論文

国際誌
2021年5月11日

Decreased grey matter volumes in unaffected mothers of individuals with autism spectrum disorder reflect the broader autism endophenotype.

Scientific reports
  • Kyung-Min An
  • ,
  • Takashi Ikeda
  • ,
  • Tetsu Hirosawa
  • ,
  • Ken Yaoi
  • ,
  • Yuko Yoshimura
  • ,
  • Chiaki Hasegawa
  • ,
  • Sanae Tanaka
  • ,
  • Daisuke N Saito
  • ,
  • Mitsuru Kikuchi

11
1
開始ページ
10001
終了ページ
10001
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1038/s41598-021-89393-z

Autism spectrum disorder (ASD) is a neurodevelopmental disorder with an early onset and a strong genetic origin. Unaffected relatives may present similar but subthreshold characteristics of ASD. This broader autism phenotype is especially prevalent in the parents of individuals with ASD, suggesting that it has heritable factors. Although previous studies have demonstrated brain morphometry differences in ASD, they are poorly understood in parents of individuals with ASD. Here, we estimated grey matter volume in 45 mothers of children with ASD (mASD) and 46 age-, sex-, and handedness-matched controls using whole-brain voxel-based morphometry analysis. The mASD group had smaller grey matter volume in the right middle temporal gyrus, temporoparietal junction, cerebellum, and parahippocampal gyrus compared with the control group. Furthermore, we analysed the correlations of these brain volumes with ASD behavioural characteristics using autism spectrum quotient (AQ) and systemizing quotient (SQ) scores, which measure general autistic traits and the drive to systemize. Smaller volumes in the middle temporal gyrus and temporoparietal junction correlated with higher SQ scores, and smaller volumes in the cerebellum and parahippocampal gyrus correlated with higher AQ scores. Our findings suggest that atypical grey matter volumes in mASD may represent one of the neurostructural endophenotypes of ASD.

リンク情報
DOI
https://doi.org/10.1038/s41598-021-89393-z
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/33976262
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113597
ID情報
  • DOI : 10.1038/s41598-021-89393-z
  • PubMed ID : 33976262
  • PubMed Central 記事ID : PMC8113597

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