association studies. This was performed by searching five databases. A three-stage screening (titles, abstract, full text) was carried out in duplicate and independently by two reviewers. Assessment was carried out according to the suggested scale for quality assessment of periodontal genetic-association studies and adapted to genetic analyses of implant-related studies leading to an overall final score 0-20 based on the summation of positive answers.
The initial search resulted in 1838 articles. Sixty-seven full-text articles were assessed for eligibility and four studies met the defined inclusion criteria. IL-6 G174C, TNF-α -308, IL-1A-889 and IL-1B+3954 and CD14-159 C/T polymorphisms were evaluated. The quality assessment scores ranged from 6 to 11 positive answers from out of a maximum score of 20. The great heterogeneity among the studies did not allow a meta-analysis.
The published evidence on genetic predisposition and implant biologic complications is limited. The small number of identified studies evaluating the association between genetic polymorphisms and peri-implant disease presented methodological and reporting inadequacies. Thus, the potential link between genetic polymorphisms and biological complications should be further investigated and clarified through well-designed clinical studies on adequately powered and appropriately included study populations.
本系统评价的目的是评估在加载后至少 12 个月的随访期内,特定基因多态性与牙种植体相关生物学并发症之间的关系。
制定了一项敏感的搜索策略,以确定与种植体相关的遗传关联研究。通过搜索五个数据库来完成此操作。由两名评审员重复且独立地进行了三阶段筛选(标题、摘要、全文)。根据牙周遗传关联研究的质量评估建议进行评估,并针对与种植体相关研究的遗传分析进行了调整,最终总分为 0-20 分,基于阳性答案的总和。
初步搜索产生了 1838 篇文章。对 67 篇全文文章进行了资格评估,符合定义的纳入标准的有四项研究。评估了 IL-6 G174C、TNF-α-308、IL-1A-889 和 IL-1B+3954 以及 CD14-159 C/T 多态性。质量评估评分范围为 20 分中的 6 到 11 个阳性答案。由于研究之间存在很大的异质性,因此不允许进行荟萃分析。
关于遗传易感性和种植体生物学并发症的已发表证据有限。评估遗传多态性与种植体周围疾病之间关联的已确定研究数量较少,存在方法学和报告方面的不足。因此,需要通过针对适当纳入研究人群的精心设计的临床研究进一步研究和阐明遗传多态性与生物学并发症之间的潜在联系。