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全基因组 SNP 与饮酒对血压的交互作用研究:韩国基因组与流行病学研究(KoGES)中的安山和安城研究。

Genome-wide interaction study of single-nucleotide polymorphisms and alcohol consumption on blood pressure: The Ansan and Ansung study of the Korean Genome and Epidemiology Study (KoGES).

机构信息

Department of Public Health Science, College of Medicine, Hanyang University, Seoul, South Korea.

Laboratory of Research and Development for Genomics, Cheil General Hospital and Women's Healthcare Center, Seoul, South Korea.

出版信息

Genet Epidemiol. 2020 Apr;44(3):300-310. doi: 10.1002/gepi.22285. Epub 2020 Feb 11.

DOI:10.1002/gepi.22285
PMID:32048322
Abstract

Hypertension is a common disease worldwide. Alcohol consumption is one of the risk factors for hypertension, however, it is unclear how alcohol consumption elevates blood pressure. Blood pressure could be affected by interactions between genetic variations and alcohol consumption. Thus, we performed a genome-wide interaction study (GWIS) to assess the effect of gene-alcohol consumption interaction on blood pressure among adults aged ≥40 years from the Ansan and Ansung cohort study (n = 6,176), a part of the Korean Genome Epidemiology Study (KoGES). As a result, rs1297184, single-nucleotide polymorphism (SNP) in locus LGR5 was significant (P  = 8.78 × 10 ) in GWIS analysis on diastolic blood pressure, but not on systolic blood pressure. However, there was a heteroscedasticity of alcohol consumption. In the GWIS analysis, applying the inverse-variance weighting to correct the systematic inflation slightly attenuated the strength of interaction (P  = 7.14 × 10 ). This interaction was replicated in the Health Examinees cohort (p = .026), a large-scale community-based cohort (n = 18,708). In conclusion, we identified a possible novel interaction between an SNP (rs1297184) and alcohol consumption on blood pressure.

摘要

高血压是一种全球性的常见疾病。饮酒是高血压的危险因素之一,但饮酒如何升高血压尚不清楚。血压可能受到基因变异与饮酒之间相互作用的影响。因此,我们进行了一项全基因组交互研究(GWIS),以评估基因-饮酒相互作用对来自安山和安城队列研究(n=6176)中年龄≥40 岁成年人血压的影响,该研究是韩国基因组流行病学研究(KoGES)的一部分。结果,在对舒张压的 GWIS 分析中,位于 LGR5 基因座的单核苷酸多态性(SNP)rs1297184 具有统计学意义(P=8.78×10-8),但对收缩压无统计学意义。然而,饮酒存在异方差性。在 GWIS 分析中,应用逆方差加权法校正系统膨胀略微减弱了相互作用的强度(P=7.14×10-7)。该相互作用在 Health Examinees 队列(p=0.026)中得到了复制,该队列是一个大规模的基于社区的队列(n=18708)。总之,我们鉴定出了一个 SNP(rs1297184)和饮酒与血压之间可能存在的新的交互作用。

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