Division of Epidemiology, Human Genetics, and Environmental Science, School of Public Health, University of Texas Health Science Center, Houston, USA.
Ann Epidemiol. 2011 Nov;21(11):815-23. doi: 10.1016/j.annepidem.2011.08.007.
To investigate the potential interaction between folate intake and the paraoxonase 1 (PON1) Q192R polymorphism with the risk of incident coronary heart disease (CHD) and ischemic stroke in the Atherosclerosis Risk in Communities study, a population-based prospective cohort of cardiovascular disease in 15,792 white and African-American subject.
Race-stratified Cox proportional hazards models were performed to examine the interaction between folate intake and the PON1 Q192R polymorphism.
A significant inverse association between folate intake and risk of incident CHD among white subjects was found (hazard rate ratio, 1.30; 95% confidence interval, 1.09-1.56; P = .004; folate intake ≤155 μg vs ≥279 μg, reference group). An interaction effect was observed between the dominant genetic model and folate intake with regards to incident ischemic stroke in white subjects (hazard rate ratio, 0.68; 95% confidence interval, 0.91-0.99; and 1.24 from 1st-4th quartile, respectively; P-trend = .05).
There was an interaction between folate intake and PON1 Q192 polymorphism with regard to the risk of ischemic stroke in white subjects. Future studies should investigate the interaction between additional polymorphisms within the PON1 gene and genetic variants in other folate metabolizing genes with folate intake on the risk of incident CHD and stroke.
在社区动脉粥样硬化风险研究中,调查叶酸摄入量与对氧磷酶 1(PON1)Q192R 多态性与冠心病(CHD)和缺血性卒中发病风险之间的潜在相互作用。这是一个基于人群的心血管疾病的白种人和非裔美国人队列研究。
按种族分层的 Cox 比例风险模型来研究叶酸摄入量与 PON1 Q192R 多态性之间的相互作用。
在白种人群中发现,叶酸摄入量与 CHD 发病风险呈显著负相关(危险率比,1.30;95%置信区间,1.09-1.56;P=0.004;叶酸摄入量≤155μg 与≥279μg,参考组)。在白种人群中,发现了显性遗传模型与叶酸摄入量对缺血性卒中发病风险的交互作用(危险率比,0.68;95%置信区间,0.91-0.99;第一至第四四分位数分别为 1.24;P 趋势=0.05)。
叶酸摄入量与 PON1 Q192 多态性之间存在交互作用,影响白种人群的缺血性卒中发病风险。未来的研究应调查 PON1 基因内的其他多态性与其他叶酸代谢基因中的遗传变异与叶酸摄入量对 CHD 和卒中发病风险的相互作用。