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Both alleles of the M235T polymorphism of the angiotensinogen gene can be a risk factor for myocardial infarction
Author(s) -
FernándezArcás N,
DieguezLucena JL,
MuñozMorán E,
RuizGaldón M,
EspinosaCaliani S,
ArandaLara P,
RiusDiaz F,
GaitánArroyo MJ,
De TeresaGalván E,
ReyesEngel A
Publication year - 2001
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1034/j.1399-0004.2001.600108.x
Subject(s) - genotype , medicine , allele , odds ratio , myocardial infarction , endocrinology , risk factor , angiotensin converting enzyme , polymorphism (computer science) , allele frequency , angiotensin ii , biology , genetics , gene , receptor , blood pressure
We have studied the role of three polymorphic genes of the renin‐angiotensin system (RAS) as independent risk factors for myocardial infarction (MI) and their correlation with three of the major coronary risk factors: serum cholesterol (CH), hypertension (HT) and smoking (SM). A population of 392 men was genotyped for the M235T polymorphism of the angiotensinogen ( AGT ) gene, the insertion/deletion of the angiotensin‐converting enzyme ( ACE ) and the all66c of the angiotensin‐II type 1 receptor ( AT 1 R ), by means of polymerase chain reaction (PCR) and restriction enzyme analysis. It was observed that the T allele frequency increased significantly in the MI with HT, CH, and SM subgroup (0.58 vs 0.31) (p<0.01). In contrast, the M allele frequency was higher in the MI without HT, CH, and SM (0.69 vs 0.42) (p<0.01). A strong association between the MM genotype and MI (p<0.001, odds ratio=4.29, confidence interval=1.95–9.42) was found when age‐matched MM control subjects were compared to MI individuals with none of the other known major coronary risk factors. Futhermore, subjects with the MM genotype showed a significantly higher plasma renin activity (PRA) profile than those with the TT genotype (p<0.001). It can be concluded that the M allele is an independent risk factor for MI and the T allele modified the risk when other major risk factors are present.