使用时间生物学表型来解决双相情感障碍的异质性。

Molecular Neuropsychiatry Pub Date : 2020-04-01 Epub Date: 2020-02-20 DOI:10.1159/000506636
Robert Gonzalez, Suzanne D Gonzalez, Michael J McCarthy
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引用次数: 15

摘要

双相情感障碍(BD)是一种神经精神情绪障碍,其特征是反复发作的躁狂和抑郁,以及睡眠、精力、食欲和认知功能的中断,这些节律性行为通常在日常周期中发生变化。季节性变化、睡眠和/或昼夜节律紊乱也可能引发双相障碍症状,这表明与生物钟相关的时间生物学因素可能是该疾病的共同特征。研究表明双相障碍存在于临床谱系中,具有不同的亚型,通常与其他精神疾病交叉。这种异质性一直是双相障碍研究的主要挑战,并导致诊断稳定性和治疗结果方面的问题。为了解决这种异质性,我们提出与时间生物学相关的生物标志物可能有助于将双相障碍分类为客观可测量的表型,从而建立更好的诊断,指导治疗,并可能导致更好的临床结果。目前,我们回顾了人类昼夜节律时间保持的生物学基础,讨论了BD与生物钟的联系,并介绍了最近的研究,这些研究评估了时间生物学测量作为建立BD表型的基础。我们的结论是,时间生物学可以为未来的研究提供信息,利用其他新技术,如基因组学、细胞生物学和高级行为分析,建立新的、更基于生物学的双相障碍表型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Using Chronobiological Phenotypes to Address Heterogeneity in Bipolar Disorder.

Bipolar disorder (BD) is a neuropsychiatric mood disorder characterized by recurrent episodes of mania and depression in addition to disruptions in sleep, energy, appetite, and cognitive functions-rhythmic behaviors that typically change on daily cycles. BD symptoms can also be provoked by seasonal changes, sleep, and/or circadian disruption, indicating that chronobiological factors linked to the circadian clock may be a common feature in the disorder. Research indicates that BD exists on a clinical spectrum, with distinct subtypes often intersecting with other psychiatric disorders. This heterogeneity has been a major challenge to BD research and contributes to problems in diagnostic stability and treatment outcomes. To address this heterogeneity, we propose that chronobiologically related biomarkers could be useful in classifying BD into objectively measurable phenotypes to establish better diagnoses, inform treatments, and perhaps lead to better clinical outcomes. Presently, we review the biological basis of circadian time keeping in humans, discuss the links of BD to the circadian clock, and pre-sent recent studies that evaluated chronobiological measures as a basis for establishing BD phenotypes. We conclude that chronobiology may inform future research using other novel techniques such as genomics, cell biology, and advanced behavioral analyses to establish new and more biologically based BD phenotypes.

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