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Changes in biomarkers and 24 hours blood pressure in hypertensive African Americans with the metabolic syndrome: Comparison of amlodipine/olmesartan versus hydrochlorothiazide/losartan
Authors:Nadya Merchant  Syed T. Rahman  Mushtaq Ahmad  Janice M. Parrott  Julie Johnson  Keith C. Ferdinand  Bobby V. Khan
Affiliation:1. Atlanta Vascular Research Foundation, Atlanta, GA;2. Morehouse University School of Medicine, Atlanta, GA;1. Division of Nephrology, Department of Medicine, Istanbul Medeniyet University School of Medicine, Istanbul, Turkey;2. Department of Medicine, Fatih University School of Medicine, Ankara, Turkey;3. Nephrology Clinic, Karaman State Hospital, Karaman, Turkey;4. Division of Nephrology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA;5. Department of Veterans Affairs Medical Center, Birmingham, Alabama, AL, USA;1. Centre d''Investigations Préventives et Cliniques (IPC Center), Paris, France;2. Paris Descartes University, AP–HP, Diagnositic and Therapeutic Center, Hôtel-Dieu, Paris, France;1. Division of Hospital Medicine, Department of Medicine, University of Miami School of Medicine, Miami, FL;2. Division of Clinical Pharmacology, Department of Medicine, University of Miami School of Medicine, Miami, FL
Abstract:We evaluated the efficacy of amlodipine and olmesartan (A/O; Azor) versus losartan and hydrochlorothiazide (L/H; Hyzaar), on changes in serum and urine biomarkers of inflammation and oxidation, neutrophil reactive oxygen species generation, and changes in systolic blood pressure (BP), diastolic BP, and heart rate as measured with 24 hours ambulatory BP monitoring in a high-risk, hypertensive African-American population with the metabolic syndrome. Sixty-six African-American subjects with Stage 1 and 2 hypertension and characteristics of the metabolic syndrome were treated in open-label, active comparator fashion for 20 weeks. After 14 weeks of therapy, treatment with A/O had a significant effect on reducing the production of reactive oxygen series, plasminogen activator inhibitor-1, F2 isoprostane, myeloperoxidase, and homeostasis model assessment for insulin resistance while L/H treatment only significantly lowered levels of plasminogen activator inhibitor-1 and homeostasis model assessment for insulin resistance. Treatment with A/O showed a trend of a more immediate and sustained systolic and diastolic BP-lowering, as well as night time BP reduction. In addition to a trend toward lower blood pressure, treatment with A/O in comparison with L/H has superior efficacy in reducing reactive oxygen species generation and production of inflammatory and oxidative biomarkers in a hypertensive African-American population with features of the metabolic syndrome.
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