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Sex differences in trajectories of cortical development in autistic children from 2-13 years of age.
Andrews, Derek S; Diers, Kersten; Lee, Joshua K; Harvey, Danielle J; Heath, Brianna; Cordero, Devani; Rogers, Sally J; Reuter, Martin; Solomon, Marjorie; Amaral, David G; Nordahl, Christine Wu.
Afiliação
  • Andrews DS; Department of Psychiatry & Behavioral Sciences, the MIND Institute, University of California, Davis, CA, USA. dandrews@ucdavis.edu.
  • Diers K; AI in Medical Imaging, German Center for Neurodegenerative Diseases, Bonn, Germany.
  • Lee JK; Department of Psychiatry & Behavioral Sciences, the MIND Institute, University of California, Davis, CA, USA.
  • Harvey DJ; Division of Biostatistics, Department of Public Health Sciences, University of California, University of California, Davis, CA, USA.
  • Heath B; Department of Psychiatry & Behavioral Sciences, the MIND Institute, University of California, Davis, CA, USA.
  • Cordero D; A.A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, MA, USA.
  • Rogers SJ; Department of Psychiatry & Behavioral Sciences, the MIND Institute, University of California, Davis, CA, USA.
  • Reuter M; AI in Medical Imaging, German Center for Neurodegenerative Diseases, Bonn, Germany.
  • Solomon M; A.A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, MA, USA.
  • Amaral DG; Department of Radiology, Harvard Medical School, Boston, MA, USA.
  • Nordahl CW; Department of Psychiatry & Behavioral Sciences, the MIND Institute, University of California, Davis, CA, USA.
Mol Psychiatry ; 2024 May 16.
Article em En | MEDLINE | ID: mdl-38755243
ABSTRACT
Previous studies have reported alterations in cortical thickness in autism. However, few have included enough autistic females to determine if there are sex specific differences in cortical structure in autism. This longitudinal study aimed to investigate autistic sex differences in cortical thickness and trajectory of cortical thinning across childhood. Participants included 290 autistic (88 females) and 139 nonautistic (60 females) individuals assessed at up to 4 timepoints spanning ~2-13 years of age (918 total MRI timepoints). Estimates of cortical thickness in early and late childhood as well as the trajectory of cortical thinning were modeled using spatiotemporal linear mixed effects models of age-by-sex-by-diagnosis. Additionally, the spatial correspondence between cortical maps of sex-by-diagnosis differences and neurotypical sex differences were evaluated. Relative to their nonautistic peers, autistic females had more extensive cortical differences than autistic males. These differences involved multiple functional networks, and were mainly characterized by thicker cortex at ~3 years of age and faster cortical thinning in autistic females. Cortical regions in which autistic alterations were different between the sexes significantly overlapped with regions that differed by sex in neurotypical development. Autistic females and males demonstrated some shared differences in cortical thickness and rate of cortical thinning across childhood relative to their nonautistic peers, however these areas were relatively small compared to the widespread differences observed across the sexes. These results support evidence of sex-specific neurobiology in autism and suggest that processes that regulate sex differentiation in the neurotypical brain contribute to sex differences in the etiology of autism.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article