Evidence map›Paper›PMID 38751343›Full record

ArticleClinical and experimental dermatology2024

Disagreement concerning atopic dermatitis subtypes between an English prospective cohort (ALSPAC) and linked electronic health records.

Julian Matthewman, Amy Mulick, Nick Dand, Daniel Major-Smith, Alasdair Henderson, Neil Pearce, Spiros Denaxas, Rita Iskandar, Amanda Roberts, Rosie P Cornish and 3 more

Abstract read
In one paragraph

Article in Clinical and experimental dermatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Agreement between parent reported and clinical coding of asthma, eczema and allergic rhinitis: The multi-ethnic Born in Bradford cohort.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2025
    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

13 authors.

Julian MatthewmanLondon School of Hygiene & Tropical Medicine, London, UK.ORCID 0000-0003-3291-2381
Amy MulickLondon School of Hygiene & Tropical Medicine, London, UK.
Nick DandDepartment of Medical and Molecular Genetics, School of Basic & Medical Biosciences, King's College London, London, UK.ORCID 0000-0002-1805-6278
Daniel Major-SmithPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Alasdair HendersonLondon School of Hygiene & Tropical Medicine, London, UK.ORCID 0000-0002-8903-4906
Neil PearceLondon School of Hygiene & Tropical Medicine, London, UK.ORCID 0000-0002-9938-7852
Spiros DenaxasInstitute of Health Informatics, UCL, London, UK.ORCID 0000-0001-9612-7791
Rita IskandarLondon School of Hygiene & Tropical Medicine, London, UK.
Amanda RobertsIndependent Patient Partner.
Rosie P CornishPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Sara J BrownCentre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
Lavinia PaternosterMRC Integrative Epidemiology Unit, Bristol Medical School, University of Bristol, Bristol, UK.
Sinéad M LanganLondon School of Hygiene & Tropical Medicine, London, UK.

Funding

ALSPACBIOMAPBritish Heart FoundationChief Scientist Office of the Scottish Government Health and Social Care DirectoratesDepartment of Health and Social CareEconomic and Social Research CouncilEngineering and Physical Sciences Research CouncilHealth and Social Care Research and Development DivisionHealth Data Research UKJohn Templeton Foundation 61917Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_19009National Institute for Health and Care Research Bristol Biomedical Research Centre NIHR203315NIHRPublic Health AgencyUK Medical Research CouncilWellcome TrustWellcome Trust 205039/Z/16/Z
6 · The paper itself

Abstract

backgroundSubtypes of atopic dermatitis (AD) have been derived from the Avon Longitudinal Study of Parents and Children (ALSPAC) based on the presence and severity of symptoms reported in questionnaires (severe-frequent, moderate-frequent, moderate-declining, mild-intermittent, unaffected-rare). Good agreement between ALSPAC and linked electronic health records (EHRs) would increase trust in the clinical validity of these subtypes and allow inference of subtypes from EHRs alone, which would enable their study in large primary care databases.

objectivesFirstly, to explore whether the presence and number of AD records in EHRs agree with AD symptom and severity reports from ALSPAC. Secondly, to explore whether EHRs agree with ALSPAC-derived AD subtypes. Thirdly, to construct models to classify ALSPAC-derived AD subtypes using EHRs.

methodsWe used data from the ALSPAC prospective cohort study from 11 timepoints until age 14 years (1991-2008), linked to local general practice EHRs. We assessed how far ALSPAC questionnaire responses and derived subtypes agreed with AD as established in EHRs using different AD definitions (e.g. diagnosis and/or prescription) and other AD-related records. We classified AD subtypes using EHRs, fitting multinomial logistic regression models, tuning hyperparameters and evaluating performance in the testing set [receiver operating characteristic (ROC) area under the curve (AUC), accuracy, sensitivity and specificity].

resultsOverall, 8828 individuals out of a total 13 898 had been assigned an AD subtype and also had linked EHRs. The number of AD-related codes in EHRs generally increased with the severity of the AD subtype. However, not all patients with the severe-frequent subtype had AD in EHRs, and many with the unaffected-rare subtype did have AD in EHRs. When predicting the ALSPAC AD subtype using EHRs, the best tuned model had an ROC AUC of 0.65, a sensitivity of 0.29 and a specificity of 0.83 (both macro-averaged). When different sets of predictors were used, individuals with missing EHR coverage were excluded, and subtypes were combined, sensitivity was not considerably improved.

conclusionsALSPAC and EHRs disagreed not only on AD subtypes, but also on whether children had AD or not. Researchers should be aware that individuals considered to have AD in one source may not be considered to have AD in another.

Indexed as

Dermatitis, AtopicElectronic Health RecordsAdolescentChildChild, PreschoolEnglandFemaleHumansInfantLogistic ModelsLongitudinal StudiesMaleProspective StudiesSeverity of Illness IndexSurveys and Questionnaires

Identifiers

PMID38751343
PMCPMC11583923

What OpenQuestion holds

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LicenceCC BY
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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.