Antunes André S L M, Reis-de-Oliveira Guilherme, Martins-de-Souza Daniel
Brazilian Biosciences National Laboratory (LNBio), Brazilian Center for Research in Energy and Materials (CNPEM), Campinas, Brazil.
Laboratory of Neuroproteomics, University of Campinas, Campinas, Brazil.
Eur Arch Psychiatry Clin Neurosci. 2025 Feb;275(1):109-122. doi: 10.1007/s00406-024-01842-8. Epub 2024 Jul 19.
COVID-19, a complex multisystem disorder affecting the central nervous system, can also have psychiatric sequelae. In addition, clinical evidence indicates that a diagnosis of a schizophrenia spectrum disorder is a risk factor for mortality in patients with COVID-19. In this study, we aimed to explore brain-specific molecular aspects of COVID-19 by using a proteomic approach. We analyzed the brain proteome of fatal COVID-19 cases and compared it with differentially regulated proteins found in postmortem schizophrenia brains. The COVID-19 proteomic dataset revealed a strong enrichment of proteins expressed by glial and neuronal cells and processes related to diseases with a psychiatric and neurodegenerative component. Specifically, the COVID-19 brain proteome enriches processes that are hallmark features of schizophrenia. Furthermore, we identified shared and distinct molecular pathways affected in both conditions. We found that brain ageing processes are likely present in both COVID-19 and schizophrenia, albeit possibly driven by distinct processes. In addition, alterations in brain cell metabolism were observed, with schizophrenia primarily impacting amino acid metabolism and COVID-19 predominantly affecting carbohydrate metabolism. The enrichment of metabolic pathways associated with astrocytic components in both conditions suggests the involvement of this cell type in the pathogenesis. Both COVID-19 and schizophrenia influenced neurotransmitter systems, but with distinct impacts. Future studies exploring the underlying mechanisms linking brain ageing and metabolic dysregulation may provide valuable insights into the complex pathophysiology of these conditions and the increased vulnerability of schizophrenia patients to severe outcomes.
新冠病毒病(COVID-19)是一种影响中枢神经系统的复杂多系统疾病,也可能有精神方面的后遗症。此外,临床证据表明,精神分裂症谱系障碍的诊断是COVID-19患者死亡的一个危险因素。在本研究中,我们旨在通过蛋白质组学方法探索COVID-19在大脑中的特定分子层面。我们分析了COVID-19死亡病例的大脑蛋白质组,并将其与死后精神分裂症大脑中差异调节的蛋白质进行比较。COVID-19蛋白质组数据集显示,神经胶质细胞和神经元细胞表达的蛋白质以及与具有精神和神经退行性成分的疾病相关的过程高度富集。具体而言,COVID-19大脑蛋白质组富集了精神分裂症的标志性特征过程。此外,我们确定了在两种情况下都受到影响的共同和不同的分子途径。我们发现,大脑衰老过程可能在COVID-19和精神分裂症中都存在,尽管可能由不同的过程驱动。此外,观察到脑细胞代谢的改变,精神分裂症主要影响氨基酸代谢,而COVID-19主要影响碳水化合物代谢。两种情况下与星形胶质细胞成分相关的代谢途径的富集表明这种细胞类型参与了发病机制。COVID-19和精神分裂症都影响神经递质系统,但影响方式不同。未来探索大脑衰老与代谢失调之间潜在机制的研究可能会为这些疾病的复杂病理生理学以及精神分裂症患者对严重后果的易感性增加提供有价值的见解。