C771G (His241Gln) Polymorphism of MLXIPL Gene, TG levels and coronary artery disease: A case control study

被引:10
作者
Ghasemi, Asghar [1 ]
Aghajani, Hasan [2 ]
Fallah, Soudabeh [1 ]
Assadi, Mehrdad [3 ]
Seifi, Morteza [1 ,4 ]
机构
[1] Univ Tehran Med Sci, Fac Med, Dept Biochem, Tehran, Iran
[2] Univ Tehran Med Sci, Fac Med, Ctr Heart, Tehran, Iran
[3] Univ Tehran Med Sci, Fac Publ Hlth, Dept Med Mycol & Parasitol, Tehran, Iran
[4] Univ Alberta, Dept Med Genet, Edmonton, AB, Canada
关键词
coronary artery disease; MLXIPL; polymorphism; ELEMENT-BINDING PROTEIN; MYOCARDIAL-INFARCTION; TRANSCRIPTION FACTOR; TRIGLYCERIDE LEVELS; CHREBP; POPULATION; EXPRESSION; GENOMICS; CHINESE; LIVER;
D O I
10.5152/akd.2014.5135
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective: It is suggested that C771G (His241Gln) polymorphism of MLXIPL gene might be a genetic risk factor for coronary artery disease (CAD); therefore, the aim of the present study was to investigate the association between C771G polymorphism of MLXIPL gene and the pathogenesis of CAD in Iranian patients with coronary artery stenosis and control subjects. Methods: Two hundred and five patients with coronary artery stenosis and 195 healthy control subjects were included in this study. MLXIPL genotypes were determined by polymerase chain reaction and restriction fragment length polymorphism (RFLP). Results: There was an association between the MLXIPL polymorphism and quantitative lipid traits in patient group. Distribution of the CC genotype of MLXIPL was more frequent in patients, (chi(2)=5.13; p<0.005) and after adjustment for classical CAD risk factors, the MLXIPL CC genotype was independently associated with CAD (OR=1.98, 95% CI, 1.12-4.11; p=0.02). Distribution of MLXIPL genotypes were significantly different as compared with the severity of stenosis (chi(2)=6.34; p<0.05). Conclusion: These results suggest that C771G polymorphism of MLXIPL gene is associated with stenosis and its severity.
引用
收藏
页码:8 / 12
页数:5
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