Berlanga C, Ortega-Soto H A, Ontiveros M, Senties H
Special Studies Clinic, Mexican Institute of Psychiatry, Tlalpan.
Psychiatry Res. 1992 Dec;44(3):257-62. doi: 10.1016/0165-1781(92)90029-3.
A double-blind clinical trial was carried out to evaluate the efficacy of S-adenosyl-L-methionine (SAMe) in speeding the onset of action of imipramine (IMI). SAMe is a naturally occurring substance that has been shown to possess antidepressant activity with a rapid mode of onset and minimal side effects. Sixty-three outpatients with moderate to severe depression were included in the study. After an initial 1-week placebo period, only 40 patients entered the active treatment phase. During the first 2 weeks of the trial, half of these patients received 200 mg/day of SAMe intramuscularly, while the other half received placebo. Simultaneously, oral IMI was administered to all patients at a fixed dose of 150 mg/day. The onset of clinical response was determined by evaluating patients every second day. By the end of week 2, the parenteral treatment was suppressed and IMI was adjusted according to individual needs. Depressive symptoms decreased earlier in the patients who were receiving the SAMe-IMI combination than in those who were receiving the placebo-IMI combination.
开展了一项双盲临床试验,以评估S-腺苷-L-蛋氨酸(SAMe)在加速丙咪嗪(IMI)起效方面的疗效。SAMe是一种天然存在的物质,已被证明具有抗抑郁活性,起效迅速且副作用极小。该研究纳入了63名中度至重度抑郁症门诊患者。在最初为期1周的安慰剂期后,只有40名患者进入积极治疗阶段。在试验的前2周,这些患者中的一半每天肌肉注射200毫克SAMe,而另一半接受安慰剂。同时,所有患者均以每天150毫克的固定剂量口服IMI。通过每隔一天对患者进行评估来确定临床反应的起效情况。到第2周末,停止非肠道治疗,并根据个体需求调整IMI。接受SAMe-IMI联合治疗的患者的抑郁症状比接受安慰剂-IMI联合治疗的患者更早减轻。