Sex differences in cognitive functioning in velocardiofacial syndrome (VCFS)

被引:44
作者
Antshel, KM
AbdulSabur, N
Roizen, N
Fremont, W
Kates, WR
机构
[1] SUNY Upstate Med Univ, Dept Psychiat & Behav Sci, Program Neurosci, Syracuse, NY 13210 USA
[2] SUNY Upstate Med Univ, Dept Pediat, Syracuse, NY 13210 USA
[3] Johns Hopkins Sch Med, Dept Psychiat, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
D O I
10.1207/s15326942dn2803_6
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Sex differences in cognitive functioning were investigated in children with velocardiofacial syndrome (VCFS), a genetic defect caused by a microdeletion on chromosome 22q.11. The study population consisted of six groups: 50 boys with VCFS (M = 11.1, SD = 2.7), 40 girls with VCFS (M = 10.8, SD = 2.5), 13 male siblings of the participant with VCFS (M = 12.3, SD = 1.9), 17 female siblings of the participant with VCFS (M = 12.2, SD = 1.9), and a race- and gender-ratio-matched sample of 28 boy community control participants (M = 10.7, SD = 2.4) and 19 girl community control participants (M = 9.2, SD = 2.3). Each participant received a psychological assessment including intellectual and academic achievement as well as structural magnetic resonance imaging of his or her brain. Our results indicate that boys with VCFS may be more cognitively affected than girls. In addition, and although cross-sectional in nature, our results document a negative association between age and cognitive functioning in girls with VCFS but not in boys. Sex differences in frontal lobe volume are generally seen in the general population between boys and girls (boys > girls) and across all three samples, this trend emerged. Relative to boys with VCFS, girls with VCFS may be less cognitively affected, although age is negatively associated with cognitive functioning in girls with VCFS but not boys, suggesting that girls with VCFS may fail to maintain this cognitive advantage over boys.
引用
收藏
页码:849 / 869
页数:21
相关论文
共 100 条
  • [21] DRISCOLL DA, 1992, AM J HUM GENET, V50, P924
  • [22] Dubal DB, 1999, J NEUROSCI, V19, P6385
  • [23] Prevalence of 22q11 microdeletion
    duMontcel, ST
    Mendizabal, H
    Ayme, S
    Levy, A
    Philip, N
    [J]. JOURNAL OF MEDICAL GENETICS, 1996, 33 (08) : 719 - 719
  • [24] ATTENTION-DEFICIT DISORDER AND SPECIFIC READING-DISABILITY - SEPARATE BUT OFTEN OVERLAPPING DISORDERS
    DYKMAN, RA
    ACKERMAN, PT
    [J]. JOURNAL OF LEARNING DISABILITIES, 1991, 24 (02) : 96 - 103
  • [25] Children and adolescents with velocardiofacial syndrome: A volumetric MRI study
    Eliez, S
    Schmitt, JE
    White, CD
    Reiss, AL
    [J]. AMERICAN JOURNAL OF PSYCHIATRY, 2000, 157 (03) : 409 - 415
  • [26] SELECTIVE FEMALE AFFLICTION IN THE DEVELOPMENTAL DISORDERS OF CHILDHOOD - A LITERATURE-REVIEW
    EME, RF
    [J]. JOURNAL OF CLINICAL CHILD PSYCHOLOGY, 1992, 21 (04): : 354 - 364
  • [27] Faraone Stephen V, 2003, World Psychiatry, V2, P104
  • [28] RELATIONS BETWEEN PRENATAL TESTOSTERONE LEVELS AND COGNITIVE-ABILITIES AT 4 YEARS
    FINEGAN, JAK
    NICCOLS, GA
    SITARENIOS, G
    [J]. DEVELOPMENTAL PSYCHOLOGY, 1992, 28 (06) : 1075 - 1089
  • [29] Genetics of autism: Complex aetiology for a heterogeneous disorder
    Folstein, SE
    Rosen-Sheidley, B
    [J]. NATURE REVIEWS GENETICS, 2001, 2 (12) : 943 - 955
  • [30] Aromatase expression by astrocytes after brain injury: Implications for local estrogen formation in brain repair
    Garcia-Segura, LM
    Wozniak, A
    Azcoitia, I
    Rodriguez, JR
    Hutchison, RE
    Hutchison, JB
    [J]. NEUROSCIENCE, 1999, 89 (02) : 567 - 578