Department of Public Health & Community Medicine, Tufts University School of Medicine, Tufts University, Boston, Massachusetts, USA.
Department of Basic & Translational Sciences, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
J Clin Periodontol. 2023 Sep;50(9):1140-1153. doi: 10.1111/jcpe.13852. Epub 2023 Jul 18.
To investigate individual susceptibility to periodontitis by conducting an epigenome-wide association study using peripheral blood.
We included 1077 African American and 457 European American participants of the Atherosclerosis Risk in Communities (ARIC) study who had completed a dental examination or reported being edentulous at Visit 4 and had available data on DNA methylation from Visit 2 or 3. DNA methylation levels were compared by periodontal disease severity and edentulism through discovery analyses and subsequent testing of individual CpGs.
Our discovery analysis replicated findings from a previous study reporting a region in gene ZFP57 (6p22.1) that was significantly hypomethylated in severe periodontal disease compared with no/mild periodontal disease in European American participants. Higher methylation levels in a separate region in an unknown gene (located in Chr10: 743,992-744,958) was associated with significantly higher odds of edentulism compared with no/mild periodontal disease in African American participants. In subsequent CpG testing, four CpGs in a region previously associated with periodontitis located within HOXA4 were significantly hypermethylated in severe periodontal disease compared with no/mild periodontal disease in African American participants (odds ratio per 1 SD increase in methylation level: cg11015251: 1.28 (1.02, 1.61); cg14359292: 1.24 (1.01, 1.54); cg07317062: 1.30 (1.05, 1.61); cg08657492: 1.25 (1.01, 1.55)).
Our study highlights epigenetic variations in ZPF57 and HOXA4 that are significantly and reproducibly associated with periodontitis. Future studies should evaluate gene regulatory mechanisms in the candidate regions of these loci.
通过对外周血进行全基因组关联研究,探讨个体易患牙周炎的情况。
我们纳入了 1077 名非裔美国人和 457 名欧洲裔美国人,他们均参加了动脉粥样硬化风险社区研究(ARIC),并在第 4 次就诊时完成了牙科检查或报告无牙,且在第 2 次或第 3 次就诊时可获得 DNA 甲基化数据。通过发现分析和对个体 CpG 的后续检测,比较了牙周病严重程度和无牙与 DNA 甲基化水平的关系。
我们的发现分析复制了之前一项研究的结果,该研究报告了基因 ZFP57(6p22.1)中的一个区域在欧洲裔美国人中,与无/轻度牙周病相比,严重牙周病患者的该区域明显呈低甲基化状态。在一个未知基因的另一个独立区域(位于 Chr10:743,992-744,958)中,较高的甲基化水平与非裔美国人的无牙或无/轻度牙周病相比,无牙的可能性显著更高。在随后的 CpG 检测中,与先前与牙周炎相关的位于 HOXA4 内的一个区域中的四个 CpG 在严重牙周病患者中与无/轻度牙周病患者相比,甲基化水平显著升高(每增加 1 个 SD 的甲基化水平的比值比:cg11015251:1.28(1.02,1.61);cg14359292:1.24(1.01,1.54);cg07317062:1.30(1.05,1.61);cg08657492:1.25(1.01,1.55))。
我们的研究强调了 ZPF57 和 HOXA4 中的表观遗传变异与牙周炎显著且可重复相关。未来的研究应评估这些基因座候选区域中的基因调控机制。