Evidence map›Paper›PMID 42180015›Full record

ArticleCrohn's & colitis 3602026

Safety of biologics and Janus kinase inhibitors in inflammatory bowel disease patients with low cardiovascular risk.

Paraj Patel, Omair Iqbal, Divyanshu Mohananey, Saffia Bajwa, Masoud Khani, Jake Luo, Daniel J Stein, Gursimran S Kochhar, Jana G Hashash, Emad Mansoor and 2 more

Abstract read
In one paragraph

Article in Crohn's & colitis 360, 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

12 authors.

Paraj PatelDivision of Gastroenterology and Hepatology, Medical College of Wisconsin, Milwaukee, WI, United States.ORCID https://orcid.org/0009-0009-7017-0519
Omair IqbalMedical College of Wisconsin, Milwaukee, WI, United States.
Divyanshu MohananeyMedical College of Wisconsin Cardiovascular Center, Medical College of Wisconsin, Milwaukee, WI, United States.ORCID https://orcid.org/0000-0003-2815-2949
Saffia BajwaDepartment of Medicine, Medical College of Wisconsin, Milwaukee, WI, United States.
Masoud KhaniHealth Informatics Program, Zilber School of Public Health, University of Wisconsin-Milwaukee, Milwaukee, WI, United States.
Jake LuoHealth Informatics Program, Zilber School of Public Health, University of Wisconsin-Milwaukee, Milwaukee, WI, United States.
Daniel J SteinDivision of Gastroenterology and Hepatology, Medical College of Wisconsin, Milwaukee, WI, United States.
Gursimran S KochharDepartment of Gastroenterology and Hepatology, Allegheny Health Network, Pittsburgh, PA, United States.
Jana G HashashDepartment of Gastroenterology and Hepatology, Mayo Clinic in Florida, Jacksonville, FL, United States.
Emad MansoorDivision of Gastroenterology and Liver Disease, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, OH, United States.
Raymond K CrossDepartment of Medicine, Division of Gastroenterology and Hepatology, University of Maryland School of Medicine, Baltimore, MD, United States.
Preetika SinhDivision of Gastroenterology and Hepatology, Medical College of Wisconsin, Milwaukee, WI, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Due to underlying chronic inflammation, inflammatory bowel disease (IBD) is associated with an increased risk of major adverse cardiovascular events (MACE). There is limited data on the role of cardiovascular (CV) risk factors and IBD medications on MACE. We aim to determine the association between MACE and IBD medications in a large national cohort of IBD patients with low baseline CV risk. Methods: We conducted a retrospective cohort study between January 1, 2015 and November 15, 2023 using the TriNetX database. Using logistic regression analysis, IBD patients exposed to biologics and small molecules were assessed for outcomes of individual and composite MACE (myocardial infarction [MI], ischemic stroke, percutaneous coronary intervention [PCI]/coronary artery bypass graft [CABG]). Outcomes were adjusted for demographics, non-advanced IBD therapies, statin use, CV risk factors, and prior history of coronary artery disease (CAD). Results: We identified 113 729 IBD patients with an average age of 42 years and low prevalence of CV risk factors (5%-6%). Anti-TNF therapy was associated with a statistically significant decreased risk of composite MACE (adjusted OR [aOR] 0.795, 95% CI, 0.670-0.930, Conclusions: In a cohort of young IBD patients with low CV risk, use of anti-TNF and anti-integrins is associated with a decreased risk of MACE, and there was no increased risk of MACE with JAK inhibitors.

Indexed as

biologicsinflammationinflammatory bowel diseaseoutcomes research

Identifiers

PMID42180015
PMCPMC13189853

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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.