Asymmetric dimethylarginine, smoking, and risk of coronary heart disease in apparently healthy men:: Prospective analysis from the population-based Monitoring of Trends and Determinants in Cardiovascular Disease/Kooperative Gesundheitsforschung in der Region Augsburg study and experimental data

被引:75
作者
Maas, Renke
Schulze, Friedrich
Baumert, Jens
Loewel, Hannelore
Hamraz, Khatera
Schwedhelm, Edzard
Koenig, Wolfgang
Boeger, Rainer H.
机构
[1] Univ Ulm, Med Ctr, Dept Internal Med Cardiol 2, D-89081 Ulm, Germany
[2] Univ Hamburg, Hosp Eppendorf, Inst Expt & Clin Pharmacol & Toxicol, D-20246 Hamburg, Germany
[3] GSF, Res Ctr Environm & Hlth, Inst Epidemiol, Neuherberg, Germany
关键词
D O I
10.1373/clinchem.2006.081893
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: An increased plasma concentration of the endogenous nitric oxide synthase inhibitor asymmetric dimethylarginine (ADMA) predicts adverse clinical outcome in patients with coronary heart disease. We investigated the association between plasma concentrations of ADMA and risk in initially healthy smoking and nonsmoking men. Methods: Participants for this nested case-control study came from the population-based Monitoring of Trends and Determinants in Cardiovascular Disease/Kooperative Gesundheitsforschung in der Region Augsburg study. ADMA, was measured by liquid chromatography-tandem mass spectrometry in 88 men with incident coronary events (fatal and nonfatal myocardial infarction and sudden cardiac death). and 254 age-matched controls, with a median (interquartile range) follow-up of 6.2 (3.3-7.9) years. Results: After adjustment for potential confounders, the relative risk for a future coronary event was 2.00 [95% confidence interval (CI) 1.27-3.16; P = 0.003] for smokers compared with nonsmokers and 1.35 (95% Cl 0.78-2.33; P = 0.282) for the top vs the bottom tertile of the ADMA distribution. In cases and controls, lower ADMA plasma concentrations Were observed in smokers. Analysis of ADMA-associated risk in smokers and nonsmokers separately revealed substantial differences: the adjusted relative risk for. future coronar y events (top vs bottom tertile of the ADMA distribution) Was 0.48 (95% Cl 0.16-1.46; P = 0.198) in smokers and 2.40 (95% Cl 1.14-5.08; P = 0.021) in nonsmokers. Exposure of human endothelium-derived EAhy 926 cells to tobacco smoke enhanced expression of the ADMA metabolizing enzyme dimethylarginine dimethylaminohydrolase 2 and reduced ADMA concentration. Conclusions: In apparently healthy men, increased ADMA predicts the risk for coronary events in nonsmokers, but not in smokers. This may be explained in part by an alteration of ADMA metabolism by tobacco smoke. (c) 2007 American Association for Clinical Chemistry.
引用
收藏
页码:693 / 701
页数:9
相关论文
共 39 条
[1]  
[Anonymous], 2000, J AM SOC NEPHROL
[2]  
[Anonymous], 1988, J CLIN EPIDEMIOL, V41, P105, DOI DOI 10.1016/0895-4356(88)90084-4
[3]  
[Anonymous], 1998, CVD Prevention
[4]   When the endothelium cannot say 'NO' anymore -: ADMA, an endogenous inhibitor of NO synthase, promotes cardiovascular disease [J].
Böger, RH .
EUROPEAN HEART JOURNAL, 2003, 24 (21) :1901-1902
[5]   PERMANENT CELL-LINE EXPRESSING HUMAN FACTOR-VIII-RELATED ANTIGEN ESTABLISHED BY HYBRIDIZATION [J].
EDGELL, CJ ;
MCDONALD, CC ;
GRAHAM, JB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (12) :3734-3737
[6]   Relationship between obesity, smoking, and the endogenous nitric oxide synthase inhibitor, asymmetric dimethylarginine [J].
Eid, HMA ;
Arnesen, H ;
Hjerkinn, EM ;
Lyberg, T ;
Seljeflot, I .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2004, 53 (12) :1574-1579
[7]   Independent association of various smoking characteristics with markers of systemic inflammation in men -: Results from a representative sample of the general population (MONICA Augsburg Survey 1994/95) [J].
Fröhlich, M ;
Sund, M ;
Löwel, H ;
Imhof, A ;
Hoffmeister, A ;
Koenig, W .
EUROPEAN HEART JOURNAL, 2003, 24 (14) :1365-1372
[8]   Effect of nicotine on the intimal hyperplasia after endothelial removal of the rabbit carotid artery [J].
Hamasaki, H ;
Sato, J ;
Masuda, H ;
Tamaoki, S ;
Isotani, E ;
Obayashi, S ;
Udagawa, T ;
Azuma, H .
GENERAL PHARMACOLOGY, 1997, 28 (05) :653-659
[9]  
Hutchinson WL, 2000, CLIN CHEM, V46, P934
[10]   Involvement of DDAH/ADMA/NOS pathway in nicotine-induced endothelial dysfunction [J].
Jiang, De-Jian ;
Jia, Su-Jie ;
Yan, Jin ;
Zhou, Zhi ;
Yuan, Qiong ;
Li, Yuan-Jian .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 349 (02) :683-693