Cao Maolin, Zhang Yifei, Chen Dan, Zhong Jiaju, Zhang Xiaoli, Yang Ling, Li Xue, Fang Liang, Liu Beizhong, Gong Fang, Zhou Chanjuan
Central Laboratory, Yongchuan Hospital of Chongqing Medical University, Chongqing, China.
Chongqing Clinical Research Center for Geriatric Disease, Chongqing, China.
Front Genet. 2023 Apr 6;14:1056186. doi: 10.3389/fgene.2023.1056186. eCollection 2023.
Dyslipidemia is an independent predictor of ischemic stroke (IS). Genetic variations in lipid-metabolism related genes may increase the risk of IS. Fatty acid-binding protein 1 (FABP1) and fatty acid-binding protein 2 (FABP2) are lipid chaperones responsible for lipid transport and metabolism. The present study aimed to determine the association between or and ischemic stroke. A total of 251 participants were recruited composed of 138 patients with ischemic stroke and 113 healthy subjects. DNA was extracted from peripheral blood samples. The rs2241883 polymorphism in and rs1799883 polymorphism in were genotyped using polymerase chain reaction-restriction fragment length polymorphism. Generalized multifactor dimensionality reduction (GMDR) was used to find out the interaction combinations between two SNPs and environmental factors. The GA genotype of FABP2 rs1799883 increased susceptibility to ischemic stroke under overdominant inheritance model ( = 0.042). After adjusting for the risk factors of IS, it was associated with a significantly higher risk of IS in the codominant inheritance model (adjust OR = 3.431, 95%CI = 1.060-11.103, = 0.04). The interactions of rs2241883 and rs1799883 were not associated with IS risk ( = 0.172). Moreover, interaction analysis of two genes (rs1799883 and rs2241883) and two environmental factors (smoking and alcohol consumption) was associated with an increased risk of IS ( = 0.011). The GA genotype of FABP2 rs1799883, interactions between rs1799883, rs2241883 and smoking and alcohol consumption were associated with IS risk in Chinese Han populations.
血脂异常是缺血性卒中(IS)的独立预测因素。脂质代谢相关基因的遗传变异可能会增加IS的风险。脂肪酸结合蛋白1(FABP1)和脂肪酸结合蛋白2(FABP2)是负责脂质运输和代谢的脂质伴侣蛋白。本研究旨在确定FABP1和FABP2与缺血性卒中之间的关联。共招募了251名参与者,其中包括138例缺血性卒中患者和113名健康受试者。从外周血样本中提取DNA。使用聚合酶链反应-限制性片段长度多态性方法对FABP1的rs2241883多态性和FABP2的rs1799883多态性进行基因分型。采用广义多因素降维法(GMDR)来找出两个单核苷酸多态性(SNP)与环境因素之间的相互作用组合。在超显性遗传模型下,FABP2 rs1799883的GA基因型增加了对缺血性卒中的易感性(P = 0.042)。在校正IS的危险因素后,在共显性遗传模型中,它与IS的风险显著升高相关(校正后的比值比= 3.431,95%可信区间= 1.060 - 11.103,P = 0.04)。FABP1 rs2241883和FABP2 rs1799883的相互作用与IS风险无关(P = 0.172)。此外,两个基因(rs1799883和rs2241883)与两个环境因素(吸烟和饮酒)的相互作用分析显示与IS风险增加相关(P = 0.011)。在中国汉族人群中,FABP2 rs1799883的GA基因型、rs1799883、rs2241883与吸烟和饮酒之间的相互作用与IS风险相关。