Associations between brain network, puberty, and behaviors in boys with Klinefelter syndrome.

Background: Klinefelter syndrome (KS), also referred to as XXY syndrome, is a significant but inadequately studied risk factor for neuropsychiatric disability. Whether alterations in functional brain connectivity or pubertal delays are associated with aberrant cognitive-behavioral outcomes in indivi...

Descripción completa

Detalles Bibliográficos
Publicado en:European Child & Adolescent Psychiatry Vol. 34; no. 2; pp. 585 - 598
Autores principales: Li, Rihui, Foland-Ross, Lara C., Jordan, Tracy, Marzelli, Matthew J., Ross, Judith L., Reiss, Allan L.
Formato: diagnostic images research tables/charts Journal Article
Publicado: Springer Nature Feb2025
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=183352864&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 183352864
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        10188827
        EJ3
      jtl: European Child & Adolescent Psychiatry
      issn: 10188827
      maglogo: N
    pubinfo:
      dt: Feb2025
      vid: 34
      iid: 2
      pid: 237
      pub: Springer Nature
      place: New York, New York
    artinfo:
      ui:
        183352864
        177988671
        183352864
        183352864
        10.1007/s00787-024-02501-y
        183352864
      ppf: 585
      ppct: 13
      formats:
        fmt:
          @attributes:
            type: P
      tig:
        atl: Associations between brain network, puberty, and behaviors in boys with Klinefelter syndrome.
      aug:
        au:
          Li, Rihui
          Foland-Ross, Lara C.
          Jordan, Tracy
          Marzelli, Matthew J.
          Ross, Judith L.
          Reiss, Allan L.
        affil: https://ror.org/01r4q9n85 Center for Cognitive and Brain Sciences, Institute of Collaborative Innovation, University of Macau, Taipa, Macao S.A.R., China
      sug:
        subj:
          Klinefelter's Syndrome In Adolescence
          Puberty
          Men
          Functional Connectivity Evaluation
          Adolescent Behavior Evaluation
          Cognition
          Funding Source
          Human
          Male
          Adolescence
          Child
          Nonexperimental Studies
          Descriptive Statistics
          Testosterone
          Magnetic Resonance Imaging
          Machine Learning
          Verbal Behavior
          Mediation Analysis
          Adolescent: 13-18 years
          Child: 6-12 years
          Male
      ab: Background: Klinefelter syndrome (KS), also referred to as XXY syndrome, is a significant but inadequately studied risk factor for neuropsychiatric disability. Whether alterations in functional brain connectivity or pubertal delays are associated with aberrant cognitive-behavioral outcomes in individuals with KS is largely unknown. In this observational study, we investigated KS-related alterations in the resting-state brain network, testosterone level, and cognitive-behavioral impairment in adolescents with Klinefelter syndrome. Methods: We recruited 46 boys with KS, ages 8 to 17 years, and 51 age-matched typically developing (TD) boys. All participants underwent resting-state functional magnetic resonance imaging scans, pubertal, and cognitive-behavioral assessments. Resting-state functional connectivity and regional brain activity of the participants were assessed. Results: We found widespread alterations in global functional connectivity among the inferior frontal gyrus, temporal-parietal area, and hippocampus in boys with KS. Aberrant regional activities, including enhanced fALFF in the motor area and reduced ReHo in the caudate, were also found in the KS group compared to the TD children. Further, using machine learning methods, brain network alterations in these regions accurately differentiated boys with KS from TD controls. Finally, we showed that the alterations of brain network properties not only effectively predict cognitive-behavioral impairment in boys with KS, but also appear to mediate the association between total testosterone level and language ability, a cognitive domain at particular risk for dysfunction in this condition. Conclusion: Our results offer an informatic neurobiological foundation for understanding cognitive-behavioral impairments in individuals with KS and contribute to our understanding of the interplay between pubertal status, brain function, and cognitive-behavioral outcome in this population.
      pubtype: Academic Journal
      doctype:
        diagnostic images
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
    refInfo:
    holdings:
      @attributes:
        islocal: N