Both Disease Activity and HLA-B27 Status Are Associated With Gut Microbiome Dysbiosis in Spondyloarthritis Patients.


Journal

Arthritis & rheumatology (Hoboken, N.J.)
ISSN: 2326-5205
Titre abrégé: Arthritis Rheumatol
Pays: United States
ID NLM: 101623795

Informations de publication

Date de publication:
01 2023
Historique:
revised: 27 04 2022
received: 28 10 2021
accepted: 30 06 2022
pubmed: 13 7 2022
medline: 30 12 2022
entrez: 12 7 2022
Statut: ppublish

Résumé

Gut microbiome dysbiosis has previously been reported in spondyloarthritis (SpA) patients and could be critically involved in the pathogenesis of this disorder. The objectives of this study were to further characterize the microbiota structure in SpA patients and to investigate the relationship between dysbiosis and disease activity in light of the putative influence of the genetic background. Shotgun sequencing was performed on fecal DNA isolated from stool samples from 2 groups of adult volunteers: SpA patients (n = 102) and healthy controls (n = 63). A subset of the healthy controls comprised the age-matched siblings of patients whose HLA-B27 status was known. Changes in gut microbiota composition were assessed based on species diversity, enterotypes, and taxonomic and functional differences. Dysbiosis was confirmed in SpA patients as compared to healthy controls. The restriction of microbiota diversity was detected in patients with the most active disease, and the abundance of several bacterial species was correlated with Bath Ankylosing Spondylitis Disease Activity Index score. Among healthy controls, significant differences in microbiota composition were also detected between the HLA-B27-positive and the HLA-B27-negative siblings of SpA patients. We highlighted a decreased abundance of several species of bacteria in SpA patients, especially those bacteria belonging to the Clostridiales order. Among the few species of bacteria showing increased abundance, Ruminococcus gnavus was one of the top differentiating species. These findings reveal that genetic background and level of disease activity are likely to influence the composition of the gut microbiota of patients with SpA. It may be appropriate for further research on chronic arthritis to focus on these key parameters.

Identifiants

pubmed: 35818337
doi: 10.1002/art.42289
pmc: PMC10099252
doi:

Substances chimiques

HLA-B27 Antigen 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

41-52

Informations de copyright

© 2022 The Authors. Arthritis & Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology.

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Auteurs

Magali Berland (M)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Victoria Meslier (V)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Samar Berreira Ibraim (S)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Emmanuelle Le Chatelier (E)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Nicolas Pons (N)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Nicolas Maziers (N)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Florence Thirion (F)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Franck Gauthier (F)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Florian Plaza Oñate (F)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Jean-Pierre Furet (JP)

AgroParisTech, Université Paris-Saclay and the Micalis Institute, INRAE, Jouy-en-Josas, France, and Paris Center for Microbiome Medicine (PaCeMM) FHU, Paris, France.

Ariane Leboime (A)

Service de Rhumatologie, Hôpital Ambroise Paré, AP-HP, Boulogne, France.

Roula Said-Nahal (R)

Service de Rhumatologie, Hôpital Ambroise Paré, AP-HP, Boulogne, France.

Florence Levenez (F)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Nathalie Galleron (N)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Benoît Quinquis (B)

Université Paris-Saclay and MetaGenoPolis, INRAE, Jouy-en-Josas, France.

Philippe Langella (P)

AgroParisTech, Université Paris-Saclay and the Micalis Institute, INRAE, Jouy-en-Josas, France, and Paris Center for Microbiome Medicine (PaCeMM) FHU, Paris, France.

Stanislav Dusko Ehrlich (SD)

Université Paris-Saclay, MetaGenoPolis, INRAE, Jouy-en-Josas, France, and the Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, UK, and Paris Center for Microbiome Medicine (PaCeMM) FHU, Paris, France.

Maxime Breban (M)

Service de Rhumatologie, Hôpital Ambroise Paré, AP-HP, Boulogne, France, Infection & Inflammation, UMR 1173, Inserm, Université de Versailles-Paris-Saclay, Montigny-le-Bretonneux, France, and Laboratoire d'Excellence Inflamex, Université Paris Descartes, Sorbonne Paris Cité, and Paris Center for Microbiome Medicine (PaCeMM) FHU, Paris, France.

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