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January 24, 2026Inflammatory Bowel Diseases0 citations

Molecular and Resting-State Brain Connectivity Links to Stress Reactivity in Ulcerative Colitis

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EMEmeran MayerJLJennifer LabusSCSteve Cole

Key Points

  • The research aims to explore the biological underpinnings of stress reactivity in ulcerative colitis through gene regulation and brain connectivity analyses.
  • Blood transcriptome profiling was conducted on 92 ulcerative colitis patients to assess gene expression and regulation.
  • Brain imaging focused on resting state connectivity in networks like the central autonomic network and emotional arousal regions.
  • Psychosocial symptoms were evaluated to categorize patients into high and low stress reactivity groups.
  • High stress reactivity was linked to increased sympathetic nervous system and HPA-axis gene activation.
  • Significant differences in brain connectivity were noted between stress reactivity groups, particularly involving the left parabrachial complex.
  • A multivariate connectivity signature correlating with inflammatory scores was identified, predicting flare risk effectively.

Abstract

Abstract BACKGROUND Perceived stress has previously been associated with increased flare risk in ulcerative colitis (UC) patients, and we have demonstrated that a psychometrically-based Stress Reactivity (SR) phenotype is associated with increased risk of flares and altered gut microbiome composition in ulcerative colitis (UC) patients. Here, we further delineate the biological basis of increased SR by investigating associations between SR with blood transcriptomic measures of sympathetic nervous system (SNS) gene regulation and resting state brain connectivity. METHODS Blood transcriptome profiling, brain imaging, and psychosocial symptom assessments were obtained in 92 (53 High SR, 39 Low SR) biopsy-confirmed UC patients. Pro-inflammatory, Type I interferon, and Conserved Transcriptional Response to Adversity (CTRA) gene expression composites were analyzed, along with genome-wide analysis of differential gene expression and transcription factor activation patterns. Resting state connectivity analyses was focused on central autonomic network (CAN) and its connection with the emotional arousal, salience, sensorimotor, default mode networks, and with brainstem regions. RESULTS In blood cell gene regulation, high SR was associated with increased activation of the SNS response pathway CREB, the HPA-axis glucocorticoid receptor (GR) pathway, and multiple immune activation pathways (STAT, IRF2/3, PPAR-gamma, PU1, and MAF) while the canonical pro-inflammatory NF-kB pathway was down-regulated. UC SR groups showed differences in the intrinsic connectivity of the CAN, with a large effect size decrease in High compared to the Low SR group in the Left(L) parabrachial complex (PBC) to L anterior insula (aINS) connectivity (Cohen’s d=-.92,p=6.48e-.05, q = 0.02). SR group differences were also observed for connectivity measures of several other brain regions Cohens D =|0.59-0.43|). Integrative multivariate analyses revealed an intrinsic CAN connectivity signature comprised by 9 features including pairwise connectivity from emotional arousal to salience regions and default mode to PBC and salience regions. Higher scores on this signature were associated with higher inflammatory composite scores, b = 0.80(SE=.12), B=.65, t = 6.50 p = 1.77e-08, and increased CREB activity, p .01. CONCLUSIONS To our knowledge, this is the first demonstration of a high SR phenotype with distinct brain and transcriptomic features that predict flare risk. The High SR group shows a profile of increased SNS and HPA-axis gene regulation, with alterations in the intrinsic connectivity of the CAN. Furthermore, across the SR groups, higher scores on a multivariate CAN signature associated with parasympathetic and sympathetic activity are linked to higher inflammatory composite scores, a consequence of greater SNS modulation of gene expression.

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Cite This Study

Mayer et al. (2026) studied this question.

synapsesocial.com/papers/69746149bb9d90c67120b23fhttps://doi.org/10.1093/ibd/izag006.122
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