4.7 Article

Distribution of Asymmetric Dimethylarginine among 980 Healthy, Older Adults of Different Ethnicities

Journal

CLINICAL CHEMISTRY
Volume 56, Issue 1, Pages 111-120

Publisher

AMER ASSOC CLINICAL CHEMISTRY
DOI: 10.1373/clinchem.2009.136200

Keywords

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Funding

  1. Donald W. Reynolds Foundation (Las Vegas, NV)
  2. Deutsche Forschungsgemeinschaft [Sy 41/1-1]
  3. Hamburg University [F-167-1]

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BACKGROUND: Endothelium-derived nitric oxide plays a crucial role in the regulation of vascular tone and the development of cardiovascular disease. The endogenous nitric oxide synthase inhibitor asymmetric dimethylarginine (ADMA) has emerged as a novel cardiovascular risk factor. ADMA appears to be an independent predictor for cardiovascular and overall mortality. However, the majority Of Studies investigating the clinical role of ADMA were performed in European study populations with few individuals of other ethnicities. METHODS: We performed a cross-sectional study of 980 healthy, older (age 60-72 years) individuals of different ethnicities living in the San Francisco Bay area and analyzed ADMA plasma concentrations and their relationship to other cardiovascular risk factors. Plasma ADMA concentrations were measured Using a recently developed, highly sensitive ELISA. RESULTS: In our entire sample, we were able to define a reference interval for ADMA plasma concentrations of 0.47 (90% Cl 0.46-0.48) mu mol/l, to 0.85 (0.84-0.89) mu mol/L. The mean ADMA concentration was 0.63 (SD 0.11) mu mol/l, (median 0.61 mu mol/L. Mean ADMA concentrations were significantly lower in African Americans (0.60 mu mol/L; P < 0.01) and mixed non-Hispanics (0.60 mu mol/L; P < 0.05) compared with whites (0.63 mu mol/L). ADMA was positively correlated with cystatin-C in both men (rho = 0.29) and women (rho = 0.37), and median plasma ADMA concentrations increased across cystatin-C quintiles. CONCLUSIONS: ADMA varies nearly 2-fold across a healthy sample of older men and women, correlates with age, body mass index, and renal function, and is different across ethnic groups. Additional studies in a wider age range and including larger ethnic subgroups would be useful. (C) 2009 American Association for Clinical Chemistry,

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