Evaluation of clinical assessments of social abilities for use in autism clinical trials by the autism biomarkers consortium for clinical trials.
autism spectrum disorder
biomarkers
clinical trials
measurement
stability
validity
Journal
Autism research : official journal of the International Society for Autism Research
ISSN: 1939-3806
Titre abrégé: Autism Res
Pays: United States
ID NLM: 101461858
Informations de publication
Date de publication:
05 2023
05 2023
Historique:
received:
20
10
2022
accepted:
11
02
2023
pmc-release:
01
05
2024
medline:
18
5
2023
pubmed:
18
3
2023
entrez:
17
3
2023
Statut:
ppublish
Résumé
Clinical trials in autism spectrum disorder (ASD) often rely on clinician rating scales and parent surveys to measure autism-related features and social behaviors. To aid in the selection of these assessments for future clinical trials, the Autism Biomarkers Consortium for Clinical Trials (ABC-CT) directly compared eight common instruments with respect to acquisition rates, sensitivity to group differences, equivalence across demographic sub-groups, convergent validity, and stability over a 6-week period. The sample included 280 children diagnosed with ASD (65 girls) and 119 neurotypical children (36 girls) aged from 6 to 11 years. Full scale IQ for ASD ranged from 60 to 150 and for neurotypical ranged from 86 to 150. Instruments measured clinician global assessment and autism-related behaviors, social communication abilities, adaptive function, and social withdrawal behavior. For each instrument, we examined only the scales that measured social or communication functioning. Data acquisition rates were at least 97.5% at T1 and 95.7% at T2. All scales distinguished diagnostic groups. Some scales significantly differed by participant and/or family demographic characteristics. Within the ASD group, most clinical instruments exhibited weak (≥ |0.1|) to moderate (≥ |0.4|) intercorrelations. Short-term stability was moderate (ICC: 0.5-0.75) to excellent (ICC: >0.9) within the ASD group. Variations in the degree of stability may inform viability for different contexts of use, such as identifying clinical subgroups for trials versus serving as a modifiable clinical outcome. All instruments were evaluated in terms of their advantages and potential concerns for use in clinical trials.
Identifiants
pubmed: 36929131
doi: 10.1002/aur.2905
pmc: PMC10192100
mid: NIHMS1876322
doi:
Substances chimiques
Biomarkers
0
Banques de données
ClinicalTrials.gov
['NCT02996669']
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
981-996Subventions
Organisme : NICHD NIH HHS
ID : P50 HD105351
Pays : United States
Organisme : NIMH NIH HHS
ID : U19 MH108206
Pays : United States
Informations de copyright
© 2023 International Society for Autism Research and Wiley Periodicals LLC.
Références
Autism. 2014 May;18(4):370-5
pubmed: 24104511
Autism. 2014 Jan;18(1):31-44
pubmed: 24019124
Autism. 2015 Jul;19(5):622-36
pubmed: 25096930
Child Psychiatry Hum Dev. 2014;45(2):185-92
pubmed: 23801256
Autism. 2021 Aug;25(6):1565-1579
pubmed: 33715473
Sci Transl Med. 2019 May 8;11(491):
pubmed: 31043522
J Autism Dev Disord. 2022 Mar;52(3):1120-1130
pubmed: 33871736
OTJR (Thorofare N J). 2021 Oct;41(4):243-250
pubmed: 33955293
Ment Retard. 1997 Feb;35(1):10-7
pubmed: 9046782
J Autism Dev Disord. 2015 Jun;45(6):1579-87
pubmed: 25398602
J Autism Dev Disord. 2014 Jan;44(1):168-79
pubmed: 23748386
J Am Acad Child Adolesc Psychiatry. 2016 Jul;55(7):602-609.e3
pubmed: 27343887
Autism Res. 2018 Mar;11(3):421-433
pubmed: 29427532
J Autism Dev Disord. 2003 Feb;33(1):31-45
pubmed: 12708578
Surgery. 2016 Jun;159(6):1638-1645
pubmed: 26962006
J Chiropr Med. 2016 Jun;15(2):155-63
pubmed: 27330520
N Engl J Med. 2002 Aug 1;347(5):314-21
pubmed: 12151468
Pediatrics. 2009 Dec;124(6):1533-40
pubmed: 19948625
Am J Ment Defic. 1985 Mar;89(5):492-502
pubmed: 3158201
J Am Acad Child Adolesc Psychiatry. 2012 Aug;51(8):788-97
pubmed: 22840550
J Autism Dev Disord. 2017 Feb;47(2):231-242
pubmed: 27815645
Psychol Bull. 1955 Jul;52(4):281-302
pubmed: 13245896
Disabil Health J. 2010 Apr;3(2):107-16
pubmed: 21122776