Evidence map›Paper›PMID 41879953›Full record

ArticleDigestive diseases and sciences2026

Risk of Autoimmune Hepatitis Among Patients with Inflammatory Bowel Disease Treated with Infliximab: A Retrospective Cohort Study Using a National Database.

Hamza Almusabeh, Zack Kovach, Laurel Lloyd, Mohamad Zaki Alzaher, Daniel Teran, Olanrewaju Adeniran, Katherine Shepherd, Khaled Elfert, Sanya Goswami, Kanwarpreet Tandon and 1 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Digestive diseases and sciences, 2026. 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

11 authors.

Hamza AlmusabehDepartment of Internal Medicine, West Virginia University School of Medicine, Morgantown, WV, USA. Hamza.Almusabeh@hsc.wvu.edu.
Zack KovachDepartment of Internal Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
Laurel LloydDepartment of Internal Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
Mohamad Zaki AlzaherHarvard Medical School, Boston, MA, USA.
Daniel TeranDepartment of Internal Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
Olanrewaju AdeniranDepartment of Internal Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
Katherine ShepherdDepartment of Internal Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
Khaled ElfertDivision of Gastroenterology and Hepatology, Department of Internal Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
Sanya GoswamiDivision of Gastroenterology and Hepatology, Department of Internal Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
Kanwarpreet TandonDivision of Gastroenterology and Hepatology, Department of Internal Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
Jennifer Hadam-VeverkaDivision of Gastroenterology and Hepatology, Department of Internal Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsInfliximab and adalimumab are widely used anti-tumor necrosis factor agents for inflammatory bowel disease, both with reported cases of drug-induced autoimmune hepatitis. However, comparative data on the risk of autoimmune hepatitis with infliximab versus adalimumab are limited. We aimed to compare the risk of autoimmune hepatitis among patients with inflammatory bowel disease treated with infliximab versus adalimumab.

methodsWe conducted a retrospective active-comparator, new-user cohort study using the TriNetX US collaborative network. Adults with Crohn's disease or ulcerative colitis who initiated infliximab or adalimumab were included. Patients with prior autoimmune hepatitis, prior exposure to the alternate anti-tumor necrosis factor agent, selected autoimmune comorbidities, or other biologic exposure were excluded. The primary outcome was new autoimmune hepatitis occurring at least 3 months after treatment initiation. Propensity score matching was performed to balance baseline covariates. A sensitivity analysis was also conducted including autoimmune comorbidities in the matching model.

resultsAfter propensity score matching, 15,298 patients remained in each group. Autoimmune hepatitis occurred in 33 patients (0.216%) treated with infliximab and 13 patients (0.085%) treated with adalimumab. Infliximab was associated with a higher risk of autoimmune hepatitis (risk ratio 2.53; 95% confidence interval (CI) 1.336-4.818; P = 0.0032). Time-to-event analysis showed similar findings (hazard ratio 2.602; 95% CI 1.369-4.945). In the sensitivity analysis, infliximab remained associated with a higher risk of autoimmune hepatitis.

conclusionsIn this large national cohort of patients with inflammatory bowel disease, infliximab was associated with a higher observed risk of autoimmune hepatitis compared with adalimumab.

Indexed as

AdalimumabColitis, UlcerativeCrohn DiseaseGastrointestinal AgentsHepatitis, AutoimmuneInflammatory Bowel DiseasesInfliximabAdultDatabases, FactualFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsUnited StatesAdalimumabGastrointestinal AgentsInfliximabAdalimumabAutoimmune hepatitisDrug-induced liver injuryInflammatory bowel diseaseInfliximabPropensity score matching

Identifiers

What OpenQuestion holds

Textmetadata
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.