Meier A, Weidmann P, Mordasini R, Riesen W, Bachmann C
Atherosclerosis. 1982 Feb;41(2-3):415-9. doi: 10.1016/0021-9150(82)90205-2.
In 18 patients with essential hypertension serum low density lipoprotein cholesterol (LDL-C) was significantly (P less than 0.001) increased following short-term chlorthalidone therapy, but not during combination therapy with chlorthalidone and a betablocker. This tendency was similar in two subgroups which were studied with an inverse sequence of drug administration. In Group I (11 men), a 22% increase (P less than 0.01) in LDL-C during chlorthalidone monotherapy was restored to normal 6 weeks after addition to a betablocker to the diuretic; in Group II (5 men, 2 postmenopausal women) LDL-C levels were increased by 41% (P less than 0.05) 6 weeks after withdrawal of the betablocker from the combination therapy. No significant changes occurred during either the treatment phase in high density lipoprotein cholesterol or apoprotein B levels. It is concluded that combination therapy with a betablocker may prevent or reverse an increase in serum LDL-C associated with short-term chlorthalidone monotherapy.
在18例原发性高血压患者中,短期服用氯噻酮治疗后,血清低密度脂蛋白胆固醇(LDL-C)显著升高(P<0.001),但氯噻酮与β受体阻滞剂联合治疗期间则未出现这种情况。在两个采用相反给药顺序进行研究的亚组中,这种趋势相似。在第一组(11名男性)中,氯噻酮单药治疗期间LDL-C升高了22%(P<0.01),在利尿剂中添加β受体阻滞剂6周后恢复正常;在第二组(5名男性,2名绝经后女性)中,联合治疗中停用β受体阻滞剂6周后,LDL-C水平升高了41%(P<0.05)。在治疗阶段,高密度脂蛋白胆固醇或载脂蛋白B水平均未发生显著变化。结论是,β受体阻滞剂联合治疗可能预防或逆转与短期氯噻酮单药治疗相关的血清LDL-C升高。