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Gut microbiome profiles in patients with nociceptive pain, neuropathic pain, and pain-free controls: a case-control study

L. Goudman, D. Vandeputte, Patrice Forget, T. Demuyser, M. Moens

Regional anesthesia and pain medicine, 2026

10 participants

Abstract

Objective Gut microbiota have been implicated in pain modulation through immune, inflammatory, and neurobiological pathways, yet whether distinct gut microbial signatures differentiate nociceptive from neuropathic low back pain remains unclear. Methods and analysis In this longitudinal study, we profiled the gut microbiome of individuals with nociceptive low back pain (n=10), neuropathic low back pain (n=10), and pain-free controls (n=10) at baseline and after 3 months. Pain patients were resampled following standard-of-care treatment, while controls were resampled to capture background temporal variation. Gut microbial profiles were characterized using 16S rRNA gene (V4) sequencing. Alpha diversity was analyzed using mixed-effects models, beta diversity using Bray–Curtis, weighted UniFrac, and centered log-ratio–Euclidean distances, and differential abundance using Analysis of Compositions of Microbiomes with Bias Correction 2 (ANCOM-BC2). Results Entropy-based alpha-diversity indices did not differ between groups or over time. Richness-based metrics suggested a possible reduction in the neuropathic-dominant group in pairwise contrasts after rarefaction, although omnibus group effects did not reach conventional statistical significance. Overall microbial community structure did not differ between pain groups and controls, and no population-specific or population-by-time effects were detected at the genus or amplicon sequence variant level. Conclusion Together, these…

How strong is the evidence?

Evidence Hub reads this as a case-control, done in people. Its evidence level is 4 of 5 (Low · observational). Observational designs can show an association but not prove cause. Reported size: 10 participants or records.

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