克罗恩病和重度抑郁症患者的共同神经生物学变化

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Hanna A Hartmann, Marja L Berthold, Shukti Ramkiran, Lukas Bündgens, Julius W Jaeger, Jana Hagen, Maria Backhaus, Maria Collée, Gereon J Schnellbächer, Tanja Veselinović, N Jon Shah, Kai M Schneider, Ravichandran Rajkumar, Irene Neuner
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引用次数: 0

摘要

背景:新出现的证据强调了中枢神经系统对肠道的深远影响。这在炎症性肠病中尤其明显,心理压力已被证明可以调节炎症反应并先于疾病发作。大脑参与克罗恩病(CD)的神经心理学相关性,以及它与重度抑郁症(MDD)重叠的神经生物学通路,仍然没有明确的定义。本研究旨在利用超高场神经成像描述这些共享机制。方法:对13例CD患者(年龄20 ~ 41岁,男性9例)、13例年龄匹配的MDD患者(20 ~ 42岁,男性9例)和13例健康对照(HC)(19 ~ 42岁,男性9例)采用7特斯拉磁共振扫描仪进行静息状态功能磁共振成像。症状严重程度的评估采用贝克抑郁量表(BDI-II)评估抑郁症,胃肠症状评定量表(GSRS)评估CD。结果:BDI-II评分在两组间差异有统计学意义(χ2 = 37.16, p)。结论:这些探索性发现揭示了CD和MDD在脑活动和连通性方面的相似异常。对这些相互作用的更深入了解可能会使综合治疗方法能够解决这些相互关联的疾病的心理和生理方面的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Shared neurobiological changes in individuals with Crohn's disease and major depressive disorder.

Background: Emerging evidence highlights the profound impact of the central nervous system on the gut. This is particularly evident in inflammatory bowel disease, where psychological stress has been shown to modulate the inflammatory response and precede disease flares. The neuropsychological correlates of the brain's involvement in Crohn's disease (CD), as well as its overlapping neurobiological pathways with major depressive disorder (MDD), remain poorly defined. This study aims to delineate these shared mechanisms using ultra-high-field neuroimaging.

Methods: Resting-state functional magnetic resonance imaging was conducted on 13 CD patients (age range: 20-41 years; 9 males), 13 age-matched MDD patients (20-42 years; 9 males), and 13 healthy controls (HC) (19-42 years; 9 males) using a 7 Tesla MR scanner. Assessments for symptom severity included the Beck Depression Inventory-II (BDI-II) for depression and the Gastrointestinal Symptom Rating Scale (GSRS) for CD.

Results: Significant differences in BDI-II scores are observed among the groups (χ2 = 37.16, p < 0.0001), with CD patients scoring higher than HCs but lower than MDD patients. Correlation shows a positive association between GSRS and BDI-II scores in CD patients. Group-level fMRI analysis of normalized fALFF maps reveals significant clusters in the precuneus cortex. Subsequent seed-based connectivity analysis using the precuneus as seed region shows increased connectivity with the left supramarginal gyrus and decreased connectivity with the precuneus and anterior cingulate gyrus in MDD and CD compared to HCs.

Conclusions: These exploratory findings reveal similar abnormalities in brain activity and connectivity in CD and MDD. A deeper understanding of these interactions may enable integrated treatment approaches that address both psychological and physiological aspects of these interconnected conditions.

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