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托吡酯辅助治疗精神分裂症的疗效与安全性:随机对照试验的荟萃分析

Efficacy and safety of adjunctive topiramate for schizophrenia: a meta-analysis of randomized controlled trials.

作者信息

Zheng W, Xiang Y-T, Xiang Y-Q, Li X-B, Ungvari G S, Chiu H F K, Correll C U

机构信息

The Affiliated Brain Hospital of Guangzhou Medical University (Guangzhou Huiai Hospital), Guangzhou, China.

The National Clinical Research Center for Mental Disorders, China & Beijing Anding Hospital, Capital Medical University, Beijing, China.

出版信息

Acta Psychiatr Scand. 2016 Nov;134(5):385-398. doi: 10.1111/acps.12631. Epub 2016 Sep 1.

Abstract

OBJECTIVE

To systematically examine the randomized controlled trial (RCT) evidence regarding efficacy and tolerability of topiramate cotreatment with antipsychotics in schizophrenia-spectrum disorders.

METHODS

Random-effects meta-analysis of RCTs of topiramate cotreatment with antipsychotics vs. placebo/ongoing antipsychotic treatment in schizophrenia-spectrum disorders. Standardized or weighted mean difference (SMD/WMD), risk ratio (RR) ±95% confidence intervals (CIs), and number needed to harm (NNH) were calculated.

RESULTS

Across 16 RCTs (n = 934, duration = 11.8 ± 5.6 weeks), topiramate outperformed the comparator regarding change/endpoint of total (SMD: -0.58, 95% CI: -0.82, -0.35, P < 0.00001), positive (SMD: -0.37, 95% CI: -0.61, -0.14, P = 0.002), negative (SMD: -0.58, 95% CI: -0.87, -0.29, P < 0.0001), and general symptoms (SMD: -0.68, 95% CI: -0.95, -0.40, P < 0.00001). Furthermore, topiramate was superior regarding body weight (WMD: -2.75 kg, 95% CI: -4.03, -1.47, P < 0.0001), body mass index (BMI) (WMD: -1.77, 95% CI: -2.38, -1.15, P < 0.00001), triglycerides (P = 0.006), and insulin levels (P < 0.00001). Superiority regarding psychopathology and body weight/BMI was consistent across Chinese/Asian and Western RCTs, double-blind and open designs, clozapine and non-clozapine cotreatment, augmentation and co-initiation RCTs, and higher and lower quality RCTs. In meta-regression analyses, topiramate's efficacy for total symptoms was moderated by shorter illness duration (P = 0.047), while weight loss was greater in prevention/co-initiation vs. intervention/augmentation RCTs (-4.11 kg, 95% CI: -6.70, -1.52 vs. -1.41 kg, 95% CI: -2.23, -0.59, P < 0.001). All-cause discontinuation was similar between topiramate and comparators (RR: 1.28, 95% CI: 0.91, 1.81, P = 0.16). While topiramate led to more concentration/attention difficulties (P = 0.03, NNH = 8, 95% CI=4-25), psychomotor slowing (P = 0.02, NNH = 7, 95% CI = 4-25), and paresthesia (P = 0.05, NNH = 2, 95% CI = 4-33), it led to less ≥7% weight gain (P = 0.0001, NNH = 2, 95% CI = 2-3) and constipation (P = 0.04, NNH = 9, 95% CI = 5-100) than the comparator.

CONCLUSIONS

These results indicate that adjunctive topiramate to antipsychotics is an effective and safe treatment choice for symptomatic improvement and weight reduction in patients with schizophrenia-spectrum disorders.

摘要

目的

系统审查关于托吡酯与抗精神病药物联合治疗精神分裂症谱系障碍的疗效和耐受性的随机对照试验(RCT)证据。

方法

对托吡酯与抗精神病药物联合治疗对比安慰剂/持续抗精神病药物治疗精神分裂症谱系障碍的RCT进行随机效应荟萃分析。计算标准化或加权平均差(SMD/WMD)、风险比(RR)±95%置信区间(CI)以及伤害所需人数(NNH)。

结果

在16项RCT(n = 934,疗程 = 11.8 ± 5.6周)中,托吡酯在总体(SMD:-0.58,95% CI:-0.82,-0.35,P < 0.00001)、阳性(SMD:-0.37,95% CI:-0.61,-0.14,P = 0.002)、阴性(SMD:-0.58,95% CI:-0.87,-0.29,P < 0.0001)和一般症状(SMD:-0.68,95% CI:-0.95,-0.40,P < 0.00001)的变化/终点方面优于对照。此外,托吡酯在体重(WMD:-2.75 kg,95% CI:-4.03,-1.47,P < 0.0001)、体重指数(BMI)(WMD:-1.77,95% CI:-2.38,-1.15,P < 0.00001)、甘油三酯(P = 0.006)和胰岛素水平(P < 0.00001)方面更具优势。在精神病理学以及体重/BMI方面的优势在中文/亚洲和西方的RCT、双盲和开放设计、氯氮平与非氯氮平联合治疗、强化和联合起始RCT以及高质量和低质量RCT中均一致。在荟萃回归分析中,托吡酯对总体症状的疗效受病程较短影响(P = 0.047),而在预防/联合起始RCT中体重减轻幅度大于干预/强化RCT(-4.11 kg,95% CI:-6.70,-1.52 vs. -1.41 kg,95% CI:-2.23,-0.59,P < 0.001)。托吡酯与对照的全因停药率相似(RR:1.28,95% CI:0.91,1.81,P = 0.16)。虽然托吡酯导致更多的注意力/集中困难(P = 0.03,NNH = 8,95% CI = 4 - 25)、精神运动迟缓(P = 用,NNH = 7,95% CI = 4 - 25)和感觉异常(P = 0.05,NNH = 2,95% CI = 4 - 33),但与对照相比,它导致≥7%体重增加(P = 0.0001,NNH = 2,95% CI = 2 - 3)和便秘(P = 0.04,NNH = 9,95% CI = 5 - 100)的情况更少。

结论

这些结果表明,抗精神病药物联合托吡酯是精神分裂症谱系障碍患者改善症状和减轻体重的一种有效且安全的治疗选择。

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