(Circulation. 1999;100:e85.)
© 1999 American Heart Association, Inc.
Circulation Electronic Pages |
The Department of Medicine, University of Queensland, Princess Alexandra Hospital, Brisbane, Australia
| Introduction |
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Recently, an analysis was performed using a prospective, longitudinal, population-based sample in which the insertion/deletion (I/D) polymorphism of the ACE gene was postulated as a sex-specific candidate gene for hypertension.1 A significant association between hypertension in males and the ACE DD genotype was observed after adjustment for all confounders (OR 1.59, P=0.02), whereas linkage between the DD genotype and diastolic blood pressure (DBP) in men was significant only when adjusted for age alone (P=0.03 and P=0.16 after and before adjustment for age alone, respectively).
In contrast, an independent prospective, population-based study found
no association between the ACE I/D polymorphism and hypertension,
nor was there any sex stratification with regard to allele or
genotype.2 Adjustment for several potential
confounders did not affect this result for isolated systolic
hypertension (systolic blood pressure [SBP]
160
mm Hg, DBP
90 mm Hg) (II versus DD OR 1.06; I versus D OR
1.09) or systolic-diastolic hypertension (SBP
160 mm Hg, DBP
90 mm Hg) (II versus DD OR 1.19; I
versus D OR 1.16).
O'Donnell et al1 used the Framingham cohort, which has a large sample size (n=3095/1044 sib pairs) and allowed use of both association analyses and pedigree-based linkage analyses, which provides considerable power to the study. The Dubbo cohort subset used by Johnson et al2 is smaller (n=33) but epidemiologically superior, with a sound geographical definition.3
The most obvious differences between these studies are the definition
of high blood pressure and the criteria used to classify
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