Literature DB >> 33510659

CNVs and Chromosomal Aneuploidy in Patients With Early-Onset Schizophrenia and Bipolar Disorder: Genotype-Phenotype Associations.

Hojka Gregoric Kumperscak1,2, Danijela Krgovic2,3, Maja Drobnic Radobuljac4,5, Nina Senica1, Andreja Zagorac3, Nadja Kokalj Vokac2,3.   

Abstract

Introduction: Early-onset schizophrenia (EOS) and bipolar disorder (EOB) start before the age of 18 years and have a more severe clinical course, a worse prognosis, and a greater genetic loading compared to the late-onset forms. Copy number variations (CNVs) are an important genetic factor in the etiology of psychiatric disorders. Therefore, this study aimed to analyze CNVs in patients with EOS and EOB and to establish genotype-phenotype relationships for contiguous gene syndromes or genes affected by identified CNVs.
Methods: Molecular karyotyping was performed in 45 patients, 38 with EOS and seven with EOB hospitalized between 2010 and 2017. The exclusion criteria were medical or neurological disorders or IQ under 70. Detected CNVs were analyzed according to the standards and guidelines of the American College of Medical Genetics. Result: Molecular karyotyping showed CNVs in four patients with EOS (encompassing the PAK2, ADAMTS3, and ADAMTSL1 genes, and the 16p11.2 microduplication syndrome) and in two patients with EOB (encompassing the ARHGAP11B and PRODH genes). In one patient with EOB, a chromosomal aneuploidy 47, XYY was found. Discussion: Our study is the first study of CNVs in EOS and EOB patients in Slovenia. Our findings support the association of the PAK2, ARHGAP11B, and PRODH genes with schizophrenia and/or bipolar disorder. To our knowledge, this is also the first report of a multiplication of the ADAMTSL1 gene and the smallest deletion of the PAK2 gene in a patient with EOS, and one of the few reports of the 47, XYY karyotype in a patient with EOB.
Copyright © 2021 Gregoric Kumperscak, Krgovic, Drobnic Radobuljac, Senica, Zagorac and Kokalj Vokac.

Entities:  

Keywords:  bipolar disorder; chromosomal aneuploidy; copy number variations; early onset; schizophrenia

Year:  2021        PMID: 33510659      PMCID: PMC7837028          DOI: 10.3389/fpsyt.2020.606372

Source DB:  PubMed          Journal:  Front Psychiatry        ISSN: 1664-0640            Impact factor:   4.157


  71 in total

1.  Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.

Authors:  Anne S Bassett; Chelsea Lowther; Daniele Merico; Gregory Costain; Eva W C Chow; Therese van Amelsvoort; Donna McDonald-McGinn; Raquel E Gur; Ann Swillen; Marianne Van den Bree; Kieran Murphy; Doron Gothelf; Carrie E Bearden; Stephan Eliez; Wendy Kates; Nicole Philip; Vandana Sashi; Linda Campbell; Jacob Vorstman; Joseph Cubells; Gabriela M Repetto; Tony Simon; Erik Boot; Tracy Heung; Rens Evers; Claudia Vingerhoets; Esther van Duin; Elaine Zackai; Elfi Vergaelen; Koen Devriendt; Joris R Vermeesch; Michael Owen; Clodagh Murphy; Elena Michaelovosky; Leila Kushan; Maude Schneider; Wanda Fremont; Tiffany Busa; Stephen Hooper; Kathryn McCabe; Sasja Duijff; Karin Isaev; Giovanna Pellecchia; John Wei; Matthew J Gazzellone; Stephen W Scherer; Beverly S Emanuel; Tingwei Guo; Bernice E Morrow; Christian R Marshall
Journal:  Am J Psychiatry       Date:  2017-07-28       Impact factor: 18.112

2.  Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample.

Authors:  Andrew McQuillin; Nicholas Bass; Adebayo Anjorin; Jacob Lawrence; Radhika Kandaswamy; Greg Lydall; Jennifer Moran; Pamela Sklar; Shaun Purcell; Hugh Gurling
Journal:  Eur J Hum Genet       Date:  2011-01-05       Impact factor: 4.246

3.  The DGCR5 long noncoding RNA may regulate expression of several schizophrenia-related genes.

Authors:  Qingtuan Meng; Kangli Wang; Tonya Brunetti; Yan Xia; Chuan Jiao; Rujia Dai; Dominic Fitzgerald; Amber Thomas; Lindsey Jay; Heather Eckart; Kay Grennan; Yuka Imamura-Kawasawa; Mingfeng Li; Nenad Sestan; Kevin P White; Chao Chen; Chunyu Liu
Journal:  Sci Transl Med       Date:  2018-12-13       Impact factor: 17.956

Review 4.  The human clinical phenotypes of altered CHRNA7 copy number.

Authors:  Madelyn A Gillentine; Christian P Schaaf
Journal:  Biochem Pharmacol       Date:  2015-06-18       Impact factor: 5.858

5.  Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.

Authors:  Detelina Grozeva; George Kirov; Dobril Ivanov; Ian R Jones; Lisa Jones; Elaine K Green; David M St Clair; Allan H Young; Nicol Ferrier; Anne E Farmer; Peter McGuffin; Peter A Holmans; Michael J Owen; Michael C O'Donovan; Nick Craddock
Journal:  Arch Gen Psychiatry       Date:  2010-04

Review 6.  CNVs in neuropsychiatric disorders.

Authors:  George Kirov
Journal:  Hum Mol Genet       Date:  2015-06-30       Impact factor: 6.150

7.  The 3q29 deletion confers >40-fold increase in risk for schizophrenia.

Authors:  J G Mulle
Journal:  Mol Psychiatry       Date:  2015-06-09       Impact factor: 15.992

8.  SlgA, encoded by the homolog of the human schizophrenia-associated gene PRODH, acts in clock neurons to regulate Drosophila aggression.

Authors:  Liesbeth Zwarts; Veerle Vulsteke; Edgar Buhl; James J L Hodge; Patrick Callaerts
Journal:  Dis Model Mech       Date:  2017-03-22       Impact factor: 5.758

Review 9.  Sex differences in the developing brain as a source of inherent risk.

Authors:  Margaret M McCarthy
Journal:  Dialogues Clin Neurosci       Date:  2016-12       Impact factor: 5.986

10.  Investigation of epigenetic regulatory networks associated with autism spectrum disorder (ASD) by integrated global LINE-1 methylation and gene expression profiling analyses.

Authors:  Chayanin Tangsuwansri; Thanit Saeliw; Surangrat Thongkorn; Weerasak Chonchaiya; Kanya Suphapeetiporn; Apiwat Mutirangura; Tewin Tencomnao; Valerie Wailin Hu; Tewarit Sarachana
Journal:  PLoS One       Date:  2018-07-23       Impact factor: 3.240

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