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精神分裂症的分子机制:来自人类遗传学的启示。

Molecular mechanisms of schizophrenia: Insights from human genetics.

机构信息

Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.

Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA; Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.

出版信息

Curr Opin Neurobiol. 2023 Aug;81:102731. doi: 10.1016/j.conb.2023.102731. Epub 2023 May 26.

Abstract

Schizophrenia is a debilitating psychiatric disorder that affects millions of people worldwide; however, its etiology is poorly understood at the molecular and neurobiological levels. A particularly important advance in recent years is the discovery of rare genetic variants associated with a greatly increased risk of developing schizophrenia. These primarily loss-of-function variants are found in genes that overlap with those implicated by common variants and are involved in the regulation of glutamate signaling, synaptic function, DNA transcription, and chromatin remodeling. Animal models harboring mutations in these large-effect schizophrenia risk genes show promise in providing additional insights into the molecular mechanisms of the disease.

摘要

精神分裂症是一种使人虚弱的精神疾病,影响着全球数百万人;然而,其病因在分子和神经生物学水平上还了解甚少。近年来一个特别重要的进展是发现了与精神分裂症发病风险大大增加相关的罕见遗传变异。这些主要的功能丧失变异存在于与常见变异相关的基因中,并且涉及谷氨酸信号转导、突触功能、DNA 转录和染色质重塑的调节。携带这些大效应精神分裂症风险基因突变的动物模型有望为该疾病的分子机制提供更多的见解。

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