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Identification of Susceptibility Variants in ADIPOR1 Gene Associated with Type 2 Diabetes, Coronary Artery Disease and the Comorbidity of Type 2 Diabetes and Coronary Artery Disease

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机构: [1]Capital Med Univ, Beijing Inst Heart Lung & Blood Vessels, Anzhen Hosp, Dept Emergency Med, Beijing, Peoples R China; [2]Beijing Hosp, Key Lab Geriatr, Beijing, Peoples R China; [3]Chinese Minist Hlth, Beijing Inst Geriatr, Beijing, Peoples R China; [4]Capital Med Univ, Beijing Ditan Hosp, Dept Cardiol, Beijing, Peoples R China; [5]Capital Med Univ, Beijing Anzhen Hosp, Beijing Inst Heart Lung & Blood Vessels, Dept Cardiol, Beijing, Peoples R China; [6]Capital Med Univ, Beijing You An Hosp, Dept Funct Tests, Beijing, Peoples R China; [7]Jiangbin Hosp, Dept Neurol, Nanning, Peoples R China; [8]Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada; [9]Guangxi Zhuang Autonomous Region Women & Children, Dept Cardiac Surg, Nanning, Peoples R China
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Objective: Adiponectin receptor 1 (encoded by ADIPOR1) is one of the major adiponectin receptors, and plays an important role in glucose and lipid metabolism. However, few studies have reported simultaneous associations between ADIPOR1 variants and type 2 diabetes (T2D), coronary artery disease (CAD) and T2D with CAD. Based on the "common soil'' hypothesis, we investigated whether ADIPOR1 polymorphisms contributed to the etiology of T2D, CAD, or T2D with CAD in a Northern Han Chinese population. Methods: Our multi-disease comparison study enrolled 657 subjects, including 165 with T2D, 173 with CAD, 174 with both T2D and CAD (T2D+CAD), and 145 local healthy controls. Six ADIPOR1 single nucleotide polymorphisms (SNPs) were genotyped and their association with disease risk was analyzed. Results: Multi-case-control comparison identified two ADIPOR1 variants: rs3737884-G, which was simultaneously associated with an increased risk of T2D, CAD, and T2D+CAD (P-value range, 9.80 x 10(-5)-6.30 x 10(-4); odds ratio (OR) range: 1.96-2.42) and 16850797-C, which was separately associated with T2D and T2D+CAD (P-value range: 0.007-0.014; OR range: 1.71-1.77). The risk genotypes of both rs3737884 and 16850797 were consistently associated with common metabolic phenotypes in all three diseases (P-value range: 4.81 x 10(-42)-0.001). We observed an increase in the genetic dose-dependent cumulative risk with increasing risk allele numbers in T2D, CAD and T2D+CAD (P-trend from 1.35 x 10(-5)-0.002). Conclusions: Our results suggest that ADIPOR1 risk polymorphisms are a strong candidate for the " common soil'' hypothesis and could partially contribute to disease susceptibility to T2D, CAD, and T2D with CAD in the Northern Han Chinese population.

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出版当年[2013]版:
大类 | 2 区 生物
小类 | 2 区 综合性期刊
最新[2023]版:
大类 | 3 区 综合性期刊
小类 | 3 区 综合性期刊
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出版当年[2012]版:
Q1 MULTIDISCIPLINARY SCIENCES
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Q1 MULTIDISCIPLINARY SCIENCES

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第一作者机构: [1]Capital Med Univ, Beijing Inst Heart Lung & Blood Vessels, Anzhen Hosp, Dept Emergency Med, Beijing, Peoples R China;
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通讯机构: [2]Beijing Hosp, Key Lab Geriatr, Beijing, Peoples R China; [3]Chinese Minist Hlth, Beijing Inst Geriatr, Beijing, Peoples R China;
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