APOC3/A5 haplotypes, lipid levels, and risk of myocardial infarction in the Central Valley of Costa Rica

 

Kaydedildi:
Detaylı Bibliyografya
Yazarlar: Ruiz Narváez, Edward A., Yang, Yadong, Nakanishi, Yukiko, Kirchdorfer, Jill, Campos Núñez, Hannia
Materyal Türü: artículo original
Yayın Tarihi:2005
Diğer Bilgiler:Genetic variation in the APOC3 and APOA5 genes has been associated with plasma triglyceride concentrations and may affect the risk of myocardial infarction (MI). To assess whether APOC3/A5 haplotypes are associated with risk of MI, we examined three single-nucleotide polymorphisms (SNPs) in APOC3 (3238C>G, −455T>C, and −482C>T) and six SNPs in the APOA5 gene (−1131T>C, c.−3A>G, c.56C>G, IVS3+476G>A, c.553G>T, and c.1259T>C) in incident cases (n = 1,703) of a first nonfatal MI matched for gender, age, and area of residence with population-based controls (n = 1,703). Conditional logistic regression models, adjusted for potential environmental confounders, were used for analysis. The common APOC3*222 haplotype was more frequent in cases than in controls (17.4% and 13.7%, respectively, P < 0.001) and was associated with increased risk of MI [odds ratio (OR) = 1.27; 95% confidence interval (95% CI), 1.09, 1.48] compared with APOC3*111 wild-type haplotype. This association was independent of the APOA5 SNPs. Although the APOC3 3238G, APOA5 −1131C, APOA5 c.−3G, and APOA5 c.1259C alleles were associated with higher triglyceride plasma concentrations, these effects could not explain the associations with MI in this population. In summary, this study supports the hypothesis that haplotypes in the APOC3 gene but not in the APOA5 gene increase susceptibility to MI.
Ülke:Kérwá
Kurum:Universidad de Costa Rica
Repositorio:Kérwá
OAI Identifier:oai:kerwa.ucr.ac.cr:10669/81228
Online Erişim:https://www.jlr.org/content/46/12/2605.full?sid=dd073ae5-e50a-4fd5-8ec2-d9a7535897b9
https://hdl.handle.net/10669/81228
Anahtar Kelime:Infarto de miocardio
Genética
Epidemiología
Factores de riesgo