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Narrative review examines neuromodulators and brain-gut therapies for disorders of gut-brain interaction

Narrative review examines neuromodulators and brain-gut therapies for disorders of gut-brain interac…
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Key Takeaway
Consider brain-gut behavior therapies as an option with efficacy comparable to pharmacologic treatments for DGBI, per a narrative review.

This narrative review synthesizes neurophysiological, psychological, pharmacological, and psychotherapeutic literature related to disorders of gut-brain interaction (DGBI), including irritable bowel syndrome and functional dyspepsia. The population examined is individuals with DGBI. The review discusses interventions including neuromodulators (e.g., tricyclic antidepressants) and brain-gut behavior therapies (BGBTs) such as cognitive behavioral therapy and gut-directed hypnotherapy, alongside dietary interventions. No specific comparator was reported for the interventions discussed.

The main findings from the synthesis indicate that neuromodulators demonstrate modest efficacy in treating DGBI, though specific effect sizes, absolute numbers, and statistical measures were not reported. Brain-gut behavior therapies were reported to exhibit comparable efficacy to pharmacologic treatments, with the added findings of sustained symptom relief and additional benefit on mood and illness-related beliefs. The review also notes that neuroimaging and genetic studies support the role of emotional and cognitive circuits in gut sensitivity, and that psychiatric comorbidity, particularly anxiety, is bidirectionally linked to DGBI and influences treatment response.

Safety and tolerability data for the interventions were not reported in this review. Key limitations stem from the nature of the publication; it is a narrative review synthesizing existing literature rather than a primary study reporting specific trial data, effect sizes, or safety outcomes. The practice relevance suggested by the authors is that DGBI represent complex, stress-sensitive conditions best managed through multidisciplinary care, integrating pharmacologic neuromodulation, psychotherapeutic interventions, and dietary strategies targeting the brain-gut axis.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedMar 2026
View Original Abstract ↓
IntroductionDisorders of gut-brain interaction (DGBI), including irritable bowel syndrome and functional dyspepsia, are chronic gastrointestinal syndromes characterized by visceral hypersensitivity and altered brain-gut signaling in the absence of known structural pathology. A significant proportion of individuals with DGBI have comorbid psychiatric conditions, especially anxiety and depression, highlighting the biopsychosocial underpinnings of these disorders.MethodsThis narrative review synthesizes the neurophysiological, psychological, pharmacological, and psychotherapeutic literature related to DGBI. We examined the role of gut-brain axis dysregulation, the prevalence and impact of psychiatric comorbidity, and evaluated current treatment modalities, including neuromodulators, brain-gut behavior therapies (BGBTs), and dietary interventions.ResultsNeuroimaging and genetic studies support the role of emotional and cognitive circuits in modulating gut sensitivity and symptom perception. Psychiatric comorbidity, particularly anxiety, is bidirectionally linked to DGBI and influences treatment response. Neuromodulators such as tricyclic antidepressants demonstrate modest efficacy. BGBTs—including cognitive behavioral therapy and gut-directed hypnotherapy—exhibit comparable efficacy to pharmacologic treatments, with sustained symptom relief and additional benefit on mood and illness-related beliefs.DiscussionDGBI represent complex, stress-sensitive conditions best managed through multidisciplinary care. Integration of pharmacologic neuromodulation, psychotherapeutic interventions, and dietary strategies targeting the brain-gut axis offers the most comprehensive approach. Future research should refine treatment matching based on symptom phenotype, psychological profile, and gut-brain biomarkers to improve long-term outcomes.
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