Analysis of the genetic association between IL27 variants and coronary artery disease in a Chinese Han population

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作者
Qian Fan
Shaofang Nie
Sihui Li
Yuhua Liao
Hongsong Zhang
Lingfeng Zha
Fan Wang
Tingting Tang
Ni Xia
Chengqi Xu
Pengyun Wang
Tian Xie
Jiangjiao Xie
Qiulun Lu
Qingxian Li
Jin Qian
Bin Li
Gang Wu
Yanxia Wu
Yan Yang
Qing K. Wang
Xin Tu
Xiang Cheng
机构
[1] Laboratory of Cardiovascular Immunology,Department of Biostatistics and Epidemiology
[2] Institute of Cardiology,Department of Medicine
[3] Union Hospital,Department of Cardiology
[4] Tongji Medical College,Department of Cardiology
[5] Huazhong University of Science and Technology,Department of Cardiology
[6] University of Pennsylvania,undefined
[7] Key Laboratory of Molecular Biophysics of Ministry of Education,undefined
[8] College of Life Science and Technology,undefined
[9] Center for Human Genome Research,undefined
[10] Cardio-X Institute,undefined
[11] Huazhong University of Science and Technology,undefined
[12] Section of Molecule Medicine,undefined
[13] University of Oklahoma Health Sciences Center,undefined
[14] Jining Medical College Affiliated Hospital,undefined
[15] Suizhou Central Hospital,undefined
[16] Xiangyang Central Hospital,undefined
[17] Renmin Hospital of Wuhan University,undefined
[18] Wuhan No. 1 Hospital,undefined
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摘要
Interleukin-27 (IL-27) is an important cytokine in inflammatory diseases, including coronary artery disease (CAD). To explore the precise role of IL-27 in CAD, we investigated the genetic association between IL27 and CAD in the GeneID Chinese Han population. A two-stage case control association analysis was performed for 3075 CAD cases and 2802 controls. Logistic regression analysis was used to adjust the traditional risk factors for CAD. Results showed that a promoter variant, rs153109, tended to be marginally associated with CAD in the discovery population (Padj = 0.028, OR = 1.27, 95%CI: 1.03–1.58). However, this association was not replicated in the validation stage (Padj = 0.559, OR = 1.04, 95%CI: 0.90–1.21). In addition, when we classified the combined population into two subgroups according to the age at disease onset or disease state, we again obtained no significant associations. Finally, we estimated the severity of coronary stenosis using the Gensini Scoring system and determined that the rs153109 genotypes were still not associated with the Gensini scores of the CAD patients. In conclusion, our study failed to find an association between common variants in the functional region of IL27 and CAD in a Chinese Han population, which indicated that IL-27 might only be an inflammatory marker during the development of CAD.
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