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CYP4F2 genetic polymorphisms are associated with coronary heart disease in a Chinese population

BACKGROUND: To explore the relationship between CYP4F2 gene polymorphism and coronary heart disease (CHD) in a Chinese Han population. METHODS: We selected 440 CHD patients and 440 control subjects to perform a case - control study. Four SNPs (rs2108622, rs3093100, rs3093105 and rs3093135) in CYP4F2...

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Detalles Bibliográficos
Autores principales: Yu, Changqing, Yan, Qingkai, Fu, Chunjiang, Shi, Weibin, Wang, Hongyong, Zeng, Chunyu, Wang, Xukai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052825/
https://www.ncbi.nlm.nih.gov/pubmed/24886380
http://dx.doi.org/10.1186/1476-511X-13-83
Descripción
Sumario:BACKGROUND: To explore the relationship between CYP4F2 gene polymorphism and coronary heart disease (CHD) in a Chinese Han population. METHODS: We selected 440 CHD patients and 440 control subjects to perform a case - control study. Four SNPs (rs2108622, rs3093100, rs3093105 and rs3093135) in CYP4F2 gene were genotyped using polymerase chain reaction - restriction fragment length polymorphism (PCR - RFLP) methods. The genotype and haplotype distributions were compared between the case and the control group. RESULTS: We found both rs2108622 and rs3093105 in CYP4F2 gene were associated with the risk for CHD (P <0.01). Haplotype analysis indicated that GGGT haplotype consisted by rs2108622-rs3093100-rs3093105-rs3093135 was associated with CHD risk (OR = 4.367, 95% CI: 2.241 ~ 8.510; P < 0.001), but GGTA haplotype was associated with decreased risk for CHD (OR = 0.450, 95% CI: 0.111 ~ 0.777; P <0.001). CONCLUSION: CYP4F2 gene polymorphisms were associated with the risk of CHD in Chinese population.