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Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease?

Identifieur interne : 003027 ( PascalFrancis/Corpus ); précédent : 003026; suivant : 003028

Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease?

Auteurs : Franck Hansmannel ; Corinne Lendon ; Florence Pasquier ; Julie Dumont ; Didier Hannequin ; Julien Chapuis ; Geoffroy Laumet ; Anne-Marie Ayral ; Daniela Galimberti ; Elio Scarpini ; Dominique Campion ; Philippe Amouyel ; Jean-Charles Lambert

Source :

RBID : Pascal:09-0082051

Descripteurs français

English descriptors

Abstract

Expression of ornithine transcarbamylase (OTC) is strongly induced in the brain of individuals suffering from Alzheimer's Disease (AD). Association studies in a population from northern France have revealed that two SNPs -389 G/A (rs5963409) and -241 A/G (rs5963411) located in the promoter of the OTC gene are associated with the risk of developing AD. In the present work, these association studies were extended to a population of 2113 AD cases and 1580 controls from northern France, western France, the United Kingdom and Italy. The rs5963409 minor allele was weakly but significantly associated with an increased risk of developing AD (OR = 1.19, p = 0.004). This association was independent of age and ApoE status. Our results support that the OTC gene may be a minor genetic determinant of AD.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0304-3940
A02 01      @0 NELED5
A03   1    @0 Neurosci. lett.
A05       @2 449
A06       @2 1
A08 01  1  ENG  @1 Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease?
A11 01  1    @1 HANSMANNEL (Franck)
A11 02  1    @1 LENDON (Corinne)
A11 03  1    @1 PASQUIER (Florence)
A11 04  1    @1 DUMONT (Julie)
A11 05  1    @1 HANNEQUIN (Didier)
A11 06  1    @1 CHAPUIS (Julien)
A11 07  1    @1 LAUMET (Geoffroy)
A11 08  1    @1 AYRAL (Anne-Marie)
A11 09  1    @1 GALIMBERTI (Daniela)
A11 10  1    @1 SCARPINI (Elio)
A11 11  1    @1 CAMPION (Dominique)
A11 12  1    @1 AMOUYEL (Philippe)
A11 13  1    @1 LAMBERT (Jean-Charles)
A14 01      @1 INSERM, U744, Institut Pasteur de Lille, Université de Lille @2 Lille @3 FRA @Z 1 aut. @Z 4 aut. @Z 6 aut. @Z 7 aut. @Z 8 aut. @Z 12 aut. @Z 13 aut.
A14 02      @1 Molecular Psychiatry Group, Queensland Institute of Medical Research @2 Brisbane @3 AUS @Z 2 aut.
A14 03      @1 EA2391, Department of Neurology, Memory Clinic, University Hospital of Lille @3 FRA @Z 3 aut.
A14 04      @1 INSERM U614, Faculty of Medicine of Rouen @3 FRA @Z 5 aut. @Z 11 aut.
A14 05      @1 Department of Neurological Sciences, University of Milan, Fondazione Ospedale Maggiore Policlinico @2 Milan @3 ITA @Z 9 aut. @Z 10 aut.
A20       @1 76-80
A21       @1 2009
A23 01      @0 ENG
A43 01      @1 INIST @2 17240 @5 354000185030790170
A44       @0 0000 @1 © 2009 INIST-CNRS. All rights reserved.
A45       @0 12 ref.
A47 01  1    @0 09-0082051
A60       @1 P @3 PR
A61       @0 A
A64 01  1    @0 Neuroscience letters
A66 01      @0 IRL
C01 01    ENG  @0 Expression of ornithine transcarbamylase (OTC) is strongly induced in the brain of individuals suffering from Alzheimer's Disease (AD). Association studies in a population from northern France have revealed that two SNPs -389 G/A (rs5963409) and -241 A/G (rs5963411) located in the promoter of the OTC gene are associated with the risk of developing AD. In the present work, these association studies were extended to a population of 2113 AD cases and 1580 controls from northern France, western France, the United Kingdom and Italy. The rs5963409 minor allele was weakly but significantly associated with an increased risk of developing AD (OR = 1.19, p = 0.004). This association was independent of age and ApoE status. Our results support that the OTC gene may be a minor genetic determinant of AD.
C02 01  X    @0 002A25
C02 02  X    @0 002B17G
C03 01  X  FRE  @0 Ornithine carbamoyltransferase @2 FE @5 01
C03 01  X  ENG  @0 Ornithine carbamoyltransferase @2 FE @5 01
C03 01  X  SPA  @0 Ornithine carbamoyltransferase @2 FE @5 01
C03 02  X  FRE  @0 Polymorphisme @5 02
C03 02  X  ENG  @0 Polymorphism @5 02
C03 02  X  SPA  @0 Polimorfismo @5 02
C03 03  X  FRE  @0 Urée @2 NK @2 FR @5 03
C03 03  X  ENG  @0 Urea @2 NK @2 FR @5 03
C03 03  X  SPA  @0 Urea @2 NK @2 FR @5 03
C03 04  X  FRE  @0 Démence d'Alzheimer @5 09
C03 04  X  ENG  @0 Alzheimer disease @5 09
C03 04  X  SPA  @0 Demencia Alzheimer @5 09
C07 01  X  FRE  @0 Transferases @2 FE
C07 01  X  ENG  @0 Transferases @2 FE
C07 01  X  SPA  @0 Transferases @2 FE
C07 02  X  FRE  @0 Enzyme @2 FE
C07 02  X  ENG  @0 Enzyme @2 FE
C07 02  X  SPA  @0 Enzima @2 FE
C07 03  X  FRE  @0 Maladie dégénérative @5 20
C07 03  X  ENG  @0 Degenerative disease @5 20
C07 03  X  SPA  @0 Enfermedad degenerativa @5 20
C07 04  X  FRE  @0 Pathologie du système nerveux @5 21
C07 04  X  ENG  @0 Nervous system diseases @5 21
C07 04  X  SPA  @0 Sistema nervioso patología @5 21
C07 05  X  FRE  @0 Pathologie de l'encéphale @5 22
C07 05  X  ENG  @0 Cerebral disorder @5 22
C07 05  X  SPA  @0 Encéfalo patología @5 22
C07 06  X  FRE  @0 Pathologie du système nerveux central @5 23
C07 06  X  ENG  @0 Central nervous system disease @5 23
C07 06  X  SPA  @0 Sistema nervosio central patología @5 23
N21       @1 061
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 09-0082051 INIST
ET : Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease?
AU : HANSMANNEL (Franck); LENDON (Corinne); PASQUIER (Florence); DUMONT (Julie); HANNEQUIN (Didier); CHAPUIS (Julien); LAUMET (Geoffroy); AYRAL (Anne-Marie); GALIMBERTI (Daniela); SCARPINI (Elio); CAMPION (Dominique); AMOUYEL (Philippe); LAMBERT (Jean-Charles)
AF : INSERM, U744, Institut Pasteur de Lille, Université de Lille/Lille/France (1 aut., 4 aut., 6 aut., 7 aut., 8 aut., 12 aut., 13 aut.); Molecular Psychiatry Group, Queensland Institute of Medical Research/Brisbane/Australie (2 aut.); EA2391, Department of Neurology, Memory Clinic, University Hospital of Lille/France (3 aut.); INSERM U614, Faculty of Medicine of Rouen/France (5 aut., 11 aut.); Department of Neurological Sciences, University of Milan, Fondazione Ospedale Maggiore Policlinico/Milan/Italie (9 aut., 10 aut.)
DT : Publication en série; Papier de recherche; Niveau analytique
SO : Neuroscience letters; ISSN 0304-3940; Coden NELED5; Irlande; Da. 2009; Vol. 449; No. 1; Pp. 76-80; Bibl. 12 ref.
LA : Anglais
EA : Expression of ornithine transcarbamylase (OTC) is strongly induced in the brain of individuals suffering from Alzheimer's Disease (AD). Association studies in a population from northern France have revealed that two SNPs -389 G/A (rs5963409) and -241 A/G (rs5963411) located in the promoter of the OTC gene are associated with the risk of developing AD. In the present work, these association studies were extended to a population of 2113 AD cases and 1580 controls from northern France, western France, the United Kingdom and Italy. The rs5963409 minor allele was weakly but significantly associated with an increased risk of developing AD (OR = 1.19, p = 0.004). This association was independent of age and ApoE status. Our results support that the OTC gene may be a minor genetic determinant of AD.
CC : 002A25; 002B17G
FD : Ornithine carbamoyltransferase; Polymorphisme; Urée; Démence d'Alzheimer
FG : Transferases; Enzyme; Maladie dégénérative; Pathologie du système nerveux; Pathologie de l'encéphale; Pathologie du système nerveux central
ED : Ornithine carbamoyltransferase; Polymorphism; Urea; Alzheimer disease
EG : Transferases; Enzyme; Degenerative disease; Nervous system diseases; Cerebral disorder; Central nervous system disease
SD : Ornithine carbamoyltransferase; Polimorfismo; Urea; Demencia Alzheimer
LO : INIST-17240.354000185030790170
ID : 09-0082051

Links to Exploration step

Pascal:09-0082051

Le document en format XML

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<div type="abstract" xml:lang="en">Expression of ornithine transcarbamylase (OTC) is strongly induced in the brain of individuals suffering from Alzheimer's Disease (AD). Association studies in a population from northern France have revealed that two SNPs -389 G/A (rs5963409) and -241 A/G (rs5963411) located in the promoter of the OTC gene are associated with the risk of developing AD. In the present work, these association studies were extended to a population of 2113 AD cases and 1580 controls from northern France, western France, the United Kingdom and Italy. The rs5963409 minor allele was weakly but significantly associated with an increased risk of developing AD (OR = 1.19, p = 0.004). This association was independent of age and ApoE status. Our results support that the OTC gene may be a minor genetic determinant of AD.</div>
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<ET>Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease?</ET>
<AU>HANSMANNEL (Franck); LENDON (Corinne); PASQUIER (Florence); DUMONT (Julie); HANNEQUIN (Didier); CHAPUIS (Julien); LAUMET (Geoffroy); AYRAL (Anne-Marie); GALIMBERTI (Daniela); SCARPINI (Elio); CAMPION (Dominique); AMOUYEL (Philippe); LAMBERT (Jean-Charles)</AU>
<AF>INSERM, U744, Institut Pasteur de Lille, Université de Lille/Lille/France (1 aut., 4 aut., 6 aut., 7 aut., 8 aut., 12 aut., 13 aut.); Molecular Psychiatry Group, Queensland Institute of Medical Research/Brisbane/Australie (2 aut.); EA2391, Department of Neurology, Memory Clinic, University Hospital of Lille/France (3 aut.); INSERM U614, Faculty of Medicine of Rouen/France (5 aut., 11 aut.); Department of Neurological Sciences, University of Milan, Fondazione Ospedale Maggiore Policlinico/Milan/Italie (9 aut., 10 aut.)</AF>
<DT>Publication en série; Papier de recherche; Niveau analytique</DT>
<SO>Neuroscience letters; ISSN 0304-3940; Coden NELED5; Irlande; Da. 2009; Vol. 449; No. 1; Pp. 76-80; Bibl. 12 ref.</SO>
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<EA>Expression of ornithine transcarbamylase (OTC) is strongly induced in the brain of individuals suffering from Alzheimer's Disease (AD). Association studies in a population from northern France have revealed that two SNPs -389 G/A (rs5963409) and -241 A/G (rs5963411) located in the promoter of the OTC gene are associated with the risk of developing AD. In the present work, these association studies were extended to a population of 2113 AD cases and 1580 controls from northern France, western France, the United Kingdom and Italy. The rs5963409 minor allele was weakly but significantly associated with an increased risk of developing AD (OR = 1.19, p = 0.004). This association was independent of age and ApoE status. Our results support that the OTC gene may be a minor genetic determinant of AD.</EA>
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