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rs2048327-G 载脂蛋白携带者的低 HDL 浓度可能使男性易患冠心病:德黑兰心脏代谢遗传研究(TCGS)。

Low HDL concentration in rs2048327-G carriers can predispose men to develop coronary heart disease: Tehran Cardiometabolic genetic study (TCGS).

机构信息

Cellular and Molecular Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Cellular and Molecular Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Gene. 2021 Apr 30;778:145485. doi: 10.1016/j.gene.2021.145485. Epub 2021 Feb 11.

Abstract

Recent genome-wide association studies (GWAS) highlighted the importance of genetic variations on SLC22A3 and MIA3 genes in developing coronary heart disease (CHD) among different ethnicities. However, the influence of these variations is not recognized within the Iranian population. Hence, in the present study, we aim to investigate two key single nucleotide polymorphisms (SNPs) on CHD incidence in this population. For this purpose, from Tehran Cardiometabolic Genetic Study (TCGS), 453 individuals with CHD were selected as a case and 453 individuals as a control that matched their age and gender. After quality control of two selected SNPs, rs2048327 (SLC22A3) and rs17465637 (MIA3), we used genotyps resulted from chip-typing technology and conducted the logistic regression analysis adjusted for non-genetic risk factors to detect the possible association of these SNPs with the CHD development. Our findings demonstrated the rs2048327-G and rs17465637-C can significantly increase the risk of CHD development about two times in only males and females, respectively. Interestingly, in the male carriers of the risk allele (G) of rs2048327, the low high-density lipoprotein (HDL) level can significantly predispose them to develop coronary heart disease in the future. According to our results, paying more attention to gender and genetic markers can help more efficient coronary heart disease screening and diagnosis.

摘要

最近的全基因组关联研究(GWAS)强调了 SLC22A3 和 MIA3 基因的遗传变异在不同种族中发生冠心病(CHD)的重要性。然而,这些变异在伊朗人群中尚未得到认可。因此,在本研究中,我们旨在研究这一人群中两个关键的单核苷酸多态性(SNP)对 CHD 发病的影响。为此,我们从德黑兰心脏代谢遗传研究(TCGS)中选择了 453 名 CHD 患者作为病例组,453 名年龄和性别相匹配的个体作为对照组。对两个选定的 SNP(rs2048327[ SLC22A3 ]和 rs17465637[ MIA3 ])进行质量控制后,我们使用芯片分型技术获得的基因型,并进行了经非遗传风险因素调整的 logistic 回归分析,以检测这些 SNP 与 CHD 发展之间的可能关联。我们的研究结果表明,rs2048327-G 和 rs17465637-C 仅在男性和女性中分别显著增加 CHD 发病风险约两倍。有趣的是,在 rs2048327 风险等位基因(G)的男性携带者中,低水平的高密度脂蛋白(HDL)可显著增加其未来发生冠心病的风险。根据我们的研究结果,关注性别和遗传标志物可以帮助更有效地进行冠心病筛查和诊断。

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