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加兰他敏治疗精神分裂症的随机对照试验的荟萃分析:显著的认知增强作用。

Meta-analysis of randomized controlled trials of galantamine in schizophrenia: significant cognitive enhancement.

机构信息

Department of Psychiatry and Behavioral Health, Stony Brook University Renaissance School of Medicine, Stony Brook, NY, 11794, USA.

Department of Population Health Sciences, Division of Biostatistics and Data Science, Augusta University, Augusta, GA, USA.

出版信息

Psychiatry Res. 2020 Sep;291:113285. doi: 10.1016/j.psychres.2020.113285. Epub 2020 Jul 10.

Abstract

Cognitive impairments are core features of schizophrenia and the best predictor of functional outcome. Cholinergic system and alpha-7 nicotinic acetylcholine (α7nACh) receptors are strongly implicated in the pathophysiologic mechanisms associated with cognitive impairments in schizophrenia. Galantamine is not only a reversible, competitive inhibitor of acetylcholinesterase but also a type I positive allosteric modulator of α7nACh receptors. The objective of this meta-analysis was to examine the efficacy of galantamine for cognitive symptoms of schizophrenia. In the meta-analysis that included six randomized controlled trials (RCTs, N=226), cognitive impairments significantly improved with galantamine compared to placebo, with a small Hedges' g effect size of 0.233. This finding is consistent with other RCTs in schizophrenia with medications with a similar mechanism of action. On the basis of the results from all the failed (although some efficacy has been shown) RCTs to date in schizophrenia, targeting only one pathophysiologic mechanism may be insufficient to detect a clinically meaningful signal. Nicotinergic medications, like any other add-on medications, are unlikely to be effective as stand-alone medications. Hence, these medications may have to be combined with other medications with complementary mechanisms such as glutamatergic/N-methyl-D-aspartate systems to detect a meaningful effect size for the three domains of psychopathology.

摘要

认知障碍是精神分裂症的核心特征,也是功能结局的最佳预测指标。胆碱能系统和α7 烟碱型乙酰胆碱 (α7nACh) 受体强烈参与与精神分裂症认知障碍相关的病理生理机制。加兰他敏不仅是乙酰胆碱酯酶的可逆、竞争性抑制剂,也是α7nACh 受体的 I 型正变构调节剂。本荟萃分析的目的是研究加兰他敏对精神分裂症认知症状的疗效。在包括六项随机对照试验 (RCT) 的荟萃分析中(N=226),与安慰剂相比,加兰他敏显著改善了认知障碍,Hedges'g 效应大小为 0.233。这一发现与其他具有类似作用机制的精神分裂症药物的 RCT 一致。基于迄今为止所有针对精神分裂症的失败(尽管已经显示出一些疗效)RCT 的结果,仅针对一种病理生理机制可能不足以检测到有临床意义的信号。烟碱能药物,就像任何其他附加药物一样,不太可能作为单一药物有效。因此,这些药物可能需要与其他具有互补机制的药物(如谷氨酸能/N-甲基-D-天冬氨酸系统)联合使用,以检测精神病理学三个领域的有意义的效应大小。

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