Positive association between PPARD rs2016520 polymorphism and coronary heart disease in a Han Chinese population

被引:7
作者
Ye, H. D. [1 ]
Li, Y. R. [1 ]
Hong, Q. X. [1 ]
Zhou, A. N. [1 ]
Zhao, Q. L. [2 ]
Xu, L. M. [1 ]
Xu, M. Q. [3 ]
Xu, X. T. [1 ]
Tang, L. L. [1 ]
Dai, D. J. [1 ]
Jiang, D. J. [1 ]
Huang, Y. [1 ]
Wang, D. W. [4 ,5 ]
Duan, S. W. [1 ]
机构
[1] Ningbo Univ, Sch Med, Zhejiang Prov Key Lab Pathophysiol, Ningbo 315211, Zhejiang, Peoples R China
[2] Ningbo Univ, Yinzhou Peoples Hosp, Ningbo 315211, Zhejiang, Peoples R China
[3] Shanghai Jiao Tong Univ, Bio X Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, Shanghai 200030, Peoples R China
[4] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Inst Hypertens, Wuhan 430074, Peoples R China
[5] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Internal Med, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
Coronary heart disease; Meta-analysis; PPARD; Polymorphism; rs2016520; ACTIVATED RECEPTOR-DELTA; ARTERY-DISEASE; RISK-FACTORS; VARIANTS; GENE; ATHEROSCLEROSIS; METAANALYSIS;
D O I
10.4238/2015.June.11.10
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
PPARD encodes peroxisome proliferator-activated receptor delta, which has been shown to play an important role in controlling lipid metabolism and atherosclerosis. In this case-control study, we explored the relationship between PPARD rs2016520 polymorphism and coronary heart disease (CHD) in a Han Chinese population. A total of 657 CHD cases and 640 controls were included in the association study. rs2016520 polymorphism genotyping was performed using the melting temperature-shift polymerase chain reaction method. The PPARD rs2016520-G allele reduced CHD risk by 17.9% (chi(2) = 5.061, P = 0.025, OR = 0.821, 95% CI = 0.692-0.975). Furthermore, a significant difference in CHD risk was observed for the PPARD rs2016520 polymorphism in the dominant model (AG + GG vs AA: chi(2) = 4.751, degrees of freedom (df) = 1, P = 0.029, OR = 0.784, 95% CI = 0.6310.976). Analysis by age suggested that the G-allele decreased CHD risk by 14.8% in ages greater than 65 years (chi(2) = 4.446, P = 0.035, OR = 0.852, 95%CI = 0.684-1.060). In contrast, meta-analysis of PPARD rs2016520 among 3732 cases and 5042 controls revealed no association between PPARD rs2016520 and CHD (P = 0.19). We found that the PPARD rs2016520-GG genotype decreased CHD risk in a Han Chinese population. Moreover, we found an association between serum high-density lipoprotein cholesterol level and PPARD rs2016520 in senior individuals aged = 65 years. The meta-analysis revealed no association between PPARD rs2016520 and CHD, suggesting ethnic differences in the association between the PPARD locus and CHD.
引用
收藏
页码:6350 / 6359
页数:10
相关论文
共 36 条
[1]  
Aberle Jens, 2006, Int J Med Sci, V3, P108
[2]   The mechanisms of action of PPARs [J].
Berger, J ;
Moller, DE .
ANNUAL REVIEW OF MEDICINE, 2002, 53 :409-435
[3]   Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls [J].
Burton, Paul R. ;
Clayton, David G. ;
Cardon, Lon R. ;
Craddock, Nick ;
Deloukas, Panos ;
Duncanson, Audrey ;
Kwiatkowski, Dominic P. ;
McCarthy, Mark I. ;
Ouwehand, Willem H. ;
Samani, Nilesh J. ;
Todd, John A. ;
Donnelly, Peter ;
Barrett, Jeffrey C. ;
Davison, Dan ;
Easton, Doug ;
Evans, David ;
Leung, Hin-Tak ;
Marchini, Jonathan L. ;
Morris, Andrew P. ;
Spencer, Chris C. A. ;
Tobin, Martin D. ;
Attwood, Antony P. ;
Boorman, James P. ;
Cant, Barbara ;
Everson, Ursula ;
Hussey, Judith M. ;
Jolley, Jennifer D. ;
Knight, Alexandra S. ;
Koch, Kerstin ;
Meech, Elizabeth ;
Nutland, Sarah ;
Prowse, Christopher V. ;
Stevens, Helen E. ;
Taylor, Niall C. ;
Walters, Graham R. ;
Walker, Neil M. ;
Watkins, Nicholas A. ;
Winzer, Thilo ;
Jones, Richard W. ;
McArdle, Wendy L. ;
Ring, Susan M. ;
Strachan, David P. ;
Pembrey, Marcus ;
Breen, Gerome ;
St Clair, David ;
Caesar, Sian ;
Gordon-Smith, Katherine ;
Jones, Lisa ;
Fraser, Christine ;
Green, Elain K. .
NATURE, 2007, 447 (7145) :661-678
[4]   Effect of Genetic Polymorphism+294T/C in Peroxisome Proliferator-Activated Receptor Delta on the Risk of Ischemic Stroke in a Tunisian Population [J].
Chehaibi, Khouloud ;
Hrira, Mohamed Yahia ;
Rouis, Mustapha ;
Najah, Mohamed ;
Jguirim-Souissi, Imen ;
Nouira, Samir ;
Slimane, Mohamed Naceur .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2013, 50 (02) :360-367
[5]   Hypermethylation of EDNRB promoter contributes to the risk of colorectal cancer [J].
Chen, Cheng ;
Wang, Lingyan ;
Liao, Qi ;
Huang, Yi ;
Ye, Huadan ;
Chen, Fei ;
Xu, Leiting ;
Ye, Meng ;
Duan, Shiwei .
DIAGNOSTIC PATHOLOGY, 2013, 8
[6]   Peroxisome Proliferator-Activated Receptor Genetic Polymorphisms and Nonalcoholic Fatty Liver Disease: Any Role in Disease Susceptibility? [J].
Dongiovanni, Paola ;
Valenti, Luca .
PPAR RESEARCH, 2013, 2013
[7]   Efficacy and safety of mirodenafil for patients with erectile dysfunction: a meta-analysis of three multicenter, randomized, double-blind, placebo-controlled clinical trials [J].
Du, Wan ;
Li, Jing ;
Fan, Ning ;
Shang, Panfeng ;
Wang, Zhiping ;
Ding, Hui .
AGING MALE, 2014, 17 (02) :107-111
[8]   The role of PPARs in atherosclerosis [J].
Duval, C ;
Chinetti, G ;
Trottein, F ;
Fruchart, JC ;
Staels, B .
TRENDS IN MOLECULAR MEDICINE, 2002, 8 (09) :422-430
[9]   Peroxisome proliferator-activated receptor delta and cardiovascular disease [J].
Ehrenborg, Ewa ;
Skogsberg, Josefin .
ATHEROSCLEROSIS, 2013, 231 (01) :95-106
[10]   Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows [J].
Excoffier, Laurent ;
Lischer, Heidi E. L. .
MOLECULAR ECOLOGY RESOURCES, 2010, 10 (03) :564-567