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

被引:6
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
    Berger, J
    Moller, DE
    [J]. 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
    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.
    [J]. 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
    Chehaibi, Khouloud
    Hrira, Mohamed Yahia
    Rouis, Mustapha
    Najah, Mohamed
    Jguirim-Souissi, Imen
    Nouira, Samir
    Slimane, Mohamed Naceur
    [J]. JOURNAL OF MOLECULAR NEUROSCIENCE, 2013, 50 (02) : 360 - 367
  • [5] Hypermethylation of EDNRB promoter contributes to the risk of colorectal cancer
    Chen, Cheng
    Wang, Lingyan
    Liao, Qi
    Huang, Yi
    Ye, Huadan
    Chen, Fei
    Xu, Leiting
    Ye, Meng
    Duan, Shiwei
    [J]. DIAGNOSTIC PATHOLOGY, 2013, 8
  • [6] Peroxisome Proliferator-Activated Receptor Genetic Polymorphisms and Nonalcoholic Fatty Liver Disease: Any Role in Disease Susceptibility?
    Dongiovanni, Paola
    Valenti, Luca
    [J]. 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
    Du, Wan
    Li, Jing
    Fan, Ning
    Shang, Panfeng
    Wang, Zhiping
    Ding, Hui
    [J]. AGING MALE, 2014, 17 (02) : 107 - 111
  • [8] The role of PPARs in atherosclerosis
    Duval, C
    Chinetti, G
    Trottein, F
    Fruchart, JC
    Staels, B
    [J]. TRENDS IN MOLECULAR MEDICINE, 2002, 8 (09) : 422 - 430
  • [9] Peroxisome proliferator-activated receptor delta and cardiovascular disease
    Ehrenborg, Ewa
    Skogsberg, Josefin
    [J]. 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
    Excoffier, Laurent
    Lischer, Heidi E. L.
    [J]. MOLECULAR ECOLOGY RESOURCES, 2010, 10 (03) : 564 - 567