A Pilot Study on Early-Onset Schizophrenia Reveals the Implication of Wnt, Cadherin and Cholecystokinin Receptor Signaling in Its Pathophysiology

被引:1
作者
Drozd, Malgorzata Marta [1 ]
Capovilla, Maria [1 ]
Previdere, Carlo [2 ]
Grossi, Mauro [1 ]
Askenazy, Florence [3 ,4 ]
Bardoni, Barbara [5 ]
Fernandez, Arnaud [1 ,3 ,4 ]
机构
[1] Univ Cote Azur, Inst Pharmacol Mol & Cellulaire, CNRS, UMR7275, Valbonne, France
[2] Univ Pavia, Dipartimento Sanita Pubbl Med Sperimentale & Fore, Unita Med Legale & Sci Forensi Antonio Fornari, Lab Genet Forense, Pavia, Italy
[3] CHU Lenval, Hop Pediat Nice, Dept Psychiat Enfant & Adolescent, Nice, France
[4] Univ Cote Azur, CoBTek, EA7276, Valbonne, France
[5] Univ Cote Azur, Inst Pharmacol Mol & Cellulaire, CNRS, INSERM,UMR7275, Valbonne, France
关键词
Early-Onset Schizophrenia; Autism Spectrum Disorder; Intellectual Disability; WNT; Cadherin; Cholecystokinin receptor; Whole Exome Sequencing; HOMOCYSTEINE METABOLISM; DISORDERS; PROTEIN; RETARDATION; CHILDREN; MUTATION; PATHWAY; GENES;
D O I
10.3389/fgene.2021.792218
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Early-Onset Schizophrenia (EOS) is a very rare mental disorder that is a form of schizophrenia occurring before the age of 18. EOS is a brain disease marked by an early onset of positive and negative symptoms of psychosis that impact development and cognitive functioning. Clinical manifestations commonly include premorbid features of Autism Spectrum Disorder (ASD), attention deficits, Intellectual Disability (ID), neurodevelopmental delay, and behavioral disturbances. After the onset of psychotic symptoms, other neuropsychiatric comorbidities are also common, including obsessive-compulsive disorder, major depressive disorder, expressive and receptive language disorders, auditory processing, and executive functioning deficits. With the purpose to better gain insight into the genetic bases of this disorder, we developed a pilot project performing whole exome sequencing of nine trios affected by EOS, ASD, and mild ID. We carried out gene prioritization by combining multiple bioinformatic tools allowing us to identify the main pathways that could underpin the neurodevelopmental phenotypes of these patients. We identified the presence of variants in genes belonging to the Wnt, cadherin and cholecystokinin receptor signaling pathways.
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页数:11
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