Microbiome Analytics of the Gut Microbiota in Patients With Juvenile Idiopathic Arthritis: A Longitudinal Observational Cohort Study

Objective To assess the composition of gut microbiota in Italian and Dutch patients with juvenile idiopathic arthritis (JIA) at baseline, with inactive disease, and with persistent activity compared to healthy controls. Methods In a multicenter, prospective, observational cohort study, fecal samples...

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Veröffentlicht in:Arthritis & rheumatology (Hoboken, N.J.) N.J.), 2019-06, Vol.71 (6), p.1000-1010
Hauptverfasser: Dijkhuizen, E. H. Pieter, Del Chierico, Federica, Malattia, Clara, Russo, Alessandra, Pires Marafon, Denise, Haar, Nienke M., Magni‐Manzoni, Silvia, Vastert, Sebastiaan J., Dallapiccola, Bruno, Prakken, Berent, Martini, Alberto, Benedetti, Fabrizio, Putignani, Lorenza
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Sprache:eng
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Zusammenfassung:Objective To assess the composition of gut microbiota in Italian and Dutch patients with juvenile idiopathic arthritis (JIA) at baseline, with inactive disease, and with persistent activity compared to healthy controls. Methods In a multicenter, prospective, observational cohort study, fecal samples were collected at baseline from 78 Italian and 21 Dutch treatment‐naive JIA patients with 0.99 and 0.71, respectively). The operational taxonomic units (OTUs) of Erysipelotrichaceae (increased in patients), Allobaculum (decreased in patients), and Faecalibacterium prausnitzii (increased in patients) showed different relative abundance in Italian patient baseline samples compared to controls after controlling for multiple comparisons. Some OTUs differed between Dutch patient samples and healthy controls, but no evidence remained after controlling for multiple comparisons. No differences were found in paired analysis between Italian patient baseline and inactive disease samples. Conclusion Our findings show evidence for dysbiosis in JIA patients. Only patient/control status, age, and geographic origin appear to be drivers of the microbiota profiles, regardless of disease activity stage, inflammation, and markers of autoimmunity.
ISSN:2326-5191
2326-5205
DOI:10.1002/art.40827