Cited by 118Autism Spectrum Disorder ResearchChild Nutrition and Feeding IssuesChild and Animal Learning Development

The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index; none of the 25 sources its claims cite is checked for support yet.

Behavioural markers for autism in infancy: Scores on the Autism Observational Scale for Infants in a prospective study of at-risk siblings

Open access

Abstract

We investigated early behavioural markers of autism spectrum disorder (ASD) using the Autism Observational Scale for Infants (AOSI) in a prospective familial high-risk (HR) sample of infant siblings (N=54) and low-risk (LR) controls (N=50). The AOSI was completed at 7 and 14 month infant visits and children were seen again at age 24 and 36 months. Diagnostic outcome of ASD (HR-ASD) versus no ASD (HR-No ASD) was determined for the HR sample at the latter timepoint. The HR group scored higher than the LR group at 7 months and marginally but non-significantly higher than the LR group at 14 months, although these differences did not remain when verbal and nonverbal developmental level were covaried. The HR-ASD outcome group had higher AOSI scores than the LR group at 14 months but not 7 months, even when developmental level was taken into account. The HR-No ASD outcome group had scores intermediate between the HR-ASD and LR groups. At both timepoints a few individual items were higher in the HR-ASD and HR-No ASD outcome groups compared to the LR group and these included both social (e.g. orienting to name) and non-social (e.g. visual tracking) behaviours. AOSI scores at 14 months but not at 7 months were moderately correlated with later scores on the autism diagnostic observation schedule (ADOS) suggesting continuity of autistic-like behavioural atypicality but only from the second and not first year of life. The scores of HR siblings who did not go on to have ASD were intermediate between the HR-ASD outcome and LR groups, consistent with the notion of a broader autism phenotype.

Overview

AI snapshot

Written from the paper’s full text.

TL;DR

In a prospective BASIS sample of 104 infants (54 high-risk [HR], 50 low-risk [LR]), AOSI scores differentiated HR from LR at 7 months but not after controlling for developmental level, while at 14 months AOSI scores differentiated HR-ASD from LR and marginally from HR-No ASD. AOSI scores at 14 months, but not 7 months, were moderately associated with later ADOS scores at 24 and 36 months in the HR group.

Key findings

  • At 7 months, HR infants had higher AOSI total scores than LR infants, F(1, 102) = 4.10, p < .045, d = .39; at 14 months the HR vs LR difference was not significant, F(1, 99) = 3.36, p = .07, d = .36. Covarying Mullen Verbal and Nonverbal T-scores attenuated HR vs LR differences at both ages (7 m: p = .37; 14 m: p = .14).
  • At 14 months, the three-group comparison was significant, F(2, 96) = 4.43, p = .014: HR-ASD scored higher than LR (p = .01, d = .81) and marginally higher than HR-No ASD (p = .07, d = .65). After covarying Mullen scores, the 14-month group difference remained, F(4, 93) = 3.85, p = .03, with HR-ASD > LR (p < .01) and HR-ASD > HR-No ASD (p = .03); HR-No ASD and LR did not differ (p = .53).
  • Individual AOSI items: at 7 months HR and LR did not differ on any item, but at 14 months HR scored higher on orientation to name (U = 931.00, p < .01). Outcome-group item differences occurred at 7 months for visual tracking (χ² = 9.99, p < .01; HR-No ASD > LR, U = 634.50, p < .01) and social referencing (χ² = 10.78, p < .01; HR-ASD > LR, U = 206.50, p < .01), and at 14 months for orientation to name (χ² = 11.50, p < .01; HR-No ASD > LR, U = 596.00, p < .01; HR-ASD > LR, U = 282.50, p < .01), engagement of attention (χ² = 9.75, p < .01; no significant post-hoc tests), and social referencing (χ² = 9.75, p < .01; no significant post-hoc tests).
  • In the HR group, AOSI at 7 months was not associated with ADOS at 24 months (r = .23, p = .10) or 36 months (r = .16, p = .27); AOSI at 14 months was associated with ADOS at 24 months (r = .30, p = .03) and 36 months (r = .38, p = .005).

Methods

  • Prospective British Autism Study of Infant Siblings (BASIS) cohort: 104 children (54 HR, 50 LR) seen at approximately 7 months (mean = 7.35, SD = 1.21), 14 months (mean = 13.79, SD = 1.46), 24 months (mean = 23.9, SD = .95), and 36 months (mean = 37.93, SD = 3.02). HR infants had an older sibling with a community clinical ASD diagnosis; LR controls had no ASD in first-degree relatives.
  • The Autism Observational Scale for Infants (AOSI), a 19-item experimenter-led semi-structured assessment, was administered at 7 and 14 months; total score maximum = 44. Double-coding agreement was excellent at 7 months (n = 92, ICC = .97) and 14 months (n = 85, ICC = .95). At 36 months, 17 HR toddlers met ICD-10 criteria for ASD (HR-ASD) and 36 did not (HR-No ASD); LR controls received no formal clinical diagnosis.
  • AOSI total scores were square-root transformed and compared using ANOVA/Tukey tests; individual items used Mann–Whitney/Kruskal–Wallis tests with p < .01; Pearson correlations examined AOSI–ADOS associations in the HR group; Mullen Verbal and Nonverbal T-scores were covaried in follow-up analyses.

Limitations

  • The paper states findings are preliminary due to modest sample size and require confirmation in larger and other independent samples. It also states assessments were non-blind to risk status at infancy and toddler assessments, although the toddler team was blind to infant AOSI scores.
  • The paper notes item-level findings should be considered exploratory because a strict correction for multiple testing was not undertaken and require replication.
  • The paper reports a recurrence rate of 32.1%, higher than the 18.7% in Ozonoff et al. (2011), and states this likely reflects the modest at-risk sample and may not be generalizable. Evident from the text: LR controls lacked a full developmental history and no ADI-R was administered, so no formal clinical diagnoses were assigned to that group.

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Integrity signals

Registry

Crossref · 10.1016/j.infbeh.2014.12.017

Cites

42 of 42 references verified0 citation errors · 0 not checkable

Statistics

10 tests recomputed · 0 with the reported and recomputed p on opposite sides of .05

Verification

Claims the paper makes

0 of 25 cited sources checked · 0 supported · 0 flagged

  • It may state two separate claims as one. 30
  • Probably not a substantial claim. 9
34 of 34

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Statistics that don’t add up

Each reported p-value recomputed from its test statistic and degrees of freedom.

  • Inconsistent p-value: F(4, 95) = .61, p = .47

    Minor

    The paper reports p = .47 here; recomputing from the test statistic and its degrees of freedom gives p = .656. The check cannot tell whether the statistic or the p-value is the misprint.

    Reported p = .47 · recomputed p = .656

  • Inconsistent p-value: F(3, 96) = 2.24, p = .14

    Minor

    The paper reports p = .14 here; recomputing from the test statistic and its degrees of freedom gives p = .089. The check cannot tell whether the statistic or the p-value is the misprint.

    Reported p = .14 · recomputed p = .089

  • Inconsistent p-value: F(3, 99) = .66, p = .37

    Minor

    The paper reports p = .37 here; recomputing from the test statistic and its degrees of freedom gives p = .579. The check cannot tell whether the statistic or the p-value is the misprint.

    Reported p = .37 · recomputed p = .579

3 of 3

Statistics recomputed

Every reported test result, recomputed from its test statistic and degrees of freedom. A result shows as not adding up only once an independent check has confirmed it.

  • Doesn’t add upF(3, 99) = 0.66reported p = .37 · recomputed p = .579

    “F(3, 99) = .66, p = .37”

  • Doesn’t add upF(3, 96) = 2.24reported p = .14 · recomputed p = .089

    “F(3, 96) = 2.24, p = .14”

  • Doesn’t add upF(4, 95) = 0.61reported p = .47 · recomputed p = .656

    “F(4, 95) = .61, p = .47”

  • Not confirmedF(1, 102) = 4.1reported p < .045 · recomputed p = .045

    “F(1, 102) = 4.10, p < .045”

  • ConsistentF(1, 99) = 3.36reported p = .07 · recomputed p = .070

    “F(1, 99) = 3.36, p = .07”

  • ConsistentF(3, 99) = 4.48reported p < .05 · recomputed p = .005

    “F(3, 99) = 4.48, p < .05”

  • ConsistentF(2, 98) = 2.94reported p = .058 · recomputed p = .058

    “F(2, 98) = 2.94, p = .058”

  • ConsistentF(2, 96) = 4.43reported p = .014 · recomputed p = .014

    “F(2, 96) = 4.43, p = .014”

  • ConsistentF(4, 93) = 3.85reported p = .03 · recomputed p = .006

    “F(4, 93) = 3.85, p = .03”

    The paper states a correction for multiple tests

  • ConsistentF(4, 95) = 4.31reported p < .05 · recomputed p = .003

    “F(4, 95) = 4.31, p < .05”

10 of 10

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

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Citations

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Metadata

Authors
Gammer, I., Bedford, R., Elsabbagh, M., Garwood, H., Pasco, G., Tucker, L., Volein, A., Johnson, M. H., & Charman, T.
Affiliations
  • King's College London (GB)
  • McGill University (CA)
  • University of London (GB)
Corresponding author
Charman, Tony
Venue
Infant Behavior and Development
Publisher
Elsevier BV
Published
2015-02
Volume
38
Pages
107-115
ISSN
0163-6383 (ISSN-L)
OpenAlex
W2159608964
Cited by
118
References
42
Citations by year
2026: 3 · 2025: 2 · 2024: 3 · 2023: 2 · 2022: 7 · 2021: 9 · 2020: 47 · 2019: 12 · 2018: 7 · 2017: 17 · 2016: 6 · 2015: 3
FWCI
6.61
Type
journal article
Language
en
Open access
Locations
  • Infant Behavior and Development (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Research Explorer (The University of Manchester) (publishedVersion)
  • BIROn (Birkbeck, University of London) (acceptedVersion)
  • Research Portal (King's College London) (submittedVersion, cc-by)
Funders
  • Autism Speaks
  • Medical Research Council (G0701484)
  • ESF
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
  • Health Sciences › Medicine › Psychiatry and Mental health › Child Nutrition and Feeding Issues
  • Social Sciences › Psychology › Developmental and Educational Psychology › Child and Animal Learning Development
Keywords
autism spectrum disorder, infant siblings, familial high risk, Autism Diagnostic Observation Schedule, visual object tracking, social orienting, broader autism phenotype
MeSH terms
Child, Child Development Disorders, Pervasive, Child, Preschool, Female, Humans, Infant, Longitudinal Studies, Male, Personality Assessment, Phenotype, Prospective Studies, Psychometrics, Risk Assessment, Genetic Predisposition to Disease, Siblings, Early Diagnosis, Early Medical Intervention

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