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干扰素调节因子 5 () 基因单倍型与早发性冠心病相关。多态性与心脏代谢参数的关联。动脉粥样硬化疾病的遗传学 (GEA) 墨西哥研究。

Interferon Regulatory Factor 5 () Gene Haplotypes Are Associated with Premature Coronary Artery Disease. Association of the Polymorphisms with Cardiometabolic Parameters. The Genetics of Atherosclerotic Disease (GEA) Mexican Study.

机构信息

Department of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez, 14080 Mexico City, Mexico.

Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, 14080 Mexico City, Mexico.

出版信息

Biomolecules. 2021 Mar 17;11(3):443. doi: 10.3390/biom11030443.

Abstract

Interferon regulatory factor 5 () has an important role in the inflammatory process, a fundamental component of coronary artery disease (CAD). Thus, the objective of this study was to evaluate the association of polymorphisms with the development of premature CAD (pCAD) and cardiometabolic parameters. polymorphisms (rs1874330, rs3778754, rs3757386, rs3757385, rs3807134, rs3807135, and rs6968563) were determined in 1116 pCAD patients and 1003 controls. Polymorphism distribution was similar in patients and controls; however, the haplotype analysis showed five haplotypes with a different distribution. (OR (odds ratio) = 1.248, = 0005) and (OR = 10.73, < 0.0001) were associated with a high risk, whereas (OR = 0.155, < 0.0001), (OR = 0.108, < 0.0001), and (OR = 0.014, < 0.0001) were associated with a low risk of pCAD. Associations with aspartate aminotransferase, hypertriglyceridemia, magnesium deficiency, triglycerides/HDL-C index, LDL-C, and adiponectin levels were observed in pCAD patients. In controls, associations with hypoalphalipoproteinemia, non-HDL-C, apolipoprotein B, hyperuricemia, TNF-α, IL-6, IL-15, valvular calcification, and subclinical hypothyroidism were observed. In summary, five haplotypes were associated with pCAD, two with high risk and three with low risk. Some polymorphisms were associated with cardiometabolic parameters in pCAD patients and control.

摘要

干扰素调节因子 5 () 在炎症过程中具有重要作用,而炎症是冠状动脉疾病 (CAD) 的一个基本组成部分。因此,本研究旨在评估 多态性与早发 CAD (pCAD) 及心脏代谢参数的相关性。在 1116 例 pCAD 患者和 1003 例对照中,测定了 多态性(rs1874330、rs3778754、rs3757386、rs3757385、rs3807134、rs3807135 和 rs6968563)。患者与对照组的多态性分布相似,但单体型分析显示,有 5 种不同分布的单体型。 (OR (比值比) = 1.248, = 0005) 和 (OR = 10.73, < 0.0001) 与高风险相关,而 (OR = 0.155, < 0.0001)、 (OR = 0.108, < 0.0001) 和 (OR = 0.014, < 0.0001) 与 pCAD 的低风险相关。在 pCAD 患者中观察到与天冬氨酸转氨酶、高甘油三酯血症、镁缺乏、甘油三酯/高密度脂蛋白胆固醇指数、LDL-C 和脂联素水平相关的相关性。在对照组中,观察到与低高密度脂蛋白血症、非高密度脂蛋白胆固醇、载脂蛋白 B、高尿酸血症、TNF-α、IL-6、IL-15、瓣膜钙化和亚临床甲状腺功能减退症相关的相关性。总之,有 5 种单体型与 pCAD 相关,其中 2 种与高风险相关,3 种与低风险相关。一些 多态性与 pCAD 患者和对照组的心脏代谢参数相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3503/8002496/c43beb943d84/biomolecules-11-00443-g001.jpg

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