Potential Candidates for Biomarkers in Bipolar Disorder: A Proteomic Approach through Systems Biology

IF 2.4 4区 医学 Q3 NEUROSCIENCES Clinical Psychopharmacology and Neuroscience Pub Date : 2022-05-31 DOI:10.9758/cpn.2022.20.2.211
P. Ziani, J. Feiten, J. Goularte, R. Colombo, Bárbara Antqueviezc, L. Géa, A. Rosa
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引用次数: 6

Abstract

Bipolar disorder (BD) is one of the most disabling diseases characterized by severe humor fluctuation. It is accompanied by cognitive and functional impairment in addiction to high suicide rates. BD is often underdiagnosed and treated incorrectly because many of the reported symptoms are not exclusive to the disorder. Once the diagnosis is exclusively clinical, it is not possible to state precisely. From that, proteomic approaches were used to identify, in a large scale, all proteins involved in cellular or tissue processes. This review aggregate data from blood proteomes, by using protein association network, of subjects with BD and healthy controls to suggest dysfunctional molecular pathways involved in disease. Original articles containing proteomic analysis were searched in PubMed. Seven studies were selected and data were extracted for posterior analysis. A protein-protein interaction network was created by STRING database. A final set of proteins in this network were employed as input in ClueGO and, the main biological process was visualized using R package pathview. The analysis revealed proteins associated with many biological processes, including growth and endocrine regulation, iron transportation, protease inhibition, protection against pathogens and cholesterol transport. Moreover, pathway analysis indicated the association of uncovered proteins with two main metabolic pathways: complement system and coagulation cascade. Thus, a better understanding on the pathophysiology of psychiatric disorders and the identification of potential biomarker candidates are essential to improve diagnostic, prognostic and design pharmacological strategies.
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双相情感障碍生物标志物的潜在候选物:通过系统生物学的蛋白质组学方法
双相情感障碍(BD)是以严重的幽默波动为特征的致残性疾病之一。它伴随着高自杀率成瘾的认知和功能损害。BD通常诊断不足,治疗不当,因为许多报告的症状并非该疾病独有。一旦诊断完全是临床诊断,就不可能准确地说明。由此,蛋白质组学方法被用于大规模识别参与细胞或组织过程的所有蛋白质。这篇综述通过使用蛋白质关联网络收集BD受试者和健康对照者的血液蛋白质组数据,以表明与疾病有关的功能失调的分子途径。在PubMed中搜索包含蛋白质组学分析的原始文章。选取7项研究,提取数据进行后验分析。STRING数据库建立了蛋白质-蛋白质相互作用网络。该网络中的最后一组蛋白质被用作ClueGO的输入,并且使用R包路径视图可视化主要的生物学过程。分析揭示了与许多生物学过程相关的蛋白质,包括生长和内分泌调节、铁转运、蛋白酶抑制、对病原体的保护和胆固醇转运。此外,通路分析表明,未覆盖的蛋白质与两种主要代谢通路有关:补体系统和凝血级联。因此,更好地了解精神疾病的病理生理学和识别潜在的候选生物标志物对于改善诊断、预后和设计药理学策略至关重要。
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来源期刊
Clinical Psychopharmacology and Neuroscience
Clinical Psychopharmacology and Neuroscience NEUROSCIENCESPHARMACOLOGY & PHARMACY-PHARMACOLOGY & PHARMACY
CiteScore
4.70
自引率
12.50%
发文量
81
期刊介绍: Clinical Psychopharmacology and Neuroscience (Clin Psychopharmacol Neurosci) launched in 2003, is the official journal of The Korean College of Neuropsychopharmacology (KCNP), and the associate journal for Asian College of Neuropsychopharmacology (AsCNP). This journal aims to publish evidence-based, scientifically written articles related to clinical and preclinical studies in the field of psychopharmacology and neuroscience. This journal intends to foster and encourage communications between psychiatrist, neuroscientist and all related experts in Asia as well as worldwide. It is published four times a year at the last day of February, May, August, and November.
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