From the John T. McDonald Department of Human Genetics, John P. Hussman Institute for Human Genomics (L.W., A.B., S.H.B., R.L.S.), Department of Neurology (T.R., S.H.B., R.L.S., C.D.), Department of Public Health Sciences (T.R., R.L.S.), and Department of Medicine (B.H.), Miller School of Medicine, University of Miami, FL; and Department of Biostatistics, Yale School of Public Health, Yale University, New Haven, CT (H.Z.).
Arterioscler Thromb Vasc Biol. 2014 Jan;34(1):219-25. doi: 10.1161/ATVBAHA.113.302706. Epub 2013 Nov 7.
Carotid intima-media thickness (cIMT), a marker for atherosclerosis, is affected by smoking and has substantial interindividual variation. We sought to identify the genetic moderators influencing the effect of smoking on cIMT.
With a multistage design using 722 379 single nucleotide polymorphisms (SNP), a genome-wide interaction study was performed in a discovery sample of 669 Hispanics, followed by replication in 589 subjects (264 Hispanics, 172 non-Hispanic blacks, 153 non-Hispanic whites). Assuming an additive genetic model, regression analysis was performed to test for smoking-SNP interaction on cIMT while controlling for age, sex, and the top 3 principal components of ancestry. The strongest interaction in Hispanics was found with a synonymous splicing SNP (rs3751383) in exon 9 of RCBTB1 (P=2.5e(-6) in discovery sample; P=0.01 in the Hispanic replication sample; P<8.8e(-9) in the combined Hispanic sample). Stratification analysis in the combined Hispanic sample showed that smoking had no effect on cIMT among rs3751383 G homozygote (P=0.15), a moderate effect among rs3751383 heterozygote (P=0.01), and a strong effect among rs3751383 A homozygote (P=2.1e(-7)). A consistent trend was observed in the non-Hispanic white and black data sets, leading to an interaction effect of P<2.9e(-9) in the meta-analysis of all 1258 subjects.
Our study represents the first genome-wide smoking-SNP interaction study of cIMT and identifies RCBTB1 as a modifier of the smoking effect on cIMT. Testing for gene-environment interactions can help uncover genetic factors that contribute to the interindividual variation in response to the same environmental exposure.
颈动脉内膜中层厚度(cIMT)是动脉粥样硬化的标志物,受吸烟影响且个体间差异较大。本研究旨在确定影响吸烟对 cIMT 影响的遗传调节因子。
采用 722379 个单核苷酸多态性(SNP)的多阶段设计,在包含 669 名西班牙裔个体的发现样本中进行全基因组交互研究,随后在包含 589 名个体(264 名西班牙裔、172 名非西班牙裔黑人、153 名非西班牙裔白人)的样本中进行复制。在控制年龄、性别和祖先的前 3 个主成分的情况下,假设加性遗传模型,通过回归分析检验吸烟-SNP 对 cIMT 的交互作用。在西班牙裔人群中,发现 RCBTB1 外显子 9 中的同义剪接 SNP(rs3751383)与吸烟的交互作用最强(在发现样本中 P=2.5e(-6);在西班牙裔复制样本中 P=0.01;在合并的西班牙裔样本中 P<8.8e(-9))。在合并的西班牙裔样本中,分层分析显示 rs3751383 纯合子(G)中吸烟对 cIMT 无影响(P=0.15),杂合子(rs3751383)中影响中等(P=0.01),纯合子(rs3751383)中影响较大(P=2.1e(-7))。在非西班牙裔白人和黑人数据集中观察到一致的趋势,导致在包含 1258 名个体的荟萃分析中交互作用的 P<2.9e(-9)。
本研究代表了首个针对 cIMT 的全基因组吸烟-SNP 交互研究,确定 RCBTB1 是吸烟对 cIMT 影响的调节因子。检测基因-环境相互作用可以帮助揭示导致对相同环境暴露的个体间差异的遗传因素。