Evidence map›Paper›PMID 42776961›Full record

ArticlePloS one2026

Moderate-to-severe chronic spontaneous urticaria is associated with increased risk of immune-mediated diseases: A population-based study.

Kimberly Smart, Andrea Ure, Nicole Johnsen, Shaliz Aflatooni, Julian A Cortes, Gabriela Palma, Yvonne Nong, Andrea J Borba, Paul C Levins, April W Armstrong

Abstract read
In one paragraph

Article in PloS one, 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

10 authors.

Kimberly SmartKeck School of Medicine, University of Southern California, Los Angeles, California, United States of America.ORCID https://orcid.org/0009-0007-6686-9971
Andrea UreUniversity of California, Davis School of Medicine, Sacramento, California, United States of America.
Nicole JohnsenDavid Geffen School of Medicine at the University of California, Los Angeles, California, United States of America.
Shaliz AflatooniUSF Morsani College of Medicine, Tampa, Florida, United States of America.
Julian A CortesUniversity of California, San Diego School of Medicine, San Diego, California, United States of America.
Gabriela PalmaDonald and Barbara Zucker School of Medicine at Hofstra/Northwell, Uniondale, New York, United States of America.
Yvonne NongDivision of Dermatology, Department of Medicine, David Geffen School of Medicine at the University of California, Los Angeles, California, United States of America.
Andrea J BorbaDivision of Dermatology, Department of Medicine, David Geffen School of Medicine at the University of California, Los Angeles, California, United States of America.
Paul C LevinsDivision of Dermatology, Department of Medicine, David Geffen School of Medicine at the University of California, Los Angeles, California, United States of America.
April W ArmstrongDivision of Dermatology, Department of Medicine, David Geffen School of Medicine at the University of California, Los Angeles, California, United States of America.ORCID https://orcid.org/0000-0003-0064-8707

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic spontaneous urticaria (CSU) is characterized by the idiopathic appearance of wheals and/or angioedema lasting more than six weeks. There is a critical need to evaluate whether the severity of CSU influences the risk of future immune-mediated comorbidities. We aim to evaluate if patients with moderate-to-severe chronic spontaneous urticaria (CSU) have an increased risk of developing immune-mediated comorbidities compared with matched patients with mild CSU. We conducted a retrospective cohort study using the TriNetX US Collaborative Network database from 2014-2026. We propensity matched patients with ≥2 ICD-10 diagnoses of idiopathic urticaria treated with omalizumab, dupilumab, or cyclosporine (moderate-to-severe disease) to age-, sex-, race-, ethnicity-, comorbidity-, and family history-matched counterparts who were never treated with biologics or cyclosporine (mild disease). After matching, 16,413 patients were included in the moderate-to-severe group, and 16,413 patients were included in the mild group. Patients with moderate-to-severe CSU had a significantly increased risk of developing rheumatoid arthritis OR=1.34 (95% CI: 1.12 to 1.60, p = 0.001) and Sjögren's syndrome OR=1.04 (1.63-2.56, p < 0.0001), after adjusting for clinical factors and multiple hypothesis testing (Bonferroni's alpha ≤0.00333). Moderate-to-severe CSU is associated with an increased risk of rheumatoid arthritis and Sjögren's syndrome compared to mild CSU.

Indexed as

Arthritis, RheumatoidChronic UrticariaUrticariaAdultAgedComorbidityCyclosporineFemaleHumansMaleMiddle AgedOmalizumabRetrospective StudiesRisk FactorsSeverity of Illness IndexCyclosporineOmalizumab

Identifiers

PMID42776961
PMCPMC13600506

What OpenQuestion holds

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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.