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Big data approaches to decomposing heterogeneity across the autism spectrum

期刊

MOLECULAR PSYCHIATRY
卷 24, 期 10, 页码 1435-1450

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41380-018-0321-0

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资金

  1. European Research Council (ERC) Starting Grant [ERC-2017-STG 755816]
  2. O'Brien Scholars Program within the Child and Youth Mental Health Collaborative at the Centre for Addiction and Mental Health (CAMH)
  3. Hospital for Sick Children, Toronto
  4. Department of Psychiatry, University of Toronto
  5. Slaight Family Child and Youth Mental Health Innovation Fund
  6. CAMH Foundation
  7. Ontario Brain Institute via the Province of Ontario Neurodevelopmental Disorders (POND) Network
  8. Autism Research Trust
  9. Medical Research Council
  10. National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research and Care East of England at Cambridgeshire and Peterborough NHS Foundation Trust
  11. Innovative Medicines Initiative 2 Joint Undertaking (JU) [777394]
  12. European Union's Horizon 2020 research and innovation program
  13. EFPIA
  14. SFARI
  15. Autistica
  16. AUTISM SPEAKS
  17. MRC [G0600977] Funding Source: UKRI

向作者/读者索取更多资源

Autism is a diagnostic label based on behavior. While the diagnostic criteria attempt to maximize clinical consensus, it also masks a wide degree of heterogeneity between and within individuals at multiple levels of analysis. Understanding this multi-level heterogeneity is of high clinical and translational importance. Here we present organizing principles to frame research examining multi-level heterogeneity in autism. Theoretical concepts such as 'spectrum' or 'autisms' reflect nonmutually exclusive explanations regarding continuous/dimensional or categorical/qualitative variation between and within individuals. However, common practices of small sample size studies and case-control models are suboptimal for tackling heterogeneity. Big data are an important ingredient for furthering our understanding of heterogeneity in autism. In addition to being 'feature-rich', big data should be both 'broad' (i.e., large sample size) and 'deep' (i.e., multiple levels of data collected on the same individuals). These characteristics increase the likelihood that the study results are more generalizable and facilitate evaluation of the utility of different models of heterogeneity. A model's utility can be measured by its ability to explain clinically or mechanistically important phenomena, and also by explaining how variability manifests across different levels of analysis. The directionality for explaining variability across levels can be bottom-up or top-down, and should include the importance of development for characterizing changes within individuals. While progress can be made with 'supervised' models built upon a priori or theoretically predicted distinctions or dimensions of importance, it will become increasingly important to complement such work with unsupervised data-driven discoveries that leverage unknown and multivariate distinctions within big data. A better understanding of how to model heterogeneity between autistic people will facilitate progress towards precision medicine for symptoms that cause suffering, and person-centered support.

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