Evidence map›Paper›PMID 41483143›Full record

ArticleJournal of gastroenterology2026

Real-world outcomes of ustekinumab, vedolizumab, and tumor necrosis factor inhibitors in very-early-onset inflammatory bowel disease: a multi-center cohort study.

Ryusuke Nambu, Itaru Iwama, Ichiro Takeuchi, Shin-Ichiro Hagiwara, Yuri Etani, Emiri Kaji, Atsushi Yoden, Fumihiko Kakuta, Yusuke Hoshi, Naoya Tsumura and 14 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of gastroenterology, 2026. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors.

Ryusuke NambuCenter for Pediatric Inflammatory Bowel Disease, Division of Gastroenterology and Hepatology, Saitama Children's Medical Center, 1-2 Shintoshin, Chuo-Ku, Saitama, 3308777, Japan. nambee1231@gmail.com.ORCID 0000-0002-7206-7111
Itaru IwamaCenter for Pediatric Inflammatory Bowel Disease, Division of Gastroenterology and Hepatology, Saitama Children's Medical Center, 1-2 Shintoshin, Chuo-Ku, Saitama, 3308777, Japan.
Ichiro TakeuchiCenter for Pediatric Inflammatory Bowel Disease, Division of Gastroenterology, National Center for Child Health and Development, Tokyo, Japan.
Shin-Ichiro HagiwaraDepartment of Gastroenterology, Nutrition and Endocrinology, Osaka Women's and Children's Hospital, Osaka, Japan.
Yuri EtaniDepartment of Gastroenterology, Nutrition and Endocrinology, Osaka Women's and Children's Hospital, Osaka, Japan.
Emiri KajiDepartment of Pediatrics, Osaka Medical and Pharmaceutical University, Osaka, Japan.
Atsushi YodenDepartment of Pediatrics, Osaka Medical and Pharmaceutical University, Osaka, Japan.
Fumihiko KakutaDepartment of Gastroenterology, Miyagi Children's Hospital, Miyagi, Japan.
Yusuke HoshiDepartment of Gastroenterology, Miyagi Children's Hospital, Miyagi, Japan.
Naoya TsumuraDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Tatsuki MizuochiDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
Hideki KumagaiDepartment of Pediatrics, Jichi Medical University, Tochigi, Japan.
Koji YokoyamaDepartment of Pediatrics, Jichi Medical University, Tochigi, Japan.
Takuya NishizawaDepartment of Pediatrics, Gunma University Graduate School of Medicine, Gunma, Japan.
Masaaki UsamiDepartment of Pediatrics School of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Ishikawa, Japan.
Yugo TakakiDepartment of Pediatric Gastroenterology and Hepatology, Japanese Red Cross Kumamoto Hospital, Kumamoto, Japan.
Ryo EbanaDepartment of Pediatrics, Okinawa Chubu Hospital, Okinawa, Japan.
Shingo KurasawaDepartment of Pediatrics, Shinshu University School of Medicine, Nagano, Japan.
Hiroki FujikawaDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, Hiroshima, Japan.
Takashi IshigeDepartment of Pediatrics, Gunma University Graduate School of Medicine, Gunma, Japan.
Takahiro KudoDepartment of Pediatrics, Faculty of Medicine, Juntendo University, Tokyo, Japan.
M Masashi YoshidaCenter for Pediatric Inflammatory Bowel Disease, Division of Gastroenterology and Hepatology, Saitama Children's Medical Center, 1-2 Shintoshin, Chuo-Ku, Saitama, 3308777, Japan.
Hirotaka ShimizuCenter for Pediatric Inflammatory Bowel Disease, Division of Gastroenterology, National Center for Child Health and Development, Tokyo, Japan.
Katsuhiro AraiCenter for Pediatric Inflammatory Bowel Disease, Division of Gastroenterology, National Center for Child Health and Development, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVery-early-onset inflammatory bowel disease (VEO-IBD), representing cases diagnosed before age 6 years, is increasing in prevalence. Although VEO-IBD often presents as severe, treatment-resistant disease requiring biologic agents, studies showing the effectiveness of biologics, such as ustekinumab (UST) and vedolizumab (VDZ), remain limited.

methodsWe retrospectively analyzed patients with VEO-IBD treated for at least a year from 13 institutions in Japan, evaluating clinical course including effectiveness of biologics, such as infliximab (IFX), adalimumab (ADL), UST, and VDZ. Patients with monogenic IBD were excluded. Steroid-free clinical remission (SFCR) and treatment persistence were assessed separately for first-line and for second-line or subsequent biologic therapies.

resultsWe studied 101 VEO-IBD patients (56% male; median age, 3.6 years), including 40 with Crohn's disease, 52 with ulcerative colitis, and 9 with unclassified IBD. Biologics were used in 67 patients, most commonly infliximab (IFX; n = 52), followed by UST (n = 38), adalimumab (ADL; n = 23), and VDZ (n = 21). As first-line therapy, IFX and ADL achieved 1-year SFCR rates of 19% and 46%, with persistence rates of 36% and 48%. Despite being used mainly as second-line or subsequent therapies, UST and VDZ showed 1-year SFCR rates of about 45% and 36%, and maintained persistence of 79% and 46%, respectively, with UST demonstrating higher persistence than TNF-α inhibitors (P < 0.01). No discontinuations due to infusion reactions or other adverse events occurred with UST or VDZ.

conclusionUST and VDZ were effective and well tolerated even when used as second-line or subsequent therapies for VEO-IBD.

Indexed as

Antibodies, Monoclonal, HumanizedGastrointestinal AgentsInflammatory Bowel DiseasesTumor Necrosis Factor InhibitorsUstekinumabAdalimumabAdolescentAge of OnsetChildChild, PreschoolCohort StudiesColitis, UlcerativeCrohn DiseaseFemaleHumansInfliximabAdalimumabAntibodies, Monoclonal, HumanizedGastrointestinal AgentsInfliximabTumor Necrosis Factor InhibitorsUstekinumabvedolizumabBiologicsPediatric inflammatory bowel diseaseVery-early-onset IBD

Identifiers

PMID41483143
PMCPMC13048906

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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.