Evidence map›Paper›PMID 40261548›Full record

ArticleDermatology and therapy2025

The Association Between Atopic Dermatitis and Select Disease Events in Adults in the United States: A Retrospective Cohort Study in the Optum Electronic Health Records Database.

Adina R Lemeshow, Alexander Egeberg, Thomas Edwards, Stephen E Schachterle, William Romero, Daniela E Myers, Shefali Vyas, Jonathan I Silverberg

Abstract read
In one paragraph

Article in Dermatology and therapy, 2025. 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

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

8 authors.

Adina R LemeshowPfizer Inc., 66 Hudson Yards East, 13/13N-2, New York, NY, 10001, USA. adina.lemeshow@pfizer.com.ORCID http://orcid.org/0000-0003-2994-1341
Alexander EgebergDepartment of Dermatology, Bispebjerg University Hospital, University of Copenhagen, Copenhagen, Denmark.
Thomas Edwards, Panalgo, Boston, MA, USA.
Stephen E SchachterlePfizer Inc., 66 Hudson Yards East, 13/13N-2, New York, NY, 10001, USA.
William RomeroPfizer Ltd., Tadworth, Surrey, UK.
Daniela E MyersPfizer Inc., 66 Hudson Yards East, 13/13N-2, New York, NY, 10001, USA.
Shefali VyasPfizer Inc., 66 Hudson Yards East, 13/13N-2, New York, NY, 10001, USA.
Jonathan I SilverbergDepartment of Dermatology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPrevious studies have reported positive associations between atopic dermatitis (AD) and select disease events; however, definitive conclusions are lacking. The aim of this study was to characterize demographic and clinical characteristics of patients with and without AD and estimate crude incidence rates (IRs) and adjusted hazard rate ratios (HRRs) of select disease events in these cohorts.

methodsThis retrospective observational analysis used Optum® Market Clarity Electronic Health Records, a US administrative healthcare database. Adults with and without AD between 2016 and 2021 with ≥ 12 months of database activity prior to index date (based on diagnosis or first treatment) were included. Each patient with AD was matched on age and index date with five patients without AD. The AD cohort was stratified by treatment prescribed within 30 days of AD diagnosis: no AD treatment; topical corticosteroids (TCS)/topical calcineurin inhibitors (TCI) only ("TCS/TCI only"); phototherapy with/without TCS/TCI ("phototherapy"); and systemic therapy, including oral corticosteroids with/without phototherapy and with/without TCS/TCI ("systemics"). Crude IRs and adjusted HRRs of infections, malignancies, cardiovascular events, mental health outcomes, asthma, fracture, and death across patient subgroups were estimated.

resultsThe total cohort comprised 161,646 adults. Among the 25,915 patients with AD, 8384 (32.35%), 13,459 (51.94%), 366 (1.41%), and 3706 (14.30%) were included in the "no AD treatment," "TCS/TCI only," "phototherapy," and "systemics" subgroups, respectively. Crude IRs/1000 patient-years were higher among patients with AD versus those without AD for serious infections (38.35 vs. 19.21), major adverse cardiovascular events (16.51 vs. 11.82), venous thromboembolism (11.12 vs. 6.89), malignancies (excluding nonmelanoma skin cancer; 17.51 vs. 15.25), and depression (63.50 vs. 44.18); similar trends were observed after controlling for potential confounding variables. When stratified by treatment, IRs and HRRs of these events were generally higher in patients in the "systemics" subgroup versus other treatment subgroups.

conclusionsOverall, certain disease event rates were higher in the population with AD versus the population without AD, with a trend towards higher rates among patients prescribed systemic therapies compared with those prescribed TCS/TCI only. This study further informs the relationship between AD and the risk of select disease events.

Indexed as

Atopic dermatitisDisease eventsElectronic health records databaseHazard rate ratiosIncidence ratesTreatment subgroups

Identifiers

PMID40261548
PMCPMC12092883

What OpenQuestion holds

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LicenceCC BY-NC
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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.