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利培酮联合阿达木单抗治疗慢性精神分裂症的随机、双盲、安慰剂对照临床试验。

Risperidone combination therapy with adalimumab for treatment of chronic schizophrenia: a randomized, double-blind, placebo-controlled clinical trial.

机构信息

Psychiatric Research Center, Roozbeh Psychiatric Hospital, Tehran University of Medical Sciences.

Department of Psychiatry, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.

出版信息

Int Clin Psychopharmacol. 2022 May 1;37(3):92-101. doi: 10.1097/YIC.0000000000000399.

Abstract

This study aimed to investigate the efficacy and safety of antitumor necrosis factor-alpha (TNF-α) therapy using adalimumab in patients with chronic schizophrenia. This is a randomized, double-blind, placebo-controlled clinical trial carried out at Roozbeh Hospital (Tehran, Iran) from June 2020 to October 2021. The patients were randomly divided into two parallel adalimumab + risperidone and placebo + risperidone groups. Participants in the intervention group received adalimumab subcutaneous injection (40 mg) by pen-injector at weeks 0 and 4. Using the Positive and Negative Symptoms Scale (PANSS), patients' positive and negative symptoms were assessed at weeks 0, 4, and 8. Forty patients (20 in each group) were included. PANSS total (t = 4.43, df = 38, P < 0.001), negative (t = 2.88, df = 38, P = 0.006), and general psychopathology (t = 4.06, df = 38, P < 0.001) scores demonstrated a significantly greater decline in adalimumab compared with the placebo group from baseline study endpoint. However, improvement of PANSS positive subscale scores showed no significant difference from the baseline study endpoint. There was no significant between-group difference regarding levels of C-reactive protein, interleukin (IL)-1β, TNF-α, IL-6, and IL-8 at baseline and also at the week 8 visit (P > 0.05 for all). The current study found adalimumab adjunctive therapy effective in treating schizophrenia, particularly its negative and general psychopathology symptoms, with no side effects.

摘要

本研究旨在探讨阿达木单抗(adalimumab)治疗慢性精神分裂症患者的疗效和安全性。这是一项在 2020 年 6 月至 2021 年 10 月在伊朗德黑兰的 Roozbeh 医院进行的随机、双盲、安慰剂对照临床试验。患者被随机分为阿达木单抗+利培酮和安慰剂+利培酮两组。干预组患者接受阿达木单抗皮下注射(40mg),每周 0 天和 4 天各一次,使用阳性和阴性症状量表(PANSS)在第 0 周、第 4 周和第 8 周评估患者的阳性和阴性症状。共有 40 名患者(每组 20 名)入组。PANSS 总分(t=4.43,df=38,P<0.001)、阴性症状(t=2.88,df=38,P=0.006)和一般精神病症状(t=4.06,df=38,P<0.001)评分显示,与安慰剂组相比,阿达木单抗组从基线研究终点显著下降。然而,从基线研究终点来看,PANSS 阳性量表评分的改善没有显著差异。两组患者在基线和第 8 周时的 C 反应蛋白、白细胞介素(IL)-1β、肿瘤坏死因子(TNF)-α、IL-6 和 IL-8 水平无显著差异(所有 P 值均>0.05)。本研究发现阿达木单抗辅助治疗精神分裂症有效,特别是对其阴性和一般精神病症状,且无副作用。

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