Literature DB >> 19665689

Association between sequence variant of c.553 G > T in the apolipoprotein A5 gene and metabolic syndrome, insulin resistance, and carotid atherosclerosis.

Kuo-Liong Chien1, Hsiu-Ching Hsu, Yen-Ching Chen, Ta-Chen Su, Yuan-Teh Lee, Ming-Fong Chen.   

Abstract

Common polymorphism of the apolipoprotein A5 gene (APOA5, c.553G>T) related to metabolic syndrome components, insulin resistance, and carotid atherosclerosis remains unclear. We investigated the associations of the APOA5 c.553G>T gene with various metabolic syndrome components and carotid artery atherosclerosis among family members. A total of 661 participants who provided complete genotyping and carotid artery measures were included in this study. Participants with APOA5 c.553T carrier (GT and TT) were more likely to have higher levels of triglycerides and apolipoprotein B, as well as lower levels of high-density lipoprotein (HDL) cholesterol, than participants with the GG genotype. Individuals who carried T alleles had an increased risk of a high level of triglycerides (multivariate odds ratio [OR], 3.86; 95% confidence interval [CI], 1.98-7.55; P<0.0001) and low levels of HDL cholesterol (OR, 2.32; 95% CI, 1.40-3.86; P=0.0012) compared with those without T alleles. The age was an effect modifier for the association between APOA5 genotype and smoking, alcohol drinking, obesity, and lipid profiles, including total, HDL, and low-density lipoprotein (LDL) cholesterol; triglycerides; and apolipoproteins. In addition, the association between APOA5 genotype and hypertriglyceridemia was significant only in adult groups (OR, 3.53; 95% CI, 1.79-6.94), and the association between APOA5 genotype and low HDL cholesterol was stable in young adolescents (OR, 2.39; 95% CI, 1.19-4.78) and adults (OR, 2.20; 95% CI, 1.17-4.15). Our findings indicated that the APOA5 c.553G>T polymorphism is associated with high triglycerides and low HDL cholesterol but not with other metabolic syndrome components or carotid atherosclerosis in this ethnic Chinese population.

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Year:  2009        PMID: 19665689     DOI: 10.1016/j.trsl.2009.06.005

Source DB:  PubMed          Journal:  Transl Res        ISSN: 1878-1810            Impact factor:   7.012


  7 in total

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Journal:  Ann Hum Genet       Date:  2018-07-19       Impact factor: 1.670

Review 2.  The paradox of ApoA5 modulation of triglycerides: evidence from clinical and basic research.

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Journal:  Clin Biochem       Date:  2012-09-19       Impact factor: 3.281

3.  Mosaicism of mitochondrial genetic variation in atherosclerotic lesions of the human aorta.

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Journal:  Biomed Res Int       Date:  2015-03-05       Impact factor: 3.411

4.  Lack of Evidence of the Role of APOA5 3'UTR Polymorphisms in Iranian Children and Adolescents with Metabolic Syndrome.

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5.  Association of single nucleotide polymorphisms with dyslipidemia in antiretroviral exposed HIV patients in a Ghanaian population: A case-control study.

Authors:  Christian Obirikorang; Emmanuel Acheampong; Lawrence Quaye; Joseph Yorke; Ernestine Kubi Amos-Abanyie; Priscilla Abena Akyaw; Enoch Odame Anto; Simon Bannison Bani; Evans Adu Asamoah; Emmanuella Nsenbah Batu
Journal:  PLoS One       Date:  2020-01-13       Impact factor: 3.240

6.  Common sequence variants in CD36 gene and the levels of triglyceride and high-density lipoprotein cholesterol among ethnic Chinese in Taiwan.

Authors:  Kuo-Liong Chien; Hsiu-Ching Hsu; Pi-Hua Liu; Hung-Ju Lin; Ming-Fong Chen
Journal:  Lipids Health Dis       Date:  2012-12-18       Impact factor: 3.876

7.  Relationship between Serum Kallistatin and Afamin and Anthropometric Factors Associated with Obesity and of Being Overweight in Patients after Myocardial Infarction and without Myocardial Infarction.

Authors:  Grzegorz Józef Nowicki; Barbara Ślusarska; Maciej Polak; Katarzyna Naylor; Tomasz Kocki
Journal:  J Clin Med       Date:  2021-12-10       Impact factor: 4.241

  7 in total

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