ArticleRheumatology (Oxford, England)2026
Prospective analysis on the gut microbiome and the risk of autoimmune rheumatic diseases in the population-based FINRISK 2002 cohort.
Article in Rheumatology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
objectivesTo examine the long-term relationship between the gut microbiome and the risk of incident autoimmune rheumatic diseases (ARDs) in the general adult population.
methodsParticipants of the FINRISK cohort (N = 6242) donated faecal samples in 2002 and were followed for incident ARD which was a composite outcome, defined as developing RA, AS or systemic connective tissue disorder. We used multivariable-adjusted models to assess the association of incident ARD with alpha diversity, community composition, prevalent taxa and prevalent predicted pathways.
resultsIncident ARD was observed in 264 (4.2%) participants over a median follow-up of 19.8 years. The top species detected in the multivariable-adjusted models were Scatocola faecipullorum, Sutterella wadsworthensis_A_565807, Alistipes_A_871404 indistinctus and CAG-217 sp000436335. However, none of the associations reached statistical significance after FDR correction. Moreover, we did not find evidence of a statistically significant association between incident ARD and alpha diversity, community composition or prevalent predicted pathways in the age- and sex-adjusted or the multivariable-adjusted models.
conclusionNo evidence of association between baseline gut microbiome composition and the risk of incident ARDs (composite outcome) in the Finnish general adult population was detected in the current study. Our null findings, however, should be interpreted with caution since our study was limited by the use of a composite outcome (rather than using individual ARDs) and a single baseline measurement of the gut microbiome. More research efforts are still required to understand the prospective relationship between gut microbiome and individual ARDs.
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