The Danish 22q11 research initiative.

Détails

ID Serval
serval:BIB_6A4680D3150A
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
The Danish 22q11 research initiative.
Périodique
BMC psychiatry
Auteur⸱e⸱s
Schmock H., Vangkilde A., Larsen K.M., Fischer E., Birknow M.R., Jepsen J.R., Olesen C., Skovby F., Plessen K.J., Mørup M., Hulme O., Baaré W.F., Didriksen M., Siebner H.R., Werge T., Olsen L.
ISSN
1471-244X (Electronic)
ISSN-L
1471-244X
Statut éditorial
Publié
Date de publication
17/09/2015
Peer-reviewed
Oui
Volume
15
Pages
220
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Résumé
Neurodevelopmental brain disorders such as schizophrenia, autism and attention deficit hyperactivity disorder are complex disorders with heterogeneous etiologies. Schizophrenia and autism are difficult to treat and often cause major individual suffering largely owing to our limited understanding of the disease biology. Thus our understanding of the biological pathogenesis needs to be substantiated to enable development of more targeted treatment options with improved efficacy. Insights into the pre-morbid disease dynamics, the morbid condition and the underlying biological disease mechanisms may come from studies of subjects with homogenous etiologies. Breakthroughs in psychiatric genetics have shown that several genetic anomalies predispose for neurodevelopmental brain disorders. We have established a Danish research initiative to study the common microdeletion at chromosome 22q11.2, which is one of the genetic anomalies that confer high risk of schizophrenia, autism and attention deficit hyperactivity disorder.
The study applies a "cause-to-outcome" strategy to identify pre-morbid pathogenesis and underlying biological disease mechanisms of psychosis and secondarily the morbid condition of autism and attention deficit hyperactivity disorder. We use a population based epidemiological design to inform on disease prevalence, environmental risk factors and familial disposition for mental health disorders and a case control study design to map the functional effects across behavioral and neurophysiological traits of the 22q11 deletion in a recruited sample of Danish individuals.
Identification of predictive pre-morbid clinical, cognitive, functional and structural brain alterations in 22q11 deletion carriers may alter current clinical practice from symptomatic therapy of manifest mental illness into early intervention strategies, which may also be applicable to at risk subjects without known etiology. Hopefully new insights into the biological disease mechanisms, which are mandatory for novel drug developments, can improve the outcome of the pharmacological interventions in psychiatry.
Mots-clé
Attention Deficit Disorder with Hyperactivity/genetics, Autistic Disorder/genetics, Case-Control Studies, Child, Child Health Services, Chromosome Aberrations, Chromosomes, Human, Pair 22, Denmark, Humans, Mental Health Services, Research Design, Schizophrenia/genetics
Pubmed
Open Access
Oui
Création de la notice
14/02/2019 10:20
Dernière modification de la notice
20/08/2019 15:25
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