Suppr超能文献

血管紧张素转换酶抑制而非血管紧张素II拮抗可降低超重高血压患者的血浆纤维蛋白原和胰岛素抵抗。

ACE inhibition but not angiotensin II antagonism reduces plasma fibrinogen and insulin resistance in overweight hypertensive patients.

作者信息

Fogari R, Zoppi A, Lazzari P, Preti P, Mugellini A, Corradi L, Lusardi P

机构信息

Department of Internal Medicine and Therapeutics, University of Pavia, Italy.

出版信息

J Cardiovasc Pharmacol. 1998 Oct;32(4):616-20. doi: 10.1097/00005344-199810000-00014.

Abstract

The aim of this study was to compare the effects of the angiotensin-converting enzyme (ACE) inhibitor perindopril and the angiotensin II antagonist losartan on insulin sensitivity and plasma fibrinogen in overweight hypertensive patients. Twenty-eight overweight mild to moderate [diastolic blood pressure (DBP) >90 and <110 mm Hg] hypertensives aged 43-64 years, after a 4-week placebo period, were randomized to perindopril, 4 mg o.d., or losartan, 50 mg o.d., for 6 weeks. Then, after a new placebo period, patients were crossed to the alternative regimen for further 6 weeks. At the end of the placebo and of the treatment periods, blood pressure was measured, plasma fibrinogen was evaluated, and insulin sensitivity was assessed by the euglycemic, hyperinsulinemic clamp technique. Glucose infusion rate (GIR) during the last 30 min of clamp and total glucose requirement (TGR) were evaluated. Both perindopril and losartan reduced SBP (by a mean of 20.2 mm Hg, p < 0.001 vs. placebo; and 15.8 mm Hg, p = 0.002 vs. placebo, respectively) and DBP (by a mean of 15.2 mm Hg, p = 0.001 vs. placebo, and 11.8 mm Hg, p = 0.01 vs. placebo respectively), with no difference between the two treatments. GIR was significantly increased by perindopril (+2.91 mg/min/kg, p = 0.042 vs. placebo), but not by losartan (+0.28 mg/min/kg, NS). TGR was not modified by losartan but was increased by perindopril (+9.3 g, p = 0.042 vs. placebo). Plasma fibrinogen levels were reduced by perindopril (-53.4 mg/dl, p = 0.022 vs. placebo) but not by losartan (-16.8 mg/dl, NS). The perindopril-induced decrease in fibrinogen was correlated with the increase in GIR (r = 0.39; p < 0.01). These findings suggest that fibrinogen decrease produced by the ACE inhibitor is related to its action on insulin sensitivity, which seems to be dependent not on angiotensin II blockade but rather on other mechanisms.

摘要

本研究旨在比较血管紧张素转换酶(ACE)抑制剂培哚普利和血管紧张素II拮抗剂氯沙坦对超重高血压患者胰岛素敏感性和血浆纤维蛋白原的影响。28例年龄在43 - 64岁的超重轻度至中度[舒张压(DBP)>90且<110 mmHg]高血压患者,经过4周的安慰剂期后,被随机分为两组,一组每日口服4 mg培哚普利,另一组每日口服50 mg氯沙坦,为期6周。然后,在新的安慰剂期后,患者交叉接受另一种治疗方案,再进行6周。在安慰剂期和治疗期结束时,测量血压,评估血浆纤维蛋白原,并通过正常血糖、高胰岛素钳夹技术评估胰岛素敏感性。评估钳夹最后30分钟的葡萄糖输注速率(GIR)和总葡萄糖需求量(TGR)。培哚普利和氯沙坦均降低收缩压(平均降低20.2 mmHg,与安慰剂相比p < 0.001;以及15.8 mmHg,与安慰剂相比p = 0.002)和舒张压(平均降低15.2 mmHg,与安慰剂相比p = 0.001;以及11.8 mmHg,与安慰剂相比p = 0.01),两种治疗之间无差异。培哚普利显著增加GIR(+2.91 mg/min/kg,与安慰剂相比p = 0.042),但氯沙坦未增加(+0.28 mg/min/kg,无统计学意义)。氯沙坦未改变TGR,但培哚普利使其增加(+9.3 g,与安慰剂相比p = 0.042)。培哚普利降低血浆纤维蛋白原水平(-53.4 mg/dl,与安慰剂相比p = 0.022),但氯沙坦未降低(-16.8 mg/dl,无统计学意义)。培哚普利引起的纤维蛋白原降低与GIR增加相关(r = 0.39;p < 0.01)。这些发现表明,ACE抑制剂引起的纤维蛋白原降低与其对胰岛素敏感性的作用有关,这似乎不依赖于血管紧张素II阻断,而是依赖于其他机制。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验