首页> 外文期刊>Hypertension research: Official journal of the Japanese Society of Hypertension >Role of angiotensin II in plasma PAI-1 changes induced by imidapril or candesartan in hypertensive patients with metabolic syndrome.
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Role of angiotensin II in plasma PAI-1 changes induced by imidapril or candesartan in hypertensive patients with metabolic syndrome.

机译:血管紧张素II在咪达普利或坎地沙坦诱导的高血压代谢综合征患者血浆PAI-1变化中的作用。

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To evaluate the relationship between plasma plasminogen activator inhibitor-1 (PAI-1) and angiotensin II (Ang II) changes during treatment with imidapril and candesartan in hypertensive patients with metabolic syndrome. A total of 84 hypertensive patients with metabolic syndrome were randomized to imidapril 10 mg or candesartan 16 mg for 16 weeks. At weeks 4 and 8, there was a dose titration to imidapril 20 mg and candesartan 32 mg in nonresponders (systolic blood pressure (SBP) >140 and/or diastolic blood pressure (DBP) >90 mm Hg). We evaluated, at baseline and after 2, 4, 8, 12 and 16 weeks, clinic blood pressure, Ang II and PAI-1 antigen. Both imidapril and candesartan induced a similar SBP/DBP reduction (-19.4/16.8 and -19.5/16.3 mm Hg, respectively, P<0.001 vs. baseline). Both drugs decreased PAI-1 antigen after 4 weeks of treatment, but only the PAI-1 lowering effect of imidapril was sustained throughout the 16 weeks (-9.3 ng ml(-1), P<0.01 vs. baseline), whereas candesartan increased PAI-1 (+6.5 ng ml(-1), P<0.05 vs. baseline and P<0.01 vs. imidapril). Imidapril significantly decreased Ang II levels (-14.6 pg ml(-1) at week 16, P<0.05 vs. baseline), whereas candesartan increased them (+24.2 pg ml(-1), P<0.01 vs. baseline and vs. imidapril). In both groups there was a positive correlation between Ang II and PAI-1 changes (r=0.61, P<0.001 at week 16 for imidapril, and r=0.37, P<0.005 at week 16 for candesartan). Imidapril reduced plasma PAI-1 and Ang II levels, whereas candesartan increased them. This suggests that the different effect of angiotensin-converting enzyme inhibitors and Ang II blockers on Ang II production has a role in their different influence on fibrinolysis.
机译:为了评估在代谢综合征的高血压患者中,使用咪达普利和坎地沙坦治疗期间血浆纤溶酶原激活物抑制剂-1(PAI-1)和血管紧张素II(Ang II)的变化。总共84例患有代谢综合征的高血压患者被随机分配至咪达普利10 mg或坎地沙坦16 mg,持续16周。在第4周和第8周,无反应者的滴定剂量为咪达普利20 mg和坎地沙坦32 mg(收缩压(SBP)> 140和/或舒张压(DBP)> 90 mm Hg)。我们在基线以及第2、4、8、12和16周后评估了临床血压,Ang II和PAI-1抗原。咪达普利和坎地沙坦均引起相似的SBP / DBP降低(分别为-19.4 / 16.8和-19.5 / 16.3 mm Hg,相对于基线,P <0.001)。两种药物在治疗4周后均降低了PAI-1抗原,但在整个16周中仅降低了咪达普利的PAI-1降低作用(-9.3 ng ml(-1),相对于基线P <0.01),而坎地沙坦则升高PAI-1(+6.5 ng ml(-1),与基线相比P <0.05,与吡虫啉相比P <0.01)。咪达普利显着降低Ang II水平(在第16周时为-14.6 pg ml(-1),与基线相比,P <0.05),而坎地沙坦则将其升高(+24.2 pg ml(-1),与基线和vs.相比,P <0.01。吡虫啉)。两组中Ang II和PAI-1变化之间均呈正相关(咪达普利,r = 0.61,在第16周时P <0.001,坎地沙坦,r = 0.37,在16周时P <0.005)。咪达普利降低血浆PAI-1和Ang II水平,而坎地沙坦则升高血浆PAI-1和Ang II水平。这表明血管紧张素转化酶抑制剂和Ang II阻断剂对Ang II产生的不同作用在其对纤维蛋白溶解的不同影响中起作用。

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