Decoding neurodevelopmental changes in schizophrenia: a comprehensive systematic review of neurogenic alterations.

IF 4.1 Q2 PSYCHIATRY
Noemí Rueda, Ana Gómez-Garrido, María Alemany-Navarro, Nathalia Garrido-Torres, Miguel Ruíz-Veguilla, Benedicto Crespo-Facorro, Susana García-Cerro
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Abstract

Schizophrenia (SCZ) is a chronic brain disorder with significant impacts on patients, families, and society, affecting health, social life, and economic well-being. Despite extensive research, the biological basis of SCZ remains unclear. However, evidence suggests that disruptions in brain development, including neurogenesis, neuronal migration, synaptogenesis, and circuit maturation, may contribute to the risk of developing SCZ later in life. This review integrates findings from in vivo and in vitro studies on SCZ tissues, providing a comprehensive overview of neurodevelopmental alterations, with a particular focus on neurogenesis. We examine alterations in brain trophic support, inflammatory states, and alterations in cell markers, molecular pathways, and genetic factors implicated in both neurogenic and broader developmental processes. Additionally, we explore anomalies in miRNAs and genetic variations, such as single nucleotide polymorphisms (SNPs) and chromosome structure alterations, linked to SCZ. This review provides a framework to guide future research on the genetic, cellular, and molecular mechanisms underlying SCZ, with particular emphasis on neurogenesis within a broader neurodevelopmental context.

解码精神分裂症的神经发育变化:对神经源性改变的全面系统回顾。
精神分裂症(SCZ)是一种慢性脑部疾病,对患者、家庭和社会产生重大影响,影响健康、社会生活和经济福祉。尽管进行了广泛的研究,但SCZ的生物学基础仍不清楚。然而,有证据表明,大脑发育的中断,包括神经发生、神经元迁移、突触发生和电路成熟,可能会增加生命后期发生SCZ的风险。这篇综述整合了SCZ组织的体内和体外研究结果,提供了神经发育改变的全面概述,特别关注神经发生。我们研究了脑营养支持、炎症状态、细胞标记物、分子通路和遗传因素的改变,这些改变与神经源性和更广泛的发育过程有关。此外,我们还探索了与SCZ相关的mirna异常和遗传变异,如单核苷酸多态性(snp)和染色体结构改变。这篇综述提供了一个框架,指导未来对SCZ的遗传、细胞和分子机制的研究,特别强调在更广泛的神经发育背景下的神经发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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