4.6 Article

Diagnostic Classification for Human Autism and Obsessive-Compulsive Disorder Based on Machine Learning From a Primate Genetic Model

Journal

AMERICAN JOURNAL OF PSYCHIATRY
Volume 178, Issue 1, Pages 65-76

Publisher

AMER PSYCHIATRIC PUBLISHING, INC
DOI: 10.1176/appi.ajp.2020.19101091

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Funding

  1. National Key R&D Program of China [2017YFC1310400, 2018YFC1313803]
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB32030000]
  3. Shanghai Municipal Science and Technology Major Project [2018SHZDZX05]
  4. National Natural Science Foundation [81571300, 81527901, 31771174]
  5. Key Realm R&D Program of Guangdong Province [2019B030335001]
  6. Wellcome Trust [104631/Z/12/Z]

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The study employed non-invasive neuroimaging methods to identify core regions associated with autism spectrum disorder and obsessive-compulsive disorder in both monkeys and human data sets, leading to diagnostic classification and prediction of symptom severity.
Objective: Psychiatric disorders commonly comprise comorbid symptoms, such as autism spectrum disorder (ASD), obsessive-compulsive disorder (OCD), and attention deficit hyperactivity disorder (ADHD), raising controversies over accurate diagnosis and overlap of their neural underpinnings. The authors used non invasive neuroimaging in humans and nonhuman primates to identify neural markers associated with DSM-5 diagnoses and quantitative measures of symptom severity. Methods: Resting-state functional connectivity data obtained from both wild-type and methyl-CpG binding protein 2 (MECP2) transgenic monkeys were used to construct monkey-derived classifiers for diagnostic classification in four human data sets (ASD: Autism Brain Imaging Data Exchange [ABIDE-I], N=1,112; ABIDE-II, N=1,114; ADHD-200 sample: N=776; OCD local institutional database: N=186). Stepwise linear regression models were applied to examine associations between functional connections of monkey-derived classifiers and dimensional symptom severity of psychiatric disorders. Results: Nine core regions prominently distributed in frontal and temporal cortices were identified in monkeys and used as seeds to construct the monkey-derived classifier that informed diagnostic classification in human autism. This same set of core regions was useful for diagnostic classification in the OCD cohort but not the ADHD cohort. Models based on functional connections of the right ventrolateral prefrontal cortex with the left thalamus and right prefrontal polar cortex predicted communication scores of ASD patients and compulsivity scores of OCD patients, respectively. Conclusions: The identified core regions may serve as a basis for building markers for ASD and OCD diagnoses, as well as measures of symptom severity. These findings may inform future development of machine-learning models for psychiatric disorders and may improve the accuracy and speed of clinical assessments.

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