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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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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