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Positive Association between APOA5 rs662799 Polymorphism and Coronary Heart Disease: A Case-Control Study and Meta-Analysis

OBJECTIVE: Apolipoprotein A5 (APOA5) is associated with plasma triglyceride (TG) levels, a risk factor for coronary heart disease (CHD). This study explored the association between CHD and the APOA5 rs662799 polymorphism. METHODS: We collected 1,521 samples (783 CHD patients and 738 controls) for th...

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Detalles Bibliográficos
Autores principales: Ye, Huadan, Zhou, Annan, Hong, Qiangxiao, Tang, Linlin, Xu, Xuting, Xin, Yanfei, Jiang, Danjie, Dai, Dongjun, Li, Yirun, Wang, Dao Wen, Duan, Shiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550406/
https://www.ncbi.nlm.nih.gov/pubmed/26309253
http://dx.doi.org/10.1371/journal.pone.0135683
Descripción
Sumario:OBJECTIVE: Apolipoprotein A5 (APOA5) is associated with plasma triglyceride (TG) levels, a risk factor for coronary heart disease (CHD). This study explored the association between CHD and the APOA5 rs662799 polymorphism. METHODS: We collected 1,521 samples (783 CHD patients and 738 controls) for this case-control study. Meta-analysis was performed using Review Manager Software and Stata Software. RESULTS: Significant differences were observed between CHD cases and controls at the level of both genotype (χ(2) = 8.964, df = 2, P = 0.011) and allele (χ(2) = 9.180, df = 1, P = 0.002, OR = 1.275, 95% CI = 1.089–1.492). A breakdown analysis by gender showed a significant association of APOA5 rs662799 with CHD in males (χ(2) = 7.770, df = 1, P = 0.005; OR = 1.331, 95% CI = 1.088–1.628). An additional meta-analysis using 21378 cases and 28428 controls established that rs662799 is significantly associated with CHD (P < 0.00001). CONCLUSION: Both our case-control study and meta-analysis confirm a significant association between APOA5 rs662799 and CHD. In addition, our results suggest a male-specific association between the APOA5 rs662799 polymorphism and CHD.