Specific changes in faecal microbiota are associated with familial Mediterranean fever.
Adiponectin
/ blood
Adult
Aged
Amyloidosis
/ microbiology
Biomarkers
Cross-Sectional Studies
Cytokines
/ blood
Enzyme-Linked Immunosorbent Assay
Familial Mediterranean Fever
/ blood
Feces
/ microbiology
Female
Gastrointestinal Microbiome
Humans
Inflammation Mediators
/ blood
Linear Models
Male
Middle Aged
Phenotype
AA amyloidosis
adipokines
familial Mediterranean fever
indoleamine 2,3-dioxygenase
microbiota
Journal
Annals of the rheumatic diseases
ISSN: 1468-2060
Titre abrégé: Ann Rheum Dis
Pays: England
ID NLM: 0372355
Informations de publication
Date de publication:
10 2019
10 2019
Historique:
received:
18
02
2019
revised:
13
07
2019
accepted:
18
07
2019
pubmed:
5
8
2019
medline:
31
3
2020
entrez:
5
8
2019
Statut:
ppublish
Résumé
Familial Mediterranean fever (FMF) can be complicated by AA amyloidosis (AAA), though it remains unclear why only some patients develop amyloidosis. We examined the gut microbiota composition and inflammatory markers in patients with FMF complicated or not by AAA. We analysed the gut microbiota of 34 patients with FMF without AAA, 7 patients with FMF with AAA, 19 patients with AAA of another origin, and 26 controls using 16S ribosomal RNA gene sequencing with the Illumina MiSeq platform. Associations between bacterial taxa and clinical phenotypes were evaluated using multivariate association with linear models statistical method. Blood levels of interleukin (IL)-1β, IL-6, tumour necrosis factor-α and adipokines were assessed by ELISA; indoleamine 2,3-dioxygenase (IDO) activity was determined by high-performance liquid chromatography. Compared with healthy subjects, specific changes in faecal microbiota were observed in FMF and AAA groups. Several operational taxonomic units (OTUs) were associated with FMF. Moreover, two OTUs were over-represented in FMF-related AAA compared with FMF without AAA. Additionally, higher adiponectin levels and IDO activity were observed in FMF-related AAA compared with FMF without AAA (p<0.05). The presence of specific changes in faecal microbiota in FMF and in FMF-related AAA suggests that intestinal microorganisms may play a role in the pathogenesis of these diseases. These findings may offer an opportunity to use techniques for gut microbiota manipulation.
Identifiants
pubmed: 31377728
pii: annrheumdis-2019-215258
doi: 10.1136/annrheumdis-2019-215258
doi:
Substances chimiques
ADIPOQ protein, human
0
Adiponectin
0
Biomarkers
0
Cytokines
0
Inflammation Mediators
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1398-1404Investigateurs
Serge Amselem
(S)
Camille Louvrier
(C)
Léa Savey
(L)
Joris Galland
(J)
Antoine Hankard
(A)
Alexandre Cez
(A)
Pierre-Antoine Michel
(PA)
Bertrand Knebelmann
(B)
Alexandre Hertig
(A)
Corinne Isnard Bagnis
(C)
Xavier Belenfant
(X)
Nicolas Martin Silva
(N)
David Saadoun
(D)
Tristan Legris
(T)
Commentaires et corrections
Type : CommentIn
Informations de copyright
© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None.