https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=pubmed&id=39515835&retmode=xml&tool=Litmetric&email=readroberts32@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09 3951583520241108
1468-20602024Nov08Annals of the rheumatic diseasesAnn Rheum DisDynamics of the gut microbiome in individuals at risk of rheumatoid arthritis: a cross-sectional and longitudinal observational study.ard-2024-22636210.1136/ard-2024-226362This work aimed to resolve the conflicting reports on Prevotellaceae abundance in the development of rheumatoid arthritis (RA) and to observe structural, functional and temporal changes in the gut microbiome in RA progressors versus non-progressors.Individuals at risk of RA were defined by the presence of anticyclic citrullinated protein (anti-CCP) antibodies and new musculoskeletal symptoms without clinical synovitis. Baseline sampling included 124 participants (30 progressed to RA), with longitudinal sampling of 19 participants (5 progressed to RA) over 15 months at five timepoints. Gut microbiome taxonomic alterations were investigated using 16S rRNA amplicon sequencing and confirmed with shotgun metagenomic DNA sequencing on 49 samples.At baseline, CCP+ at risk progressors showed significant differences in Prevotellaceae abundance compared with non-progressors, contingent on intrinsic RA risk factors and time to progression. Longitudinal sampling revealed gut microbiome instability in progressors 10 months before RA onset, a phenomenon absent in non-progressors. This may indicate a late microbial shift before RA onset, with Prevotellaceae contributing but not dominating these changes. Structural changes in the gut microbiome during arthritis development were associated with increased amino acid metabolism.These data suggest conflicting reports on Prevotellaceae overabundance are likely due to sampling within a heterogeneous population along a dynamic disease spectrum, with certain Prevotellaceae strains/clades possibly contributing to the establishment and/or progression of RA. Gut microbiome changes in RA may appear at the transition to clinical arthritis as a late manifestation, and it remains unclear whether they represent a primary or secondary phenomenon.© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ on behalf of EULAR.RooneyChristopher MCM0000-0002-3640-853XLeeds Institute of Medical Research, University of Leeds, Leeds, UK c.rooney@leeds.ac.uk.JefferyIan BIB4D Pharma PLC, Cork, Ireland.MankiaKulveerK0000-0002-7945-6582University of Leeds, Leeds Institute of Rheumatic and Musculoskeletal Medicine, Leeds, UK.NIHR Leeds Musculoskeletal Biomedical Research Centre, Leeds, UK.WilcoxMark HMHLeeds Institute of Medical Research, University of Leeds, Leeds, UK.EmeryPaulP0000-0002-7429-8482University of Leeds, Leeds Institute of Rheumatic and Musculoskeletal Medicine, Leeds, UK.NIHR Leeds Musculoskeletal Biomedical Research Centre, Leeds, UK.engJournal Article20241108
EnglandAnn Rheum Dis03723550003-4967IMAnti-Citrullinated Protein AntibodiesRheumatoid ArthritisRisk FactorsCompeting interests: CMR has received funding from Versus Arthritis and Leeds Cares and in-kind support from 4D Pharma PLC. KM has received grants from Gilead, Lilly, Serac Healthcare, AstraZeneca and DeepCure; consulting fees from AbbVie, UCB, Lilly, Galapagos, Serac Healthcare, Zura Bio and DeepCure; and honoraria from AbbVie, UCB, Lilly, Galapagos, Serac Healthcare, Zura Bio and DeepCure. PE has received grants from AbbVie, BMS, Lilly, Novartis, Pfizer and Samsung; and consulting fees from AbbVie, Activia, AstraZeneca, BMS, Boehringer Ingelheim, Galapagos, Gilead, Immunovant, Janssen, Lilly and Novartis.
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