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Association of a genetic variant in the apolipoprotein A5 gene with the metabolic syndrome in Chinese
Author(s) -
Ong Kwok Leung,
Jiang Chao Qiang,
Liu Bin,
Jin Ya Li,
Tso Annette W.K.,
Tam Sidney,
Wong Ka Sing,
Tomlinson Brian,
Cheung Bernard M.Y.,
Lin Jie Ming,
Yue Xiao Jun,
Lam Karen S.L.,
Lam Tai Hing,
Thomas Graham Neil
Publication year - 2011
Publication title -
clinical endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.055
H-Index - 147
eISSN - 1365-2265
pISSN - 0300-0664
DOI - 10.1111/j.1365-2265.2010.03899.x
Subject(s) - single nucleotide polymorphism , medicine , metabolic syndrome , odds ratio , cohort , apolipoprotein b , endocrinology , snp , obesity , genetics , biology , genotype , cholesterol , gene
Summary Objective Single nucleotide polymorphisms (SNPs) in the apolipoprotein A5 gene ( APOA5 ) are associated with hypertriglyceridaemia in our population. We studied the associations of SNPs in APOA5 with the metabolic syndrome (MetS) in the Hong Kong and Guangzhou Chinese. Methods We genotyped five tagging SNPs in 1330 unrelated subjects from the Hong Kong Cardiovascular Risk Factor Prevalence Study cohort with follow‐up after a median interval of 6·4 years; 1952 subjects from the Guangzhou Biobank Cohort Study‐Cardiovascular Disease Subcohort were used to replicate the findings. The MetS was defined according to the consensus criteria proposed jointly by several organizations in 2009. Results The SNP rs662799 (−1131T>C) was associated with the MetS (odds ratio = 1·47, P = 0·00082) and the number of its components present (regression coefficient = 0·204, P = 4·6 × 10 −5 ) after adjusting for age, sex, smoking, drinking and education in Hong Kong subjects at baseline. Similar association of this SNP was found in Hong Kong subjects at follow‐up ( P = 0·010 and 0·00021, respectively) and in Guangzhou subjects ( P = 0·0041 and 0·017, respectively). The association of rs662799 with the number of the MetS components was significant regardless of age, sex, obesity and alcohol drinking, but almost disappeared after further adjusting for plasma triglycerides. Conclusion Our results showed that the −1131T>C polymorphism in APOA5 was associated with the MetS because of its strong effect on plasma triglycerides. This may partly explain the higher cardiovascular risk in people with this polymorphism.