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重度抑郁症快感缺乏中皮质厚度改变的转录底物

Transcriptional substrates of cortical thickness alterations in anhedonia of major depressive disorder.

作者信息

Liang Sugai, Gao Yuan, Palaniyappan Lena, Song Xue-Mei, Zhang Tian, Han Jin-Fang, Tan Zhong-Lin, Li Tao

机构信息

Affiliated Mental Health Center & Hangzhou Seventh People's Hospital, School of Medicine, Zhejiang University, Hangzhou 310013, China.

Affiliated Mental Health Center & Hangzhou Seventh People's Hospital, School of Medicine, Zhejiang University, Hangzhou 310013, China; Interdisciplinary Institute of Neuroscience and Technology, School of Medicine, Zhejiang University, Hangzhou 310027, China.

出版信息

J Affect Disord. 2025 Jun 15;379:118-126. doi: 10.1016/j.jad.2025.03.003. Epub 2025 Mar 6.

Abstract

BACKGROUND

Anhedonia is a core symptom of major depressive disorder (MDD), which has been shown to be associated with abnormalities in cortical morphology. However, the correlation between cortical thickness (CT) changes with anhedonia in MDD and gene expression remains unclear.

METHODS

We investigated the link between brain-wide gene expression and CT correlates of anhedonia in individuals with MDD, using 7 Tesla neuroimaging and a publicly available transcriptomic dataset. The interest-activity score was used to evaluation MDD with high anhedonia (HA) and low anhedonia (LA). Nineteen patients with HA, nineteen patients with LA, and twenty healthy controls (HC) were enrolled. We investigated CT alterations of anhedonia subgroups relative to HC and related cortical gene expression, enrichment and specific cell types. We further used Neurosynth and von Economo-Koskinas atlas to assess the meta-analytic cognitive functions and cytoarchitectural variation associated with anhedonia-related cortical changes.

RESULTS

Both patient subgroups exhibited widespread CT reduction, with HA manifesting more pronounced changes. Gene expression related to anhedonia had significant spatial correlations with CT differences. Transcriptional signatures related to anhedonia-associated cortical thinning were connected to mitochondrial dysfunction and enriched in adipogenesis, oxidative phosphorylation, mTORC1 signaling pathways, involving neurons, astrocytes, and oligodendrocytes. These CT alterations were significantly correlated with meta-analytic terms involving somatosensory processing and pain perception. HA had reduced CT within the somatomotor and ventral attention networks, and in agranular cortical regions.

LIMITATIONS

These include measuring anhedonia using interest-activity score and employing a cross-sectional design.

CONCLUSIONS

This study sheds light on the molecular basis underlying gene expression associated with anhedonia in MDD, suggesting directions for targeted therapeutic interventions.

摘要

背景

快感缺失是重度抑郁症(MDD)的核心症状,已被证明与皮质形态异常有关。然而,MDD中皮质厚度(CT)变化与快感缺失之间的相关性以及基因表达仍不清楚。

方法

我们使用7特斯拉神经影像学和公开可用的转录组数据集,研究了MDD患者全脑基因表达与快感缺失的CT相关性之间的联系。兴趣活动评分用于评估高快感缺失(HA)和低快感缺失(LA)的MDD患者。招募了19名HA患者、19名LA患者和20名健康对照(HC)。我们研究了快感缺失亚组相对于HC的CT改变以及相关的皮质基因表达、富集情况和特定细胞类型。我们进一步使用Neurosynth和冯·埃科诺莫-科斯金纳斯图谱来评估与快感缺失相关的皮质变化相关的元分析认知功能和细胞结构变异。

结果

两个患者亚组均表现出广泛的CT降低,HA表现出更明显的变化。与快感缺失相关的基因表达与CT差异具有显著的空间相关性。与快感缺失相关的皮质变薄相关的转录特征与线粒体功能障碍有关,并在脂肪生成、氧化磷酸化、mTORC1信号通路中富集,涉及神经元、星形胶质细胞和少突胶质细胞。这些CT改变与涉及体感处理和疼痛感知的元分析术语显著相关。HA在躯体运动和腹侧注意网络以及无颗粒皮质区域的CT降低。

局限性

这些局限性包括使用兴趣活动评分来测量快感缺失以及采用横断面设计。

结论

本研究揭示了MDD中与快感缺失相关的基因表达的分子基础,为靶向治疗干预提供了方向。

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