Reduced false positives in autism screening via digital biomarkers inferred from deep comorbidity patterns

  • Dmytro Onishchenko
  • , Yi Huang
  • , James van Horne
  • , Peter J. Smith
  • , Michael M. Msall
  • , Ishanu Chattopadhyay

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Here, we develop digital biomarkers for autism spectrum disorder (ASD), computed from patterns of past medical encounters, identifying children at high risk with an area under the receiver operating characteristic exceeding 80% from shortly after 2 years of age for either sex, and across two independent patient databases. We leverage uncharted ASD comorbidities, with no requirement of additional blood work, or procedures, to estimate the autism comorbid risk score (ACoR), during the earliest years when interventions are the most effective. ACoR has superior predictive performance to common questionnaire-based screenings and can reduce their current socioeconomic, ethnic, and demographic biases. In addition, we can condition on current screening scores to either halve the state-of-the-art false-positive rate or boost sensitivity to over 60%, while maintaining specificity above 95%. Thus, ACoR can significantly reduce the median diagnostic age, reducing diagnostic delays and accelerating access to evidence-based interventions.

Original languageEnglish
JournalScience advances
Volume7
Issue number41
DOIs
StatePublished - Oct 2021

Bibliographical note

Publisher Copyright:
Copyright © 2021 The Authors, some rights reserved.

Funding

We acknowledge Professor Andrey Rzhetsky for inspiring us to investigate the notion of uncharted comorbidity patterns modulating autism risk. This work is funded, in part, by the Defense Advanced Research Projects Agency (DARPA) project number HR00111890043/P00004. The claims made in this study do not reflect the position or the policy of the U.S. Government. The UCM dataset is provided by the Clinical Research Data Warehouse (CRDW) maintained by the Center for Research Informatics (CRI) at the University of Chicago. The Center for Research Informatics is funded by the Biological Sciences Division, the Institute for Translational Medicine/CTSA (NIH UL1 TR000430) at the University of Chicago.

FundersFunder number
Center for Research Informatics, University of Chicago
National Institutes of Health
Defense Advanced Research Projects AgencyHR00111890043/P00004
Defense Advanced Research Projects Agency
National Center for Advancing Translational SciencesUL1TR000430
National Center for Advancing Translational Sciences
University of Chicago
Georgia Clinical and Translational Science Alliance
Instituto Nacional de Ciência e Tecnologia Translacional em Medicina

    ASJC Scopus subject areas

    • General

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