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抗高血压药物对血脂和脂蛋白的影响,I. 利尿剂。

The effects of antihypertensive drugs on serum lipids and lipoproteins, I. Diuretics.

作者信息

Ames R P

出版信息

Drugs. 1986 Sep;32(3):260-78. doi: 10.2165/00003495-198632030-00003.

Abstract

Potassium-losing diuretic drugs, when used in the treatment of hypertension, cause unfavourable short term alterations in blood lipid and lipoprotein concentrations. The disturbance is characterised by increases in total cholesterol of 4 to 13%, in low density lipoprotein (LDL) cholesterol of 7 to 29%, in very-low density lipoprotein (VLDL) cholesterol of 7 to 56%, and in total triglyceride of 14 to 37%. The disturbance is variable among patients and over time in individual patients; it is absent in some. In long term treatment the data are fragmentary, but total cholesterol and triglycerides usually return to baseline values or below. The variability of the lipid response to diuretics has several consequences: firstly, it necessitates a sizeable study population (minimum of 30 patients) in order to document convincingly its presence or absence; secondly, lipoprotein fractions must be examined to define the pattern of the disturbance; and thirdly, the subsidence of the diuretic-induced lipid effects in long term treatment may be more apparent than real because even larger decreases have been noted in untreated groups in the few studies that wisely included these important controls for comparison. While the cause of the lipid-lipoprotein aberration is unclear, existing data suggest that certain attributes of the study population influence the response, i.e. age, habitual diet, hormonal milieu (gender), baseline cholesterol concentrations, and induced glucose intolerance. The apparent absence of lipid alterations with indapamide needs to be substantiated and compared with low doses of a standard thiazide-type drug. The lipid-lipoprotein effects of diuretics seem inconsequentially small, but they may contribute to the disappointing failure of diuretic-based regimens to lower the incidence of coronary heart disease in hypertensive patients. Nevertheless, diuretic-based treatment remains the only therapeutic regimen of proven benefit to congestive heart failure in patients with hypertension, and it is superior to beta-blockade in preventing stroke. Hence, alternative antihypertensive drug regimens must be compared prospectively with diuretics in order to verify any theoretic superiority.

摘要

失钾性利尿药用于治疗高血压时,会引起血脂和脂蛋白浓度在短期内出现不利变化。这种紊乱的特征是总胆固醇升高4%至13%,低密度脂蛋白(LDL)胆固醇升高7%至29%,极低密度脂蛋白(VLDL)胆固醇升高7%至56%,总甘油三酯升高14%至37%。这种紊乱在患者之间存在差异,且在个体患者中会随时间变化;有些患者没有这种情况。在长期治疗中,数据不完整,但总胆固醇和甘油三酯通常会恢复到基线值或更低。利尿剂对脂质反应的变异性有几个后果:首先,为了令人信服地证明其存在或不存在,需要相当大的研究人群(至少30名患者);其次,必须检查脂蛋白组分以确定紊乱模式;第三,长期治疗中利尿剂引起的脂质效应的消退可能比实际情况更明显,因为在少数明智地纳入这些重要对照进行比较的研究中,未治疗组的下降幅度甚至更大。虽然脂质 - 脂蛋白异常的原因尚不清楚,但现有数据表明,研究人群的某些特征会影响反应,即年龄、习惯饮食、激素环境(性别)、基线胆固醇浓度和诱发的葡萄糖不耐受。吲达帕胺明显不存在脂质改变这一点需要得到证实,并与低剂量的标准噻嗪类药物进行比较。利尿剂对脂质 - 脂蛋白的影响似乎微不足道,但它们可能导致基于利尿剂的治疗方案在降低高血压患者冠心病发病率方面令人失望地失败。然而,基于利尿剂的治疗仍然是对高血压合并充血性心力衰竭患者唯一已证实有益的治疗方案,并且在预防中风方面优于β受体阻滞剂。因此,必须将替代的抗高血压药物方案与利尿剂进行前瞻性比较,以验证任何理论上的优越性。

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