Medical School, Hangzhou Normal University, Hangzhou 310000, China.
Medical School, Shihezi University, Shihezi 832000, China.
Int J Environ Res Public Health. 2019 Mar 4;16(5):786. doi: 10.3390/ijerph16050786.
Coronary artery disease has become a major health concern over the past several decades. We aimed to explore the association of single nucleotide polymorphisms (SNPs) in the ATP-binding cassette subfamily A member 1 () and lifestyle factors with coronary artery disease (CAD) in dyslipidemia. This nested case-control study included 173 patients with CAD and 500 matched control individuals (1:3, case: control) from a district in southern China. We collected medical reports, lifestyle details, and blood samples of individuals with dyslipidemia and used the polymerase chain reaction-ligase detection reaction method to genotype the SNPs. The CC genotype of the additive and recessive models of rs4149339, together with regular intake of fried foods or dessert, increased the risk of CAD (adjusted odd ratio (OR) = 1.91, = 0.030; adjusted OR = 1.97, = 0.017; adjusted OR = 1.80, = 0.002; adjusted OR = 1.98, = 0.001). The AT + AA genotype of the dominant model of rs4743763 and moderate/heavy physical activity reduced the risk of CAD (adjusted OR = 0.66, = 0.030; adjusted OR = 0.44, = 0.001). The CT + CC genotype of the dominant model of rs2472386 reduced the risk of CAD only in males (adjusted OR = 0.36, = 0.001). The interaction between rs4149339 and rs4743763 of and haplotype CTT (comprising rs4149339, rs4743763, and rs2472386) appeared to increase the risk of CAD (relative excess risk due to interaction (RERI) = 3.19, = 0.045; OR = 1.49, = 0.019). Polymorphisms of rs4149339, rs4743763 and rs2472386 in and three lifestyle factors (physical activity, fried food intake, and dessert intake) were associated with CAD in people with dyslipidemia in southern China. These results provide the theoretical basis for gene screening and the prevention of chronic cardiovascular diseases.
在过去的几十年中,冠状动脉疾病已成为一个主要的健康关注点。我们旨在探讨单核苷酸多态性(SNP)在 ATP 结合盒亚家族 A 成员 1(ABCA1)中的作用以及生活方式因素与血脂异常患者冠状动脉疾病(CAD)之间的关联。这项巢式病例对照研究包括 173 名 CAD 患者和 500 名匹配的对照个体(1:3,病例对照),他们来自中国南方的一个地区。我们收集了血脂异常患者的医疗报告、生活方式细节和血液样本,并使用聚合酶链反应-连接酶检测反应方法对 SNP 进行基因分型。rs4149339 的加性和隐性模型的 CC 基因型,以及经常食用油炸食品或甜点,增加了 CAD 的风险(调整后的比值比(OR)=1.91,=0.030;调整后的 OR = 1.97,=0.017;调整后的 OR = 1.80,=0.002;调整后的 OR = 1.98,=0.001)。rs4743763 的显性模型的 AT+AA 基因型和中度/剧烈体力活动降低了 CAD 的风险(调整后的 OR = 0.66,=0.030;调整后的 OR = 0.44,=0.001)。rs2472386 的显性模型的 CT+CC 基因型仅降低了男性 CAD 的风险(调整后的 OR = 0.36,=0.001)。rs4149339 和 rs4743763 之间的相互作用以及包含 rs4149339、rs4743763 和 rs2472386 的单倍型 CTT 似乎增加了 CAD 的风险(交互超额风险归因(RERI)=3.19,=0.045;OR = 1.49,=0.019)。ABCA1 中的 rs4149339、rs4743763 和 rs2472386 多态性以及三种生活方式因素(体力活动、油炸食品摄入和甜点摄入)与中国南方血脂异常患者的 CAD 相关。这些结果为基因筛查和预防慢性心血管疾病提供了理论依据。