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September 1, 1994Journal of Clinical Investigation140 citationsOpen Access

Different frequencies of angiotensin-converting enzyme genotypes in older hypertensive individuals.

BMBrian J. MorrisRZRobert Y.L. ZeeASA. P. Schrader

Structured PICO

Does the frequency of the ACE DD genotype decrease with age in patients with severe familial hypertension?

P
Population
118 Caucasian subjects with severe, early onset, familial hypertension and 196 age-, sex- and body mass index-matched normotensive controls.
I
Intervention
Assessment of angiotensin I-converting enzyme (ACE) insertion/deletion (I/D) polymorphism
C
Comparator
Normotensive controls and comparison across age groups (<50, 50-59, and >=60 years)
O
Outcome
Frequency of the ACE DD genotype and D allele across age groupssurrogate

The frequency of the ACE DD genotype decreases significantly with age in patients with severe familial hypertension, suggesting it may be associated with premature death in this high-risk population.

Abstract

The frequency of the D allele of an insertion/deletion (I/D) polymorphism of the angiotensin I-converting enzyme (ACE) gene has been reported to be elevated in myocardial infarction and other patients. We therefore hypothesized that death rate of DD individuals should be increased in the population as a whole and this should be evident as a decrease in DD frequency with age. This hypothesis was tested in 118 Caucasian subjects who were already at high risk of cardiovascular events by having severe, early onset, familial hypertension (HT). A group of 196 age-, sex- and body mass index-matched normotensives (NTs) was used as a control. In the NT group II, ID, and DD genotype frequencies were similar for different age groups. DD frequency was 0.42 in NTs, but in HTs was 0.28, 0.26, and 0.10 for the age groups or = 60 yr, respectively. Corresponding D allele frequencies were 0.52, 0.46, and 0.40 in the respective age groups of HTs, compared with 0.61 in NTs (by chi 2-analysis, P = 0.1, 0.047, and 0.0006, respectively). In HTs aged > or = 60, DD frequency was only 14% of expected. Plasma ACE activity tracked similarly with I/D genotype in HTs (P = 0.027; n = 35) as in NTs (P = 0.0001; n = 94) and Michaelis constant was identical for DD and II. Neither blood pressure, body mass index, nor sex bore any relationship with I/D genotype. In conclusion, in a group of severely HT patients not selected for cardiac pathology, there appeared to be a marked, selective decrease, in subgroups of increasing age, in frequency of the ACE DD genotype. One possibility suggested by this data might be that DD increases risk of premature death, at least in HTs who have two HT parents.

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Cite This Study

Morris et al. (1994) studied this question.

synapsesocial.com/papers/6a7047d4e71d69abee088163https://doi.org/10.1172/jci117423
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1DECREASE WITH AGE IN FREQUENCY OF THE HOMOZYGOUS DELETIONAL ANGIOTENSIN‐CONVERTING ENZYME GENOTYPE IN HYPERTENSIVE PATIENTS*1998 · 4 citations
  2. 2HYPOTHESIS: AN ANGIOTENSIN CONVERTING ENZYME/GENOTYPE, PRESENT IN ONE IN THREE CAUCASIANS, IS ASSOCIATED WITH AN INCREASED MORTALITY RATE1996 · 17 citations
  3. 3Cardiovascular effects of I/D angiotensin-converting enzyme gene polymorphism in healthy subjects2005 · 21 citations
  4. 4Insertion/deletion (I/D) polymorphism at the locus for angiotensin I‐converting enzyme and myocardial infarction1993 · 107 citations
  5. 5Cardiovascular effects of I/D angiotensin-converting enzyme gene polymorphism in healthy subjects. Findings after six years follow up2005 · 1 citations