Cargando…
Use of MRP8/14 in clinical practice as a predictor of outcome after methotrexate withdrawal in patients with juvenile idiopathic arthritis
The objective of this study was to determine the effectiveness of MRP8/14 as a predictor of disease flare in patients with juvenile idiopathic arthritis (JIA) following the withdrawal of methotrexate (MTX) in a routine clinical setting. All MRP8/14 tests performed at a single centre in a 27-month pe...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474586/ https://www.ncbi.nlm.nih.gov/pubmed/35486225 http://dx.doi.org/10.1007/s10067-022-06165-4 |
_version_ | 1784789751626203136 |
---|---|
author | Sumner, Emma J. Almeida, Beverley Palman, Jason Bale, Peter Heard, Clare Holzinger, Dirk Roth, Johannes Foell, Dirk Robinson, Emily Ursu, Simona Wallace, Chris Gilmour, Kimberly Wedderburn, Lucy R. Ralph, Elizabeth |
author_facet | Sumner, Emma J. Almeida, Beverley Palman, Jason Bale, Peter Heard, Clare Holzinger, Dirk Roth, Johannes Foell, Dirk Robinson, Emily Ursu, Simona Wallace, Chris Gilmour, Kimberly Wedderburn, Lucy R. Ralph, Elizabeth |
author_sort | Sumner, Emma J. |
collection | PubMed |
description | The objective of this study was to determine the effectiveness of MRP8/14 as a predictor of disease flare in patients with juvenile idiopathic arthritis (JIA) following the withdrawal of methotrexate (MTX) in a routine clinical setting. All MRP8/14 tests performed at a single centre in a 27-month period were considered for analysis. Patients were assessed against criteria for inactive disease and subsequent disease flare. Decisions on whether or not to stop treatment were recorded. MRP8/14 results were assessed in conjunction with clinical information. Clinicians were also surveyed to investigate if MRP8/14 influenced their decision to discontinue MTX where this was available at that time point. One hundred four cases met the inclusion criteria during the study period. Although there was no significant difference in flares between patients with an elevated or low MRP8/14 value, in those who stopped MTX (n = 22), no patients with a low MRP8/14 (≤ 4000 ng/ml) result flared (follow-up time 12 months). Clinicians reported that for patients with clinically inactive disease and an elevated MRP8/14 result (> 4000 ng/ml), none would advise withdrawal of MTX. Low MRP8/14 was interpreted favourably when considering stopping MTX treatment in patients with JIA. Implementation of MRP8/14 testing has changed clinical practice at this centre. However, the observation that some patients in our cohort who had an elevated MRP8/14 value did not flare after stopping MTX for non-disease-related reasons highlights the need for further biomarkers to predict the risk of flare off medication in JIA and aid clinicians in treatment decisions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10067-022-06165-4. |
format | Online Article Text |
id | pubmed-9474586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-94745862022-09-16 Use of MRP8/14 in clinical practice as a predictor of outcome after methotrexate withdrawal in patients with juvenile idiopathic arthritis Sumner, Emma J. Almeida, Beverley Palman, Jason Bale, Peter Heard, Clare Holzinger, Dirk Roth, Johannes Foell, Dirk Robinson, Emily Ursu, Simona Wallace, Chris Gilmour, Kimberly Wedderburn, Lucy R. Ralph, Elizabeth Clin Rheumatol Brief Report The objective of this study was to determine the effectiveness of MRP8/14 as a predictor of disease flare in patients with juvenile idiopathic arthritis (JIA) following the withdrawal of methotrexate (MTX) in a routine clinical setting. All MRP8/14 tests performed at a single centre in a 27-month period were considered for analysis. Patients were assessed against criteria for inactive disease and subsequent disease flare. Decisions on whether or not to stop treatment were recorded. MRP8/14 results were assessed in conjunction with clinical information. Clinicians were also surveyed to investigate if MRP8/14 influenced their decision to discontinue MTX where this was available at that time point. One hundred four cases met the inclusion criteria during the study period. Although there was no significant difference in flares between patients with an elevated or low MRP8/14 value, in those who stopped MTX (n = 22), no patients with a low MRP8/14 (≤ 4000 ng/ml) result flared (follow-up time 12 months). Clinicians reported that for patients with clinically inactive disease and an elevated MRP8/14 result (> 4000 ng/ml), none would advise withdrawal of MTX. Low MRP8/14 was interpreted favourably when considering stopping MTX treatment in patients with JIA. Implementation of MRP8/14 testing has changed clinical practice at this centre. However, the observation that some patients in our cohort who had an elevated MRP8/14 value did not flare after stopping MTX for non-disease-related reasons highlights the need for further biomarkers to predict the risk of flare off medication in JIA and aid clinicians in treatment decisions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10067-022-06165-4. Springer International Publishing 2022-04-29 2022 /pmc/articles/PMC9474586/ /pubmed/35486225 http://dx.doi.org/10.1007/s10067-022-06165-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Brief Report Sumner, Emma J. Almeida, Beverley Palman, Jason Bale, Peter Heard, Clare Holzinger, Dirk Roth, Johannes Foell, Dirk Robinson, Emily Ursu, Simona Wallace, Chris Gilmour, Kimberly Wedderburn, Lucy R. Ralph, Elizabeth Use of MRP8/14 in clinical practice as a predictor of outcome after methotrexate withdrawal in patients with juvenile idiopathic arthritis |
title | Use of MRP8/14 in clinical practice as a predictor of outcome after methotrexate withdrawal in patients with juvenile idiopathic arthritis |
title_full | Use of MRP8/14 in clinical practice as a predictor of outcome after methotrexate withdrawal in patients with juvenile idiopathic arthritis |
title_fullStr | Use of MRP8/14 in clinical practice as a predictor of outcome after methotrexate withdrawal in patients with juvenile idiopathic arthritis |
title_full_unstemmed | Use of MRP8/14 in clinical practice as a predictor of outcome after methotrexate withdrawal in patients with juvenile idiopathic arthritis |
title_short | Use of MRP8/14 in clinical practice as a predictor of outcome after methotrexate withdrawal in patients with juvenile idiopathic arthritis |
title_sort | use of mrp8/14 in clinical practice as a predictor of outcome after methotrexate withdrawal in patients with juvenile idiopathic arthritis |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474586/ https://www.ncbi.nlm.nih.gov/pubmed/35486225 http://dx.doi.org/10.1007/s10067-022-06165-4 |
work_keys_str_mv | AT sumneremmaj useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT almeidabeverley useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT palmanjason useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT balepeter useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT heardclare useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT holzingerdirk useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT rothjohannes useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT foelldirk useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT robinsonemily useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT ursusimona useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT wallacechris useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT gilmourkimberly useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT wedderburnlucyr useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis AT ralphelizabeth useofmrp814inclinicalpracticeasapredictorofoutcomeaftermethotrexatewithdrawalinpatientswithjuvenileidiopathicarthritis |