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
  • [41] 22q11.2 deletion syndrome in diverse populations
    Kruszka, Paul
    Addissie, Yonit A.
    McGinn, Daniel E.
    Porras, Antonio R.
    Biggs, Elijah
    Share, Matthew
    Crowley, T. Blaine
    Chung, Brian H. Y.
    Mok, Gary T. K.
    Mak, Christopher C. Y.
    Muthukumarasamy, Premala
    Thong, Meow-Keong
    Sirisena, Nirmala D.
    Dissanayake, Vajira H. W.
    Paththinige, C. Sampath
    Prabodha, L. B. Lahiru
    Mishra, Rupesh
    Shotelersuk, Vorasuk
    Ekure, Ekanem Nsikak
    Sokunbi, Ogochukwu Jidechukwu
    Kalu, Nnenna
    Ferreira, Carlos R.
    Duncan, Jordann-Mishael
    Patil, Siddaramappa Jagdish
    Jones, Kelly L.
    Kaplan, Julie D.
    Abdul-Rahman, Omar A.
    Uwineza, Annette
    Mutesa, Leon
    Moresco, Angelica
    Gabriela Obregon, Maria
    Richieri-Costa, Antonio
    Gil-da-Silva-Lopes, Vera L.
    Adeyemo, Adebowale A.
    Summar, Marshall
    Zackai, Elaine H.
    McDonald-McGinn, Donna M.
    Linguraru, Marius George
    Muenke, Maximilian
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (04) : 879 - 888
  • [42] Clozapine Use in 22q11.2 Deletion Syndrome
    Colijn, Mark Ainsley
    JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2024, 44 (02) : 168 - 178
  • [43] Neurological manifestation of 22q11.2 deletion syndrome
    Bayat, Michael
    Bayat, Allan
    NEUROLOGICAL SCIENCES, 2022, 43 (03) : 1695 - 1700
  • [44] Surgical Considerations in 22Q11.2 Deletion Syndrome
    Kirschner, Richard E.
    Baylis, Adriane L.
    CLINICS IN PLASTIC SURGERY, 2014, 41 (02) : 271 - +
  • [45] Clinical Manifestations of 22q11.2 Deletion Syndrome
    Cirillo, Annapaola
    Lioncino, Michele
    Maratea, Annachiara
    Passariello, Annalisa
    Fusco, Adelaide
    Fratta, Fiorella
    Monda, Emanuele
    Caiazza, Martina
    Signore, Giovanni
    Esposito, Augusto
    Baban, Anwar
    Versacci, Paolo
    Putotto, Carolina
    Marino, Bruno
    Pignata, Claudio
    Cirillo, Emilia
    Giardino, Giuliana
    Sarubbi, Berardo
    Limongelli, Giuseppe
    Russo, Maria Giovanna
    HEART FAILURE CLINICS, 2022, 18 (01) : 155 - 164
  • [46] Deletion Syndrome 22q11.2: A Systematic Review
    Cortes-Martin, Jonathan
    Lopez Penuela, Nuria
    Carlos Sanchez-Garcia, Juan
    Montiel-Troya, Maria
    Diaz-Rodriguez, Lourdes
    Rodriguez-Blanque, Raquel
    CHILDREN-BASEL, 2022, 9 (08):
  • [47] Chromatin Modifications in 22q11.2 Deletion Syndrome
    Zhang, Zhe
    Shi, LiHua
    Song, Li
    Maurer, Kelly
    Zhao, Xue
    Zackai, Elaine H.
    McGinn, Daniel E.
    Crowley, T. Blaine
    McGinn, Donna M. McDonald
    Sullivan, Kathleen E.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2021, 41 (08) : 1853 - 1864
  • [48] Complement Activation in 22q11.2 Deletion Syndrome
    Grinde, Dina
    Overland, Torstein
    Lima, Kari
    Schjalm, Camilla
    Mollnes, Tom Eirik
    Abrahamsen, Tore G.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2020, 40 (03) : 515 - 523
  • [49] Longitudinal perspectives on the psychosis spectrum in 22q11.2 deletion syndrome
    Tang, Sunny X.
    Gur, Raquel E.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (10) : 2192 - 2202
  • [50] Molecular Screening for 22Q11.2 Deletion Syndrome in Patients With Congenital Heart Disease
    Huber, Janaina
    Peres, Vivian Catarino
    de Castro, Alexandre Luz
    dos Santos, Tiago Jeronimo
    Beltrao, Lauro da Fontoura
    de Baumont, Angelica Cerveira
    Cossio, Silvia Liliana
    Dalberto, Tiago Pires
    Riegel, Mariluce
    Canedo, Andres Delgado
    Schaan, Beatriz D'Agord
    Pellanda, Lucia Campos
    PEDIATRIC CARDIOLOGY, 2014, 35 (08) : 1356 - 1362