A quantitative MRI study of posterior fossa development in velocardiofacial syndrome

被引:58
作者
Eliez, S [1 ]
Schmitt, JE [1 ]
White, CD [1 ]
Wellis, VG [1 ]
Reiss, AL [1 ]
机构
[1] Stanford Univ, Dept Psychiat & Behav Sci, Sch Med, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
velocardiofacial; VCFS; 22q11.2; brain; MRI;
D O I
10.1016/S0006-3223(00)01005-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Velocardiofacial syndrome (VCFS) has been identified as a risk factor for developing schizophrenia. Qualitative neuroimaging studies indicated that VCFS was frequently associated with abnormal development of structures in the posterior fossa of the brain. The objective of this investigation was to identify the specific structures affected in the posterior fossa and investigate the association of these neuroanatomic variations with behaviors potentially related to later-onset psychiatric disorders. Methods: Twenty-four children and adolescents with VCFS individually matched for age and gender with 24 control subjects received magnetic resonance imaging scans. Analysis of covariance models were used to investigate regional brain differences. Association between brain areas and behaviors measured on the Child Behavior Checklist (CBCL) were assessed using simple regression models. Results: Children with VCFS had significantly smaller size of vermal lobules VI-VII and the pens after adjusting for overall brain size. There were no significant associations between scores on the CBCL and measures of neuroanatomic variation within the VCFS group. Conclusions: Structural alterations of the posterior fossa in VCFS are specifically limited to cerebellar vermis lobules VI-VII and pens. Previous literature has suggested that the vermis is involved in social cognition, and alteration of lobules VI-VII could therefore partially explain the neurobehavioral profile associated with VCFS. Biol Psychiatry 2001;49:540-546 (C) 2001 Society of Biological Psychiatry.
引用
收藏
页码:540 / 546
页数:7
相关论文
共 58 条
  • [1] Achenbach T.M., 1991, MANUAL CHILD BEHAV C
  • [2] FURTHER DELINEATION OF BRAIN ANOMALIES IN VELO-CARDIO-FACIAL SYNDROME
    ALTMAN, DH
    ALTMAN, NR
    MITNICK, RJ
    SHPRINTZEN, RJ
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 60 (02): : 174 - 175
  • [3] 22q11 deletion syndrome: A genetic subtype of schizophrenia
    Bassett, AS
    Chow, EWC
    [J]. BIOLOGICAL PSYCHIATRY, 1999, 46 (07) : 882 - 891
  • [4] INHIBITION OF OCULAR DOMINANCE COLUMN FORMATION BY INFUSION OF NT-4/5 OR BDNF
    CABELLI, RJ
    HOHN, A
    SHATZ, CJ
    [J]. SCIENCE, 1995, 267 (5204) : 1662 - 1666
  • [5] Carlson C, 1997, AM J HUM GENET, V60, P851
  • [6] Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia
    Chow, EWC
    Mikulis, DJ
    Zipursky, RB
    Scutt, LE
    Weksberg, R
    Bassett, AS
    [J]. BIOLOGICAL PSYCHIATRY, 1999, 46 (10) : 1436 - 1442
  • [7] EFFECTS OF AGE AND COMMUNICATION LEVEL ON EYE CONTACT IN FRAGILE-X MALES AND NON-FRAGILE-X AUTISTIC MALES
    COHEN, IL
    VIETZE, PM
    SUDHALTER, V
    JENKINS, EC
    BROWN, WT
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1991, 38 (2-3): : 498 - 502
  • [8] COHEN IL, 1988, AM J MENT RETARD, V92, P436
  • [9] Devriendt K, 1996, DEV MED CHILD NEUROL, V38, P949
  • [10] Prevalence of 22q11 microdeletion
    duMontcel, ST
    Mendizabal, H
    Ayme, S
    Levy, A
    Philip, N
    [J]. JOURNAL OF MEDICAL GENETICS, 1996, 33 (08) : 719 - 719