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阿利吉仑和氯沙坦对代谢综合征合并高血压患者纤溶和胰岛素敏感性的不同影响。

Different effects of aliskiren and losartan on fibrinolysis and insulin sensitivity in hypertensive patients with metabolic syndrome.

机构信息

Department of Internal Medicine and Therapeutics, Centro Ipertensione e Fisiopatologia Cardiovascolare, University of Pavia, Pavia, Italy.

出版信息

Horm Metab Res. 2010 Nov;42(12):892-6. doi: 10.1055/s-0030-1263123. Epub 2010 Sep 2.

Abstract

The aim of this study was to compare the effect of aliskiren and losartan on fibrinolysis and insulin sensitivity (IS) in hypertensive patients with metabolic syndrome. After 2-week placebo period, 76 outpatients with mild to moderate hypertension and metabolic syndrome were randomized to aliskiren 300 mg od or losartan 100 mg od for 12 weeks. Clinic blood pressure (BP), plasma PAI-1 antigen, and tPA activity were evaluated after 2, 4, 8, and 12 weeks of treatment. At the end of each treatment period patients performed an euglycemic hyperinsulinemic clamp and IS was assessed by glucose infusion rate (GIR). Both aliskiren and losartan induced a significant and similar SBP/DBP reduction (-15.6/10.7 mmHg and -15.5/10.5 mmHg, p<0.001 vs. baseline, respectively). Both drugs decreased PAI-1 antigen and activity after 2 weeks of treatment; subsequently, only the decreasing effect of aliskiren was sustained throughout the 12 weeks [-7.5 ng/ml (-31%) p<0.05 vs. baseline], while with losartan PAI-1 increased at week 12 [+3.6 ng/ml (+15%), p<0.05 vs. baseline and p<0.01 vs. aliskiren)]. The tPA activity showed no significant change with aliskiren and a decrease with losartan [-0.04 IU/ml (-8%), p<0.05 vs. baseline and p<0.01 vs. aliskiren]. Aliskiren significantly increased GIR [+1.4 mg/min/kg (+28%), p<0.01 vs. baseline] while losartan did not change it [+0.2 mg/min/kg (+4%), NS vs. baseline, p<0.05 vs. aliskiren)]. These results indicated that in this type of patients, despite similar BP reduction, aliskiren improved the fibrinolytic balance as well as IS, while losartan worsened the fibrinolytic balance and did not affect IS. The clinical relevance of these different effects remains to be clarified.

摘要

本研究旨在比较阿利吉仑和氯沙坦对合并代谢综合征的高血压患者纤溶和胰岛素敏感性(IS)的影响。在 2 周安慰剂期后,76 例轻中度高血压合并代谢综合征的门诊患者被随机分为阿利吉仑 300mg 每日 1 次或氯沙坦 100mg 每日 1 次治疗 12 周。在治疗 2、4、8 和 12 周后评估临床血压(BP)、血浆 PAI-1 抗原和 tPA 活性。在每个治疗期末,患者行正葡萄糖高胰岛素钳夹试验,并通过葡萄糖输注率(GIR)评估 IS。阿利吉仑和氯沙坦均显著且相似地降低 SBP/DBP(分别为-15.6/10.7mmHg 和-15.5/10.5mmHg,p<0.001 与基线相比)。两种药物在治疗 2 周后均降低 PAI-1 抗原和活性;随后,只有阿利吉仑的降低作用持续整个 12 周[-7.5ng/ml(-31%),p<0.05 与基线相比],而氯沙坦在第 12 周时 PAI-1 增加[+3.6ng/ml(+15%),p<0.05 与基线相比,p<0.01 与阿利吉仑相比)]。tPA 活性在阿利吉仑治疗中无明显变化,而在氯沙坦治疗中下降[-0.04IU/ml(-8%),p<0.05 与基线相比,p<0.01 与阿利吉仑相比]。阿利吉仑显著增加 GIR[+1.4mg/min/kg(+28%),p<0.01 与基线相比],而氯沙坦未改变 GIR[+0.2mg/min/kg(+4%),与基线相比无统计学意义(NS),p<0.05 与阿利吉仑相比]。这些结果表明,在这种类型的患者中,尽管血压降低相似,阿利吉仑改善了纤溶平衡和 IS,而氯沙坦恶化了纤溶平衡且不影响 IS。这些不同影响的临床意义仍有待阐明。

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