Translational Psychiatry Program, Faillace Department of Psychiatry and Behavioral Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston (UTHealth), Houston, TX, USA.
Laboratory of Experimental Pathophysiology, Graduate Program in Health Sciences, Health Sciences Unit, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.
Curr Top Behav Neurosci. 2021;48:215-237. doi: 10.1007/7854_2020_173.
Bipolar disorder (BD) is a severe, debilitating psychiatric condition with onset in adolescence or young adulthood and often follows a relapsing and remitting course throughout life. The concept of neuroprogression in BD refers to the progressive path with an identifiable trajectory that takes place with recurrent mood episodes, which eventually leads to cognitive, functional, and clinical deterioration in the course of BD. Understanding the biological basis of neuroprogression helps to explain the subset of BD patients who experience worsening of their disorder over time. Additionally, the study of the neurobiological mechanisms underpinning neuroprogression will help BD staging based on systems biology. Replicated epidemiological studies have suggested inflammatory mechanisms as primary contributors to the neuroprogression of mood disorders. It is known that dysregulated inflammatory/immune pathways are often associated with BD pathophysiology. Hence, in this chapter, we focus on the evidence for the involvement of inflammation and immune regulated pathways in the neurobiological consequences of BD neuroprogression. Herein we put forth the evidence of immune markers from autoimmune disorders, chronic infections, and gut-brain axis that lead to BD neuroprogression. Further, we highlighted the peripheral and central inflammatory components measured along with BD progression.
双相情感障碍 (BD) 是一种严重的、使人衰弱的精神疾病,发病于青少年或成年早期,且通常在一生中呈现反复发作和缓解的过程。BD 中的神经进展概念是指一种具有可识别轨迹的渐进过程,伴随着反复发作的情绪发作,最终导致 BD 病程中的认知、功能和临床恶化。了解神经进展的生物学基础有助于解释随着时间的推移,BD 患者中存在病情恶化的亚组。此外,对神经生物学机制的研究将有助于基于系统生物学对 BD 进行分期。经过复制的流行病学研究表明,炎症机制是情绪障碍神经进展的主要原因。众所周知,失调的炎症/免疫途径通常与 BD 病理生理学有关。因此,在这一章中,我们重点关注炎症和免疫调节途径在 BD 神经进展的神经生物学后果中的作用。在这里,我们提出了自身免疫性疾病、慢性感染和肠脑轴中与 BD 神经进展相关的炎症标志物的证据。此外,我们还强调了随着 BD 进展而测量的外周和中枢炎症成分。