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J Clin Periodontol. 2023 Sep;50(9):1140-1153. doi: 10.1111/jcpe.13852. Epub 2023 Jul 18.
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Blood Leukocyte DNA Methylation Markers of Periodontal Disease and Risk of Lung Cancer in a Case-Control Study Nested in the CLUE II Cohort.病例对照研究巢式 CLUE II 队列中牙周病的血白细胞 DNA 甲基化标志物与肺癌风险。
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本文引用的文献

1
Epigenome-wide meta-analysis of BMI in nine cohorts: Examining the utility of epigenetically predicted BMI.基于九项队列的 BMI 全基因组表观遗传元分析:检验表观遗传预测 BMI 的效用。
Am J Hum Genet. 2023 Feb 2;110(2):273-283. doi: 10.1016/j.ajhg.2022.12.014. Epub 2023 Jan 16.
2
The Role of Zinc Finger Proteins in Various Oral Conditions.锌指蛋白在各种口腔状况中的作用。
ScientificWorldJournal. 2022 Apr 15;2022:4612054. doi: 10.1155/2022/4612054. eCollection 2022.
3
Enhanced cell deconvolution of peripheral blood using DNA methylation for high-resolution immune profiling.利用 DNA 甲基化增强外周血的细胞去卷积,实现高分辨率免疫分析。
Nat Commun. 2022 Feb 9;13(1):761. doi: 10.1038/s41467-021-27864-7.
4
MiR-150 Attenuates Maladaptive Cardiac Remodeling Mediated by Long Noncoding RNA MIAT and Directly Represses Profibrotic .miR-150 通过长链非编码 RNA MIAT 减轻病理性心脏重构并直接抑制成纤维细胞增殖
Circ Heart Fail. 2022 Apr;15(4):e008686. doi: 10.1161/CIRCHEARTFAILURE.121.008686. Epub 2022 Jan 10.
5
Blood DNA Methylation and Incident Coronary Heart Disease: Evidence From the Strong Heart Study.血液 DNA 甲基化与冠心病事件:来自“强健心脏研究”的证据。
JAMA Cardiol. 2021 Nov 1;6(11):1237-1246. doi: 10.1001/jamacardio.2021.2704.
6
The ARIC (Atherosclerosis Risk In Communities) Study: JACC Focus Seminar 3/8.ARIC(社区动脉粥样硬化风险研究):JACC 重点研讨会 3/8。
J Am Coll Cardiol. 2021 Jun 15;77(23):2939-2959. doi: 10.1016/j.jacc.2021.04.035.
7
Differential DNA methylation and mRNA transcription in gingival tissues in periodontal health and disease.牙周健康和疾病中牙龈组织的差异 DNA 甲基化和 mRNA 转录。
J Clin Periodontol. 2021 Sep;48(9):1152-1164. doi: 10.1111/jcpe.13504. Epub 2021 Jul 11.
8
DNA Methylation and Expression Profiles of Whole Blood in Parkinson's Disease.帕金森病全血的DNA甲基化与表达谱
Front Genet. 2021 Apr 26;12:640266. doi: 10.3389/fgene.2021.640266. eCollection 2021.
9
ZNF718, HOXA4, and ZFP57 are differentially methylated in periodontitis in comparison with periodontal health: Epigenome-wide DNA methylation pilot study.ZNF718、HOXA4 和 ZFP57 在牙周炎与牙周健康中的甲基化程度存在差异:全基因组 DNA 甲基化初步研究。
J Periodontal Res. 2021 Aug;56(4):710-725. doi: 10.1111/jre.12868. Epub 2021 Mar 4.
10
Nutrition as a Key Modifiable Factor for Periodontitis and Main Chronic Diseases.营养作为牙周炎和主要慢性疾病的关键可改变因素。
J Clin Med. 2021 Jan 7;10(2):197. doi: 10.3390/jcm10020197.

采用外周血白细胞进行的表观基因组全基因组关联研究,在社区动脉粥样硬化风险研究中确定了与牙周病和无牙症相关的基因组区域。

Epigenome-wide association study using peripheral blood leukocytes identifies genomic regions associated with periodontal disease and edentulism in the Atherosclerosis Risk in Communities study.

机构信息

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.

出版信息

J Clin Periodontol. 2023 Sep;50(9):1140-1153. doi: 10.1111/jcpe.13852. Epub 2023 Jul 18.

DOI:10.1111/jcpe.13852
PMID:37464577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10528731/
Abstract

AIM

To investigate individual susceptibility to periodontitis by conducting an epigenome-wide association study using peripheral blood.

MATERIALS AND METHODS

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.

RESULTS

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)).

CONCLUSIONS

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.

摘要

目的

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。

材料与方法

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。

结果

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))。

结论

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。