Balldin J, Berggren U, Engel J, Eriksson M, Hård E, Söderpalm B
Department of Clinical Neuroscience, University of Göteborg, Sweden.
Alcohol Clin Exp Res. 1994 Oct;18(5):1133-6. doi: 10.1111/j.1530-0277.1994.tb00093.x.
The effect of the selective serotonin reuptake inhibitor citalopram (40 mg daily dose) on alcohol intake was investigated in a double-blind, placebo-controlled cross-over study. Thirty men with heavy alcohol consumption (mean daily alcohol intake 111 +/- 51 g pure alcohol) completed the study. After a 2-week baseline period, subjects were randomly allocated to treatment with either citalopram or placebo for 5 weeks. In the total sample of heavy drinkers, no difference was found between citalopram and placebo treatment in alcohol consumption or days of abstinence. However, the response to citalopram was negatively correlated (rs = -0.67, p < 0.01) with baseline levels of mean daily alcohol intake. Therefore, we divided the total sample into two subgroups with baseline mean daily alcohol intake above and below median (107 g pure alcohol), respectively. In the group with the higher baseline values (138 +/- 25 g pure alcohol), citalopram was not different from placebo in reducing the daily alcohol intake, but in subjects with the lower baseline values (85 +/- 15 g pure alcohol), citalopram was significantly (p < 0.01) superior to placebo. Consequently, citalopram at the present dose appears capable of reducing alcohol intake only in a subgroup of heavy drinkers with a mean daily consumption of between 60 and 100 g pure alcohol.
在一项双盲、安慰剂对照的交叉研究中,研究了选择性5-羟色胺再摄取抑制剂西酞普兰(每日剂量40毫克)对酒精摄入量的影响。30名重度饮酒男性(平均每日酒精摄入量为111±51克纯酒精)完成了该研究。在为期2周的基线期后,受试者被随机分配接受西酞普兰或安慰剂治疗5周。在重度饮酒者的总样本中,西酞普兰和安慰剂治疗在酒精消费量或戒酒天数方面未发现差异。然而,对西酞普兰的反应与平均每日酒精摄入量的基线水平呈负相关(rs = -0.67,p < 0.01)。因此,我们将总样本分为两个亚组,分别以平均每日酒精摄入量高于和低于中位数(107克纯酒精)为基线。在基线值较高的组(138±25克纯酒精)中,西酞普兰在减少每日酒精摄入量方面与安慰剂没有差异,但在基线值较低的受试者(85±15克纯酒精)中,西酞普兰显著(p < 0.01)优于安慰剂。因此,目前剂量的西酞普兰似乎仅能在平均每日消费量为60至100克纯酒精的重度饮酒者亚组中减少酒精摄入量。