Systemic HypertensionCardiovascular risk factors, angiotensin-converting enzyme gene I/D polymorphism, and left ventricular mass in systemic hypertension☆
Section snippets
Subjects
All patients were preliminarily asked to give their informed consent to enter the study. After excluding subjects with coronary heart disease (as judged by clinical examination, standard 12-lead electrocardiogram and/or presence of wall motion abnormality by 2-dimensional echocardiography), valvular heart disease (2-dimensional Doppler echocardiography), secondary hypertension, dilated cardiomyopathy, left bundle branch block, thyroid disease, or treatment with oral contraceptives, 225
Genotype frequencies and clinical characteristics of the study population
Table Ilists the characteristics of the study population stratified according to ACE I/D genotypes. Homozygosity for the D allele (DD genotype) was present in 33%; homozygosity for the I allele (II) was found in 16%. These frequencies were compared with those predicted from the Hardy-Weinberg equilibrium in the general population. No significant difference was observed (chi-square), nor was any difference found in clinical or ambulatory blood pressure or in left ventricular geometry. The
Discussion
In a case-control study, Cambien et al16 reported that the association between myocardial infarction and the DD genotype of the ACE gene could be detected only in patients without major cardiovascular risk factors (low-risk patients). This finding has recently been confirmed by coronary angiography in a large cohort of 920 men.21 Moreover, in the study by Mattu et al,22 a significant association between DD genotype and coronary lesions was detected only in low-risk patients.
The role of
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This study was supported in part by Grant MURST-185/1995-1996 of the Italian Ministry of University and Research.