C. Hengstenberg et al., Evaluation of the aldosterone synthase (CYP11B2) gene polymorphism in patients with myocardial infarction, HYPERTENSIO, 35(3), 2000, pp. 704-709
Citations number
20
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Left ventricular remodeling after myocardial infarction involves activation
of the renin-angiotensin-aldosterone system. Recently,the biallelic -344T/
C polymorphism of the aldosterone synthase gene was associated with increas
ed aldosterone levels, arterial hypertension, diastolic dysfunction, and le
ft ventricular dilatation. We hypothesized that this polymorphism may also
affect left ventricular geometry and function after myocardial infarction.
By using a standardized questionnaire, as well as anthropometric and echoca
rdiographic measurements, we thus studied 606 patients (533 men and 73 wome
n) who had a myocardial infarction before the age of 60 years. The aldoster
one synthase gene polymorphism was analyzed after polymerase chain reaction
amplification and restriction enzyme digestion. The results demonstrated t
hat there was no association of the aldosterone synthase gene polymorphism
with echocardiographically determined left ventricular dimensions, wall thi
cknesses, or indexes of systolic or diastolic function. Furthermore, anthro
pometric data, including blood pressure levels, were balanced between the d
ifferent genotypes. Finally, the allele frequency was similar for patients
with myocardial infarction and a sample group from the normal population (n
=1675). The data indicate that the allele status of the aldosterone synthas
e gene polymorphism is not useful for the identification of patients with m
yocardial infarction who have impaired left ventricular function or unfavor
able remodeling.