Epigenetics of spondyloarthritis.

Ankylosing spondylitis DNA methylation Epigenetics Histone modification Micro-RNA Spondyloarthritis

Journal

Joint bone spine
ISSN: 1778-7254
Titre abrégé: Joint Bone Spine
Pays: France
ID NLM: 100938016

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 19 05 2020
accepted: 03 06 2020
pubmed: 14 6 2020
medline: 29 6 2021
entrez: 14 6 2020
Statut: ppublish

Résumé

Spondyloarthritis (SpA) is a chronic inflammatory disorder resulting from a combination of genetic predisposition and environmental factors. Despite recent advances, a substantial fraction of its genetic basis remains poorly understood. Several mechanisms have been proposed to account for this unexplained heritability, including epigenetics which can play a role at the interface between genetic and environmental susceptibility factors. Epigenetics refers to changes in gene expression that are not encoded in the DNA sequence itself. Such mechanisms may include DNA methylation, histone modifications and non-coding RNAs. Disruption of one of these systems can lead to inappropriate gene expression, which in turn might favour the development of disease. Thanks to recent technological progress, there has been a growing interest in the field of epigenetics in complex diseases, including SpA. However, epigenetic studies face some methodological limitations that hamper interpretation of their results: small sample size, absence of biological replication, lack of adequate controls for potential confounders, studies not performed in the most relevant cell/tissues. In the future, integration of epigenetics with other "omics" data will probably be necessary to improve our understanding of SpA pathogenesis. These issues need to be addressed before considering the use of epigenetic marks in clinical routine, as biomarkers or as drug targets.

Identifiants

pubmed: 32534204
pii: S1297-319X(20)30113-5
doi: 10.1016/j.jbspin.2020.06.003
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

565-571

Informations de copyright

Copyright © 2020 Société française de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.

Auteurs

Bilade Cherqaoui (B)

Inserm, UMR 1173, infection et inflammation, université Paris-Saclay, UVSQ, 78180 Montigny-le-Bretonneux, France; Laboratoire d'excellence Inflamex, université Paris Descartes, Sorbonne-Paris-Cité, Paris, France.

Frédéric Crémazy (F)

Inserm, UMR 1173, infection et inflammation, université Paris-Saclay, UVSQ, 78180 Montigny-le-Bretonneux, France; Laboratoire d'excellence Inflamex, université Paris Descartes, Sorbonne-Paris-Cité, Paris, France.

Christophe Hue (C)

Inserm, UMR 1173, infection et inflammation, université Paris-Saclay, UVSQ, 78180 Montigny-le-Bretonneux, France; Laboratoire d'excellence Inflamex, université Paris Descartes, Sorbonne-Paris-Cité, Paris, France.

Henri-Jean Garchon (HJ)

Inserm, UMR 1173, infection et inflammation, université Paris-Saclay, UVSQ, 78180 Montigny-le-Bretonneux, France; Laboratoire d'excellence Inflamex, université Paris Descartes, Sorbonne-Paris-Cité, Paris, France; Genetics department, Ambroise-Paré hospital, AP-HP, 92100 Boulogne-Billancourt, France.

Maxime Breban (M)

Inserm, UMR 1173, infection et inflammation, université Paris-Saclay, UVSQ, 78180 Montigny-le-Bretonneux, France; Laboratoire d'excellence Inflamex, université Paris Descartes, Sorbonne-Paris-Cité, Paris, France; Rheumatology department, Ambroise-Paré hospital, AP-HP, 92100 Boulogne-Billancourt, France.

Félicie Costantino (F)

Inserm, UMR 1173, infection et inflammation, université Paris-Saclay, UVSQ, 78180 Montigny-le-Bretonneux, France; Laboratoire d'excellence Inflamex, université Paris Descartes, Sorbonne-Paris-Cité, Paris, France; Rheumatology department, Ambroise-Paré hospital, AP-HP, 92100 Boulogne-Billancourt, France. Electronic address: felicie.costantino@aphp.fr.

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