Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion

被引:58
|
作者
Vorstman, Jacob A. S. [1 ]
Breetvelt, Elemi J. [1 ]
Thode, Kirstin I. [2 ]
Chow, Eva W. C. [3 ,4 ]
Bassett, Anne S. [3 ,4 ]
机构
[1] Univ Med Ctr Utrecht, Dept Psychiat, Rudolf Magnus Inst Neurosci, Utrecht, Netherlands
[2] Malcolm Grow Med Ctr, Dept Psychiat, Andrews AFB, MD USA
[3] Ctr Addict & Mental Hlth, Clin Genet Res Program, Toronto, ON, Canada
[4] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
Pleiotropy; Copy number variant (CNV); Autism; Schizophrenia; 22q11.2 deletion syndrome; COPY NUMBER VARIATIONS; NEURODEVELOPMENTAL HYPOTHESIS; DISORDERS; MICRODELETION; ADULTS; PHENOTYPE; SUSCEPTIBILITY; ASSOCIATION; CHILDREN; 16P11.2;
D O I
10.1016/j.schres.2012.10.010
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Copy number variants (CNVs) associated with neuropsychiatric disorders are increasingly being identified. While the initial reports were relatively specific, i.e. implicating vulnerability for a particular neuropsychiatric disorder, subsequent studies suggested that most of these CNVs can increase the risk for more than one neuropsychiatric disorder. Possibly, the different neuropsychiatric phenotypes associated with a single genetic variant are really distinct phenomena, indicating pleiotropy. Alternatively, seemingly different disorders could represent the same phenotype observed at different developmental stages or the same underlying pathogenesis with different phenotypic expressions. Aims: To examine the relation between autism and schizophrenia in patients sharing the same CNV. Method: We interviewed parents of 78 adult patients with the 22q11.2 deletion (22q11.2DS) to examine if autistic symptoms during childhood were associated with psychosis in adulthood. We used Chi-square, T-tests and logistic regression while entering cognitive level, gender and age as covariates. Results: The subgroup of 22q11.2DS patients with probable ASD during childhood did not show an increased risk for psychosis in adulthood. The average SRS scores were highly similar between those with and those without schizophrenia. Conclusions: ASD and schizophrenia associated with 22q11.2DS should be regarded as two unrelated, distinct phenotypic manifestations, consistent with true neuropsychiatric pleiotropy. 22q11.2DS can serve as a model to examine the mechanisms associated with neuropsychiatric pleiotropy associated with other CNVs. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:55 / 59
页数:5
相关论文
共 50 条
  • [31] Functional outcomes of adults with 22q11.2 deletion syndrome
    Butcher, Nancy J.
    Chow, Eva W. C.
    Costain, Gregory
    Karas, Dominique
    Ho, Andrew
    Bassett, Anne S.
    GENETICS IN MEDICINE, 2012, 14 (10) : 836 - 843
  • [32] How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report
    Kazutaka Ohi
    Ryota Hashimoto
    Hidenaga Yamamori
    Yuka Yasuda
    Michiko Fujimoto
    Noriko Nakatani
    Kouzin Kamino
    Masatoshi Takeda
    Annals of General Psychiatry, 12
  • [33] Distal 22q11.2 Microduplication Combined With Typical 22q11.2 Proximal Deletion: A Case Report
    Molck, Miriam Coelho
    Vieira, Tarsis Paiva
    Simioni, Milena
    Sgardioli, Ilaria Cristina
    dos Santos, Ana Paula
    Xavier, Ana Carolina
    Gil-da-Silva-Lopes, Vera Lucia
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2015, 167 (01) : 215 - 220
  • [34] How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report
    Ohi, Kazutaka
    Hashimoto, Ryota
    Yamamori, Hidenaga
    Yasuda, Yuka
    Fujimoto, Michiko
    Nakatani, Noriko
    Kamino, Kouzin
    Takeda, Masatoshi
    ANNALS OF GENERAL PSYCHIATRY, 2013, 12
  • [35] AN OVERVIEW OF CORRELATIONS BETWEEN SCHIZOPHRENIA AND 22Q11.2 DELETION SYNDROME
    Armando, Marco
    Pontillo, Maria
    De Crescenzo, Franco
    Correale, Cinzia
    De Simoni, Enrica
    Papaleo, Francesco
    Saba, Riccardo
    Vicari, Stefano
    CLINICAL NEUROPSYCHIATRY, 2013, 10 (01): : 3 - 10
  • [36] Convergent Brain Mechanisms in 22q11.2 Deletion Syndrome and Schizophrenia
    Ching, Christopher
    Sun, Daqiang
    Reina, Julio Villalon
    Martinez, Kenia
    Jonas, Rachel K.
    Lin, Amy
    Kushan, Leila
    van Erp, Theo
    Turner, Jessica
    Thompson, Paul M.
    Bearden, Carrie
    BIOLOGICAL PSYCHIATRY, 2018, 83 (09) : S50 - S50
  • [37] The importance of understanding cognitive trajectories: the case of 22q11.2 deletion syndrome
    Swillen, Ann
    CURRENT OPINION IN PSYCHIATRY, 2016, 29 (02) : 133 - 137
  • [38] Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times
    Habel, Alex
    Herriot, Richard
    Kumararatne, Dinakantha
    Allgrove, Jeremy
    Baker, Kate
    Baxendale, Helen
    Bu'Lock, Frances
    Firth, Helen
    Gennery, Andrew
    Holland, Anthony
    Illingworth, Claire
    Mercer, Nigel
    Pannebakker, Merel
    Parry, Andrew
    Roberts, Anne
    Tsai-Goodman, Beverly
    EUROPEAN JOURNAL OF PEDIATRICS, 2014, 173 (06) : 757 - 765
  • [39] Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
    Cleynen, Isabelle
    Engchuan, Worrawat
    Hestand, Matthew S.
    Heung, Tracy
    Holleman, Aaron M.
    Johnston, H. Richard
    Monfeuga, Thomas
    McDonald-McGinn, Donna M.
    Gur, Raquel E.
    Morrow, Bernice E.
    Swillen, Ann
    Vorstman, Jacob A. S.
    Bearden, Carrie E.
    Chow, Eva W. C.
    van den Bree, Marianne
    Emanuel, Beverly S.
    Vermeesch, Joris R.
    Warren, Stephen T.
    Owen, Michael J.
    Chopra, Pankaj
    Cutler, David J.
    Duncan, Richard
    Kotlar, Alex, V
    Mulle, Jennifer G.
    Voss, Anna J.
    Zwick, Michael E.
    Diacou, Alexander
    Golden, Aaron
    Guo, Tingwei
    Lin, Jhih-Rong
    Wang, Tao
    Zhang, Zhengdong
    Zhao, Yingjie
    Marshall, Christian
    Merico, Daniele
    Jin, Andrea
    Lilley, Brenna
    Salmons, Harold, I
    Oanh Tran
    Holmans, Peter
    Pardinas, Antonio
    Walters, James T. R.
    Demaerel, Wolfram
    Boot, Erik
    Butcher, Nancy J.
    Costain, Gregory A.
    Lowther, Chelsea
    Evers, Rens
    van Amelsvoort, Therese A. M. J.
    van Duin, Esther
    MOLECULAR PSYCHIATRY, 2021, 26 (08) : 4496 - 4510
  • [40] Pediatric healthcare costs for patients with 22q11.2 deletion syndrome
    Benn, Peter
    Iyengar, Sushma
    Crowley, Terrence Blaine
    Zackai, Elaine H.
    Burrows, Evanette K.
    Moshkevich, Solomon
    McDonald-McGinn, Donna M.
    Sullivan, Kathleen E.
    Demko, Zachary
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2017, 5 (06): : 631 - 638