Genetic imbalance in patients with cervical ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
Genetic imbalance in patients with cervical artery dissection
Auteur(s) :
Grond-Ginsbach, Caspar [Auteur]
Chen, Bowang [Auteur]
Krawczak, Michael [Auteur]
Pjontek, Rastislav [Auteur]
Ginsbach, Philip [Auteur]
Jiang, Yanxiang [Auteur]
Abboud, Sherine [Auteur]
Arnold, Marie-Luise [Auteur]
Bersano, Anna [Auteur]
Brandt, Tobias [Auteur]
Caso, Valeria [Auteur]
Debette, Stéphanie [Auteur]
Dichgans, Martin [Auteur]
Gschwendtner, Andreas [Auteur]
Giacalone, Giacomo [Auteur]
Martin, Juan-Jose [Auteur]
Metso, Antti J. [Auteur]
Metso, Tiina M. [Auteur]
Grau, Armin J. [Auteur]
Kloss, Manja [Auteur]
Lichy, Christoph [Auteur]
Pezzini, Alessandro [Auteur]
Traenka, Christopher [Auteur]
Schreiber, Stefan [Auteur]
Thijs, Vincent N. S. [Auteur]
Touze, Emmanuel [Auteur]
Del Zotto, Elisabetta [Auteur]
Tatlisumak, Turgut [Auteur]
LEYS, Didier [Auteur]
Troubles cognitifs dégénératifs et vasculaires - U 1171 - EA 1046 [TCDV]
Troubles cognitifs dégénératifs et vasculaires - U1171
Lyrer, Philippe A. [Auteur]
Engelter, Stefan T. [Auteur]
Chen, Bowang [Auteur]
Krawczak, Michael [Auteur]
Pjontek, Rastislav [Auteur]
Ginsbach, Philip [Auteur]
Jiang, Yanxiang [Auteur]
Abboud, Sherine [Auteur]
Arnold, Marie-Luise [Auteur]
Bersano, Anna [Auteur]
Brandt, Tobias [Auteur]
Caso, Valeria [Auteur]
Debette, Stéphanie [Auteur]
Dichgans, Martin [Auteur]
Gschwendtner, Andreas [Auteur]
Giacalone, Giacomo [Auteur]
Martin, Juan-Jose [Auteur]
Metso, Antti J. [Auteur]
Metso, Tiina M. [Auteur]
Grau, Armin J. [Auteur]
Kloss, Manja [Auteur]
Lichy, Christoph [Auteur]
Pezzini, Alessandro [Auteur]
Traenka, Christopher [Auteur]
Schreiber, Stefan [Auteur]
Thijs, Vincent N. S. [Auteur]
Touze, Emmanuel [Auteur]
Del Zotto, Elisabetta [Auteur]
Tatlisumak, Turgut [Auteur]
LEYS, Didier [Auteur]
Troubles cognitifs dégénératifs et vasculaires - U 1171 - EA 1046 [TCDV]
Troubles cognitifs dégénératifs et vasculaires - U1171
Lyrer, Philippe A. [Auteur]
Engelter, Stefan T. [Auteur]
Titre de la revue :
Current genomics
Nom court de la revue :
Curr. Genomics
Numéro :
18
Pagination :
206-213
Date de publication :
2017-01-01
ISSN :
1389-2029
Mot(s)-clé(s) en anglais :
Cardiovascular system development
Copy number variation
Cervical artery dissection
Rare genetic variation
Copy number variation
Cervical artery dissection
Rare genetic variation
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
BACKGROUND: Genetic and environmental risk factors are assumed to contribute to the susceptibility to cervical artery dissection (CeAD). To explore the role of genetic imbalance in the etiology of CeAD, copy number variants ...
Lire la suite >BACKGROUND: Genetic and environmental risk factors are assumed to contribute to the susceptibility to cervical artery dissection (CeAD). To explore the role of genetic imbalance in the etiology of CeAD, copy number variants (CNVs) were identified in high-density microarrays samples from the multicenter CADISP (Cervical Artery Dissection and Ischemic Stroke Patients) study and from control subjects from the CADISP study and the German PopGen biobank. Microarray data from 833 CeAD patients and 2040 control subjects (565 subjects with ischemic stroke due to causes different from CeAD and 1475 disease-free individuals) were analyzed. Rare genic CNVs were equally frequent in CeAD-patients (16.4%; n=137) and in control subjects (17.0%; n=346) but differed with respect to their genetic content. Compared to control subjects, CNVs from CeAD patients were enriched for genes associated with muscle organ development and cell differentiation, which suggests a possible association with arterial development. CNVs affecting cardiovascular system development were more common in CeAD patients than in control subjects (p=0.003; odds ratio (OR) =2.5; 95% confidence interval (95% CI) =1.4-4.5) and more common in patients with a familial history of CeAD than in those with sporadic CeAD (p=0.036; OR=11.2; 95% CI=1.2-107). CONCLUSIONS: The findings suggest that rare genetic imbalance affecting cardiovascular system development may contribute to the risk of CeAD. Validation of these findings in independent study populations is warranted.Lire moins >
Lire la suite >BACKGROUND: Genetic and environmental risk factors are assumed to contribute to the susceptibility to cervical artery dissection (CeAD). To explore the role of genetic imbalance in the etiology of CeAD, copy number variants (CNVs) were identified in high-density microarrays samples from the multicenter CADISP (Cervical Artery Dissection and Ischemic Stroke Patients) study and from control subjects from the CADISP study and the German PopGen biobank. Microarray data from 833 CeAD patients and 2040 control subjects (565 subjects with ischemic stroke due to causes different from CeAD and 1475 disease-free individuals) were analyzed. Rare genic CNVs were equally frequent in CeAD-patients (16.4%; n=137) and in control subjects (17.0%; n=346) but differed with respect to their genetic content. Compared to control subjects, CNVs from CeAD patients were enriched for genes associated with muscle organ development and cell differentiation, which suggests a possible association with arterial development. CNVs affecting cardiovascular system development were more common in CeAD patients than in control subjects (p=0.003; odds ratio (OR) =2.5; 95% confidence interval (95% CI) =1.4-4.5) and more common in patients with a familial history of CeAD than in those with sporadic CeAD (p=0.036; OR=11.2; 95% CI=1.2-107). CONCLUSIONS: The findings suggest that rare genetic imbalance affecting cardiovascular system development may contribute to the risk of CeAD. Validation of these findings in independent study populations is warranted.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
CHU Lille
CNRS
Inserm
Université de Lille
CNRS
Inserm
Université de Lille
Collections :
Équipe(s) de recherche :
Troubles cognitifs dégénératifs et vasculaires
Date de dépôt :
2019-11-27T14:31:53Z