Evidence map›Paper›PMID 26715450›Full record

ArticleDiagnostic pathology2015

MDR-1 and MRP-1 activity in peripheral blood leukocytes of rheumatoid arthritis patients.

Tamás Micsik, András Lőrincz, János Gál, Richard Schwab, István Peták

Open access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

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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

5 authors at 3 institutions in 1 country.

Tamás Micsik1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary. micsikt@mail.korb1.sote.hu.
András LőrinczRational Drug Design Laboratories CRC, Semmelweis University, Budapest, Hungary. lorincz2.andras@ttk.mta.hu.
János GálDepartment of Rheumatology, Bács-Kiskun County Hospital, Kecskemét, Budapest, Hungary. galj@kmk.hu.
Richard SchwabKPS Medical Biotechnology and Healthcare Services Ltd, Budapest, Hungary. schwab@kps.hu.
István PetákKPS Medical Biotechnology and Healthcare Services Ltd, Budapest, Hungary. Istvan.petak@oncompassmedicine.com.
National Healthcare Service Center · HUSemmelweis University · HUBács-Kiskun Megyei Kórház · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRheumatoid Arthritis is a chronic disease leading to decreased quality of life with a rather variable response rate to Disease Modifying Anti Rheumatic Drugs. Methotrexate (MTX) is the gold standard therapy in Rheumatoid Arthritis. The Multidrug resistance Related Protein and Multi Drug Resistance protein 1, also called P-glycoprotein-170 transporters can alter the intracellular concentration of different drugs. Methotrexate is an MRP1 substrate and thus the functional activity of MRP1 might have a clinical impact on the efficiency of the Methotrexate-therapy in Rheumatoid Arthritis.

methodsWe have compared the functional Multidrug Activity Factors (MAF) of the MDR1 and MRP1 transporters of Peripheral Blood Leukocytes of 59 Rheumatoid Arthritis patients with various response rate to MTX-therapy (MTX-responder, MTX-resistant and MTX-intolerant RA-groups) and 47 non-RA controls in six different leukocyte subpopulations (neutrophil leukocytes, monocytes, lymphocytes, CD4+, CD8+ and CD19+ cells). There was a decreased MAF of RA patients compared to non- Rheumatoid Arthritis patients and healthy controls in the leukocyte subpopulations. There was a significant difference between the MAF values of the MTX-responder and MTX intolerant groups. But we have not found significant differences between the MAF values of the MTX-responder and MTX-resistant Rheumatoid Arthritis -groups.

resultsOur results suggest that MDR1 and MRP1 functional activity does not seem to affect the response rate to MTX-therapy of Rheumatoid Arthritis-patients, but it might be useful in predicting MTX-side effects. We have demonstrated the decreased functional MDR-activity on almost 60 Rheumatoid Arthritis patients, which can be interpreted as a sign of the immune-suppressive effect of the MTX-treatment.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidATP-Binding Cassette, Sub-Family C ProteinsATP Binding Cassette Transporter, Subfamily BBiomarkersCase-Control StudiesHumansLeukocytesMethotrexateRemission InductionTreatment OutcomeABCB1 protein, humanAntirheumatic AgentsATP-Binding Cassette, Sub-Family C ProteinsATP Binding Cassette Transporter, Subfamily BBiomarkersMethotrexatemultidrug resistance-associated protein 1

Identifiers

PMID26715450
PMCPMC4696293
OpenAlexW2214034182

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Registered trials

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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.