4.6 Article

Cortical and Subcortical Brain Morphometry Differences Between Patients With Autism Spectrum Disorder and Healthy Individuals Across the Lifespan: Results From the ENIGMA ASD Working Group

期刊

AMERICAN JOURNAL OF PSYCHIATRY
卷 175, 期 4, 页码 359-369

出版社

AMER PSYCHIATRIC PUBLISHING, INC
DOI: 10.1176/appi.ajp.2017.17010100

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资金

  1. NIH [U54 EB020403]
  2. cross-NIH alliance that funds Big Data to Knowledge Centers of Excellence (BD2K)
  3. European Community [278948]
  4. European Union [115300, FP7-HEALTH-2009-2.2.1-2-241909, FP7-HEALTH-2009-2.2.1-3-242114, FP7-HEALTH-2013-2.2.1-2-603196, FP7-HEALTH-2013-2.2.1-2-602478]
  5. European Federation of Pharmaceutical Industries and Associations
  6. Ontario Brain Institute [IDS-I l-02]
  7. Alva Foundation
  8. Autism Speaks
  9. Brain Canada
  10. Canadian Institutes of Health Research
  11. Department of Defense
  12. National Centers of Excellence, NIH
  13. Ontario Brain Institute
  14. Physicians' Services Incorporated (PSI) Foundation
  15. Sanofi-Aventis
  16. SynapDx
  17. AMO Pharma
  18. European Regional Development Fund
  19. CIBERSAM
  20. Madrid Regional Government [S2010/BMD-2422 AGES]
  21. European Union Structural Funds
  22. Otsuka
  23. Pfizer
  24. Roche
  25. Servier
  26. Shire
  27. Takeda
  28. Schering-Plough
  29. Vifor
  30. MRC [MR/N026063/1] Funding Source: UKRI

向作者/读者索取更多资源

Objective: Neuroimaging studies show structural differences in both cortical and subcortical brain regions in children and adults with autism spectrum disorder (ASD) compared with healthy subjects. Findings are inconsistent, however, and it is unclear how differences develop across the lifespan. The authors investigated brain morphometry differences between individuals with ASD and healthy subjects, cross-sectionally across the lifespan, in a large multinational sample from the Enhancing Neuroimaging Genetics Through Meta-Analysis (ENIGMA) ASD working group. Method: The sample comprised 1,571 patients with ASD and 1,651 healthy control subjects (age range, 2-64 years) from 49 participating sites. MRI scans were preprocessed at individual sites with a harmonized protocol based on a validated automated-segmentation software program. Mega-analyses were used to test for case-control differences in subcortical volumes, cortical thickness, and surface area. Development of brain morphometry over the lifespan was modeled using a fractional polynomial approach. Results: The case-control mega-analysis demonstrated that ASD was associated with smaller subcortical volumes of the pallidum, putamen, amygdala, and nucleus accumbens (effect sizes [Cohen'sd], 0.13 to -0.13), as well as increased cortical thickness in the frontal cortex and decreased thickness in the temporal cortex (effect sizes, -20.21 to 0.20). Analyses of age effects indicate that the development of cortical thickness is altered in ASD, with the largest differences occurring around adolescence. No age-by-ASD interactions were observed in the subcortical partitions. Conclusions: The ENIGMA ASD working group provides the largest study of brain morphometry differences in ASD to date, using a well-established, validated, publicly available analysis pipeline. ASD patients showed altered morphometry in the cognitive and affective parts of the striatum, frontal cortex, and temporal cortex. Complex developmental trajectories were observed for the different regions, with a developmental peak around adolescence. These findings suggest an interplay in the abnormal development of the striatal, frontal, and temporal regions in ASD across the lifespan.

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