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首页> 外文期刊>European journal of gastroenterology and hepatology >Effects of losartan and amlodipine alone or combined with simvastatin in hypertensive patients with nonalcoholic hepatic steatosis
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Effects of losartan and amlodipine alone or combined with simvastatin in hypertensive patients with nonalcoholic hepatic steatosis

机译:氯沙坦和氨氯地平单独或与辛伐他汀联合治疗对非酒精性肝脂肪变性高血压患者的作用

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Objectives: The inhibition of the renin-angiotensin system and of the 3-hydroxy-3-methylglutaryl-coenzyme A reductase could improve hepatic steatosis. The aim of this study was to evaluate the effects of losartan or amlodipine alone or combined with simvastatin on hepatic steatosis degree, and on insulin sensitivity in normocholesterolemic, hypertensive patients with nonalcoholic hepatic steatosis. Methods: Patients were treated with losartan, 100 mg/day, or amlodipine, 10 mg/day, for 6 months; subsequently simvastatin, 20 mg/day was added to both treatments for a further 6 months. The patients performed an ultrasound examination [steatosis degree, subcutaneous adipose tissue (SAT) and visceral adipose tissue (VAT) diameter], an euglycemic hyperinsulinemic clamp [glucose infusion rate (GIR)], and a blood sample (fasting plasma glucose, fasting plasma insulin, triglycerides, and inflammatory parameters) at baseline, and after 6 and 12 months, respectively. Results: Both losartan and amlodipine induced a significant and similar systolic blood pressure/diastolic blood pressure reduction (P<0.001 vs. baseline). Losartan significantly increased GIR (P<0.05 vs. baseline) compared with amlodipine therapy, and the addition of simvastatin to losartan further increased GIR compared with the simvastatin added to amlodipine therapy (P<0.01 and P<0.05 vs. baseline, respectively). Losartan significantly decreased the steatosis degree, SAT, and VAT diameter compared with amlodipine therapy (P<0.05 vs. baseline with losartan for all). The addition of simvastatin to losartan therapy further decreased the steatosis degree, SAT, and VAT diameter. Conclusion: Losartan and simvastatin combination significantly improved the hepatic steatosis indices compared with amlodipine and simvastatin combination.
机译:目的:抑制肾素-血管紧张素系统和3-羟基-3-甲基戊二酰辅酶A还原酶可以改善肝脂肪变性。这项研究的目的是评估氯沙坦或氨氯地平单独或与辛伐他汀联用对非胆固醇性肝脂肪变性的正常胆固醇血症,高血压患者的肝脏脂肪变性程度和胰岛素敏感性的影响。方法:患者接受100毫克/天的氯沙坦或10毫克/天的氨氯地平治疗6个月;随后将辛伐他汀(20毫克/天)添加到两种治疗中,持续6个月。患者进行了超声检查[脂肪变性程度,皮下脂肪组织(SAT)和内脏脂肪组织(VAT)直径],血糖正常的高胰岛素钳夹[葡萄糖输注率(GIR)]和血液样本(空腹血糖,空腹血浆)在基线时以及分别在6个月和12个月后注射胰岛素,甘油三酸酯和炎症参数)。结果:氯沙坦和氨氯地平均引起明显和相似的收缩压/舒张压降低(相对于基线,P <0.001)。与氨氯地平治疗相比,氯沙坦显着提高了GIR(相对于基线,P <0.05),与氨氯地平治疗中加入的辛伐他汀相比,氯沙坦中添加辛伐他汀进一步提高了GIR(相对于基线,P <0.01和P <0.05)。与氨氯地平治疗相比,氯沙坦显着降低了脂肪变性程度,SAT和增值税直径(与氯沙坦治疗组的基线相比,P <0.05)。在氯沙坦治疗中加入辛伐他汀可进一步降低脂肪变性程度,SAT和增值税直径。结论:与氨氯地平联合辛伐他汀相比,氯沙坦联合辛伐他汀能显着改善肝脂肪变性指数。

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