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The autism inpatient collection: methods and preliminary sample description

BACKGROUND: Individuals severely affected by autism spectrum disorder (ASD), including those with intellectual disability, expressive language impairment, and/or self-injurious behavior (SIB), are underrepresented in the ASD literature and extant collections of phenotypic and biological data. An und...

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Autores principales: Siegel, Matthew, Smith, Kahsi A., Mazefsky, Carla, Gabriels, Robin L., Erickson, Craig, Kaplan, Desmond, Morrow, Eric M., Wink, Logan, Santangelo, Susan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640153/
https://www.ncbi.nlm.nih.gov/pubmed/26557975
http://dx.doi.org/10.1186/s13229-015-0054-8
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author Siegel, Matthew
Smith, Kahsi A.
Mazefsky, Carla
Gabriels, Robin L.
Erickson, Craig
Kaplan, Desmond
Morrow, Eric M.
Wink, Logan
Santangelo, Susan L.
author_facet Siegel, Matthew
Smith, Kahsi A.
Mazefsky, Carla
Gabriels, Robin L.
Erickson, Craig
Kaplan, Desmond
Morrow, Eric M.
Wink, Logan
Santangelo, Susan L.
author_sort Siegel, Matthew
collection PubMed
description BACKGROUND: Individuals severely affected by autism spectrum disorder (ASD), including those with intellectual disability, expressive language impairment, and/or self-injurious behavior (SIB), are underrepresented in the ASD literature and extant collections of phenotypic and biological data. An understanding of ASD’s etiology and subtypes can only be as complete as the studied samples are representative. METHODS: The Autism Inpatient Collection (AIC) is a multi-site study enrolling children and adolescents with ASD aged 4–20 years admitted to six specialized inpatient psychiatry units. Enrollment began March, 2014, and continues at a rate of over 400 children annually. Measures characterizing adaptive and cognitive functioning, communication, externalizing behaviors, emotion regulation, psychiatric co-morbidity, self-injurious behavior, parent stress, and parent self-efficacy are collected. ASD diagnosis is confirmed by the Autism Diagnostic Observation Schedule – 2 (ADOS-2) and extensive inpatient observation. Biological samples from probands and their biological parents are banked and processed for DNA extraction and creation of lymphoblastoid cell lines. RESULTS: Sixty-one percent of eligible subjects were enrolled. The first 147 subjects were an average of 12.6 years old (SD 3.42, range 4–20); 26.5 % female; 74.8 % Caucasian, and 81.6 % non-Hispanic/non-Latino. Mean non-verbal intelligence quotient IQ = 70.9 (SD 29.16, range 30–137) and mean adaptive behavior composite score = 55.6 (SD 12.9, range 27–96). A majority of subjects (52.4 %) were non- or minimally verbal. The average Aberrant Behavior Checklist - Irritability Subscale score was 28.6, well above the typical threshold for clinically concerning externalizing behaviors, and 26.5 % of the sample engaged in SIB. Females had more frequent and severe SIB than males. CONCLUSIONS: Preliminary data indicate that the AIC has a rich representation of the portion of the autism spectrum that is understudied and underrepresented in extant data collections. More than half of the sample is non- or minimally verbal, over 40 % have intellectual disability, and over one quarter exhibit SIB. The AIC is a substantial new resource for study of the full autism spectrum, which will augment existing data on higher-functioning cohorts and facilitate the identification of genetic subtypes and novel treatment targets. The AIC investigators welcome collaborations with other investigators, and access to the AIC phenotypic data and biosamples may be requested through the Simons Foundation (www.sfari.org).
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spelling pubmed-46401532015-11-11 The autism inpatient collection: methods and preliminary sample description Siegel, Matthew Smith, Kahsi A. Mazefsky, Carla Gabriels, Robin L. Erickson, Craig Kaplan, Desmond Morrow, Eric M. Wink, Logan Santangelo, Susan L. Mol Autism Research BACKGROUND: Individuals severely affected by autism spectrum disorder (ASD), including those with intellectual disability, expressive language impairment, and/or self-injurious behavior (SIB), are underrepresented in the ASD literature and extant collections of phenotypic and biological data. An understanding of ASD’s etiology and subtypes can only be as complete as the studied samples are representative. METHODS: The Autism Inpatient Collection (AIC) is a multi-site study enrolling children and adolescents with ASD aged 4–20 years admitted to six specialized inpatient psychiatry units. Enrollment began March, 2014, and continues at a rate of over 400 children annually. Measures characterizing adaptive and cognitive functioning, communication, externalizing behaviors, emotion regulation, psychiatric co-morbidity, self-injurious behavior, parent stress, and parent self-efficacy are collected. ASD diagnosis is confirmed by the Autism Diagnostic Observation Schedule – 2 (ADOS-2) and extensive inpatient observation. Biological samples from probands and their biological parents are banked and processed for DNA extraction and creation of lymphoblastoid cell lines. RESULTS: Sixty-one percent of eligible subjects were enrolled. The first 147 subjects were an average of 12.6 years old (SD 3.42, range 4–20); 26.5 % female; 74.8 % Caucasian, and 81.6 % non-Hispanic/non-Latino. Mean non-verbal intelligence quotient IQ = 70.9 (SD 29.16, range 30–137) and mean adaptive behavior composite score = 55.6 (SD 12.9, range 27–96). A majority of subjects (52.4 %) were non- or minimally verbal. The average Aberrant Behavior Checklist - Irritability Subscale score was 28.6, well above the typical threshold for clinically concerning externalizing behaviors, and 26.5 % of the sample engaged in SIB. Females had more frequent and severe SIB than males. CONCLUSIONS: Preliminary data indicate that the AIC has a rich representation of the portion of the autism spectrum that is understudied and underrepresented in extant data collections. More than half of the sample is non- or minimally verbal, over 40 % have intellectual disability, and over one quarter exhibit SIB. The AIC is a substantial new resource for study of the full autism spectrum, which will augment existing data on higher-functioning cohorts and facilitate the identification of genetic subtypes and novel treatment targets. The AIC investigators welcome collaborations with other investigators, and access to the AIC phenotypic data and biosamples may be requested through the Simons Foundation (www.sfari.org). BioMed Central 2015-11-10 /pmc/articles/PMC4640153/ /pubmed/26557975 http://dx.doi.org/10.1186/s13229-015-0054-8 Text en © Siegel et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Siegel, Matthew
Smith, Kahsi A.
Mazefsky, Carla
Gabriels, Robin L.
Erickson, Craig
Kaplan, Desmond
Morrow, Eric M.
Wink, Logan
Santangelo, Susan L.
The autism inpatient collection: methods and preliminary sample description
title The autism inpatient collection: methods and preliminary sample description
title_full The autism inpatient collection: methods and preliminary sample description
title_fullStr The autism inpatient collection: methods and preliminary sample description
title_full_unstemmed The autism inpatient collection: methods and preliminary sample description
title_short The autism inpatient collection: methods and preliminary sample description
title_sort autism inpatient collection: methods and preliminary sample description
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640153/
https://www.ncbi.nlm.nih.gov/pubmed/26557975
http://dx.doi.org/10.1186/s13229-015-0054-8
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