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Clinical Investigation
JAMA. 2002;287(11):1420-1426. doi: 10.1001/jama.287.11.1420

Relationship Between Insulin Resistance and an Endogenous Nitric Oxide Synthase Inhibitor

  1. Markus C. Stühlinger, MD;
  2. Fahim Abbasi, MD;
  3. James W. Chu, MD;
  4. Cindy Lamendola, MSN, ANP;
  5. Tracey L. McLaughlin, MD;
  6. John P. Cooke, MD, PhD;
  7. Gerald M. Reaven, MD;
  8. Philip S. Tsao, PhD
  1. Author Affiliations: Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, Calif. Dr Stühlinger is now with the Division of Cardiology, University of Innsbruck, Innsbruck, Austria.

Abstract

Context  Increased levels of asymmetric dimethylarginine (ADMA) are associated with endothelial dysfunction and increased risk of cardiovascular disease. Several cardiovascular risk factors are associated with reduced sensitivity to insulin, but elevated ADMA concentrations have not been fully linked to the metabolic syndrome.

Objective  To evaluate the relationship between insulin sensitivity and plasma ADMA concentrations, and to determine whether a pharmacological treatment that increases insulin sensitivity would also modulate ADMA concentrations.

Design, Setting, and Subjects  Cross-sectional study, containing a nonrandomized controlled trial component, of 64 healthy volunteers without diabetes (42 women, 22 men; 48 with normal blood pressure and 16 with hypertension), which was conducted at a university medical center between October 2000 and July 2001.

Intervention  Rosiglitazone (4 mg/d for 4 weeks and then 4 mg twice daily for 8 weeks), an insulin-sensitizing agent, was given to 7 insulin-resistant subjects with hypertension. These subjects were studied before and after 12-week treatment.

Main Outcome Measures  Insulin sensitivity measured by the insulin suppression test, and fasting plasma levels of low-density lipoprotein cholesterol, triglycerides, high-density lipoprotein cholesterol, glucose, insulin, and ADMA concentrations.

Results  Plasma ADMA concentrations were positively correlated with impairment of insulin-mediated glucose disposal in nondiabetic, normotensive subjects (r = 0.73; P<.001). Consistent with the metabolic syndrome, ADMA levels were also positively correlated with fasting triglyceride levels (r = 0.52; P<.001) but not with low-density lipoprotein cholesterol levels (r = 0.19; P = .20). Plasma ADMA concentrations increased in insulin-resistant subjects independent of hypertension. Pharmacological treatment improved insulin sensitivity and reduced mean (SD) plasma ADMA concentrations from 1.50 (0.30) to 1.05 (0.33) µmol/L (P = .001).

Conclusion  A significant relationship exists between insulin resistance and plasma concentrations of ADMA. Pharmacological intervention with rosiglitazone enhanced insulin sensitivity and reduced ADMA levels. Increases in plasma ADMA concentrations may contribute to the endothelial dysfunction observed in insulin-resistant patients.

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