Evidence map›Paper›PMID 28116118›Full record

ArticleJournal of pharmaceutical health care and sciences2017

Drug interaction between methotrexate and salazosulfapyridine in Japanese patients with rheumatoid arthritis.

Morihiro Okada, Hiroshi Fujii, Yukio Suga, Satoshi Morito, Masae Okada, Jun Nishigami, Mitsuhiro Kawano, Tsutomu Shimada, Yoshimichi Sai

Open access · goldAbstract read
In one paragraph

Article in Journal of pharmaceutical health care and sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 4 institutions in 1 country.

Morihiro OkadaDepartment of Pharmacy, Japan Community Healthcare Organization Kanazawa Hospital, Ha-15 Oki-machi, Kanazawa, 920-8610 Japan.
Hiroshi FujiiDivision of Rheumatology, Kanazawa University Graduate School of Medicine, 13-1 Takara-machi, Kanazawa, 920-8641 Japan.
Yukio SugaInstitute of Medical, Pharmaceutical and Health Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8641 Japan.
Satoshi MoritoDepartment of Pharmacy, Social Welfare Organization Saiseikai Kanazawa Hospital, 13-6 Akatsuti-machi, Kanazawa, 920-0353 Japan.
Masae OkadaDepartment of Pharmacy, Japan Community Healthcare Organization Kanazawa Hospital, Ha-15 Oki-machi, Kanazawa, 920-8610 Japan.
Jun NishigamiDepartment of Pharmacy, Japan Community Healthcare Organization Kanazawa Hospital, Ha-15 Oki-machi, Kanazawa, 920-8610 Japan.
Mitsuhiro KawanoDivision of Rheumatology, Kanazawa University Graduate School of Medicine, 13-1 Takara-machi, Kanazawa, 920-8641 Japan.
Tsutomu ShimadaDepartment of Medicinal Informatics, Graduate School of Medical Sciences, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8641 Japan.
Yoshimichi SaiDepartment of Medicinal Informatics, Graduate School of Medical Sciences, Kanazawa University, 13-1 Takara-machi, Kanazawa, 920-8641 Japan.
Kanazawa University · JPKanazawa Hospital · JPJapan Community Healthcare Organization · JPKanazawa University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMethotrexate (MTX) and salazosulfapyridine (SASP) are disease-modifying drugs that are commonly used in the treatment of rheumatoid arthritis (RA), and combination therapy with MTX and SASP is recommended for RA patients who show an inadequate response to monotherapy with either drug. This study was designed to examine the interaction between the two drugs from the viewpoint of serum MTX concentration in Japanese RA patients, who were receiving combination therapy with relatively low doses of MTX and SASP.

methodsThis is a 24-week open-label intervention study of stable RA patients (

resultsSerum MTX concentration in RA patients who discontinued SASP increased more than 2-fold within 4 weeks, and the higher level was maintained thereafter. No significant differences were detected in SDAI, DAS28-CRP, MMP-3 or inflammatory cytokines. Most participants reported no change in physical condition after withdrawal of SASP, and most preferred MTX monotherapy for future treatment.

conclusionsWithdrawal of SASP from patients receiving SASP/MTX caused a rapid, marked increase of serum MTX concentration, without any apparent change in disease parameters or side effects. Our results suggest that SASP can be discontinued without adverse effects in stable RA patients receiving combination therapy, at least among Japanese patients receiving relatively low doses of the two drugs.

trial registrationUMIN000024507. October 21, 2016 retrospectively registered.

Indexed as

MTXPolypharmacyRheumatoid arthritisSASP

Identifiers

PMID28116118
PMCPMC5244515
OpenAlexW2572803118

What OpenQuestion holds

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LicenceCC BY
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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.