Yoshihiko Ichikawa1. 1. Department of Cardiovascular Medicine, Otaru Municipal Second Hospital. yichikawa@sapmed.ac.jp
Abstract
OBJECTIVE: Metabolic syndrome (MetS) is a cluster of metabolic abnormalities that includes hyperglycemia, dyslipidemia, hypertension and increased waist circumference. Individuals with this syndrome are at increased risk for development of cardiovascular disease. Since an insulin-resistance state has a critical role in the development of MetS, there is growing concern about insulin-sensitizing effects of antihypertensives, including angiotensin II receptor blockers (ARBs). Telmisartan has been reported to have an effect on the activity of peroxisome proliferator-activated receptor gamma, a well-known target for insulin-sensitizing antidiabetic drugs. The aim of this study was to determine the effects of administration of two different ARBs at low doses (telmisartan at 20 mg/day and valsartan at 40 mg/day) on insulin sensitivity. METHODS:Patients with MetS meeting the Japanese criteria were treated with telmisartan or valsartan for 4 weeks in combination with lifestyle modification. RESULTS: A significant reduction in blood pressure was found after 4 weeks of both treatments. The homeostasis model assessment of insulin resistance (HOMA-R) was significantly reduced by telmisartan compared to the baseline value (3.11+/-2.06 vs 2.56+/-1.48, p=0.031) but was not significantly changed by valsartan. A statistically significant correlation was found between HOMA-R at baseline and changes in HOMA-R after 4 weeks of treatment only in telmisartan-treated subjects. Body mass index, glycosylated hemoglobin and lipid profile were not changed by either treatment. CONCLUSION: Our data revealed that treatment with telmisartan even at a low dose improves insulin sensitivity in hypertensive patients with MetS. This ameliorating effect of telmisartan on glucose metabolism clinically deserves to be considered.
RCT Entities:
OBJECTIVE:Metabolic syndrome (MetS) is a cluster of metabolic abnormalities that includes hyperglycemia, dyslipidemia, hypertension and increased waist circumference. Individuals with this syndrome are at increased risk for development of cardiovascular disease. Since an insulin-resistance state has a critical role in the development of MetS, there is growing concern about insulin-sensitizing effects of antihypertensives, including angiotensin II receptor blockers (ARBs). Telmisartan has been reported to have an effect on the activity of peroxisome proliferator-activated receptor gamma, a well-known target for insulin-sensitizing antidiabetic drugs. The aim of this study was to determine the effects of administration of two different ARBs at low doses (telmisartan at 20 mg/day and valsartan at 40 mg/day) on insulin sensitivity. METHODS:Patients with MetS meeting the Japanese criteria were treated with telmisartan or valsartan for 4 weeks in combination with lifestyle modification. RESULTS: A significant reduction in blood pressure was found after 4 weeks of both treatments. The homeostasis model assessment of insulin resistance (HOMA-R) was significantly reduced by telmisartan compared to the baseline value (3.11+/-2.06 vs 2.56+/-1.48, p=0.031) but was not significantly changed by valsartan. A statistically significant correlation was found between HOMA-R at baseline and changes in HOMA-R after 4 weeks of treatment only in telmisartan-treated subjects. Body mass index, glycosylated hemoglobin and lipid profile were not changed by either treatment. CONCLUSION: Our data revealed that treatment with telmisartan even at a low dose improves insulin sensitivity in hypertensivepatients with MetS. This ameliorating effect of telmisartan on glucose metabolism clinically deserves to be considered.
Authors: Giuliano Tocci; Andrea Ferrucci; Jasmine Passerini; Maurizio Averna; Paolo Bellotti; Graziella Bruno; Francesco Cosentino; Gaetano Crepaldi; Cristina Giannattasio; Maria Grazia Modena; Giulio Nati; Antonio Tiengo; Bruno Trimarco; Diego Vanuzzo; Massimo Volpe Journal: High Blood Press Cardiovasc Prev Date: 2011-06-01
Authors: Kelly Putnam; Robin Shoemaker; Frederique Yiannikouris; Lisa A Cassis Journal: Am J Physiol Heart Circ Physiol Date: 2012-01-06 Impact factor: 4.733