DELETION POLYMORPHISM OF THE ANGIOTENSIN-CONVERTING ENZYME GENE IS INDEPENDENTLY ASSOCIATED WITH LEFT-VENTRICULAR MASS AND GEOMETRIC REMODELING IN SYSTEMIC HYPERTENSION
Ag. Gharavi et al., DELETION POLYMORPHISM OF THE ANGIOTENSIN-CONVERTING ENZYME GENE IS INDEPENDENTLY ASSOCIATED WITH LEFT-VENTRICULAR MASS AND GEOMETRIC REMODELING IN SYSTEMIC HYPERTENSION, The American journal of cardiology, 77(15), 1996, pp. 1315-1319
An insertion/deletion (I/D) polymorphism of the angiotensin-converting
enzyme (ACE) gene is associated with myocardial infarction, cardiomyo
pathy, and left ventricular (LV) hypertrophy. LV mass and geometry are
related to cardiovascular morbidity and mortality. Two-dimensional di
rected M-mode echocardiograms and 24-hour ambulatory blood pressure mo
nitoring were performed in 67 hypertensive subjects. Echocardiographic
measurements were assessed in blinded fashion. LV mass index and rela
tive wall thickness were calculated. ACE genotypes were determined by
polymerase chain reaction amplification of deoxyribonucleic acid prepa
red from leukocytes, using primers that encompass the polymorphic segm
ent. Systolic ambulatory blood pressure was higher in subjects with th
e II genotype. All other patient characteristics were similar across g
enotype groups. After adjustment for other covariables, the DD and ID
genotypes were associated with significantly higher LV mass index than
was the II genotype. Adjusted relative wall thickness was also higher
in subjects with the DD genotype than in subjects with the ID and II
genotypes. On multiple regression analysis, systolic ambulatory blood
pressure, gender, body mass index, and the ACE genotype were each inde
pendently related to LV mass index (R(2)=0.53). Systolic ambulatory bl
ood pressure, race, and ACE genotype were each independently related t
o relative wall thickness (R(2)=0.34). The ACE genotype explained an a
dditional 3% and 4% of the variations of LV mass index and relative wa
ll thickness, respectively. In conclusion, ACE polymorphism accounted
for a small but statistically significant proportion of the variation
in LV mass and geometry in our hypertensive subjects.