Tryptophan metabolites are associated with gut-brain alterations in functional dyspepsia
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Background and aims:
Microbiota is thought to contribute to the pathophysiology of disorders of gut-brain interaction, including functional dyspepsia (FD), although comprehensive human data covering the entire microbiota-gut-brain axis are scarce. We aimed to study the relationships among microbiota-produced metabolites including tryptophan metabolites and short-chain fatty acids (SCFA), and functional brain connectivity in FD, in relation to symptomatology.
Methods:
In 46 patients with Rome IV-diagnosed FD and 30 healthy controls (HC), targeted metabolomics using chromatography and mass spectrometry was conducted to quantify metabolites in blood, urine, and stool. Associations with gut microbiota and symptomatology were tested using 16S rRNA gene sequencing-based fecal quantitative microbiota profiling and validated symptom questionnaires. Resting-state functional magnetic resonance imaging in 27 patients and 36 HC enabled analysis of functional connectivity in selected brain networks.
Results
Patients with FD exhibited distinct profiles of tryptophan metabolites and SCFA with higher urinary indole-3-acetate (IAA, P =0.018), lower serum kynurenine ( P =0.030) and lower plasma propionate ( P =0.0055) concentrations. FD-specific metabolite alterations were associated with more severe GI and psychological symptoms. The fecal microbiota profile was similar between FD and HC. Complementary analyses demonstrated significant alterations in resting-state brain connectivity of 44 predefined regions between FD and HC, while a connectivity-based classifier could accurately discriminate FD from HC (96% sensitivity, 100% specificity). Differences in connectivity measures mediated the higher urinary IAA levels in FD.
Conclusion
Dysregulated functional brain connectivity in FD supports an objective diagnosis, while alterations in specific tryptophan metabolite and SCFA levels highlight their potential as prognostic, predictive, or therapeutic biomarkers, and warrant further investigation on microbiota modulating therapies for FD.
ClinicalTrials.gov identifier: NCT03545243
