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    Clustering of co-occurring conditions in autism spectrum disorder during early childhood: A retrospective analysis of medical claims data

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    Author
    Vargason, Troy
    Frye, Richard E
    McGuinness, Deborah L
    Hahn, Juergen
    Affiliation
    Univ Arizona, Coll Med
    Issue Date
    2019-05-31
    Keywords
    k-means clustering
    autism spectrum disorder
    co-occurring condition
    comorbidity
    medical claims
    retrospective analysis
    
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    Show full item record
    Publisher
    WILEY
    Citation
    Vargason, T., Frye, R. E., McGuinness, D. L., & Hahn, J. (2019). Clustering of co‐occurring conditions in autism spectrum disorder during early childhood: A retrospective analysis of medical claims data. Autism Research.
    Journal
    AUTISM RESEARCH
    Rights
    Copyright © 2019 International Society for Autism Research, Wiley Periodicals, Inc.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Individuals with autism spectrum disorder (ASD) are frequently affected by co‐occurring medical conditions (COCs), which vary in severity, age of onset, and pathophysiological characteristics. The presence of COCs contributes to significant heterogeneity in the clinical presentation of ASD between individuals and a better understanding of COCs may offer greater insight into the etiology of ASD in specific subgroups while also providing guidance for diagnostic and treatment protocols. This study retrospectively analyzed medical claims data from a private United States health plan between years 2000 and 2015 to investigate patterns of COC diagnoses in a cohort of 3,278 children with ASD throughout their first 5 years of enrollment compared to 279,693 children from the general population without ASD diagnoses (POP cohort). Three subgroups of children with ASD were identified by k‐means clustering using these COC patterns. The first cluster was characterized by generally high rates of COC diagnosis and comprised 23.7% (n = 776) of the cohort. Diagnoses of developmental delays were dominant in the second cluster containing 26.5% (n = 870) of the cohort. Children in the third cluster, making up 49.8% (n = 1,632) of the cohort, had the lowest rates of COC diagnosis, which were slightly higher than rates observed in the POP cohort. A secondary analysis using these data found that gastrointestinal and immune disorders showed similar longitudinal patterns of prevalence, as did seizure and sleep disorders. These findings may help to better inform the development of diagnostic workup and treatment protocols for COCs in children with ASD. Autism Res 2019, 12: 1272–1285. © 2019 International Society for Autism Research, Wiley Periodicals, Inc.
    Note
    12 month embargo; published online: 31 May 2019
    ISSN
    1939-3792
    PubMed ID
    31149786
    DOI
    10.1002/aur.2128
    Version
    Final accepted manuscript
    Sponsors
    NIAID NIH HHS [R01 AI110642]; NIH HHS [R01AI110642]; Rensselaer Institute for Data Exploration and Applications
    ae974a485f413a2113503eed53cd6c53
    10.1002/aur.2128
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