双相情感障碍老年人大脑结构的神经影像学研究:综述。

Journal of psychiatry and brain science Pub Date : 2022-01-01 Epub Date: 2022-08-25 DOI:10.20900/jpbs.20220006
Niroop Rajashekar, Hilary P Blumberg, Luca M Villa
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引用次数: 1

摘要

躁郁症(BD)是一种常见的情绪障碍,可对晚年生活造成严重后果,包括情绪和认知症状导致的痛苦和损伤、痴呆症风险升高以及特别高的自杀风险。为了改善晚年抑郁症的治疗效果,我们需要进一步了解患有晚年抑郁症(OABD)的老年人的大脑回路差异及其与衰老过程的关系。高分辨率结构和弥散加权磁共振成像(MRI)研究中有关灰质和白质发现的现有文献表明,年轻群体中的 BD 与皮质和皮质下大脑区域内的灰质减少有关,而皮质和皮质下大脑区域是情绪处理和调节的附属区域,同时也与连接这些大脑区域的白质束结构完整性降低有关。虽然针对 OABD 的神经影像学研究较少,但在年轻样本中发现的许多大脑结构差异似乎也存在于 OABD 中。此外,还有初步迹象表明,至少在 OABD 的一部分患者中,随着年龄的增长,灰质和白质的衰退更为明显,这可能会导致更多的脑部差异,从而造成不良后果。临床前和临床数据支持情绪稳定药物的神经可塑性和保护作用,这表明治疗可以逆转和/或预防大脑变化的进展,从而减轻症状。未来的神经影像学研究将采用纵向设计,并采取大规模、多站点的举措,提供详细的临床和治疗数据,从而有望减轻 OABD 患者的痛苦、认知功能障碍和自杀。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuroimaging Studies of Brain Structure in Older Adults with Bipolar Disorder: A Review.

Bipolar disorder (BD) is a common mood disorder that can have severe consequences during later life, including suffering and impairment due to mood and cognitive symptoms, elevated risk for dementia and an especially high risk for suicide. Greater understanding of the brain circuitry differences involved in older adults with BD (OABD) in later life and their relationship to aging processes is required to improve outcomes of OABD. The current literature on gray and white matter findings, from high resolution structural and diffusion-weighted magnetic resonance imaging (MRI) studies, has shown that BD in younger age groups is associated with gray matter reductions within cortical and subcortical brain regions that subserve emotion processing and regulation, as well as reduced structural integrity of white matter tracts connecting these brain regions. While fewer neuroimaging studies have focused on OABD, it does appear that many of the structural brain differences found in younger samples are present in OABD. There is also initial suggestion that there are additional brain differences, for at least a subset of OABD, that may result from more pronounced gray and white matter declines with age that may contribute to adverse outcomes. Preclinical and clinical data supporting neuro-plastic and -protective effects of mood-stabilizing medications, suggest that treatments may reverse and/or prevent the progression of brain changes thereby reducing symptoms. Future neuroimaging research implementing longitudinal designs, and large-scale, multi-site initiatives with detailed clinical and treatment data, holds promise for reducing suffering, cognitive dysfunction and suicide in OABD.

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