Evidence map›Paper›PMID 27096285›Full record

ArticleJAMA psychiatry2016

Evaluation of Quantified Social Perception Circuit Activity as a Neurobiological Marker of Autism Spectrum Disorder.

Malin Björnsdotter, Nancy Wang, Kevin Pelphrey, Martha D Kaiser

Open access · bronzeAbstract read
In one paragraph

Article in JAMA psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 3 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

16 citing papers in PubMed, 3 syntheses or guidelines pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Meta-Analysis of the RDoC Social Processing Domain across Units of Analysis in Children and Adolescents.Journal of clinical child and adolescent psychology : the official journal for the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53
    Pooled it
  4. Article
  5. Article
  6. Article
  7. Copy Number Variation Informs fMRI-based Prediction of Autism Spectrum Disorder.Machine learning in clinical neuroimaging : 6th international workshop, MLCN 2023, held in conjunction with MICCAI 2023, Vancouver, BC, Canada, October 8, 2023, proceedings. MLCN (Workshop) (6th : 2023 : Vancouver, B.C.) · 2023
    Article
  8. Article
  9. Article
  10. Neural correlates of gentle skin stroking in early infancy.Developmental cognitive neuroscience · 2019
    Article
  11. Prediction of severity and treatment outcome for ASD from fMRI.Predictive Intelligence in Medicine. PRIME (Workshop) · 2018
    Article
  12. Article
  13. Grey matter correlates of autistic traits in women with anorexia nervosa.Journal of psychiatry & neuroscience : JPN · 2018
    Article
  14. Charting a Course for Autism Biomarkers.Biological psychiatry · 2017
    Article
  15. Article
  16. 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

4 authors at 3 institutions in 2 countries.

Malin BjörnsdotterCenter for Social and Affective Neuroscience, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden2Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.
Nancy WangCenter for Translational Developmental Neuroscience, Child Study Center, Yale School of Medicine, New Haven, Connecticut.
Kevin PelphreyAutism And Neurodevelopment Disorders Institute, The George Washington University and Children's National Medical Center, Washington, DC.
Martha D KaiserCenter for Translational Developmental Neuroscience, Child Study Center, Yale School of Medicine, New Haven, Connecticut.
Yale University · USGeorge Washington University · USUniversity of Gothenburg · SE

Funding

Multimodal Developmental Neurogenetics of Females with ASDR01MH100028 · NIMH · YALE UNIVERSITY · PI Allison Elizabeth Jack, LAUREN KENWORTHY · 2012 to 2026
$37.8M
NIMH NIH HHS R01 MH100028
6 · The paper itself

Abstract

importanceAutism spectrum disorder (ASD) is marked by social disability and is associated with dysfunction in brain circuits supporting social cue perception. The degree to which neural functioning reflects individual-level behavioral phenotype is unclear, slowing the search for functional neuroimaging biomarkers of ASD.

objectiveTo examine whether quantified neural function in social perception circuits may serve as an individual-level marker of ASD in children and adolescents. DESIGN, SETTING, AND

participantsThe cohort study was conducted at the Yale Child Study Center and involved children and adolescents diagnosed as having ASD and typically developing participants. Participants included a discovery cohort and a larger replication cohort. Individual-level social perception circuit functioning was assessed as functional magnetic resonance imaging brain responses to point-light displays of coherent vs scrambled human motion. MAIN OUTCOMES AND MEASURES: Outcome measures included performance of quantified brain responses in affected male and female participants in terms of area under the receiver operating characteristic curve (AUC), sensitivity and specificity, and correlations between brain responses and social behavior.

resultsOf the 39 participants in the discovery cohort aged 4 to 17 years, 22 had ASD and 30 were boys. Of the 75 participants in the replication cohort aged 7 to 20 years, 37 had ASD and 52 were boys. A relative reduction in social perception circuit responses was identified in discovery cohort boys with ASD at an AUC of 0.75 (95% CI, 0.52-0.89; P = .01); however, typically developing girls and girls with ASD could not be distinguished (P = .54). The results were confirmed in the replication cohort, where brain responses were identified in boys with ASD at an AUC of 0.79 (95% CI, 0.64-0.91; P < .001) and failed to distinguish affected and unaffected girls (P = .82). Across both cohorts, boys were identified at an AUC of 0.77 (95% CI, 0.64-0.86) with corresponding sensitivity and specificity of 76% each. Additionally, brain responses were associated with social behavior in boys but not in girls. CONCLUSIONS AND RELEVANCE: Quantified social perception circuit activity is a promising individual-level candidate neural marker of the male ASD behavioral phenotype. Our findings highlight the need to better understand effects of sex on social perception processing in relation to ASD phenotype manifestations.

Indexed as

Social BehaviorSocial PerceptionAdolescentAutism Spectrum DisorderBiomarkersBrainCase-Control StudiesChildCohort StudiesHumansMaleMotion PerceptionNerve NetSensitivity and SpecificityStatistics as TopicBiomarkers

Identifiers

PMID27096285
PMCPMC6475601
OpenAlexW2339404930

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.