Evidence map›Paper›PMID 38060978›Full record

ArticleThe British journal of dermatology2024

Atopic dermatitis, cognitive function and psychiatric comorbidities across early childhood and adolescence in a population-based UK birth cohort.

Patrick G Sockler, Stephen R Hooper, Katrina Abuabara, Emily Z Ma, Sarah Radtke, Aaron Bao, Elle Kim, Rashelle J Musci, Karin Kartawira, Joy Wan

Open access · greenAbstract read
In one paragraph

Article in The British journal of dermatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% of its field
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. The Psychology of Atopic Dermatitis.Journal of clinical medicine · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 1 country.

Patrick G SocklerDepartments of Dermatology.ORCID 0000-0003-2569-9447
Stephen R HooperDepartment of Health Sciences, School of Medicine, University of North Carolina-Chapel Hill, Chapel Hill, NC, USA.
Katrina AbuabaraDepartment of Dermatology, University of California-San Francisco School of Medicine, San Francisco, CA, USA.
Emily Z MaUniversity of Maryland School of Medicine, Baltimore, MD, USA.
Sarah RadtkeChild and Adolescent Psychiatry, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Aaron BaoDepartments of Dermatology.
Elle KimDepartments of Dermatology.
Rashelle J MusciMental Health.
Karin KartawiraDepartments of Dermatology.
Joy WanDepartments of Dermatology.ORCID 0000-0002-0189-0442
Johns Hopkins University · USMassachusetts Department of Mental Health · USUniversity of California, San Francisco · USUniversity of Maryland, Baltimore · USUniversity of North Carolina at Chapel Hill · USUniversity of Pennsylvania · US

Funding

Impact of Pediatric Atopic Dermatitis on Neurocognitive FunctionK23AR077629 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI WAN, JOY · 2021 to 2025
$858k
Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_19009NIAMS NIH HHS K23 AR077629NIH HHS K23AR077629Wellcome Trust
6 · The paper itself

Abstract

backgroundAtopic dermatitis (AD) may affect cognitive function, but studies are limited and inconsistent. The effect of AD severity on cognition remains underexplored and few previous studies have examined clinically validated or repeated measures of cognition throughout childhood.

objectivesTo evaluate the relationship of AD activity and severity with validated measures of general cognition in a longitudinal birth cohort.

methodsWe conducted cross-sectional analyses using data from the Avon Longitudinal Study of Parents and Children (ALSPAC), a UK cohort of 14 975 individuals followed prospectively since their birth in 1991-92. AD was assessed 11 times between the age of 6 and 166 months. Mothers were asked if their child had an 'itchy, dry skin rash in the joints and creases', and AD status was time-updated accordingly as 'never', 'maybe', 'inactive', 'active/mild' or 'active/moderate-severe'. General cognition [i.e. intelligence quotient (IQ)] was measured at 18, 49, 103 and 186 months of age using the Griffiths Mental Development Scales (GMDS), Wechsler Preschool and Primary Scale of Intelligence (WPPSI), Wechsler Intelligence Scale for Children (WISC) and Wechsler Abbreviated Scale of Intelligence (WASI), respectively. Multivariable linear regression was used to compare IQ with respect to nearest time-updated AD status. Secondary analyses were stratified by the presence or absence of psychiatric or learning disorders. An exploratory longitudinal analysis of IQ across all four outcome assessments was conducted using generalized estimating equations.

resultsNo significant associations between AD status and full-scale IQ scores on the GMDS, WPPSI, WISC and WASI were observed after adjustment for sociodemographic factors, atopic comorbidities and sleep characteristics. However, at 8 years of age, WISC Performance IQ was slightly, although statistically significantly, lower among children with active/moderate-severe AD [β coefficient -2.16, 95% confidence interval (CI) -4.12 to -0.19] and Verbal IQ was slightly, but statistically significantly, higher among those with inactive AD (β coefficient 1.31, 95% CI 0.28-2.34) compared with those without AD. Analyses stratified by psychiatric or learning disorders, and exploratory longitudinal analyses of cognition revealed similar findings.

conclusionsWe did not find any clinically meaningful associations between AD activity and severity and general cognitive function during early childhood and adolescence. Future studies should incorporate objective measures of AD severity and investigate outcomes beyond IQ.

Indexed as

Dermatitis, AtopicLearning DisabilitiesAdolescentBirth CohortChildChild, PreschoolCognitionCross-Sectional StudiesFemaleHumansLongitudinal StudiesUnited Kingdom

Identifiers

PMID38060978
PMCPMC10941325
OpenAlexW4389426524

What OpenQuestion holds

Textmetadata
LicenceTDM
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.