4.5 Article

Regional Gray Matter Volume Changes in Brains of Patients With Ulcerative Colitis

Journal

INFLAMMATORY BOWEL DISEASES
Volume 28, Issue 4, Pages 599-610

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/ibd/izab252

Keywords

ulcerative colitis; neuroimaging; GMV; voxel-based morphometry; MRI

Funding

  1. National Natural Science Foundation of China [81771918]
  2. Shaanxi National Science Foundation [2020JM-197]

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The study identified differences in gray matter volume between patients with UC and healthy controls, with decreased GMV in several regions and increased GMV in others. These changes were predominantly found in active UC patients and were partially associated with levels of anxiety and depression and clinical stage.
Background Ulcerative colitis (UC) and Crohn's disease (CD) are 2 subtypes of inflammatory bowel disease (IBD). Several studies have reported brain abnormalities in IBD patients. This study aims to identify differences of gray matter volume (GMV) between patients with UC and healthy controls (HCs). Methods Fifty-seven patients with UC and 40 HCs underwent structural magnetic resonance imaging. Voxel-based morphometry method was used to detect GMV differences. Receiver operating characteristic (ROC) curve was applied to investigate reliable biomarkers for identifying patients with UC from HCs. Regression analysis was used to examine relationships between the structure alternations and clinical symptoms. Results Compared with HCs, patients with UC showed decreased GMV in the insula, thalamus, pregenual anterior cingulate cortex, hippocampus/parahippocampus, amygdala, and temporal pole; they showed increased GMV in the putamen, supplementary motor area, periaqueductal gray, hypothalamus, and precentral gyrus. Receiver operating characteristic analysis showed the highest classification power of thalamus. The inclusion of anxiety and depression as covariates eliminated the differences in the right insula, pregenual anterior cingulate cortex, supplementary motor area, and precentral gyrus. Most of the GMV changes were found in active patients with UC, with few changes in patients with UC in remission. We also found significantly negative correlation between UC duration and GMV in several regions. Conclusion The current neuroimaging findings were involved in visceral sensory pathways and were partially associated with the levels of anxiety and depression and clinical stage of patients with UC. This study might provide evidence for possible neuromechanisms of UC.

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