Blood transcriptomic biomarkers of alcohol consumption and cardiovascular disease risk factors: the Framingham Heart Study.
Blood transcriptomic biomarkers of alcohol consumption and cardiovascular disease risk factors: the Framingham Heart Study.
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饮酒和心血管疾病危险因素的血液转录组生物标志物:弗雷明汉心脏研究。
DOI:
10.1093/hmg/ddac237
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发表时间:
2023
影响因子:
3.5
通讯作者:
Liu,Chunyu
中科院分区:
文献类型:
--
作者:
Ma,Jiantao;Huang,Allen;Yan,Kaiyu;Li,Yi;Sun,Xianbang;Joehanes,Roby;Huan,Tianxiao;Levy,Daniel;Liu,Chunyu
BackgroundThe relations of alcohol consumption and gene expression remain to be elucidated.Materials and MethodsWe examined cross-sectional associations between alcohol consumption and whole blood derived gene expression levels and between alcohol-associated genes and obesity, hypertension, and diabetes in 5531 Framingham Heart Study (FHS) participants.ResultsWe identified 25 alcohol-associated genes. We further showed cross-sectional associations of 16 alcohol-associated genes with obesity, nine genes with hypertension, and eight genes with diabetes atP< 0.002. For example, we observed decreased expression ofPROK2(β= −0.0018; 95%CI: −0.0021, −0.0007;P= 6.5e − 5) andPAX5(β= −0.0014; 95%CI: −0.0021, −0.0007;P= 6.5e − 5) per 1 g/day increase in alcohol consumption. Consistent with our previous observation on the inverse association of alcohol consumption with obesity and positive association of alcohol consumption with hypertension, we found thatPROK2was positively associated with obesity (OR = 1.42; 95%CI: 1.17, 1.72;P= 4.5e − 4) andPAX5was negatively associated with hypertension (OR = 0.73; 95%CI: 0.59, 0.89;P= 1.6e − 3). We also observed that alcohol consumption was positively associated with expression ofABCA13(β= 0.0012; 95%CI: 0.0007, 0.0017;P= 1.3e − 6) andABCA13was positively associated with diabetes (OR = 2.57; 95%CI: 1.73, 3.84;P= 3.5e − 06); this finding, however, was inconsistent with our observation of an inverse association between alcohol consumption and diabetes.ConclusionsWe showed strong cross-sectional associations between alcohol consumption and expression levels of 25 genes in FHS participants. Nonetheless, complex relationships exist between alcohol-associated genes and CVD risk factors.