Department of Psychiatry, NYU Langone Health, 1 Park Avenue, New York, NY 10016, United States of America; Nathan Kline Institute for Psychiatric Research, 140 Old Orangeburg Road, Orangeburg, NY 10962, United States of America.
Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, 55 Fruit Street, Boston, MA 02144, United States of America.
Schizophr Res. 2019 Jun;208:331-337. doi: 10.1016/j.schres.2019.01.028. Epub 2019 Jan 30.
Antidepressants are frequently prescribed in first episode schizophrenia (FES) patients for negative symptoms or for subsyndromal depressive symptoms, but therapeutic benefit has not been established, despite evidence of efficacy in later-stage schizophrenia. We conducted a 52 week, placebo-controlled add-on trial of citalopram in patients with FES who did not meet criteria for major depression to determine whether maintenance therapy with citalopram would improve outcomes by preventing or improving negative and depressive symptoms. Primary outcomes were negative symptoms measured by the Scale for Assessment of Negative Symptoms and depressive symptoms measured by the Calgary Depression Scale for Schizophrenia; both were analyzed by an intent-to-treat, mixed effects, area-under-the-curve analysis to assess the cumulative effects of symptom improvement and symptom prevention over a one-year period. Ninety-five patients were randomized and 52 (54%) completed the trial. Negative symptoms were reduced with citalopram compared to placebo (p = .04); the effect size of citalopram versus placebo was 0.32 for participants with a duration of untreated psychosis (DUP) of <18 weeks (median split) and 0.52 with a DUP >18 weeks. Rates of new-onset depression did not differ between groups; improvement in depressive symptoms was greater with placebo than citalopram (p = .02). Sexual side effects were more common with citalopram, but overall treatment-emergent side effects were not increased compared to placebo. In conclusion, citalopram may reduce levels of negative symptoms, particularly in patients with longer DUP, but we found no evidence of benefit for subsyndromal depressive symptoms.
抗抑郁药常用于首发精神分裂症(FES)患者的阴性症状或亚综合征抑郁症状,但尽管有后期精神分裂症疗效的证据,但并未确定其治疗益处。我们进行了一项为期 52 周、安慰剂对照的西酞普兰附加治疗 FES 患者的试验,这些患者不符合重性抑郁的标准,以确定西酞普兰的维持治疗是否可以通过预防或改善阴性和抑郁症状来改善结局。主要结局是通过阴性症状量表(Scale for Assessment of Negative Symptoms)评估的阴性症状和通过精神分裂症卡尔加里抑郁量表(Calgary Depression Scale for Schizophrenia)评估的抑郁症状;两者均通过意向治疗、混合效应、曲线下面积分析进行分析,以评估一年内症状改善和症状预防的累积效应。95 名患者被随机分配,52 名(54%)完成了试验。与安慰剂相比,西酞普兰可降低阴性症状(p=0.04);对于未治疗精神病持续时间(DUP)<18 周(中位数分割)的参与者,西酞普兰与安慰剂相比的效应大小为 0.32,DUP>18 周的参与者为 0.52。新发抑郁的发生率在两组之间没有差异;与西酞普兰相比,安慰剂改善抑郁症状的效果更好(p=0.02)。西酞普兰更常见的是性副作用,但与安慰剂相比,总体治疗相关副作用并未增加。总之,西酞普兰可能会降低阴性症状的水平,尤其是在 DUP 较长的患者中,但我们没有发现亚综合征抑郁症状有获益的证据。