Evidence map›Paper›PMID 42629386›Full record

ArticlePediatric research2026

Phenotypes of atopic dermatitis and long-term body mass index trajectories.

Yasutaka Kuniyoshi

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric research, 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

1 author.

Yasutaka KuniyoshiDepartment of Social Services and Healthcare Management, International University of Health and Welfare, Otawara, Japan. yasutakakuniyoshi@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEvidence linking atopic dermatitis (AD) to obesity is inconsistent, partly because prior studies overlooked the disease's clinical heterogeneity. This study aimed to identify longitudinal AD and body mass index (BMI) trajectories from childhood to adolescence and examine their concurrent associations.

methodsData from 20,158 children in a Japanese nationwide birth cohort followed for 13 years were analyzed. Group-based trajectory modeling identified five AD phenotypes and three BMI z-score trajectories. Associations were analyzed using sex-stratified multinomial logistic regression.

resultsThree BMI trajectories with similar patterns were identified for both sexes: "Stable," "High-Decreasing," and "Low-Increasing." With BMI as outcome, in boys, "Early-onset transient" (adjusted odds ratio [aOR], 1.37; 95% confidence interval [CI], 1.16-1.63) and "Early-onset persistent" (aOR, 1.18; 1.06-1.31) AD phenotypes were associated with the "High-Decreasing" BMI, while "Late-onset" AD was associated with the "Low-Increasing" BMI trajectory (aOR, 1.51; 1.07-2.14). In girls, "Late-onset" AD was associated with the "Low-Increasing" (aOR, 1.88; 1.35-2.64) and "High-Decreasing" (aOR, 1.45; 1.06-1.98) BMI; early-onset phenotypes showed no significant associations.

conclusionThe longitudinal clinical course of childhood AD is concurrently associated with distinct, sex-specific BMI trajectories, highlighting a parallel relationship between cutaneous symptom development and somatic growth. IMPACT: Longitudinal phenotypes of childhood atopic dermatitis (AD) are associated with distinct, sex-specific body mass index (BMI) trajectories. Using a 13-year nationwide birth cohort, we show a parallel relationship between the AD course and somatic growth. Early-onset AD phenotypes are associated with a "catch-down" BMI in boys, whereas late-onset AD phenotypes are associated with upward BMI shifts in both sexes. Recognizing these parallel developmental patterns helps clinicians holistically monitor children with AD.

Identifiers

What OpenQuestion holds

Textmetadata
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.