Evidence map›Paper›PMID 39155522›Full record

ArticleIntestinal research2025

Tuberculosis risk in patients with Crohn's disease on biologics: a retrospective analysis of the Japanese Medical Claims Database.

Koji Fujimoto, Shuhei Hosomi, Yumie Kobayashi, Rieko Nakata, Yu Nishida, Masaki Ominami, Yuji Nadatani, Shusei Fukunaga, Koji Otani, Fumio Tanaka and 2 more

Abstract read
In one paragraph

Article in Intestinal research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Methylglyoxal AttenuatesInternational journal of molecular sciences · 2026
    Article
  3. Observational
  4. Article
  5. Review
  6. Article
  7. Prevalence of Latent and Active Tuberculosis Infection in Inflammatory Bowel Disease Patients Who Received Biological Treatment.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2026
    Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Koji FujimotoDepartment of Gastroenterology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
Shuhei HosomiDepartment of Gastroenterology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Yumie KobayashiDepartment of Gastroenterology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Rieko NakataDepartment of Gastroenterology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Yu NishidaDepartment of Gastroenterology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Masaki OminamiDepartment of Gastroenterology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Yuji NadataniDepartment of Gastroenterology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Shusei FukunagaDepartment of Gastroenterology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Koji OtaniDepartment of Gastroenterology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Fumio TanakaDepartment of Gastroenterology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Satoko OhfujiDepartment of Public Health, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Yasuhiro FujiwaraDepartment of Gastroenterology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsTreatment using tumor necrosis factor-α (TNF-α) inhibitors is one of the risk factors for active tuberculosis (TB) in patients with Crohn's disease (CD). Biologics, such as ustekinumab (UST) and vedolizumab (VDZ), are less likely to cause opportunistic infections. However, large-scale studies for active TB and biologics other than TNF-α inhibitors are limited. We aimed to investigate the association between biologics and active TB utilizing a Japanese medical claims database.

methodsWe analyzed retrospectively the association of the risk of active TB development with treatment using TNF-α inhibitors and other biologics (UST and VDZ) in patients with CD using the Japanese Medical Data Vision (MDV) database between April 2008 and June 2022. The durations of each biologic and biologic-free treatment were calculated for each patient. Univariate and multivariate analyses were performed using the Cox proportional hazards model, with the utilization of biologics considered as time-dependent covariates.

resultsWe included 28,811 patients with CD in MDV database. Finally, 17,169 patients were analyzed. In total, 7,064 patients were categorized as biologic-naïve, while 10,105 were classified as biologic-experienced. Seventeen patients developed active TB, including 7 on infliximab, 5 on adalimumab, and 5 on no biologics. None of the patients treated with UST and VDZ developed active TB. Multivariate analysis suggested that TNF-α inhibitors were the risk factors for active TB (hazard ratio, 3.66; P= 0.020).

conclusionsTNF-α inhibitors, but not UST or VDZ, are risk factors for active TB in Japanese patients with CD.

Indexed as

Biological productsCrohn diseaseInsurance claim reviewTuberculosisTumor necrosis factor-alpha

Identifiers

PMID39155522
PMCPMC12332282

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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.