Evidence map›Paper›PMID 32033577›Full record

ArticlePediatric rheumatology online journal2020

Pharmacological conditioning for juvenile idiopathic arthritis: a potential solution to reduce methotrexate intolerance.

Rosanne M Smits, Dieuwke S Veldhuijzen, Henriet van Middendorp, Petra C E Hissink Muller, Wineke Armbrust, Elizabeth Legger, Nico M Wulffraat, Andrea W M Evers

Open access · goldAbstract read
In one paragraph

Article in Pediatric rheumatology online journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Evaluation of Methotrexate Intolerance in Children With Morphea.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Rosanne M SmitsHealth, Medical and Neuropsychology unit, Leiden University, Leiden, P.O. Box 9500, The Netherlands. R.M.Smits@fsw.leidenuniv.nl.ORCID http://orcid.org/0000-0003-2682-2654
Dieuwke S VeldhuijzenHealth, Medical and Neuropsychology unit, Leiden University, Leiden, P.O. Box 9500, The Netherlands.
Henriet van MiddendorpHealth, Medical and Neuropsychology unit, Leiden University, Leiden, P.O. Box 9500, The Netherlands.
Petra C E Hissink MullerDepartment Pediatric Rheumatology and Immunology, Leiden University Medical Center, Leiden, P.O. Box 9600, The Netherlands.
Wineke ArmbrustDepartment Pediatric Rheumatology and Immunology, University Medical Centre Groningen, Groningen, P.O. Box 30.001, The Netherlands.
Elizabeth LeggerDepartment Pediatric Rheumatology and Immunology, University Medical Centre Groningen, Groningen, P.O. Box 30.001, The Netherlands.
Nico M WulffraatDepartment Pediatric Rheumatology and Immunology, University Medical Center Utrecht, Utrecht, P.O. Box 85090, The Netherlands.
Andrea W M EversHealth, Medical and Neuropsychology unit, Leiden University, Leiden, P.O. Box 9500, The Netherlands.
Leiden University · NLUniversity Medical Center Groningen · NLLeiden University Medical Center · NLUniversity Medical Center Utrecht · NL

Funding

European Research Council ERC-2013-CoG-617700Nederlandse Organisatie voor Wetenschappelijk Onderzoek 01 6.V I CL770. L52ReumaNederland 16-3-401
6 · The paper itself

Abstract

backgroundMethotrexate (MTX) therapy has proven to be a successful and safe treatment for Juvenile Idiopathic Arthritis (JIA). Despite the high efficacy rates of MTX, treatment outcomes are often complicated by burdensome gastro-intestinal side effects. Intolerance rates for MTX in children are high (approximately 50%) and thus far no conclusive effective treatment strategies to control for side effects have been found. To address this need, this article proposes an innovative research approach based on pharmacological conditioning, to reduce MTX intolerance. PRESENTATION OF THE HYPOTHESIS: A collaboration between medical psychologists, pediatric rheumatologists, pharmacologists and patient groups was set up to develop an innovative research design that may be implemented to study potential improved control of side effects in JIA, by making use of the psychobiological principles of pharmacological conditioning. In pharmacological conditioning designs, learned positive associations from drug therapies (conditioning effects) are integrated in regular treatment regimens to maximize treatment outcomes. Medication regimens with immunosuppressant drugs that made use of pharmacological conditioning principles have been shown to lead to optimized therapeutic effects with reduced drug dosing, which might ultimately cause a reduction in side effects. TESTING THE HYPOTHESIS: This research design is tailored to serve the needs of the JIA patient group. We developed a research design in collaboration with an interdisciplinary research group consisting of patient representatives, pediatric rheumatologists, pharmacologists, and medical psychologists. IMPLICATIONS OF THE HYPOTHESIS: Based on previous experimental and clinical findings of pharmacological conditioning with immune responses, we propose that the JIA patient group is particularly suited to benefit from a pharmacological conditioning design. Moreover, findings from this study may potentially also be promising for other patient groups that endure long-lasting drug therapies.

Indexed as

AnimalsAntirheumatic AgentsArthritis, JuvenileDrug ToleranceHumansImmunityImmunosuppressive AgentsMethotrexateModels, TheoreticalAntirheumatic AgentsImmunosuppressive AgentsMethotrexateConditioned immune suppressionJuvenile idiopathic arthritisMethotrexate intolerancePharmacological conditioningSide effects

Identifiers

PMID32033577
PMCPMC7006148
OpenAlexW3007377858

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.