Tunset Mette Elise, Haslene-Hox Hanne, Larsen Jeanette Brun, Kondziella Daniel, Nygård Mona, Pedersen Sindre Andre, Vaaler Arne, Llorente Alicia
Department of Psychosis and Rehabilitation, Division of Mental Healthcare, St. Olavs University Hospital, Trondheim, Norway; Department of Mental Health- Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Department of Biotechnology and Nanomedicine, SINTEF, Trondheim, Norway.
J Psychiatr Res. 2025 Feb;182:373-390. doi: 10.1016/j.jpsychires.2025.01.037. Epub 2025 Jan 17.
Biomarkers for the diagnosis and clinical management of psychiatric disorders are currently lacking. Extracellular vesicles (EVs), lipid membrane-encapsulated vesicles released by cells, hold promise as a source of biomarkers due to their ability to carry molecules that reflect the status of their donor cells and their ubiquitous presence in biofluids. This review examines the literature on EVs in biofluids from psychiatric disorder patients, and discuss how the published studies contribute to our understanding of the pathophysiology of these conditions and to the discovery of potential biomarkers. We analyzed 46 studies on blood-borne EVs; no investigations on cerebrospinal fluid-derived EVs were found. A significant number of studies lacked optimal description of the methodology and/or characterization of the isolated EVs. Moreover, many studies aimed to capture brain-derived EVs, but often capture-proteins with low brain specificity were used. Considering biomarkers, miRNAs were the most investigated molecular type, but based on the studies analyzed it was not possible to identify robust biomarker candidates for the investigated disorders. Additionally, we describe the contribution of EV studies in illuminating the pathophysiology of psychiatric disorders, including research on insulin resistance, inflammation, mitochondrial dysfunction, and the microbiota. We conclude that there is a shortage of studies with detailed methodology description and EV sample characterization in psychiatric research. To exploit the potential of EVs to investigate psychiatric disorders and identify biomarkers more studies and validated protocols using capture proteins with high specificity to brain cells are needed. The review protocol was pre-registered in the PROSPERO database under the registration number CRD42021277534.
目前缺乏用于精神疾病诊断和临床管理的生物标志物。细胞外囊泡(EVs)是细胞释放的脂质膜包裹的囊泡,由于其能够携带反映供体细胞状态的分子且在生物流体中普遍存在,有望成为生物标志物的来源。本综述考察了有关精神疾病患者生物流体中EVs的文献,并讨论已发表的研究如何有助于我们理解这些疾病的病理生理学以及发现潜在的生物标志物。我们分析了46项关于血源性EVs的研究;未发现关于脑脊液来源的EVs的研究。大量研究缺乏对方法学的最佳描述和/或对分离出的EVs的表征。此外,许多研究旨在捕获脑源性EVs,但通常使用脑特异性低的捕获蛋白。考虑到生物标志物,微小RNA(miRNAs)是研究最多的分子类型,但基于所分析的研究,无法为所研究的疾病确定可靠的生物标志物候选物。此外,我们描述了EVs研究在阐明精神疾病病理生理学方面的贡献,包括关于胰岛素抵抗、炎症、线粒体功能障碍和微生物群的研究。我们得出结论,精神疾病研究中缺乏对方法学进行详细描述和对EVs样本进行表征的研究。为了利用EVs在研究精神疾病和识别生物标志物方面的潜力,需要更多的研究以及使用对脑细胞具有高特异性的捕获蛋白的经过验证的方案。该综述方案已在PROSPERO数据库中预注册,注册号为CRD42021277534。