Asymmetric and symmetric dimethylarginines are of similar predictive value for cardiovascular risk in the general population

被引:61
作者
Kiechl, Stefan [2 ]
Lee, Terry [3 ]
Santer, Peter [4 ]
Thompson, Graham
Tsimikas, Sotirios [5 ]
Egger, Georg [6 ]
Holt, David W. [3 ]
Willeit, Johann [2 ]
Xu, Qingbo
Mayr, Manuel [1 ]
机构
[1] Kings Coll London, Div Cardiovasc, BHF Ctr, London SE5 9NU, England
[2] Med Univ Innsbruck, Dept Neurol, Innsbruck, Austria
[3] Univ London, Analyt Unit, London, England
[4] Bruneck Hosp, Dept Lab Med, Brunico, Italy
[5] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[6] Bruneck Hosp, Dept Internal Med, Brunico, Italy
关键词
Mass spectrometry; Risk factors; Atherosclerosis; Dimethylarginines; RENAL-FUNCTION; NATURAL COURSE; ARTERY; ATHEROSCLEROSIS; MARKER; DYSFUNCTION; MORTALITY; DISEASE; EVENTS; STROKE;
D O I
10.1016/j.atherosclerosis.2008.10.040
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Asymmetric dimethylarginine (ADMA) has raised considerable interest, as it is an endogenous inhibitor of nitric oxide synthesis. While increased plasma levels of ADMA have been reported in different cardiovascular disease states, its association with symmetric dimethylarginine (SDMA) has not been evaluated in a prospective population-based study. Methods and results: We performed a mass spectrometry-based analysis of ADMA and SDMA in the plasma of 572 participants of the Bruneck study. Levels of ADMA and SDMA were significantly correlated with each other (r=0.189, p<0.001). Age and parameters of renal function, however, showed a stronger influence on SDMA than on ADMA. Both ADMA and SDMA were predictive of cardiovascular disease in multivariate analysis and the associated hazard ratios over the 5-year observation period were of similar strength: 3,86 (1.36-10.9) and 7.91 (1.94-32.3) for ADMA and SDMA, respectively (p=0.011 and 0.004). Separate analyses focused on quintile groups of SDMA revealed that the increase in cardiovascular risk was mainly confined to the top category (>0.80 mu mol/L). Conclusion: This study argues against an exclusive ADMA effect in mediating cardiovascular risk. Instead, SDMA, its supposedly inactive counterpart, has similar diagnostic value in this large prospective cohort. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:261 / 265
页数:5
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