大麻二酚、认知和精神分裂症:叙述性综述

Trevor R. Norman
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摘要

精神分裂症是一种严重的精神障碍,约占总人口的 1%。精神分裂症具有多种症状,大多对抗精神病药物治疗有反应。认知功能障碍被认为是该病的核心特征,目前的抗精神病药物对认知功能障碍的治疗反应较差。改善认知功能是一个重要的治疗目标,因为这与更好的就业和生活质量相关。已有研究通过辅助药物治疗来改善认知功能,但效果有限。大麻二酚(CBD)已在精神分裂症认知障碍的临床前模型中显示出前景。另一方面,在精神分裂症患者小群体中进行的有限研究表明,作为抗精神病药物治疗的辅助药物,对认知功能没有明显的临床益处。有一项试验将 CBD 作为一种独立的治疗药物与抗精神病药物阿米舒必利进行了比较,结果显示,两种药物在认知能力方面都有显著变化,但在统计学上没有明显差异。因此可以得出结论,临床前研究结果未能应用于临床。然而,临床前研究结果本身是基于在多种认知模型中进行的一组限定性研究,并且使用了不同的剂量和给药途径。在一系列临床研究中也存在同样的方法问题。患者在病程、所使用的 CBD 配方和剂量以及大麻素治疗时间等方面的异质性可能会影响积极的研究结果。有限的临床数据库使得 CBD 对精神分裂症认知影响的益处(或缺乏益处)并不确定。要全面评估 CBD 治疗精神分裂症认知障碍的潜在风险和益处,还需要在比目前调查的更大患者群体中继续开展研究,并考虑进行剂量范围研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cannabidiol, cognition and schizophrenia: a narrative review
Schizophrenia is a serious mental disorder affecting about 1% of the population. It is characterised by multiple symptoms which are mostly responsive to treatment with antipsychotic medications. Cognitive impairment is regarded as a core feature of illness which is mostly poorly responsive to treatment with the current antipsychotic medications. Improving cognitive function is an important treatment goal as it is associated with better outcomes in employment and quality of life. Adjunctive pharmacological treatments have been examined to improve measures of cognition but with limited success. Cannabidiol (CBD), has shown promise in preclinical models of cognitive deficits of schizophrenia. On the other hand, limited studies in small groups of patients with schizophrenia have shown no significant clinical benefits for cognitive function as an adjunct to ongoing treatment with antipsychotics. A single trial, in which CBD as a standalone treatment was compared to the antipsychotic medication amisulpride, showed significant changes in cognitive measures for both agents, with no statistically significant difference between them. It might therefore be concluded that the preclinical findings have failed to translate to the clinic. However, the preclinical findings themselves are based on a circumscribed set of studies in multiple cognitive models and have used varying doses and routes of drug administration. The same general methodological issues are present in the suite of clinical studies. Issues such as patient heterogeneity in terms of illness duration, formulation and dose of CBD employed, and length of cannabinoid treatment might militate positive findings. The limited clinical database available makes the benefits (or lack thereof) of CBD for the cognitive effects of schizophrenia uncertain. Continued research in much larger patient populations than have so far been investigated as well as a consideration of dose ranging studies are required to fully assess the potential risks against the benefits of CBD treatment for cognitive deficits in schizophrenia.
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