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

<h4>Aim</h4>To identify differentially methylated positions (DMPs) and regions (DMRs) that predict response to Methotrexate (MTX) in early rheumatoid arthritis (RA) patients.<h4>Materials and methods</h4>DNA from baseline peripheral blood mononuclear cells was extracted from...

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Main Authors: Helen R Gosselt, Costanza L Vallerga, Pooja R Mandaviya, Erik Lubberts, Johanna M W Hazes, Robert de Jonge, Sandra G Heil
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0247709
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spelling doaj-736434ab899447cabb519e42f9e129032021-03-23T05:30:41ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01163e024770910.1371/journal.pone.0247709Epigenome wide association study of response to methotrexate in early rheumatoid arthritis patients.Helen R GosseltCostanza L VallergaPooja R MandaviyaErik LubbertsJohanna M W HazesRobert de JongeSandra G Heil<h4>Aim</h4>To identify differentially methylated positions (DMPs) and regions (DMRs) that predict response to Methotrexate (MTX) in early rheumatoid arthritis (RA) patients.<h4>Materials and methods</h4>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.<h4>Results</h4>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.<h4>Conclusion</h4>No baseline genome-wide significant differences were identified as biomarker for MTX (combination) therapy response; hence meta-analyses are required.https://doi.org/10.1371/journal.pone.0247709
collection DOAJ
language English
format Article
sources DOAJ
author Helen R Gosselt
Costanza L Vallerga
Pooja R Mandaviya
Erik Lubberts
Johanna M W Hazes
Robert de Jonge
Sandra G Heil
spellingShingle Helen R Gosselt
Costanza L Vallerga
Pooja R Mandaviya
Erik Lubberts
Johanna M W Hazes
Robert de Jonge
Sandra G Heil
Epigenome wide association study of response to methotrexate in early rheumatoid arthritis patients.
PLoS ONE
author_facet Helen R Gosselt
Costanza L Vallerga
Pooja R Mandaviya
Erik Lubberts
Johanna M W Hazes
Robert de Jonge
Sandra G Heil
author_sort Helen R Gosselt
title Epigenome wide association study of response to methotrexate in early rheumatoid arthritis patients.
title_short Epigenome wide association study of response to methotrexate in early rheumatoid arthritis patients.
title_full Epigenome wide association study of response to methotrexate in early rheumatoid arthritis patients.
title_fullStr Epigenome wide association study of response to methotrexate in early rheumatoid arthritis patients.
title_full_unstemmed Epigenome wide association study of response to methotrexate in early rheumatoid arthritis patients.
title_sort epigenome wide association study of response to methotrexate in early rheumatoid arthritis patients.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2021-01-01
description <h4>Aim</h4>To identify differentially methylated positions (DMPs) and regions (DMRs) that predict response to Methotrexate (MTX) in early rheumatoid arthritis (RA) patients.<h4>Materials and methods</h4>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.<h4>Results</h4>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.<h4>Conclusion</h4>No baseline genome-wide significant differences were identified as biomarker for MTX (combination) therapy response; hence meta-analyses are required.
url https://doi.org/10.1371/journal.pone.0247709
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