ACE I/D gene polymorphism: presence of the ACE D allele increases the risk of coronary artery disease in younger individuals

被引:61
作者
Gardemann, A
Fink, M
Stricker, J
Nguyen, QD
Humme, J
Katz, N
Tillmanns, H
Hehrlein, FW
Rau, M
Haberbosch, W
机构
[1] Univ Giessen Klinikum, Inst Klin Chem & Pathobiochem, D-35392 Giessen, Germany
[2] Univ Giessen, Abt Kardiol & Angiol, D-35392 Giessen, Germany
[3] Univ Giessen, Klin Herz & Gefasschirurg, D-35392 Giessen, Germany
[4] Max Planck Inst Expt & Klin Forsch, Bad Nauheim, Germany
关键词
ACE I/D gene polymorphism; cardiovascular diseases; myocardial infarction; risk factors; renin-angiotensin-aldosterone system; Gensini score;
D O I
10.1016/S0021-9150(98)00040-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Presence of the D allele or homozygosity for the deletion (D) allele of the ACE insertion/deletion (I/D) polymorphism has been discussed as potent risk factor for coronary artery disease (CAD) and myocardial infarction (MI). Methods and results: In 2267 male Caucasians the relation of the ACE I/D gene polymorphism to CAD and MI were investigated. An association of the D allele to CAD was detected in younger subjects (e.g. < 61.7 years, mean value), but not in older patients (e.g. greater than or equal to 61.7 years). Additional exclusion of individuals with other cardiovascular risk factors (e.g. high BMI) produced an even stronger association of the D allele to CAD. In contrast, a relation of this polymorphism to non-fatal MI was only observed in older subjects; additional limitation to individuals without cardiovascular risk factors (e.g. BMI and/or diabetes) yielded a further enhancement of this association to MI. In younger subjects (e.g. < 61.7 years) the gene polymorphism was not related to non-fatal MI even after exclusion of additional risk factors. Conclusions: The present large case-control study strengthens the assumption of an association of the ACE D allele with the risk of ischemic heart disease. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:153 / 159
页数:7
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