Department of Geriatric Psychiatry, Shanghai Mental Health Center, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Aust N Z J Psychiatry. 2012 Feb;46(2):153-60. doi: 10.1177/0004867411433213.
Cerebrolysin is a nootropic drug with unique neurotrophic activities directly affecting cerebral neurons. This study evaluated the efficacy and safety of cerebrolysin added to risperidone in patients with schizophrenia dominated by negative symptoms.
The trial was a double-blind, placebo-controlled, parallel-group design. A total of 109 patients who met the DSM-IV diagnostic criteria for schizophrenia were randomly assigned to cerebrolysin (cerebrolysin plus risperidone, n=55) or placebo (risperidone only, n=54) groups. Intravenous infusions of 30 ml cerebrolysin or placebo were given once daily from Monday to Friday for 4 weeks. Efficacy was assessed with measurements including the Positive and Negative Symptoms Scale (PANSS), Wechsler Memory Scale (WMS), modified Chinese Wechsler Adult Intelligence Scale (mWAIS). and Clinical Global Impression (CGI).
Patients in both groups demonstrated improvements in psychiatric symptoms and cognitive and memory performance as assessed by PANSS, mWAIS, and WMS over the trial. There was no difference in rates of change in the PANSS total score or negative score between the two treatment groups. Patients treated with cerebrolysin showed significantly greater improvements in cognitive and memory function from week 2. No severe treatment adverse events were observed in either group. The frequency of adverse events was comparable between the two groups at the end of the treatment.
Cerebrolysin added to risperidone did not augment the efficacy of risperidone in treating the psychotic symptoms of schizophrenia patients over an 8-week trial. Cerebrolysin at 30 ml per day as an adjunctive treatment was safe and may improve cognitive and memory functions of patients with schizophrenia dominated by negative symptoms.
脑活素是一种具有独特神经营养作用的益智药,可直接影响大脑神经元。本研究评估了脑活素联合利培酮治疗以阴性症状为主的精神分裂症患者的疗效和安全性。
该试验为双盲、安慰剂对照、平行分组设计。共有 109 名符合 DSM-IV 精神分裂症诊断标准的患者被随机分为脑活素(脑活素联合利培酮,n=55)或安慰剂(仅利培酮,n=54)组。两组患者均给予脑活素 30ml 或安慰剂静脉滴注,每天 1 次,连续 5 天,共 4 周。采用阳性和阴性症状量表(PANSS)、韦氏记忆量表(WMS)、改良韦氏成人智力量表(mWAIS)和临床总体印象量表(CGI)评估疗效。
两组患者在整个试验过程中均表现出精神病症状和认知记忆功能的改善,PANSS、mWAIS 和 WMS 评分均有所下降。两组患者的 PANSS 总分和阴性评分变化率无差异。脑活素治疗组在第 2 周时认知和记忆功能的改善明显优于对照组。两组均未观察到严重的治疗不良事件。治疗结束时,两组不良反应的发生率相当。
在 8 周的试验中,脑活素联合利培酮并未增强利培酮治疗精神分裂症患者阳性症状的疗效。脑活素 30ml/天作为辅助治疗是安全的,可能改善以阴性症状为主的精神分裂症患者的认知和记忆功能。