Tezcan Hakan, Yavuz Dilek, Toprak Ahmet, Akpinar Ihsan, Koç Mehmet, Deyneli Oguzhan, Akalin Sema
Department of Internal Medicine, Marmara University School of Medicine, Istanbul, Turkey.
J Renin Angiotensin Aldosterone Syst. 2003 Jun;4(2):119-23. doi: 10.3317/jraas.2003.012.
Evidence suggests an association between insulin resistance, hypertension and impaired endothelial function. Studies have shown that insulin resistance precedes the development of hypertension. By improving insulin sensitivity, it may be possible to improve hypertension and the subsequent damage to vessel walls. Some data indicates beneficial effects of angiotensin-converting enzyme (ACE) inhibitors on insulin sensitivity and endothelial function. We aimed to investigate these effects of ACE inhibition in the same group of patients with essential hypertension.
Nine non-smoking, untreated hypertensive patients (38.3+9 years, 4/5 male/female) and 12 age-matched healthy subjects (35.2+6.7 years, 5/7 male/female) were included in the study. Hypertensive patients were given enalapril maleate (5 40 mg/day) for six months. The following parameters were studied at baseline and at the end of treatment period. Whole body insulin sensitivity was measured by a formula derived from an oral glucose tolerance test and named as the insulin sensitivity index (ISI). Insulin was measured by chemiluminescence and glucose by a glucose oxidase method. Endothelial function was evaluated as flow-mediated dilatation (FMD) of the brachial artery by ultrasonography and expressed as a percentage change relative to baseline diameter. Endothelial- independent vasodilatation was measured after sublingual nitroglycerine.
FMD was impaired in the hypertensive group compared with healthy subjects (7.3+3.1% vs. 15.3+4.8%, p<0.0005), and ISI values were 1.18+0.6 vs. 4.4+0.9 (p<0.0001) respectively. Both insulin sensitivity and FMD improved after the treatment period compared with baseline values, FMD increased from 7.3+3.1% to 16.0+2.9% (p<0.0005) and ISI from 1.18+0.6 to 4.2+1.0 (p<0.0001). FMD and ISI showed a significant positive correlation (r=0.67, p<0.001) in the hypertensive group.
Patients with essential hypertension have impaired endothelial function and decreased whole body insulin sensitivity compared with healthy subjects. Treatment for six months with enalapril maleate seems to improve both FMD and ISI. This study confirms the beneficial effects of ACE inhibition on both endothelial function and insulin sensitivity tested in the same group of essential hypertensive patients. The mechanism of these favourable effects of ACE inhibition needs to be clarified.
有证据表明胰岛素抵抗、高血压与内皮功能受损之间存在关联。研究显示胰岛素抵抗先于高血压的发生。通过改善胰岛素敏感性,有可能改善高血压及随后的血管壁损伤。一些数据表明血管紧张素转换酶(ACE)抑制剂对胰岛素敏感性和内皮功能有有益作用。我们旨在研究ACE抑制在同一组原发性高血压患者中的这些作用。
9名不吸烟、未接受治疗的高血压患者(38.3±9岁,4名男性/5名女性)和12名年龄匹配的健康受试者(35.2±6.7岁,5名男性/7名女性)纳入本研究。高血压患者服用马来酸依那普利(5~40mg/天),为期6个月。在基线期和治疗期末研究以下参数。通过口服葡萄糖耐量试验得出的公式测量全身胰岛素敏感性,并命名为胰岛素敏感性指数(ISI)。采用化学发光法测量胰岛素,用葡萄糖氧化酶法测量葡萄糖。通过超声检查评估肱动脉的血流介导的血管舒张(FMD)来评价内皮功能,并表示为相对于基线直径的百分比变化。舌下含服硝酸甘油后测量非内皮依赖性血管舒张。
与健康受试者相比,高血压组的FMD受损(7.3±3.1%对15.3±4.8%,p<0.0005),ISI值分别为1.18±0.6对4.4±0.9(p<0.0001)。与基线值相比,治疗期后胰岛素敏感性和FMD均有所改善,FMD从7.3±3.1%增加到16.0±2.9%(p<0.0005),ISI从1.18±0.6增加到4.2±1.0(p<0.0001)。高血压组中FMD和ISI呈显著正相关(r=0.67,p<0.001)。
与健康受试者相比,原发性高血压患者存在内皮功能受损和全身胰岛素敏感性降低。马来酸依那普利治疗6个月似乎可改善FMD和ISI。本研究证实了ACE抑制对同一组原发性高血压患者的内皮功能和胰岛素敏感性均有有益作用。ACE抑制这些有利作用的机制有待阐明。