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卡托普利和氢氯噻嗪固定复方在抗高血压治疗中的“脂质保护”作用。

A "lipo-protective" effect of a fixed combination of captopril and hydrochlorothiazide in antihypertensive therapy.

作者信息

Ratheiser K, Dusleag J, Seitl K, Titscher G, Klein W

机构信息

I. Medizinische Universitätsklinik, Vienna, Austria.

出版信息

Clin Cardiol. 1992 Sep;15(9):647-54. doi: 10.1002/clc.4960150906.

Abstract

Increases of triglycerides and total cholesterol have been reported during treatment with antihypertensive drugs, most notably with beta blockers and diuretics. ACE inhibitors, on the other hand, are not known for having a negative effect on lipid profile. To evaluate the effects of a fixed combination of captopril and hydrochlorothiazide on lipid metabolism, blood pressure, and quality of life, we performed an open prospective study. A total of 2,154 patients with or without hypercholesterolemia, but not receiving lipid lowering drugs, were enrolled. Of the 1891 evaluable patients at baseline, 34.1% had a moderate risk with total cholesterol between 5.2 and 6.5 mmol/l (mean 5.8 mmol/l) and 41.3% had a high coronary heart disease (CHD) risk with total cholesterol higher than 6.5 mmol/l (mean 7.3 mmol/l). After six months of treatment, the median cholesterol level in the moderate risk group decreased from 5.8 to 5.4 mmol/l (p less than 0.0003) and in the high risk group from 7.3 to 6.3 mmol/l (p less than 0.0001). Triglycerides also decreased, whereas high density lipoprotein (HDL) increased in both risk groups. Systolic and diastolic blood pressure fell as expected and quality of life improved. The fixed combination was well tolerated. We observed a significant improvement of lipid profile in patients with mild to moderate hypertension while undergoing treatment with the fixed combination of captopril and hydrochlorothiazide. We suggest that captopril may balance the negative effects of hydrochlorothiazide on lipid metabolism in patients with hypertension and concomitant hyperlipidemia.

摘要

据报道,在使用抗高血压药物治疗期间,甘油三酯和总胆固醇会升高,最明显的是使用β受体阻滞剂和利尿剂时。另一方面,人们并不认为血管紧张素转换酶(ACE)抑制剂会对血脂谱产生负面影响。为了评估卡托普利和氢氯噻嗪固定组合对脂质代谢、血压和生活质量的影响,我们进行了一项开放性前瞻性研究。总共纳入了2154例有或无高胆固醇血症但未服用降脂药物的患者。在基线时可评估的1891例患者中,34.1%有中度风险,总胆固醇在5.2至6.5 mmol/l之间(平均5.8 mmol/l),41.3%有高冠心病(CHD)风险,总胆固醇高于6.5 mmol/l(平均7.3 mmol/l)。治疗六个月后,中度风险组的胆固醇中位数水平从5.8 mmol/l降至5.4 mmol/l(p<0.0003),高风险组从7.3 mmol/l降至6.3 mmol/l(p<0.0001)。两个风险组的甘油三酯也有所下降,而高密度脂蛋白(HDL)有所增加。收缩压和舒张压如预期下降,生活质量得到改善。该固定组合耐受性良好。我们观察到,在使用卡托普利和氢氯噻嗪固定组合治疗轻度至中度高血压患者时,血脂谱有显著改善。我们认为,卡托普利可能会平衡氢氯噻嗪对高血压合并高脂血症患者脂质代谢的负面影响。

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