Efficacy for Psychopathology and Body Weight and Safety of Topiramate-Antipsychotic Cotreatment in Patients With Schizophrenia Spectrum Disorders: Results From a Meta-Analysis of Randomized Controlled Trials

被引:32
作者
Correll, Christoph U. [1 ,2 ,3 ,4 ]
Maayan, Lawrence [5 ]
Kane, John [1 ,2 ,3 ,4 ]
De Hert, Marc [6 ]
Cohen, Dan [7 ]
机构
[1] North Shore Long Isl Jewish Hlth Syst, Psychiat Res, Zucker Hillside Hosp, Glen Oaks, NY USA
[2] Hofstra North Shore LIJ Sch Med, Hempstead, NY USA
[3] Feinstein Inst Med Res, Manhasset, NY USA
[4] Albert Einstein Coll Med, Bronx, NY 10467 USA
[5] Nathan S Kline Inst Psychiat Res, Orangeburg, NY 10962 USA
[6] Katholieke Univ Leuven, Dept Neurosci, Univ Psychiat Ctr, Leuven, Belgium
[7] Mental Hlth Org North Holland North, Dept Community Mental Hlth, Heerhugowaard, Netherlands
关键词
Neuropsychiatric Disorders; Anepsychoecs; Schizophrenia; Weight; ADD-ON THERAPY; TREATMENT-RESISTANT SCHIZOPHRENIA; DOUBLE-BLIND; NEGATIVE SYMPTOMS; METABOLIC ABNORMALITIES; OBESE SUBJECTS; SCHIZOAFFECTIVE DISORDER; ATYPICAL ANTIPSYCHOTICS; ANTIEPILEPTIC DRUGS; PHYSICAL ILLNESS;
D O I
10.4088/JCP.15r10373
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: To meta-analyze the efficacy and tolerability of topiramate-antipsychotic cotreatment in schizophrenia. Data Sources: PubMed/MEDLINE database were searched until September 5, 2015, using the keywords topiramate AND antipsych* OR neurolept* OR specific antipsychotic names. Study Selection: Randomized controlled trials (RCTs) of topiramate-antipsychotic cotreatment versus placebo and ongoing antipsychotic treatment in patients with schizophrenia spectrum disorders were included. Data Extraction: Two evaluators extracted data. Standardized mean difference (SMD), weighted mean difference (WMD), and risk ratio (RR) +/- 95% CIs were calculated. Results: In 8 RCTs, lasting a mean +/- SD of 13.6 +/- 4.9 weeks, 439 patients were randomized to topiramate (100-400 mg/d) versus placebo (trials = 7) or ongoing antipsychotic treatment (trial = 1). Topiramate outperformed the comparator regarding total psychopathology (trials = 6, n = 269, SMD = -0.57 [95% CI, -1.01 to -0.14], P = .01), positive symptoms (trials = 4, n = 190, SMD = -0.56 [95% CI, -1.0 to -0.11], P = .01), negative symptoms (trials = 4, n = 190, SMD = -0.62 [95% CI, -1.13 to -0.10], P = .02) general psychopathology (trials = 3, n = 179, SMD = -0.69 [95% CI, -1.27 to -0.11], P = .02), body weight (trials = 7, n = 327, WMD = -3.14 kg [95% CI, -5.55 to -0.73], P = .01), and body mass index (BMI) (trials = 4, n = 198, WMD = -1.80 [95% CI, -2.77 to -0.84], P = .0003). Topiramate's efficacy for total psychopathology and weight reduction effects were not mediated/moderated by trial duration, topiramate dose, sex, age, inpatient status, baseline Positive and Negative Syndrome Scale, or baseline BMI. Conversely, clozapine-topiramate cotreatment moderated greater efficacy, but less weight loss, compared to topiramate-nonclozapine antipsychotic combinations. All-cause discontinuation was similar between topiramate and control groups (trials = 7, RR = 1.24 [95% CI, 0.76 to 2.02], P = .39). Topiramate trended only toward more paresthesia than placebo (trials = 4, RR = 2.03 [95 % CI, 0.99 to 4.18], P = .05). Conclusions: Topiramate-antipsychotic cotreatment significantly reduced total, positive, negative, and general psychopathology and weight/BMI in patients with schizophrenia spectrum disorder while being well tolerated. However, larger studies are needed to confirm and extend these findings. (C) Copyright 2016 Physicians Postgraduate Press, Inc.
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页码:E746 / +
页数:14
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