TY - JOUR
T1 - Cortical and subcortical brain morphometry differences between patients with autism spectrum disorder and healthy individuals across the lifespan
T2 - Results from the ENIGMA ASD working group
AU - Van Rooij, Daan
AU - Anagnostou, Evdokia
AU - Arango, Celso
AU - Auzias, Guillaume
AU - Behrmann, Marlene
AU - Busatto, Geraldo F.
AU - Calderoni, Sara
AU - Daly, Eileen
AU - Deruelle, Christine
AU - Di Martino, Adriana
AU - Dinstein, Ilan
AU - Duran, Fabio Luis Souza
AU - Durston, Sarah
AU - Ecker, Christine
AU - Fair, Damien
AU - Fedor, Jennifer
AU - Fitzgerald, Jackie
AU - Freitag, Christine M.
AU - Gallagher, Louise
AU - Gori, Ilaria
AU - Haar, Shlomi
AU - Hoekstra, Liesbeth
AU - Jahanshad, Neda
AU - Jalbrzikowski, Maria
AU - Janssen, Joost
AU - Lerch, Jason
AU - Luna, Beatriz
AU - Martinho, Mauricio Moller
AU - McGrath, Jane
AU - Muratori, Filippo
AU - Murphy, Clodagh M.
AU - Murphy, Declan G.M.
AU - O'Hearn, Kirsten
AU - Oranje, Bob
AU - Parellada, Mara
AU - Retico, Alessandra
AU - Rosa, Pedro
AU - Rubia, Katya
AU - Shook, Devon
AU - Taylor, Margot
AU - Thompson, Paul M.
AU - Tosetti, Michela
AU - Wallace, Gregory L.
AU - Zhou, Fengfeng
AU - Buitelaar, Jan K.
N1 - Publisher Copyright:
© 2018 American Psychiatric Association. All rights reserved.
PY - 2018/4/1
Y1 - 2018/4/1
N2 - 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, crosssectionally 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],0.13to-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.
AB - 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, crosssectionally 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],0.13to-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.
UR - http://www.scopus.com/inward/record.url?scp=85044833149&partnerID=8YFLogxK
U2 - 10.1176/appi.ajp.2017.17010100
DO - 10.1176/appi.ajp.2017.17010100
M3 - Article
AN - SCOPUS:85044833149
SN - 0002-953X
VL - 175
SP - 359
EP - 369
JO - American Journal of Psychiatry
JF - American Journal of Psychiatry
IS - 4
ER -