Kardia Sharon L R, Bielak Lawrence F, Lange Leslie A, Cheverud James M, Boerwinkle Eric, Turner Stephen T, Sheedy Patrick F, Peyser Patricia A
Department of Epidemiology, University of Michigan, Ann Arbor, MI 48104-3028, USA.
Med Sci Monit. 2006 Apr;12(4):CR150-8. Epub 2006 Mar 28.
Coronary artery calcification (CAC) is an important indicator of future coronary artery disease events. Since elevated blood pressure (BP) is an important predictor of CAC, genetic polymorphisms in the renin-angiotensin system and their interaction may play a role in explaining CAC quantity variation.
MATERIAL/METHODS: As part of the Epidemiology of Coronary Artery Calcification Study, 166 asymptomatic women and 166 asymptomatic men were genotyped for the insertion/deletion polymorphism in the angiotensin-converting enzyme (ACE) gene and the -6 promoter polymorphism of the angiotensinogen (AGT) gene. We used a novel method to detect gene-gene interaction and compared it to the standard two-way analysis of variance (ANOVA) method.
Based on a two-way ANOVA model, there was no evidence for epistasis for either systolic BP or CAC in either men or women. However, using a novel method, we found evidence of significant gene-gene interaction in systolic BP in men and gene-gene interaction in both systolic BP levels and CAC quantity in women.
Our study demonstrates that new methods of assessing epistasis maybe important in understanding the complex genetics of systolic blood pressure as well as subclinical coronary atherosclerosis.
冠状动脉钙化(CAC)是未来冠状动脉疾病事件的重要指标。由于血压升高(BP)是CAC的重要预测因素,肾素-血管紧张素系统中的基因多态性及其相互作用可能在解释CAC数量变化中起作用。
材料/方法:作为冠状动脉钙化流行病学研究的一部分,对166名无症状女性和166名无症状男性进行了血管紧张素转换酶(ACE)基因插入/缺失多态性和血管紧张素原(AGT)基因-6启动子多态性的基因分型。我们使用一种新方法来检测基因-基因相互作用,并将其与标准的双向方差分析(ANOVA)方法进行比较。
基于双向ANOVA模型,无论是男性还是女性,收缩压或CAC均无上位性证据。然而,使用一种新方法,我们发现男性收缩压存在显著基因-基因相互作用的证据,女性收缩压水平和CAC数量均存在基因-基因相互作用的证据。
我们的研究表明,评估上位性的新方法可能对理解收缩压的复杂遗传学以及亚临床冠状动脉粥样硬化很重要。