Key result
The angiotensin converting enzyme DD genotype was not associated with coronary artery disease (OR 0.81, P>0.05) or myocardial infarction (OR 1.16, P>0.05) among Turkish patients.
Why the study?
Does the angiotensin converting enzyme gene polymorphism affect the risk and extent of coronary artery disease and myocardial infarction in Turkish patients?
Observational (n=393)
Does the angiotensin converting enzyme gene polymorphism affect the risk and extent of coronary artery disease and myocardial infarction in Turkish patients?
Odds Ratio: 0.81
p-value: p=> 0.05
The ACE DD genotype is associated with the angiographic extent of coronary atherosclerosis, but not with the overall presence of CAD or MI in Turkish patients.
ACE DD genotype not linked to CAD or MI presence; leaves open possible association with atherosclerosis extent in Turks.
OBJECTIVE: To evaluate the effects of the angiotensin converting enzyme gene polymorphism on the presence and extent of coronary artery disease and myocardial infarction among Turkish patients. METHODS: In total 393 consecutive patients undergoing coronary angiography were evaluated for cardiac risk factors including the lipoprotein profile, lipoprotein (a), apoprotein B, and apoprotein A1 levels. The angiotensin converting enzyme genotype was determined by polymerase chain reaction. The extent of coronary atherosclerosis was determined from the angiograms using the Gensini and Leaman scores. RESULTS: The angiotensin converting enzyme genotype was found not to be associated either with coronary artery disease (odds ratio 0.81, P > 0.05) or with myocardial infarction (odds ratio 1.16, P > 0.05). Exclusion of high-risk individuals failed to reveal any association for these subgroups. Furthermore, there was no association between aneurysm formation and the genotype (P > 0.05). The lipid parameters were also not affected by the genotype (P > 0.05). However, the extent of coronary atherosclerosis determined by the Gensini score was related significantly to the genotype by multivariate analysis (P = 0.007). CONCLUSION: The DD genotype is not associated with coronary artery disease and myocardial infarction among these angiographically assessed Turkish patients, even when low-risk subgroups are analysed. Nonetheless, the extent of coronary atherosclerosis in patients with coronary artery disease is affected by their genotype.
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Tokgözoğlu et al. (1997) conducted an observational in Coronary artery disease and myocardial infarction (n=393). Angiotensin converting enzyme gene polymorphism (DD genotype) vs. Non-DD genotypes was evaluated on Presence of coronary artery disease (OR 0.81, p=> 0.05). The angiotensin converting enzyme DD genotype was not associated with coronary artery disease (OR 0.81, P>0.05) or myocardial infarction (OR 1.16, P>0.05) among Turkish patients.
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