Evidence map›Paper›PMID 41245094›Full record

ArticleTherapeutic advances in drug safety2025

Methotrexate use and risk of abnormal alanine aminotransferase elevation in children with rare inflammatory diseases: a self-controlled case series analysis using a pediatric electronic health record database in Japan.

Masayoshi Nakakuni, Azusa Hara, Kosuke Nakano, Seiji Mitsui, Naoko Deguchi, Seiko Miyazaki

Abstract read
In one paragraph

Article in Therapeutic advances in drug safety, 2025. 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
–field-weighted citation impact
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.

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

6 authors.

Masayoshi NakakuniDepartment of Multicenter Collaboration, Center for Clinical Research and Development, National Center for Child Health and Development, Okura, Setagaya-ku, Tokyo 157-8535, Japan.ORCID https://orcid.org/0000-0003-0324-6084
Azusa HaraLaboratory of Social Pharmacy and Epidemiology, Division of Social Pharmacy and Public Health, Showa Pharmaceutical University, Machida-shi, Tokyo, Japan.ORCID https://orcid.org/0000-0001-6958-7864
Kosuke NakanoDepartment of Multicenter Collaboration, Center for Clinical Research and Development, National Center for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Seiji MitsuiDepartment of Multicenter Collaboration, Center for Clinical Research and Development, National Center for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Naoko DeguchiDepartment of Multicenter Collaboration, Center for Clinical Research and Development, National Center for Child Health and Development, Setagaya-ku, Tokyo, Japan.
Seiko MiyazakiDepartment of Multicenter Collaboration, Center for Clinical Research and Development, National Center for Child Health and Development, Okura, Setagaya-ku, Tokyo 157-8535, Japan.ORCID https://orcid.org/0000-0001-7641-4566

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Methotrexate (MTX) is commonly prescribed for pediatric inflammatory diseases. However, clinical data on MTX-induced liver injury in children with rare inflammatory diseases currently remain limited. Objectives: To examine the association between MTX treatment and abnormal liver function in children with inflammatory diseases and to characterize the clinical course of suspected MTX-induced liver injury cases. Design: A self-controlled case series analysis. Methods: This study was conducted on children aged <15 years with juvenile idiopathic arthritis, psoriasis, or inflammatory bowel disease between April 2016 and March 2024. Data were obtained from the Pediatric Medical Information Collection System database, which integrates electronic medical records from over 40 pediatric medical institutions in Japan. The risk period was defined as the 7-day interval following MTX administration. In addition, this analysis compared the incidence of outcomes during the risk period with the baseline period within the same individuals. The outcome was alanine aminotransferase (ALT) elevation, defined as serum ALT levels exceeding three times the upper limit of normal. The age-adjusted incidence rate ratio (aIRR) was calculated, and clinical courses were assessed following ALT elevation. Results: Among 3696 children with inflammatory diseases, 587 received MTX treatment, while 81 developed abnormal ALT elevation. An increased risk of ALT elevation was observed (aIRR: 2.27, 95% confidence interval: 1.45-3.55). Among 45 patients with ALT elevation observed during the risk period, the normalization occurred in 35 patients. The 11 patients experienced a relapse of ALT elevation, while no patients receiving folic acid supplementation showed a relapse of ALT elevation. Conclusion: Methotrexate treatment in children with inflammatory diseases increases the risk of liver enzyme elevation, highlighting the necessity of liver function monitoring. Folic acid supplementation may help mitigate the exacerbation of MTX-induced liver injury in pediatric patients.

Indexed as

alanine aminotransferaseliver functionmethotrexatepediatric inflammatory disease

Identifiers

PMID41245094
PMCPMC12612511

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.