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Hindi Research Article
A Comparative Study of Olmesartan and Valsartan on Insulin Sensitivity in Hypertensive Patients with Diabetes Mellitus or Impaired Glucose Tolerance (OVIS Study)
| Sadatoshi Biro1*, Tetsunori Saikawa2, Takatoshi Otonari3, Yasunori Sawayama4, Masato Ageta5, Hachiro Obata6, Suminori Kono7 and Jun Sasaki8 | |
| 1Tsukasa Health Care Hospital, Kagoshima, Japan | |
| 2Japan Community Health Care Organization Yufuin Hospital, Yufu, Japan | |
| 3Otonari Clinic, Fukuoka, Japan | |
| 4Hara Sanshin Hospital, Fukuoka, Japan | |
| 5Ageta Clinic, Nichinan, Japan | |
| 6Okino Hospital, Kagoshima, Japan | |
| 7Kyushu University, Faculty of Medical Sciences, Fukuoka, Japan | |
| 8International University of Health and Welfare, Graduate School of Pharmaceutical Medicine, Fukuoka, Japan | |
| Corresponding Author : | Dr. Sadatoshi Biro Tsukasa Health Care Hospital Kagoshima, Japan Tel: 81-92-711-1126 E-mail: birou@peace.ocn.ne.jp |
| Received July 08, 2014; Accepted July 23, 2014; Published July 25, 2014 | |
| Citation: Biro S, Saikawa T, Otonari T, Sawayama Y, Ageta M, et al. (2014) A Comparative Study of Olmesartan and Valsartan on Insulin Sensitivity in Hypertensive Patients with Diabetes Mellitus or Impaired Glucose Tolerance (OVIS Study). Clin Pharmacol Biopharm 3:118. doi:10.4172/2167-065X.1000118 | |
| Copyright: © 2014 Biro S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | |
Abstract
Activation of renin angiotensin system is implicated in insulin resistance. In mega trials, it has been suggested that angiotensin receptor blockers may be beneficial on insulin sensitivity in hypertensive patients. We conducted a multicenter, open-label, parallel-group trial to compare the effects of olmesartan and valsartan on insulin sensitivity and adiponectin levels in 206 hypertensive patients with diabetes mellitus or impaired glucose tolerance. Patients were randomly assigned to either olmesartan 20 mg/day or valsartan 80 mg/day treatment for 24 weeks. Blood pressure, fasting glucose, fasting insulin, glycosylated hemoglobin (HbA1c), homeostasis model assessment for insulin resistance (HOMA-IR), and serum adiponectin levels were measured. The efficacy was evaluated in 197 patients (olmesartan, n=98; valsartan, n=99). At baseline, all parameters except for systolic blood pressure (SBP) and serum triglyceride did not differ between the 2 groups. HbA1c decreased slightly after a 24-week treatment with valsartan, but not olmesartan, while the decrease did not significantly differ in the two groups. There was no difference in the change from the baseline between olmesartan and valsartan groups concerning fasting glucose, fasting insulin, HOMA-IR, and adiponectin levels after 24-week treatment. The decrease in SBP tended to be greater in the olmesartan group than in the valsartan group even with adjustment for the baseline difference. In conclusion, there was no significant difference in insulin sensitivity or adiponectin levels between the olmesartan and valsartan groups. In the standard dose, olmesartan significantly decreased SBP as compared with valsartan.
