Evidence map›Paper›PMID 40922787›Full record

ArticleJAACAP open2025

Describing Multidomain Health Outcomes in Autistic Children in the ECHO Program.

Elizabeth A Kaplan-Kahn, Juliette Rando, Jennifer L Ames, Traci A Bekelman, Carlos A Camargo, Lisa A Croen, Stephen R Dager, Aisha S Dickerson, Anne L Dunlop, Amy J Elliott and 17 more

Abstract read
In one paragraph

Article in JAACAP open, 2025. 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

27 authors.

Elizabeth A Kaplan-KahnCenter for Autism Research at Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Juliette RandoA.J. Drexel Autism Institute at Drexel University, Philadelphia, Pennsylvania.
Jennifer L AmesKaiser Permanente Northern California, Oakland, California.
Traci A BekelmanColorado School of Public Health at University of Colorado Denver, Denver, Colorado.
Carlos A CamargoMassachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Lisa A CroenKaiser Permanente Northern California, Oakland, California.
Stephen R DagerCenter on Human Development and Disability at University of Washington, Seattle, Washington.
Aisha S DickersonJohns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Anne L DunlopEmory University School of Medicine, Atlanta, Georgia.
Amy J ElliottAvera Research Institute and the Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota.
Angelo P GiardinoUniversity of Utah School of Medicine, Salt Lake City, Utah.
Heather Cody HazlettUniversity of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Irva Hertz-PicciottoUniversity of California Davis, Davis, California.
Deborah HirtzUniversity of Vermont School of Medicine, Burlington, Vermont.
Robert M JosephChobanian & Avedisian School of Medicine at Boston University, Boston, Massachusetts.
Rebecca J LandaKennedy Krieger Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Cindy T McEvoyOregon Health & Science University School of Medicine, Portland, Oregon.
Daniel S MessingerUniversity of Miami, Miami, Florida.
Daphne Koinis-MitchellHasbro Children's Hospital at Brown University, Providence, Rhode Island.
Jenae M NeiderhiserPennsylvania State University, University Park, Pennsylvania.
Craig J NewschafferPennsylvania State University, University Park, Pennsylvania.
Jessie B NorthrupUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Sally OzonoffUniversity of California Davis, Davis, California.
Rebecca J SchmidtUniversity of California Davis, Davis, California.
Heather E VolkBloomberg School of Public Health at Johns Hopkins University, Baltimore, Maryland.
Kristen LyallA.J. Drexel Autism Institute at Drexel University, Philadelphia, Pennsylvania.
program collaborators for Environmental influences on Child Health Outcomes (ECHO)

Funding

Early Life Exposure to Endocrine Disrupting Chemicals and Child Growth, Adiposity, and NeurodevelopmentUH3OD023289 · OD · KAISER FOUNDATION RESEARCH INSTITUTE · PI ASSIAMIRA FERRARA, Monique Marie Hedderson · 2018 to 2026
$25.1M
BUILDS MARBLES: Biorepository Upkeep and Infrastructure for Longitudinal Data Sharing for MARBLESR24ES028533 · NIEHS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Brittany D. Chambers Butcher, Rebecca Jean Schmidt · 2017 to 2026
$2.3M
BUILDS MARBLES: Biorepository Upkeep and Infrastructure for Longitudinal Data Sharing for MARBLESU24ES028533 · NIEHS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHAMBERS BUTCHER, BRITTANY D., SCHMIDT, REBECCA JEAN · 2023 to 2025
$1.2M
NIEHS NIH HHS R24 ES028533NIEHS NIH HHS U24 ES028533NIH HHS UH3 OD023289
6 · The paper itself

Abstract

Objective: The goal of this study is to characterize health outcomes across 3 domains-overall well-being, behavioral health, and physical health-in a large sample of autistic and non-autistic children and adolescents in the Environmental influences on Child Health Outcomes (ECHO) program. Method: First, we examined differences in health outcomes between autistic (N = 286) and non-autistic (N = 4,225) children and adolescents in the ECHO Program. Using a subsample of 1,809 participants (116 autistic participants) with complete outcome data, we conducted latent profile analyses (LPAs) to define profiles of health outcomes for autistic children and adolescents and for the combined sample of autistic and non-autistic participants. Finally, we examined demographic factors in relation to the health outcome profiles. Results: Autistic participants demonstrated poorer health outcomes than non-autistic participants for most outcome measures across the domains of overall well-being, behavioral health, and physical health. In the combined sample LPA, 3 profiles, representing more positive health (n = 566, 31.3%), poorer health (n = 462, 25.5%), and mixed health (n = 781, 43.2%), were identified. The profile with the poorer health outcomes had the highest proportion of autistic participants (n = 64, 13.9%). However, within the autistic group, LPA revealed 2 profiles of autistic participants, with 1 profile (n = 70, 60.3%) having more positive health outcomes across all domains. Conclusion: Although autistic participants demonstrated poorer health outcomes than non-autistic participants on most measures, examining latent profiles within the group of autistic participants highlighted variability in the health outcomes among autistic youth. Results emphasize the importance of examining variability within autistic samples to better understand multidimensional health influences and outcomes of individuals on the autism spectrum. Diversity & Inclusion Statement: One or more of the authors of this paper self-identifies as a member of one or more historically underrepresented sexual and/or gender groups in science.

Identifiers

PMID40922787
PMCPMC12414301

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.