Angiotensin converting enzyme DD genotype is associated with acute coronary syndrome severity and sudden cardiac death in Taiwan: a case-control emergency room study

• Published in: BMC cardiovascular disorders Vol. 12; no. 1; p. 6
• Main Authors: Chen, Ying-Hsin, Liu, Jui-Ming, Hsu, Ren-Jun, Hu, Sheng-Chuan, Harn, Horng-Jyh, Chen, Shee-Ping, Jeng, Jing-Ren, Wu, Chieh-Lin, Ho, Jar-Yi, Yu, Cheng-Ping
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 15.02.2012; BioMed Central; BMC
• Subjects: Acute coronary syndrome; Acute Coronary Syndrome - etiology; Acute Coronary Syndrome - genetics; Acute Coronary Syndrome - mortality; Adult; Aged; Aged, 80 and over; Angina pectoris; Angiotensin converting enzyme; Cardiac arrest; Cardiovascular disease; Case-Control Studies; Coronary heart disease; Death, Sudden, Cardiac - epidemiology; Death, Sudden, Cardiac - etiology; Emergency medical care; Emergency Service, Hospital; Female; Genetic aspects; Genotype; Heart attacks; Humans; Male; Middle Aged; Mortality; Myocardial Infarction - etiology; Myocardial Infarction - genetics; Myocardial Infarction - mortality; Peptidyl-Dipeptidase A - genetics; Pharmacogenomics; Physiological aspects; Polymorphism, Genetic; Risk Factors; Sudden cardiac death; Taiwan; Taiwan
• ISSN: 1471-2261; 1471-2261
• DOI: 10.1186/1471-2261-12-6

Angiotensin converting enzyme (ACE) gene insertion/deletion (I/D) polymorphisms have been associated with acute coronary syndrome (ACS); however, several controversial results have also been found in different studied populations. This hospital-based, emergency room, case-control study in Taiwan retrospectively investigated 111 ACS patients, and 195 non-coronary subjects as a control group, to study the effects of ACE I/D polymorphism in the most urgent ACS patients. ACE I/D polymorphisms were determined by polymerase chain reaction-based assays and their associations with ACS risk, severity, and sudden cardiac death were determined. The ACE DD genotype was associated with ACS incidence. The DD genotype was associated with a significant 4-fold higher risk of ACS in multivariate analysis (odds ratio (OR) = 4.295; 95% confidence interval (CI): 1.436-12.851, p = 0.009), and a 3.35-fold higher risk of acute myocardial infarction. DD genotype carriers also had more than 3-fold higher risks of stenosis in all the three coronary arteries, left anterior descending artery infarction, and anterior wall infarction. In addition, the DD genotype was also associated with a higher risk of sudden cardiac death (OR = 6.484, 95% CI: 1.036-40.598, p = 0.046). This study demonstrated that the ACE DD genotype is an independent risk factor for ACS, and in particular, for acute myocardial infarction. In addition, the ACE DD genotype is also associated with greater ACS severity and a higher risk of sudden cardiac death. ACE genotyping is recommended for patients with a history of ACS, and more intensive preventive care is suggested for patients with the DD genotype.