Key result
The DD ACE genotype was strongly associated with the development of left ventricular dysfunction in chronic alcohol abusers compared to those with an I allele (OR 16.4).
Why the study?
Does the ACE DD genotype increase the risk of developing left ventricular dysfunction in chronic alcohol abusers?
Case-Control (n=57)
No
Does the ACE DD genotype increase the risk of developing left ventricular dysfunction in chronic alcohol abusers?
Odds Ratio: 16.4
The ACE DD genotype is strongly associated with the development of alcoholic cardiomyopathy in chronic alcohol abusers, indicating a genetic susceptibility to alcohol-induced myocardial damage.
Suggests ACE DD genotype identifies high-risk alcohol abusers; hypothesis-generating and requires prospective validation before clinical use.
BACKGROUND: Chronic alcohol abuse has a dose-dependent toxic effect on the myocardium, leading to alcoholic cardiomyopathy. The fact that only a minority of persons with chronic alcoholism have this condition suggests the possibility of a genetic vulnerability. In this context, polymorphism of the angiotensin-converting enzyme (ACE) gene has been implicated in cardiac dysfunction. OBJECTIVE: To compare the ACE genotypes of alcoholic persons who have cardiomyopathy with those of comparable alcohol abusers who have normal cardiac function. DESIGN: Case-control study over a 2-year period. SETTING: An academic tertiary referral hospital in Barcelona, Spain. PATIENTS: 30 alcoholic men with symptomatic cardiomyopathy and 27 alcoholic men with normal cardiac function. MEASUREMENTS: Ethanol intake, cardiac status, left ventricular ejection fraction (LVEF), and ACE gene polymorphism. RESULTS: The DD ACE genotype was present in 57% of alcoholic persons with an LVEF less than 0.50 and in 7% of those with normal cardiac function. Compared with persons who had an I allele, the odds ratio for development of left ventricular dysfunction in alcoholic persons with the DD genotype was 16.4. CONCLUSIONS: Vulnerability to cardiomyopathy among chronic alcohol abusers is partially genetic and is related to presence of the ACE DD genotype. This finding demonstrates genetic susceptibility to alcohol-induced myocardial damage.
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Joaquim Fernández‐Solà (2002) conducted a case-control in Alcoholic cardiomyopathy (n=57). DD ACE genotype vs. I allele was evaluated on development of left ventricular dysfunction (OR 16.4). The DD ACE genotype was strongly associated with the development of left ventricular dysfunction in chronic alcohol abusers compared to those with an I allele (OR 16.4).
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