2011
DOI: 10.1177/1470320310391326
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The association between circulating angiotensin-converting enzyme and cardiovascular risk in the elderly: a cross-sectional study

Abstract: Introduction: A polymorphism in the angiotensin-converting enzyme gene (ACE I/D polymorphism) has been associated with increased risk for cardiovascular disease (CVD). This polymorphism affects the level of circulating ACE, but there is great individual variation, even between those with the same genotype. Few previous studies have investigated the link between circulating ACE and cardiovascular risk. The aim of this study was to investigate this association, and to examine the relationship between ACE level, … Show more

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Cited by 23 publications
(13 citation statements)
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“…Our analysis showed that both in cases and controls, ACE activities were highest in II carriers, then in DD carriers, and lowest in ID carriers. This result was consistent with part of Ljungberg’s [26] report that several individuals within the II group had considerably higher plasma ACE level than most DD carriers, but not in concordance with the great majority of the researches for most of them reported that ACE activities were significantly higher in patients with DD genotype versus the two other groups ID and II, and ID genotype usually showed intermediate levels and II genotype lowest levels [7-10]. Though ACE activities appeared to be affected by the I/D polymorphism, the I/D polymorphism was reported to be accounted for 47% of the total phenotypic variance of ACE activity, indicating that the ACE gene locus might be the major locus that determined ACE activity.…”
Section: Discussionsupporting
confidence: 91%
“…Our analysis showed that both in cases and controls, ACE activities were highest in II carriers, then in DD carriers, and lowest in ID carriers. This result was consistent with part of Ljungberg’s [26] report that several individuals within the II group had considerably higher plasma ACE level than most DD carriers, but not in concordance with the great majority of the researches for most of them reported that ACE activities were significantly higher in patients with DD genotype versus the two other groups ID and II, and ID genotype usually showed intermediate levels and II genotype lowest levels [7-10]. Though ACE activities appeared to be affected by the I/D polymorphism, the I/D polymorphism was reported to be accounted for 47% of the total phenotypic variance of ACE activity, indicating that the ACE gene locus might be the major locus that determined ACE activity.…”
Section: Discussionsupporting
confidence: 91%
“…The strong gene‐diet interaction we have identified may help to explain inconsistent results in the relationship between ACE levels or ACE genotype associations and blood pressure and CVD . The assumption that ACE levels are associated with blood pressure is due to the facts that ACE catalyzes the production of angiotensin II and ACE inhibitors effectively reduce blood pressure; however, this is not consistently supported by all studies . A stratification of total and saturated fat intake by ACE genotype would be expected to improve the risk estimates obtained in these studies.…”
Section: Discussionmentioning
confidence: 89%
“…Despite huge interindividual variability in circulating ACE levels depending on the ACE genotype, circulating levels are reported to be stable within given individuals . However, ACE circulating concentrations or activity levels, which are highly correlated, were shown to be increased in obesity and decreased by weight loss . In addition to its predominant expression in pulmonary endothelium as a primary source of circulating levels, ACE is also expressed in adipose tissue with increased expression in response to overfeeding …”
Section: Introductionmentioning
confidence: 99%
“…10 Given its role in BP regulation, it is reasonable to assume that genetic variations in the RAAS influence BP and its response to exercise. Indeed, earlier studies already demonstrated that individuals with the deletion polymorphism (DD) of the angiotensin converting enzyme (ACE) gene have higher circulating ACE levels compared with individuals with the insertion polymorphism (II), [28][29][30] resulting in a higher BP and an increased risk for hypertension in DD homozygotes. [31][32][33][34] Less is known about the role of the RAAS system and its polymorphisms in BP reduction following a single exercise session.…”
Section: Introductionmentioning
confidence: 99%