Structural Connectivity and Emotion Recognition Impairment in Children and Adolescents with Chromosome 22q11.2 Deletion Syndrome

被引:0
|
作者
Ashley F. P. Sanders
Diana A. Hobbs
Tracey A. Knaus
Elliott A. Beaton
机构
[1] University of New Orleans,Department of Psychology
[2] Washington University School of Medicine in St. Louis,Department of Psychiatry
[3] Washington University School of Medicine in St. Louis,Department of Radiology
来源
Journal of Autism and Developmental Disorders | 2023年 / 53卷
关键词
Brain imaging; DiGeorge syndrome; Emotion processing; Face processing; Genetic deletion; Velocardiofacial syndrome;
D O I
暂无
中图分类号
学科分类号
摘要
Children with chromosome 22q11.2 deletion syndrome (22q11.2DS) exhibit impaired ability to process and understand emotions in others. We measured structural connectivity in children and adolescents with 22q11.2DS (n = 28) and healthy controls (n = 29). Compared to controls, those with 22q11.2DS had poorer social skills and more difficulty recognizing facial emotions. Children with 22q11.2DS also had higher fractional anisotropic diffusion in right amygdala to fusiform gyrus white matter pathways. Right amygdala to fusiform gyrus fractional anisotropy values partially mediated the relationship between 22q11.2DS and social skills, as well as the relationship between 22q11.2DS and emotion recognition accuracy. These findings provide insight into the neural origins of social skills deficits seen in 22q11.2DS and may serve as a biomarker for risk of future psychiatric problems.
引用
收藏
页码:4021 / 4034
页数:13
相关论文
共 50 条
  • [31] T Cell Transcriptome in Chromosome 22q11.2 Deletion Syndrome
    Raje, Nikita R.
    Noel-MacDonnell, Janelle R.
    Shortt, Katherine A.
    Gigliotti, Nicole M.
    Chan, Marcia A.
    Heruth, Daniel P.
    JOURNAL OF IMMUNOLOGY, 2022, 209 (05) : 874 - 885
  • [32] Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions
    Shashi, V.
    Veerapandiyan, A.
    Schoch, K.
    Kwapil, T.
    Keshavan, M.
    Ip, E.
    Hooper, S.
    JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2012, 56 (09) : 865 - 878
  • [33] Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome
    Beaton, Elliott A.
    Qin, Yufeng
    Nguyen, Vy
    Johnson, Joel
    Pinter, Joseph D.
    Simon, Tony J.
    PSYCHIATRY RESEARCH-NEUROIMAGING, 2010, 181 (02) : 108 - 113
  • [34] A child with chromosome 22q11.2 deletion syndrome and a bilobed gallbladder
    James R. Clarke
    Matthias H. Schmidt
    Marian B. Macken
    Charlotte Morley
    Elizabeth A. Cummings
    Pediatric Radiology, 2007, 37
  • [35] A child with chromosome 22q11.2 deletion syndrome and a bilobed gallbladder
    Clarke, James R.
    Schmidt, Matthias H.
    Macken, Marian B.
    Morley, Charlotte
    Cummings, Elizabeth A.
    PEDIATRIC RADIOLOGY, 2007, 37 (02) : 213 - 215
  • [36] Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome
    Allen, T. M.
    Hersh, J.
    Schoch, K.
    Curtiss, K.
    Hooper, S. R.
    Shashi, V.
    JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2014, 58 (01) : 31 - 47
  • [37] Cognitive development in children with 22q11.2 deletion syndrome
    Duijff, Sasja N.
    Klaassen, Petra W. J.
    de Veye, Henriette F. N. Swanenburg
    Beemer, Frits A.
    Sinnema, Gerben
    Vorstman, Jacob A. S.
    BRITISH JOURNAL OF PSYCHIATRY, 2012, 200 (06) : 462 - 468
  • [38] Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
    Yael Schonherz
    Maayan Davidov
    Ariel Knafo
    Hadas Zilkha
    Gal Shoval
    Gil Zalsman
    Amos Frisch
    Abraham Weizman
    Doron Gothelf
    Journal of Neurodevelopmental Disorders, 2014, 6
  • [39] Cardiovascular Anomalies Associated With Chromosome 22q11.2 Deletion Syndrome
    Momma, Kazuo
    AMERICAN JOURNAL OF CARDIOLOGY, 2010, 105 (11) : 1617 - 1624
  • [40] Behavior in preschool children with the 22q11.2 deletion syndrome
    Klaassen, Petra
    Duijff, Sasja
    de Veye, Henriette Swanenburg
    Vorstman, Jacob
    Beemer, Frits
    Sinnema, Gerben
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2013, 161A (01) : 94 - 101