Saint-Georges Zacharie, MacDonald Julia, Al-Khalili Roya, Hamati Rami, Solmi Marco, Keshavan Matcheri S, Tuominen Lauri, Guimond Synthia
The University of Ottawa Institute of Mental Health Research at the Royal, Ottawa, ON, Canada.
Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.
Mol Psychiatry. 2025 May 20. doi: 10.1038/s41380-025-03023-y.
BACKGROUND/OBJECTIVES: Studies have shown widespread alterations in different components of the cholinergic system in schizophrenia, but to date the evidence has not been systematically reviewed and summarized. Here, we systematically review imaging and post-mortem studies on the central cholinergic system in schizophrenia/schizoaffective disorder.
SUBJECTS/METHODS: Searches were performed in Embase and Medline. Study designs included cross-sectional case control studies comparing individuals with schizophrenia/schizoaffective disorder to control population. Risk of bias was assessed with the NIH/NHLBI tool for Quality Assessment of Case-Control Studies. The current study followed the PRISMA 2020 guidelines (PROSPERO: CRD42023402126).
A total of 3259 studies were screened and 61 met eligibility criteria for the systematic review, including 8 in vivo neuroimaging and 53 post-mortem studies. About 74% of these studies described significant alterations, most often reductions in either muscarinic or nicotinic receptor levels in schizophrenia. We also conducted 3 meta-analyses showing reductions in M1/M4 muscarinic receptors in the striatum (g = -0.809, k = 3, n = 108), hippocampus (g = -0.872, k = 3, n = 84), and fronto-cingulate cortex (g = -0.438, k = 4, n = 295). Six neuroimaging studies reported associations with clinical symptom severity measures, and four investigations with cognitive dysfunction.
Our review demonstrates a widespread decrease in muscarinic and nicotinic receptor levels in schizophrenia, evident in both neuroimaging and post-mortem studies. Our meta-analyses show large to moderate effects for the reductions in M1/M4 muscarinic receptors in the striatum, hippocampus, and fronto-cingulate cortex. Limitations and future directions for the field are discussed.
背景/目的:研究表明,精神分裂症患者胆碱能系统的不同组成部分存在广泛改变,但迄今为止,相关证据尚未得到系统的综述和总结。在此,我们系统地综述了精神分裂症/分裂情感性障碍患者中枢胆碱能系统的影像学和尸检研究。
受试者/方法:在Embase和Medline数据库中进行检索。研究设计包括将精神分裂症/分裂情感性障碍患者与对照人群进行比较的横断面病例对照研究。使用美国国立卫生研究院/美国国立心肺血液研究所(NIH/NHLBI)的病例对照研究质量评估工具评估偏倚风险。本研究遵循PRISMA 2020指南(国际前瞻性系统评价注册平台:CRD42023402126)。
共筛选出3259项研究,其中61项符合系统综述的纳入标准,包括8项活体神经影像学研究和53项尸检研究。这些研究中约74%描述了显著改变,最常见的是精神分裂症患者毒蕈碱或烟碱受体水平降低。我们还进行了3项荟萃分析,结果显示纹状体中M1/M4毒蕈碱受体减少(g = -0.809,k = 3,n = 108),海马体中减少(g = -0.872,k = 3,n = 84),额扣带回皮质中减少(g = -0.438,k = 4,n = 295)。六项神经影像学研究报告了与临床症状严重程度指标的关联,四项研究报告了与认知功能障碍的关联。
我们的综述表明,精神分裂症患者毒蕈碱和烟碱受体水平普遍降低,这在神经影像学和尸检研究中均很明显。我们的荟萃分析显示,纹状体、海马体和额扣带回皮质中M1/M4毒蕈碱受体减少具有较大至中等程度的效应。本文还讨论了该领域的局限性和未来研究方向。