Vitale Cristiana, Mercuro Giuseppe, Castiglioni Carlotta, Cornoldi Alessandra, Tulli Arianna, Fini Massimo, Volterrani Maurizio, Rosano Giuseppe M C
Department of Medical Sciences and Rehabilitation, IRCCS San Raffaele, Rome, Italy.
Cardiovasc Diabetol. 2005 May 15;4:6. doi: 10.1186/1475-2840-4-6.
Metabolic syndrome is a cluster of common cardiovascular risk factors that includes hypertension and insulin resistance. Hypertension and diabetes mellitus are frequent comorbidities and, like metabolic syndrome, increase the risk of cardiovascular events. Telmisartan, an antihypertensive agent with evidence of partial peroxisome proliferator-activated receptor activity-gamma (PPARgamma) activity, may improve insulin sensitivity and lipid profile in patients with metabolic syndrome.
In a double-blind, parallel-group, randomized study, patients with World Health Organization criteria for metabolic syndrome received once-daily doses of telmisartan (80 mg, n = 20) or losartan (50 mg, n = 20) for 3 months. At baseline and end of treatment, fasting and postprandial plasma glucose, insulin sensitivity, glycosylated haemoglobin (HBA1c) and 24-hour mean systolic and diastolic blood pressures were determined.
Telmisartan, but not losartan, significantly (p < 0.05) reduced free plasma glucose, free plasma insulin, homeostasis model assessment of insulin resistance and HbAic. Following treatment, plasma glucose and insulin were reduced during the oral glucose tolerance test by telmisartan, but not by losartan. Telmisartan also significantly reduced 24-hour mean systolic blood pressure (p < 0.05) and diastolic blood pressure (p < 0.05) compared with losartan.
As well as providing superior 24-hour blood pressure control, telmisartan, unlike losartan, displayed insulin-sensitizing activity, which may be explained by its partial PPARgamma activity.
代谢综合征是一组常见的心血管危险因素,包括高血压和胰岛素抵抗。高血压和糖尿病是常见的合并症,与代谢综合征一样,会增加心血管事件的风险。替米沙坦是一种具有部分过氧化物酶体增殖物激活受体γ(PPARγ)活性证据的抗高血压药物,可能改善代谢综合征患者的胰岛素敏感性和血脂谱。
在一项双盲、平行组、随机研究中,符合世界卫生组织代谢综合征标准的患者每日服用一次替米沙坦(80毫克,n = 20)或氯沙坦(50毫克,n = 20),持续3个月。在基线和治疗结束时,测定空腹和餐后血浆葡萄糖、胰岛素敏感性、糖化血红蛋白(HBA1c)以及24小时平均收缩压和舒张压。
替米沙坦而非氯沙坦显著(p < 0.05)降低了游离血浆葡萄糖、游离血浆胰岛素、胰岛素抵抗的稳态模型评估值和HbAic。治疗后,替米沙坦可降低口服葡萄糖耐量试验期间的血浆葡萄糖和胰岛素水平,而氯沙坦则无此作用。与氯沙坦相比,替米沙坦还显著降低了24小时平均收缩压(p < 0.05)和舒张压(p < 0.05)。
与氯沙坦不同,替米沙坦除了能提供更好的24小时血压控制外,还具有胰岛素增敏活性,这可能与其部分PPARγ活性有关。