Evidence map›Paper›PMID 33826159›Full record

ArticleJournal of child psychology and psychiatry, and allied disciplines2021

Diagnostic shifts in autism spectrum disorder can be linked to the fuzzy nature of the diagnostic boundary: a data-driven approach.

Birkan Tunç, Juhi Pandey, Tanya St John, Shoba S Meera, Jennifer E Maldarelli, Lonnie Zwaigenbaum, Heather C Hazlett, Stephen R Dager, Kelly N Botteron, Jessica B Girault and 8 more

Open access · greenAbstract read
In one paragraph

Article in Journal of child psychology and psychiatry, and allied disciplines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Overall prognosis of preschool autism spectrum disorder diagnoses.The Cochrane database of systematic reviews · 2022
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
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

18 authors at 9 institutions in 3 countries.

Birkan TunçCenter for Autism Research, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.ORCID 0000-0002-2294-4024
Juhi PandeyCenter for Autism Research, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Tanya St JohnDepartment of Speech and Hearing Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0003-2448-5797
Shoba S MeeraDepartment of Speech Pathology and Audiology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.ORCID 0000-0001-8867-9457
Jennifer E MaldarelliCenter for Autism Research, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Lonnie ZwaigenbaumDepartment of Pediatrics, University of Alberta, Edmonton, AB, Canada.ORCID 0000-0001-9607-0799
Heather C HazlettThe Carolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Stephen R DagerDepartment of Radiology and Bioengineering, University of Washington, Seattle, WA, USA.
Kelly N BotteronDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.
Jessica B GiraultThe Carolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Robert C McKinstryMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO, USA.ORCID 0000-0003-3578-4899
Ragini VermaDiCIPHR (Diffusion and Connectomics in Precision Healthcare Research) Lab, Department of Radiology, University of Pennsylvania, Philadelphia, PA, USA.
Jed T ElisonInstitute of Child Development, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0002-6246-1000
John R PruettDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.
Joseph PivenThe Carolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Annette M EstesDepartment of Speech and Hearing Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0003-2687-4155
Robert T SchultzCenter for Autism Research, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.ORCID 0000-0001-9817-3425
IBIS Network
Children's Hospital of Philadelphia · USUniversity of North Carolina at Chapel Hill · USUniversity of Washington · USWashington University in St. Louis · USMallinckrodt (United States) · USNational Institute of Mental Health and Neurosciences · INUniversity of Alberta · CAUniversity of Minnesota · USUniversity of Pennsylvania · US

Funding

Cellular and molecular mechanisms governing cortical surface area overgrowth in iPSC-derived neural cells from longitudinally characterized individuals with autismR01HD055741 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Joseph Piven · 2007 to 2026
$52.6M
MRI-Based Presymptomatic Prediction of ASD, and Early Infant to School-Age Brain-Behavior Trajectories, Mechanisms, and Related OutcomesR01MH118362 · NIMH · WASHINGTON UNIVERSITY · PI John R Pruett · 2019 to 2026
$16.3M
A Longitudinal MRI Study Characterizing Very Early Brain Development in Infants with Down SyndromeR01HD088125 · NICHD · WASHINGTON UNIVERSITY · PI MARRUS, NATASHA · 2018 to 2024
$13.9M
The Intellectual and Developmental Disabilities Research Center (IDDRC) at CHOP/PennP50HD105354 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI Michael Byrne Robinson · 2021 to 2026
$9.2M
Washington University Intellectual and Developmental Disabilities Research Center-Administrative Down Syndrome SupplementU54HD087011 · NICHD · WASHINGTON UNIVERSITY · PI WOZNIAK, DAVID FRANCIS · 2015 to 2019
$7.1M
The Intellectual and Developmental Disabilities Research Center at CHOP/PennU54HD086984 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI ROBERTS, TIMOTHY P · 2016 to 2020
$6.3M
Toward Scalable Biomarker-Based Prediction of ASD in High-Risk InfantsR01MH121462 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JESTE, SHAFALI SPURLING · 2019 to 2023
$4.0M
Harmonization for multisite Connectomics: parsing heterogeneity and creating markers in ASDR01MH117807 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI VERMA, RAGINI · 2019 to 2023
$3.6M
Development and neural mechanisms of repetitive behavior and sensory responsivity in autismR01MH116961 · NIMH · UNIVERSITY OF MINNESOTA · PI WOLFF, JASON J · 2018 to 2022
$2.8M
Investigating Air Pollution Effects on the Developing Brain and ASDR01ES026961 · NIEHS · JOHNS HOPKINS UNIVERSITY · PI VOLK, HEATHER E · 2016 to 2020
$2.7M
Biomedical Image Computing and Informatics ClusterS10OD023495 · OD · UNIVERSITY OF PENNSYLVANIA · PI DAVATZIKOS, CHRISTOS · 2017 to 2017
$1.9M
The fusiform and amygalda in the pathobiology of autismR01MH073084 · NIMH · YALE UNIVERSITY · PI SCHULTZ, ROBERT THOMAS · 2005 to 2009
$1.6M
NICHD NIH HHS P50 HD105354NICHD NIH HHS R01 HD055741NICHD NIH HHS R01 HD088125NICHD NIH HHS U54 HD086984NICHD NIH HHS U54 HD087011NIEHS NIH HHS R01 ES026961NIH HHS S10 OD023495NIMH NIH HHS K01 MH122779NIMH NIH HHS R01 MH073084NIMH NIH HHS R01 MH116961NIMH NIH HHS R01 MH117807NIMH NIH HHS R01 MH118362NIMH NIH HHS R01 MH121462
6 · The paper itself

Abstract

backgroundDiagnostic shifts at early ages may provide invaluable insights into the nature of separation between autism spectrum disorder (ASD) and typical development. Recent conceptualizations of ASD suggest the condition is only fuzzily separated from non-ASD, with intermediate cases between the two. These intermediate cases may shift along a transition region over time, leading to apparent instability of diagnosis.

methodsWe used a cohort of children with high ASD risk, by virtue of having an older sibling with ASD, assessed at 24 months (N = 212) and 36 months (N = 191). We applied machine learning to empirically characterize the classification boundary between ASD and non-ASD, using variables quantifying developmental and adaptive skills. We computed the distance of children to the classification boundary.

resultsChildren who switched diagnostic labels from 24 to 36 months, in both directions, (dynamic group) had intermediate phenotypic profiles. They were closer to the classification boundary compared to children who had stable diagnoses, both at 24 months (Cohen's d = .52) and at 36 months (d = .75). The magnitude of change in distance between the two time points was similar for the dynamic and stable groups (Cohen's d = .06), and diagnostic shifts were not associated with a large change. At the individual level, a few children in the dynamic group showed substantial change.

conclusionsOur results suggested that a diagnostic shift was largely due to a slight movement within a transition region between ASD and non-ASD. This fact highlights the need for more vigilant surveillance and intervention strategies. Young children with intermediate phenotypes may have an increased susceptibility to gain or lose their diagnosis at later ages, calling attention to the inherently dynamic nature of early ASD diagnoses.

Indexed as

Autism Spectrum DisorderChild, PreschoolCohort StudiesEarly DiagnosisHumansPhenotypeSiblingsAutism spectrum disordersdiagnosisinfancymachine learningstability

Identifiers

PMID33826159
PMCPMC8601115
OpenAlexW3148037832

What Socratic 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 Socratic graph.