Li Qu, Liu Xu, Zhu Ruixia, He Zhiyi
Department of Neurology, First Affiliated Hospital of China Medical University, Shenyang, China.
Department of Neurology, First Affiliated Hospital of China Medical University, Shenyang, China.
J Stroke Cerebrovasc Dis. 2015 Jun;24(6):1397-404. doi: 10.1016/j.jstrokecerebrovasdis.2015.02.024. Epub 2015 Apr 15.
The adenosine triphosphate (ATP)-binding cassette transporter G1 (ABCG1), a member of the superfamily of ATP-binding cassette transporters, is involved in the transport of cholesterol and phospholipids in macrophages. As such, ABCG1 plays a crucial role in the development of atherosclerosis in humans. In this study, we investigate the association between ABCG1 polymorphisms and the risk of developing ischemic stroke in a Chinese Han population.
This case-control study included 389 ischemic stroke patients and 380 healthy subjects. ABCG1 rs1378577 and rs57137919 polymorphisms were analyzed by a polymerase chain reaction-ligation detection reaction.
We found that the genotypic distribution and allelic frequency of these polymorphisms were similar in patients and controls. In a subgroup with hypertriglyceridemia (144 patients and 115 controls), the frequency of rs1378577 GG genotype and G allele as well as rs57137919 AA genotype was lower in the patient group compared with that in the control group (P = .018, P = .035, and P = .023, respectively). Logistic regression analysis revealed a reduced risk of ischemic stroke in a recessive model for both rs1378577 and rs57137919. Subtype analyses demonstrated that rs1378577 TG and GG genotypes and the G allele were associated with reduced risk of atherothrombotic stroke (P = .030, P = .006, and P = .004, respectively), even after adjusting for confounding factors in a dominant model.
Data from the present study demonstrate that ABCG1 polymorphisms are associated with reduced risk of developing ischemic stroke in hypertriglyceridemic population and atherothrombotic stroke in this cohort of Chinese Han population.
三磷酸腺苷(ATP)结合盒转运体G1(ABCG1)是ATP结合盒转运体超家族的成员之一,参与巨噬细胞中胆固醇和磷脂的转运。因此,ABCG1在人类动脉粥样硬化的发展中起着关键作用。在本研究中,我们调查了ABCG1基因多态性与中国汉族人群缺血性中风发病风险之间的关联。
本病例对照研究纳入了389例缺血性中风患者和380例健康受试者。通过聚合酶链反应-连接检测反应分析ABCG1 rs1378577和rs57137919基因多态性。
我们发现这些多态性的基因型分布和等位基因频率在患者和对照组中相似。在高甘油三酯血症亚组(144例患者和115例对照)中,患者组rs1378577 GG基因型和G等位基因以及rs57137919 AA基因型的频率低于对照组(分别为P = 0.018、P = 0.035和P = 0.023)。逻辑回归分析显示,在rs1378577和rs57137919的隐性模型中,缺血性中风风险降低。亚组分析表明,即使在显性模型中调整混杂因素后,rs1378577 TG和GG基因型以及G等位基因与动脉粥样硬化血栓形成性中风风险降低相关(分别为P = 0.030、P = 0.006和P = 0.004)。
本研究数据表明,ABCG1基因多态性与高甘油三酯血症人群缺血性中风发病风险降低以及该中国汉族人群队列中的动脉粥样硬化血栓形成性中风风险降低相关。