Examining overlap and homogeneity in ASD, ADHD, and OCD: a data-driven, diagnosis-agnostic approach

The validity of diagnostic labels of autism spectrum disorder (ASD), attention-deficit/hyperactivity disorder (ADHD), and obsessive compulsive disorder (OCD) is an open question given the mounting evidence that these categories may not correspond to conditions with distinct etiologies, biologies, or...

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Veröffentlicht in:Translational psychiatry 2019-11, Vol.9 (1), p.318-11, Article 318
Hauptverfasser: Kushki, Azadeh, Anagnostou, Evdokia, Hammill, Christopher, Duez, Pierre, Brian, Jessica, Iaboni, Alana, Schachar, Russell, Crosbie, Jennifer, Arnold, Paul, Lerch, Jason P.
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Sprache:eng
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Zusammenfassung:The validity of diagnostic labels of autism spectrum disorder (ASD), attention-deficit/hyperactivity disorder (ADHD), and obsessive compulsive disorder (OCD) is an open question given the mounting evidence that these categories may not correspond to conditions with distinct etiologies, biologies, or phenotypes. The objective of this study was to determine the agreement between existing diagnostic labels and groups discovered based on a data-driven, diagnosis-agnostic approach integrating cortical neuroanatomy and core-domain phenotype features. A machine learning pipeline, called bagged-multiview clustering, was designed to discover homogeneous subgroups by integrating cortical thickness data and measures of core-domain phenotypic features of ASD, ADHD, and OCD. This study was conducted using data from the Province of Ontario Neurodevelopmental Disorders (POND) Network, a multi-center study in Ontario, Canada. Participants ( n  = 226) included children between the ages of 6 and 18 with a diagnosis of ASD ( n  = 112, median [IQR] age = 11.7[4.8], 21% female), ADHD ( n  = 58, median [IQR] age = 10.2[3.3], 14% female), or OCD ( n  = 34, median [IQR] age = 12.1[4.2], 38% female), as well as typically developing controls ( n  = 22, median [IQR] age = 11.0[3.8], 55% female). The diagnosis-agnostic groups were significantly different than each other in phenotypic characteristics (SCQ: χ 2 (9) = 111.21, p  
ISSN:2158-3188
2158-3188
DOI:10.1038/s41398-019-0631-2