精神疾病的中间内表型和表观遗传机制。

Imaging neuroscience (Cambridge, Mass.) Pub Date : 2025-10-08 eCollection Date: 2025-01-01 DOI:10.1162/IMAG.a.914
Thomas Leon Kremer, David Antonio Grimaldi, Henri Fleischer, Emanuel Schwarz, Andreas Meyer-Lindenberg, Urs Braun, Heike Tost
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引用次数: 0

摘要

人类神经成像和表观遗传学研究已经准备好推进生物精神病学。利用成像遗传学的概念,分析人类神经成像和表观遗传学数据之间的关联,为研究将环境与精神疾病风险和保护联系起来的多尺度生物学机制提供了一个有吸引力的框架。一个基本的假设是,环境压力会导致表观遗传变化,从而导致细胞群的改变,而细胞群的改变反过来又可以通过人类神经成像来测量大脑结构和功能的变化。然而,与基因型不同,表观遗传学在个体内部、细胞类型之间或随时间变化而变化,因此在推断观察到的关联的即时性和方向性时需要谨慎。在这篇综述中,我们讨论了该方法框架的最新进展和挑战。未来的研究应该解决因果假设,并通过观察到的关联的复杂背景化和对纵向数据的严格分析来解释精神病理学中的个体差异。这些进展对于全面了解心理健康风险和保护的生物学因素至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intermediate endophenotypes and epigenetic mechanisms of psychiatric disorders.

Human neuroimaging and epigenetic research stand ready to advance biological psychiatry. Drawing on the concept of imaging genetics, the analysis of associations between human neuroimaging and epigenetic data provides an attractive framework for investigating multi-scale biological mechanisms linking the environment to psychiatric risk and protection. A basic assumption is that environmental stress causes epigenetic changes that lead to alterations in cellular ensembles, which in turn can be measured as changes in brain structure and function using human neuroimaging. However, unlike genotypes, epigenetics varies within individuals, between cell types, or over time, and thus caution is required when inferring the immediacy and directionality of observed associations. In this review, we discuss recent advances and challenges to this methodological framework. Future studies should address causal hypotheses and explain within-individual variance in psychopathology through sophisticated contextualization of observed associations and rigorous analyses of longitudinal data. These advances will be critical for developing a comprehensive understanding of the biological contributions to mental health risk and protection.

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