Sinkeviciute Igne, Begemann Marieke, Prikken Merel, Oranje Bob, Johnsen Erik, Lei Wan U, Hugdahl Kenneth, Kroken Rune A, Rau Carina, Jacobs Jolien D, Mattaroccia Silvia, Sommer Iris E
Division of Psychiatry, Haukeland University Hospital, PB 1400, 5021, Bergen, Norway.
NORMENT Centre of Excellence, University of Oslo, Oslo, Norway.
NPJ Schizophr. 2018 Oct 25;4(1):22. doi: 10.1038/s41537-018-0064-6.
Cognitive impairment is a core feature of schizophrenia, which is predictive for functional outcomes and is, therefore, a treatment target in itself. Yet, literature on efficacy of different pharmaco-therapeutic options is inconsistent. This quantitative review provides an overview of studies that investigated potential cognitive enhancers in schizophrenia. We included pharmacological agents, which target different neurotransmitter systems and evaluated their efficacy on overall cognitive functioning and seven separate cognitive domains. In total, 93 studies with 5630 patients were included. Cognitive enhancers, when combined across all different neurotransmitter systems, which act on a large number of different mechanisms, showed a significant (yet small) positive effect size of 0.10 (k = 51, p = 0.023; 95% CI = 0.01 to 0.18) on overall cognition. Cognitive enhancers were not superior to placebo for separate cognitive domains. When analyzing each neurotransmitter system separately, agents acting predominantly on the glutamatergic system showed a small significant effect on overall cognition (k = 29, Hedges' g = 0.19, p = 0.01), as well as on working memory (k = 20, Hedges' g = 0.13, p = 0.04). A sub-analysis of cholinesterase inhibitors (ChEI) showed a small effect on working memory (k = 6, Hedges' g = 0.26, p = 0.03). Other sub-analyses were positively nonsignificant, which may partly be due to the low number of studies we could include per neurotransmitter system. Overall, this meta-analysis showed few favorable effects of cognitive enhancers for patients with schizophrenia, partly due to lack of power. There is a lack of studies involving agents acting on other than glutamatergic and cholinergic systems, especially of those targeting the dopaminergic system.
认知障碍是精神分裂症的核心特征,它可预测功能结局,因此其本身就是一个治疗靶点。然而,关于不同药物治疗方案疗效的文献并不一致。这项定量综述概述了研究精神分裂症潜在认知增强剂的研究。我们纳入了针对不同神经递质系统的药物,并评估了它们对整体认知功能和七个独立认知领域的疗效。总共纳入了93项研究,涉及5630名患者。作用于大量不同机制的所有不同神经递质系统的认知增强剂联合使用时,对整体认知显示出显著(但较小)的正效应量0.10(k = 51,p = 0.023;95% CI = 0.01至0.18)。认知增强剂在各个独立认知领域并不优于安慰剂。当分别分析每个神经递质系统时,主要作用于谷氨酸能系统的药物对整体认知显示出较小的显著效应(k = 29,Hedges' g = 0.19,p = 0.01),对工作记忆也有显著效应(k = 20,Hedges' g = 0.13,p = 0.04)。胆碱酯酶抑制剂(ChEI)的亚组分析显示对工作记忆有较小效应(k = 6,Hedges' g = 0.26,p = 0.03)。其他亚组分析结果虽为阳性但不显著,这可能部分归因于我们每个神经递质系统能够纳入的研究数量较少。总体而言,这项荟萃分析显示认知增强剂对精神分裂症患者的有益作用较少,部分原因是样本量不足。缺乏涉及作用于谷氨酸能和胆碱能系统以外的药物的研究,尤其是针对多巴胺能系统的药物。