Omics approaches open new horizons in major depressive disorder: from biomarkers to precision medicine

Fabiola Stolfi, Hugo Abreu, Riccardo Sinella, Sara Nembrini, Sara Centonze, Virginia Landra, C. Brasso, G. Cappellano, Paola Rocca, A. Chiocchetti
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Abstract

Major depressive disorder (MDD) is a recurrent episodic mood disorder that represents the third leading cause of disability worldwide. In MDD, several factors can simultaneously contribute to its development, which complicates its diagnosis. According to practical guidelines, antidepressants are the first-line treatment for moderate to severe major depressive episodes. Traditional treatment strategies often follow a one-size-fits-all approach, resulting in suboptimal outcomes for many patients who fail to experience a response or recovery and develop the so-called “therapy-resistant depression”. The high biological and clinical inter-variability within patients and the lack of robust biomarkers hinder the finding of specific therapeutic targets, contributing to the high treatment failure rates. In this frame, precision medicine, a paradigm that tailors medical interventions to individual characteristics, would help allocate the most adequate and effective treatment for each patient while minimizing its side effects. In particular, multi-omic studies may unveil the intricate interplays between genetic predispositions and exposure to environmental factors through the study of epigenomics, transcriptomics, proteomics, metabolomics, gut microbiomics, and immunomics. The integration of the flow of multi-omic information into molecular pathways may produce better outcomes than the current psychopharmacological approach, which targets singular molecular factors mainly related to the monoamine systems, disregarding the complex network of our organism. The concept of system biomedicine involves the integration and analysis of enormous datasets generated with different technologies, creating a “patient fingerprint”, which defines the underlying biological mechanisms of every patient. This review, centered on precision medicine, explores the integration of multi-omic approaches as clinical tools for prediction in MDD at a single-patient level. It investigates how combining the existing technologies used for diagnostic, stratification, prognostic, and treatment-response biomarkers discovery with artificial intelligence can improve the assessment and treatment of MDD.
Omics 方法为重度抑郁症开辟了新天地:从生物标记物到精准医学
重度抑郁障碍(MDD)是一种反复发作的情绪障碍,是全球第三大致残原因。在重度抑郁障碍的发病过程中,多种因素可能同时起作用,从而使诊断变得复杂。根据实用指南,抗抑郁药是中度至重度重度抑郁发作的一线治疗药物。传统的治疗策略通常采用 "一刀切 "的方法,结果导致许多患者的治疗效果不理想,他们无法获得应答或康复,并发展成所谓的 "治疗耐受性抑郁症"。患者的生物和临床变异性很高,而且缺乏可靠的生物标志物,这阻碍了找到特定的治疗目标,导致治疗失败率居高不下。在这种情况下,精准医学--一种根据个体特征量身定制医疗干预措施的范例--将有助于为每位患者分配最适当、最有效的治疗,同时最大限度地减少副作用。特别是,多组学研究可以通过表观基因组学、转录物组学、蛋白质组学、代谢组学、肠道微生物组学和免疫组学的研究,揭示遗传倾向和环境因素暴露之间错综复杂的相互作用。目前的精神药理学方法主要针对与单胺系统有关的单一分子因素,而忽视了我们机体的复杂网络,与之相比,将多组学信息流整合到分子通路中可能会产生更好的结果。系统生物医学的概念涉及整合和分析利用不同技术生成的大量数据集,创建 "患者指纹",从而确定每位患者的潜在生物机制。这篇综述以精准医学为中心,探讨了如何整合多组学方法,将其作为临床工具,在单个患者层面预测 MDD。它探讨了如何将用于诊断、分层、预后和治疗反应生物标志物发现的现有技术与人工智能相结合,以改善 MDD 的评估和治疗。
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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