Epigenome wide association study of response to methotrexate in early rheumatoid arthritis patients

AIM: To identify differentially methylated positions (DMPs) and regions (DMRs) that predict response to Methotrexate (MTX) in early rheumatoid arthritis (RA) patients. MATERIALS AND METHODS: DNA from baseline peripheral blood mononuclear cells was extracted from 72 RA patients. DNA methylation, quan...

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Detalles Bibliográficos
Autores principales: Gosselt, Helen R., Vallerga, Costanza L., Mandaviya, Pooja R., Lubberts, Erik, Hazes, Johanna M. W., de Jonge, Robert, Heil, Sandra G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946177/
https://www.ncbi.nlm.nih.gov/pubmed/33690661
http://dx.doi.org/10.1371/journal.pone.0247709
Descripción
Sumario:AIM: To identify differentially methylated positions (DMPs) and regions (DMRs) that predict response to Methotrexate (MTX) in early rheumatoid arthritis (RA) patients. MATERIALS AND METHODS: DNA from baseline peripheral blood mononuclear cells was extracted from 72 RA patients. DNA methylation, quantified using the Infinium MethylationEPIC, was assessed in relation to response to MTX (combination) therapy over the first 3 months. RESULTS: Baseline DMPs associated with response were identified; including hits previously described in RA. Additionally, 1309 DMR regions were observed. However, none of these findings were genome-wide significant. Likewise, no specific pathways were related to response, nor could we replicate associations with previously identified DMPs. CONCLUSION: No baseline genome-wide significant differences were identified as biomarker for MTX (combination) therapy response; hence meta-analyses are required.

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