Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome

被引:14
|
作者
Deng, Yi [1 ,2 ]
Goodrich-Hunsaker, Naomi J. [1 ,2 ]
Cabaral, Margarita [1 ,2 ]
Amaral, David G. [1 ,2 ]
Buonocore, Michael H. [3 ]
Harvey, Danielle [4 ]
Kalish, Kristopher [5 ]
Carmichael, Owen T. [5 ,6 ]
Schumann, Cynthia M. [1 ,2 ]
Lee, Aaron [1 ,2 ]
Dougherty, Robert F. [7 ]
Perry, Lee M. [7 ]
Wandell, Brian A. [7 ]
Simon, Tony J. [1 ,2 ]
机构
[1] Univ Calif Davis, Dept Psychiat & Behav Sci, Sacramento, CA 95817 USA
[2] Univ Calif Davis, MIND Inst, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Sch Med, Dept Radiol, Sacramento, CA 95817 USA
[4] Univ Calif Davis, Dept Publ Hlth Sci, Div Biostat, Davis, CA 95616 USA
[5] Univ Calif Davis, Grad Grp Comp Sci, Davis, CA 95616 USA
[6] Univ Calif Davis, Sch Med, Dept Neurol, Sacramento, CA 95817 USA
[7] Stanford Univ, Dept Psychol, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
Chromosome; 22q11.2; deletion; Connectivity; Hippocampal formation; Tractography; Velo-cardio-facial Syndrome; CARDIO-FACIAL SYNDROME; HIPPOCAMPAL VOLUME REDUCTION; VELOCARDIOFACIAL SYNDROME DELETION; CORPUS-CALLOSUM MORPHOLOGY; CORTICAL THICKNESS; ANXIETY; MRI; ADOLESCENTS; SCHIZOPHRENIA; GYRIFICATION;
D O I
10.1016/j.pscychresns.2015.02.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The fornix is the primary subcortical output fiber system of the hippocampal formation. In children with 22q11.2 deletion syndrome (22q11.2DS), hippocampal volume reduction has been commonly reported, but few studies as yet have evaluated the integrity of the fornix. Therefore, we investigated the fornix of 45 school-aged children with 22q11.2DS and 38 matched typically developing (TD) children. Probabilistic diffusion tensor imaging (DTI) tractography was used to reconstruct the body of the fornix in each child's brain native space. Compared with children, significantly lower fractional anisotropy (FA) and higher radial diffusivity (RD) was observed bilaterally in the body of the fornix in children with 22q11.2DS. Irregularities were especially prominent in the posterior aspect of the fornix where it emerges from the hippocampus. Smaller volumes of the hippocampal formations were also found in the 22q11.2DS group. The reduced hippocampal volumes were correlated with lower fornix FA and higher fornix RD in the right hemisphere. Our findings provide neuroanatomical evidence of disrupted hippocampal connectivity in children with 22q11.2DS, which may help to further understand the biological basis of spatial impairments, affective regulation, and other factors related to the ultra-high risk for schizophrenia in this population. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:106 / 114
页数:9
相关论文
共 50 条
  • [1] Disrupted anatomic networks in the 22q11.2 deletion syndrome
    Schmitt, J. Eric
    Yi, James
    Calkins, Monica E.
    Ruparel, Kosha
    Roalf, David R.
    Cassidy, Amy
    Souders, Margaret C.
    Satterthwaite, Theodore D.
    McDonald-McGinn, Donna M.
    Zackai, Elaine H.
    Gur, Ruben C.
    Emanuel, Beverly S.
    Gur, Raquel E.
    NEUROIMAGE-CLINICAL, 2016, 12 : 420 - 428
  • [2] Meta-analysis of magnetic resonance imaging studies in chromosome 22q11.2 deletion syndrome (velocardiofacial syndrome)
    Tan, Giles M.
    Arnone, Danilo
    McIntosh, Andrew M.
    Ebmeier, Klaus P.
    SCHIZOPHRENIA RESEARCH, 2009, 115 (2-3) : 173 - 181
  • [3] COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome
    Shashi, Vandana
    Howard, Timothy D.
    Keshavan, Matcheri S.
    Kaczorowski, Jessica
    Berry, Margaret N.
    Schoch, Kelly
    Spence, Edward J.
    Kwapil, Thomas R.
    PSYCHIATRY RESEARCH, 2010, 178 (02) : 433 - 436
  • [4] Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
    Schonherz, Yael
    Davidov, Maayan
    Knafo, Ariel
    Zilkha, Hadas
    Shoval, Gal
    Zalsman, Gil
    Frisch, Amos
    Weizman, Abraham
    Gothelf, Doron
    JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2014, 6
  • [5] 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
  • [6] 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
  • [7] Children With Chromosome 22q11.2 Deletion Syndrome Exhibit Impaired Spatial Working Memory
    Wong, Ling M.
    Riggins, Tracy
    Harvey, Danielle
    Cabaral, Margarita
    Simon, Tony J.
    AJIDD-AMERICAN JOURNAL ON INTELLECTUAL AND DEVELOPMENTAL DISABILITIES, 2014, 119 (02): : 115 - 132
  • [8] 22q11.2 deletion syndrome
    McDonald-McGinn, Donna M.
    Sullivan, Kathleen E.
    Marino, Bruno
    Philip, Nicole
    Swillen, Ann
    Vorstman, Jacob A. S.
    Zackai, Elaine H.
    Emanuel, Beverly S.
    Vermeesch, Joris R.
    Morrow, Bernice E.
    Scambler, Peter J.
    Bassett, Anne S.
    NATURE REVIEWS DISEASE PRIMERS, 2015, 1
  • [9] Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome?
    Baker, Kate
    Vorstman, Jacob A. S.
    CURRENT OPINION IN NEUROLOGY, 2012, 25 (02) : 131 - 137
  • [10] An Examination of the Relationship of Anxiety and Intelligence to Adaptive Functioning in Children with Chromosome 22q11.2 Deletion Syndrome
    Angkustsiri, Kathleen
    Leckliter, Ingrid
    Tartaglia, Nicole
    Beaton, Elliott A.
    Enriquez, Janice
    Simon, Tony J.
    JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS, 2012, 33 (09) : 713 - 720