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Updated: May 25, 2026

Assessing Endothelial Vasodilator Function with the Endo-PAT 2000
Published on: October 15, 2010
Carvedilol-lisinopril combination therapy and endothelial function in obese individuals with hypertension
Aaron S Kelly1, J Michael Gonzalez-Campoy1, Kyle D Rudser1
1From the Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN ; 1 Minnesota Center for Obesity, Metabolism and Endocrinology, Eagan, MN ; 2 the Division of Biostatistics, University of Minnesota School of Public Health, Minneapolis, MN ; 3 Allina Hospitals and Clinics, St. Paul, MN ; 4 and the Department of Research, St. Paul Heart Clinic, St. Paul, MN 5.
Abstract:
The authors hypothesized that carvedilol controlled-release plus lisinopril combination therapy (C+L) would increase endothelial function and decrease oxidative stress to a greater extent than hydrochlorothiazide plus lisinopril combination therapy (H+L) in obese patients with hypertension. Twenty-five abdominally obese patients (aged 54.4±7.3 years; 14 women) with hypertension/prehypertension were enrolled in a 7-month (two 3-month treatment periods separated by a 1-month washout), randomized, double-blind, controlled, crossover clinical trial comparing C+L vs H+L. Endothelial function, measured by digital reactive hyperemic index (RHI), circulating oxidized low-density lipoprotein (oxLDL), 8-isoprostane, and asymmetric dimethylarginine (ADMA) were obtained at baseline, post-period 1, post-washout, and post-period 2. Analyses were adjusted for baseline measurements by analysis of covariance, with robust variance estimation for confidence intervals and P values. C+L treatment compared to H+L treatment significantly improved RHI (0.74, 95% confidence interval, 0.31-1.19, P =.001). This difference persisted after adjustment for the change in systolic blood pressure. No significant treatment differences were observed for oxLDL, 8-isoprostane, or ADMA. These data provide evidence that independent of blood pressure-lowering, C+L therapy improves endothelial function to a greater extent than H+L therapy. Levels of oxidative stress were not significantly different between treatments, suggesting that other mechanisms may be responsible for the improvement in endothelial function.
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