Zin C, Copertari P, Landi E, San Martin C, Lopes M, Feruglio F, Alcocer L
French Hospital, Capital Federal, Argentina.
J Cardiovasc Pharmacol. 1987;10 Suppl 3:S113-8.
The serotonergic antagonist ketanserin (K) was compared to methyldopa (M) in a four-center international study in 119 hypertensive patients over 50 years of age. After a 4-week placebo run-in period, patients randomly received K (20-40 mg b.i.d.) or M (250-500 mg b.i.d.) for 3 months. The drugs were given in monotherapy for at least 1 month, then a diuretic could be added if blood pressure remained abnormally high. For the patients on monotherapy, active drug was replaced by placebo at the end of the 3-month period until the patients were hypertensive again. K and M had a similar effect on systolic blood pressure, but diastolic blood pressure was reduced significantly more by K than by M. Significantly more patients had their blood pressure normalized in the K group (75%) than in the M group (49%). The twice daily dosage schedule caused trough blood pressure control with both drugs. No rebound hypertension occurred at discontinuation of treatment. Monotherapy with K caused a decrease in heart rate (-5 beats/min) while M produced no change. Body weight decreased with K (-0.5 kg) and increased with M (+ 0.4 kg). No important hematological or biochemical changes were seen with either drug. Slightly fewer patients reported adverse reactions during K monotherapy (40%) than with M (45%). In the latter group mainly central side effects were observed. The data confirm K to be an effective first-line antihypertensive agent with a favorable side-effect profile.
在一项针对119名50岁以上高血压患者的四中心国际研究中,将5-羟色胺能拮抗剂酮色林(K)与甲基多巴(M)进行了比较。在为期4周的安慰剂导入期后,患者随机接受K(20 - 40毫克,每日两次)或M(250 - 500毫克,每日两次)治疗3个月。药物以单一疗法给药至少1个月,如果血压仍异常高,则可加用利尿剂。对于接受单一疗法的患者,在3个月疗程结束时将活性药物替换为安慰剂,直至患者再次出现高血压。K和M对收缩压有相似的作用,但K使舒张压降低的幅度明显大于M。K组(75%)血压恢复正常的患者明显多于M组(49%)。两种药物每日两次的给药方案均能实现谷值血压控制。停药时未发生反跳性高血压。K单一疗法导致心率下降(-5次/分钟),而M则无变化。体重随K降低(-0.5千克),随M增加(+0.4千克)。两种药物均未出现重要的血液学或生化变化。接受K单一疗法的患者报告不良反应(40%)的人数略少于接受M治疗的患者(45%)。在后一组中主要观察到中枢性副作用。这些数据证实K是一种有效的一线抗高血压药物,副作用较小。