首页> 外文期刊>Advances in therapy. >Telmisartan improves lipid metabolism and adiponectin production but does not affect glycemic control in hypertensive patients with type 2 diabetes.
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Telmisartan improves lipid metabolism and adiponectin production but does not affect glycemic control in hypertensive patients with type 2 diabetes.

机译:替米沙坦可改善2型糖尿病高血压患者的脂质代谢和脂联素生成,但不影响血糖控制。

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Angiotensin II receptor blockers as a class are reported to act as insulin sensitizers. Of these, telmisartan has been shown to have additional unique peroxisome proliferator-activated receptor-gamma-mediated, insulin-sensitizing properties. In this study, investigators explored the effects of telmisartan on glycemic control and lipid metabolism in hypertensive patients with type 2 diabetes who had switched to telmisartan from another angiotensin II receptor blocker. The study subjects were 42 hypertensive outpatients with type 2 diabetes who were being treated with candesartan 8 mg/d and who agreed to switch to treatment with telmisartan 40 mg/d. Relevant laboratory variables were measured 6 mo before treatment switching, at the time of switching, and 6 mo after switching. No significant differences were noted in blood pressure, body mass index, or glycosylated hemoglobin among subjects before and after therapy was switched. No adverse reactions such as edema or hepatic toxicity were noted. No significant changes in fasting plasma glucose, fasting insulin, HOMA-R (insulin resistance as measured by the homeostasis model), preheparin lipoprotein lipase mass, high-density lipoprotein cholesterol, and free fatty acids were noted. Triglyceride levels were significantly decreased, however, and adiponectin levels were significantly increased (8.1+/-3.1 microg/mL at switching; 8.6+/-3.0 microg/mL 6 mo after switching; P<.01) after the switch to telmisartan therapy. Study results show that telmisartan did not affect glycemic control, but it improved lipid metabolism and adiponectin production in patients with type 2 diabetes, suggesting that AT(1)-receptor antagonism and selective peroxisome proliferator-activated receptor-gamma activation by telmisartan combine to account for observed effects on lipid metabolism and adiponectin production.
机译:据报道,血管紧张素II受体阻滞剂可作为胰岛素增敏剂。其中,替米沙坦已显示具有其他独特的过氧化物酶体增殖物激活的受体-γ介导的胰岛素敏感性。在这项研究中,研究人员探讨了替米沙坦对从另一种血管紧张素II受体阻滞剂转为替米沙坦的高血压2型糖尿病患者的血糖控制和脂质代谢的影响。研究对象为42例2型糖尿病高血压门诊患者,他们接受坎地沙坦8 mg / d的治疗,并同意改用替米沙坦40 mg / d的治疗。在治疗切换前,切换时和切换后6mo测量相关的实验室变量。在治疗前后,受试者之间的血压,体重指数或糖基化血红蛋白没有显着差异。没有观察到诸如水肿或肝毒性的不良反应。空腹血糖,空腹胰岛素,HOMA-R(通过稳态模型测量的胰岛素抵抗),肝素前脂蛋白脂肪酶质量,高密度脂蛋白胆固醇和游离脂肪酸均无显着变化。但是,在转用替米沙坦治疗后,甘油三酸酯水平显着降低,脂联素水平显着提高(切换时为8.1 +/- 3.1 microg / mL;切换后为6 mo时为8.6 +/- 3.0 microg / mL; P <.01) 。研究结果表明,替米沙坦不影响血糖控制,但改善2型糖尿病患者的脂质代谢和脂联素生成,提示替米沙坦对AT(1)受体的拮抗作用和选择性过氧化物酶体增殖物激活的受体-γ激活相结合。用于观察对脂质代谢和脂联素产生的影响。

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