Department of Clinical and Molecular Endocrinology, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.
Hypertens Res. 2010 Aug;33(8):796-801. doi: 10.1038/hr.2010.107. Epub 2010 Jun 17.
Telmisartan, a selective antagonist for angiotensin type1 receptor and a partial agonist for peroxisome proliferator-activated receptor-gamma, decreases blood pressure and has been shown to improve glucose and lipid metabolism, suggesting potential cardiovascular protective effects. In this study, we investigated whether long-term treatment with telmisartan improved endothelial function in 35 hypertensive patients with type 2 diabetes mellitus (T2DM). Office and home early morning blood pressure levels and flow-mediated vasodilation (FMD) were evaluated before and after 12 months of treatment with telmisartan. Blood samples were also obtained for measurement of several biochemical parameters and of adiponectin (AN) and highly sensitive C-reactive protein (hs-CRP) before and after treatment. After 12 months of treatment, office and morning blood pressure levels had significantly decreased, and levels of plasma glucose, glycosylated hemoglobin, total cholesterol, triglyceride and low-density lipoprotein cholesterol had also significantly decreased. Plasma AN and high-density lipoprotein cholesterol levels increased, but hs-CRP levels decreased. Furthermore, FMD significantly increased; changes in percent FMD showed a significant negative correlation with changes in systolic and diastolic blood pressure and a significant positive correlation with changes in AN. Stepwise multivariate regression analysis revealed that changes in plasma AN and office systolic blood pressure were both independent determinants for endothelial function after telmisartan treatment. In conclusion, this study shows that long-term treatment with telmisartan improves not only blood pressure and glucose and lipid metabolism but also endothelial function in hypertensive patients with T2DM, possibly by increased circulating AN and decreased blood pressure.
替米沙坦是血管紧张素受体 1 型的选择性拮抗剂和过氧化物酶体增殖物激活受体-γ的部分激动剂,可降低血压,并已被证明可改善葡萄糖和脂质代谢,提示其具有潜在的心血管保护作用。在这项研究中,我们调查了长期使用替米沙坦是否能改善 35 例 2 型糖尿病(T2DM)高血压患者的内皮功能。在替米沙坦治疗 12 个月前后,评估了诊室血压和清晨家庭血压水平以及血流介导的血管扩张(FMD)。治疗前后还采集了血液样本,用于测量几种生化参数以及脂联素(AN)和高敏 C 反应蛋白(hs-CRP)。治疗 12 个月后,诊室血压和清晨血压水平显著下降,血浆葡萄糖、糖化血红蛋白、总胆固醇、甘油三酯和低密度脂蛋白胆固醇水平也显著下降。血浆 AN 和高密度脂蛋白胆固醇水平升高,hs-CRP 水平降低。此外,FMD 显著增加;FMD 的变化与收缩压和舒张压的变化呈显著负相关,与 AN 的变化呈显著正相关。逐步多元回归分析显示,血浆 AN 和诊室收缩压的变化均是替米沙坦治疗后内皮功能的独立决定因素。总之,这项研究表明,长期使用替米沙坦不仅可改善 T2DM 高血压患者的血压、血糖和脂质代谢,还可改善内皮功能,可能是通过增加循环 AN 和降低血压。