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XKR6 rs7014968 SNP Increases Serum Total Cholesterol Levels and the Risk of Coronary Heart Disease and Ischemic Stroke

机译:XKR6 RS7014968 SNP增加血清总胆固醇水平和冠心病风险和缺血性卒中的风险

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The X Kell blood group complex subunit-related family member 6 (XKR6) gene single-nucleotide polymorphisms (SNPs) have been associated with serum lipid profiles and the risk of coronary heart disease (CHD) and ischemic stroke (IS) in several previous studies, but the association between the XKR6 rs7014968 SNP and serum lipid levels and the risk of CHD and IS has not been detected previously. This study aims to explore the association between the XKR6 rs7014968 SNP and serum lipid traits and the susceptibility to CHD and IS in the Guangxi Han Chinese population. Snapshot technology was used to determine the genotypes of the XKR6 rs7014968 SNP in 624 controls, 588 patients with CHD, and 544 patients with IS. The XKR6 rs7014968C allele carriers in the control group had higher serum total cholesterol (TC) levels than the C allele noncarriers (P = .025). The XKR6 rs7014968C allele carriers also had an increased risk of CHD and IS (P 60 years, body mass index (BMI) 24 kg/m 2 , and hypertension subgroups had a higher risk of CHD than those in the subgroup counterparts. The patients with the rs7014968C allele in the male, BMI 24 kg/m 2 , smoker, and hypertension subgroups also had a higher risk of IS than those in the subgroup counterparts. These results suggest that the XKR6 rs7014968 SNP is likely to increase the risk of CHD and IS by increasing serum TC levels in our study populations.
机译:X kell血液组复杂亚基相关的家庭成员6(XKR6)基因单核苷酸多态性(SNPs)已经与血清脂质谱和冠心病(CHD)和缺血性中风(IS)的风险有关但先前,XKR6 RS7014968 SNP和血清脂质水平与血清​​脂质水平之间的关联以及尚未检测到CHD的风险。本研究旨在探讨XKR6 RS7014968 SNP和血清脂质特征的关联以及对CHD的易感性,是在广西汉族人口中。 Snapshot技术用于确定XKR6 RS7014968 SNP的基因型,在624次控制中,588例CHD患者和544名患者。对照组的XKR6 RS7014968C等位基因载体具有比C等位基因非载体(P = .025)更高的血清总胆固醇(TC)水平。 XKR6 RS7014968C等位基因载体也具有增加的CHD风险,并且是(P 60岁,体重指数(BMI)> 24kg / m 2,高血压亚组的风险较高,而不是亚组对应物中的那些。患者在雄性,BMI> 24公斤/平方米,吸烟者和高血压子群中的rs7014968C等位基因也比亚组对应物中的风险更高。这些结果表明XKR6 RS7014968 SNP可能会增加风险CHD并通过增加我们的研究人口中的血清TC水平。

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