4.7 Article

Connectivity alterations in autism reflect functional idiosyncrasy

Journal

COMMUNICATIONS BIOLOGY
Volume 4, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s42003-021-02572-6

Keywords

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Funding

  1. Healthy Brains for Healthy Lives (HBHL) postdoctoral fellowship
  2. Fonds de la Recherche due Quebec - Sante (FRQ-S)
  3. National Research Foundation of Korea [NRF-2020R1A6A3A03037088]
  4. Montreal Neurological Institute and Hospital (MNI)
  5. FRQ-S
  6. National Science and Engineering Research Council of Canada (NSERC) [1304413]
  7. Canadian Institutes of Health Research [CIHR FDN-154298]
  8. SickKids Foundation [NI17-039]
  9. Azrieli Center for Autism Research (ACAR-TACC)
  10. BrainCanada (Azrieli Future Leaders)
  11. Tier-2 Canada Research Chairs program
  12. CIHR fellowship
  13. Savoy Foundation
  14. CIHR
  15. Helmholtz Foundation
  16. Healthy Brains for Healthy Lives initiative
  17. Healthy Brains Healthy Lives initiative (Canada First Research Excellence fund)
  18. Google (Research/Teaching Award)
  19. Canadian Institute of Health Research (CIHR)
  20. CIFAR Artificial Intelligence Chairs program (Canada Institute for Advanced Research)
  21. NIH [AG068563A]
  22. Max Planck Society (Otto Hahn Award)

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Benkarim et al. developed a new method to analyze inter-individual variability in functional network organization in Autism Spectrum Disorder (ASD) and found increased idiosyncrasy in default mode, somatomotor, and attention networks, but reduced idiosyncrasy in lateral temporal cortices. The study also revealed that idiosyncrasy increased with age and significantly correlated with symptom severity in ASD.
Benkarim et al devise an approach to profile inter-individual variability in functional network organization and test whether such idiosyncrasy contributes to the connectivity alterations found in Autism Spectrum Disorder. Their approach provides potential biomarkers to study atypical brain development and may be used to consolidate prior research findings on the variable nature of connectome level anomalies in autism. Autism spectrum disorder (ASD) is commonly understood as an alteration of brain networks, yet case-control analyses against typically-developing controls (TD) have yielded inconsistent results. Here, we devised a novel approach to profile the inter-individual variability in functional network organization and tested whether such idiosyncrasy contributes to connectivity alterations in ASD. Studying a multi-centric dataset with 157 ASD and 172 TD, we obtained robust evidence for increased idiosyncrasy in ASD relative to TD in default mode, somatomotor and attention networks, but also reduced idiosyncrasy in lateral temporal cortices. Idiosyncrasy increased with age and significantly correlated with symptom severity in ASD. Furthermore, while patterns of functional idiosyncrasy were not correlated with ASD-related cortical thickness alterations, they co-localized with the expression patterns of ASD risk genes. Notably, we could demonstrate that patterns of atypical idiosyncrasy in ASD closely overlapped with connectivity alterations that are measurable with conventional case-control designs and may, thus, be a principal driver of inconsistency in the autism connectomics literature. These findings support important interactions between inter-individual heterogeneity in autism and functional signatures. Our findings provide novel biomarkers to study atypical brain development and may consolidate prior research findings on the variable nature of connectome level anomalies in autism.

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