Psychiatric Research Center, Roozbeh Psychiatric Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Psychosis Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Int J Neuropsychopharmacol. 2020 Dec 29;23(12):775-782. doi: 10.1093/ijnp/pyaa006.
Patients with schizophrenia can generally manifest a broad variety of primary negative symptoms. The current study aimed to assess the efficacy and tolerability of resveratrol add-on therapy in the treatment of negative symptoms in patients with stable schizophrenia.
In a randomized, double-blind, and placebo-controlled setting, schizophrenia patients were assigned to receive either 200 mg/d resveratrol or matched placebo in addition to a stable dose of risperidone for 8 weeks. Patients were assessed using the positive and negative syndrome scale, the extrapyramidal symptom rating scale, and Hamilton Depression Rating Scale over the trial period. The primary outcome was considered as the change in positive and negative subscale score from baseline to week 8 between the treatment arms.
A total 52 patients completed the trial (26 in each arm). Baseline characteristics of both groups were statistically similar (P > .05). Despite the statistically similar behavior of positive symptoms between the groups across time (Greenhouse-Geisser corrected: F = 1.76, df = 1.88, P = .180), the resveratrol group demonstrated greater improvement in negative, general psychopathology, and total scores (Greenhouse-Geisser corrected: F = 12.25, df = 2.04, P < .001; F = 5.42, df = 1.56, P = .011; F = 7.64, df = 1.48, P = .003). HDRS scores and its changes, ESRS score, and frequency of other complications were not significantly different between resveratrol and placebo groups.
Adding resveratrol to risperidone can exhibit remarkable efficacy and safety in terms of management of schizophrenia-related negative symptoms.
精神分裂症患者通常表现出广泛的原发性阴性症状。本研究旨在评估白藜芦醇附加疗法在治疗稳定精神分裂症患者阴性症状方面的疗效和耐受性。
在随机、双盲、安慰剂对照的环境下,将精神分裂症患者分为两组,分别接受白藜芦醇 200mg/d 或匹配的安慰剂,同时服用稳定剂量的利培酮 8 周。在试验期间,使用阳性和阴性症状量表、锥体外系症状评定量表和汉密尔顿抑郁量表对患者进行评估。主要结局为治疗组从基线到第 8 周阳性和阴性子量表评分的变化。
共有 52 名患者完成了试验(每组 26 名)。两组的基线特征在统计学上相似(P>0.05)。尽管两组的阳性症状在整个时间过程中的表现相似(经绿house-geisser 校正:F=1.76,df=1.88,P=0.180),但白藜芦醇组在阴性、一般精神病学和总分方面表现出更大的改善(经绿house-geisser 校正:F=12.25,df=2.04,P<0.001;F=5.42,df=1.56,P=0.011;F=7.64,df=1.48,P=0.003)。白藜芦醇和安慰剂组之间的 HDRS 评分及其变化、ESRS 评分以及其他并发症的发生率没有显著差异。
在管理与精神分裂症相关的阴性症状方面,将白藜芦醇添加到利培酮中可表现出显著的疗效和安全性。