Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease?
Identifieur interne : 003027 ( PascalFrancis/Corpus ); précédent : 003026; suivant : 003028Is 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 LambertSource :
- Neuroscience letters [ 0304-3940 ] ; 2009.
Descripteurs français
- Pascal (Inist)
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 |
|
---|
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:09-0082051Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease?</title>
<author><name sortKey="Hansmannel, Franck" sort="Hansmannel, Franck" uniqKey="Hansmannel F" first="Franck" last="Hansmannel">Franck Hansmannel</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Lendon, Corinne" sort="Lendon, Corinne" uniqKey="Lendon C" first="Corinne" last="Lendon">Corinne Lendon</name>
<affiliation><inist:fA14 i1="02"><s1>Molecular Psychiatry Group, Queensland Institute of Medical Research</s1>
<s2>Brisbane</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Pasquier, Florence" sort="Pasquier, Florence" uniqKey="Pasquier F" first="Florence" last="Pasquier">Florence Pasquier</name>
<affiliation><inist:fA14 i1="03"><s1>EA2391, Department of Neurology, Memory Clinic, University Hospital of Lille</s1>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Dumont, Julie" sort="Dumont, Julie" uniqKey="Dumont J" first="Julie" last="Dumont">Julie Dumont</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Hannequin, Didier" sort="Hannequin, Didier" uniqKey="Hannequin D" first="Didier" last="Hannequin">Didier Hannequin</name>
<affiliation><inist:fA14 i1="04"><s1>INSERM U614, Faculty of Medicine of Rouen</s1>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Chapuis, Julien" sort="Chapuis, Julien" uniqKey="Chapuis J" first="Julien" last="Chapuis">Julien Chapuis</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Laumet, Geoffroy" sort="Laumet, Geoffroy" uniqKey="Laumet G" first="Geoffroy" last="Laumet">Geoffroy Laumet</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Ayral, Anne Marie" sort="Ayral, Anne Marie" uniqKey="Ayral A" first="Anne-Marie" last="Ayral">Anne-Marie Ayral</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Galimberti, Daniela" sort="Galimberti, Daniela" uniqKey="Galimberti D" first="Daniela" last="Galimberti">Daniela Galimberti</name>
<affiliation><inist:fA14 i1="05"><s1>Department of Neurological Sciences, University of Milan, Fondazione Ospedale Maggiore Policlinico</s1>
<s2>Milan</s2>
<s3>ITA</s3>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Scarpini, Elio" sort="Scarpini, Elio" uniqKey="Scarpini E" first="Elio" last="Scarpini">Elio Scarpini</name>
<affiliation><inist:fA14 i1="05"><s1>Department of Neurological Sciences, University of Milan, Fondazione Ospedale Maggiore Policlinico</s1>
<s2>Milan</s2>
<s3>ITA</s3>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Campion, Dominique" sort="Campion, Dominique" uniqKey="Campion D" first="Dominique" last="Campion">Dominique Campion</name>
<affiliation><inist:fA14 i1="04"><s1>INSERM U614, Faculty of Medicine of Rouen</s1>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Amouyel, Philippe" sort="Amouyel, Philippe" uniqKey="Amouyel P" first="Philippe" last="Amouyel">Philippe Amouyel</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Lambert, Jean Charles" sort="Lambert, Jean Charles" uniqKey="Lambert J" first="Jean-Charles" last="Lambert">Jean-Charles Lambert</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">09-0082051</idno>
<date when="2009">2009</date>
<idno type="stanalyst">PASCAL 09-0082051 INIST</idno>
<idno type="RBID">Pascal:09-0082051</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">003027</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease?</title>
<author><name sortKey="Hansmannel, Franck" sort="Hansmannel, Franck" uniqKey="Hansmannel F" first="Franck" last="Hansmannel">Franck Hansmannel</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Lendon, Corinne" sort="Lendon, Corinne" uniqKey="Lendon C" first="Corinne" last="Lendon">Corinne Lendon</name>
<affiliation><inist:fA14 i1="02"><s1>Molecular Psychiatry Group, Queensland Institute of Medical Research</s1>
<s2>Brisbane</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Pasquier, Florence" sort="Pasquier, Florence" uniqKey="Pasquier F" first="Florence" last="Pasquier">Florence Pasquier</name>
<affiliation><inist:fA14 i1="03"><s1>EA2391, Department of Neurology, Memory Clinic, University Hospital of Lille</s1>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Dumont, Julie" sort="Dumont, Julie" uniqKey="Dumont J" first="Julie" last="Dumont">Julie Dumont</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Hannequin, Didier" sort="Hannequin, Didier" uniqKey="Hannequin D" first="Didier" last="Hannequin">Didier Hannequin</name>
<affiliation><inist:fA14 i1="04"><s1>INSERM U614, Faculty of Medicine of Rouen</s1>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Chapuis, Julien" sort="Chapuis, Julien" uniqKey="Chapuis J" first="Julien" last="Chapuis">Julien Chapuis</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Laumet, Geoffroy" sort="Laumet, Geoffroy" uniqKey="Laumet G" first="Geoffroy" last="Laumet">Geoffroy Laumet</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Ayral, Anne Marie" sort="Ayral, Anne Marie" uniqKey="Ayral A" first="Anne-Marie" last="Ayral">Anne-Marie Ayral</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Galimberti, Daniela" sort="Galimberti, Daniela" uniqKey="Galimberti D" first="Daniela" last="Galimberti">Daniela Galimberti</name>
<affiliation><inist:fA14 i1="05"><s1>Department of Neurological Sciences, University of Milan, Fondazione Ospedale Maggiore Policlinico</s1>
<s2>Milan</s2>
<s3>ITA</s3>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Scarpini, Elio" sort="Scarpini, Elio" uniqKey="Scarpini E" first="Elio" last="Scarpini">Elio Scarpini</name>
<affiliation><inist:fA14 i1="05"><s1>Department of Neurological Sciences, University of Milan, Fondazione Ospedale Maggiore Policlinico</s1>
<s2>Milan</s2>
<s3>ITA</s3>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Campion, Dominique" sort="Campion, Dominique" uniqKey="Campion D" first="Dominique" last="Campion">Dominique Campion</name>
<affiliation><inist:fA14 i1="04"><s1>INSERM U614, Faculty of Medicine of Rouen</s1>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Amouyel, Philippe" sort="Amouyel, Philippe" uniqKey="Amouyel P" first="Philippe" last="Amouyel">Philippe Amouyel</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Lambert, Jean Charles" sort="Lambert, Jean Charles" uniqKey="Lambert J" first="Jean-Charles" last="Lambert">Jean-Charles Lambert</name>
<affiliation><inist:fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">Neuroscience letters</title>
<title level="j" type="abbreviated">Neurosci. lett.</title>
<idno type="ISSN">0304-3940</idno>
<imprint><date when="2009">2009</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Neuroscience letters</title>
<title level="j" type="abbreviated">Neurosci. lett.</title>
<idno type="ISSN">0304-3940</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alzheimer disease</term>
<term>Ornithine carbamoyltransferase</term>
<term>Polymorphism</term>
<term>Urea</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Ornithine carbamoyltransferase</term>
<term>Polymorphisme</term>
<term>Urée</term>
<term>Démence d'Alzheimer</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><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>
</front>
</TEI>
<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0304-3940</s0>
</fA01>
<fA02 i1="01"><s0>NELED5</s0>
</fA02>
<fA03 i2="1"><s0>Neurosci. lett.</s0>
</fA03>
<fA05><s2>449</s2>
</fA05>
<fA06><s2>1</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease?</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>HANSMANNEL (Franck)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>LENDON (Corinne)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>PASQUIER (Florence)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>DUMONT (Julie)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>HANNEQUIN (Didier)</s1>
</fA11>
<fA11 i1="06" i2="1"><s1>CHAPUIS (Julien)</s1>
</fA11>
<fA11 i1="07" i2="1"><s1>LAUMET (Geoffroy)</s1>
</fA11>
<fA11 i1="08" i2="1"><s1>AYRAL (Anne-Marie)</s1>
</fA11>
<fA11 i1="09" i2="1"><s1>GALIMBERTI (Daniela)</s1>
</fA11>
<fA11 i1="10" i2="1"><s1>SCARPINI (Elio)</s1>
</fA11>
<fA11 i1="11" i2="1"><s1>CAMPION (Dominique)</s1>
</fA11>
<fA11 i1="12" i2="1"><s1>AMOUYEL (Philippe)</s1>
</fA11>
<fA11 i1="13" i2="1"><s1>LAMBERT (Jean-Charles)</s1>
</fA11>
<fA14 i1="01"><s1>INSERM, U744, Institut Pasteur de Lille, Université de Lille</s1>
<s2>Lille</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Molecular Psychiatry Group, Queensland Institute of Medical Research</s1>
<s2>Brisbane</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>EA2391, Department of Neurology, Memory Clinic, University Hospital of Lille</s1>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="04"><s1>INSERM U614, Faculty of Medicine of Rouen</s1>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
<sZ>11 aut.</sZ>
</fA14>
<fA14 i1="05"><s1>Department of Neurological Sciences, University of Milan, Fondazione Ospedale Maggiore Policlinico</s1>
<s2>Milan</s2>
<s3>ITA</s3>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
</fA14>
<fA20><s1>76-80</s1>
</fA20>
<fA21><s1>2009</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>17240</s2>
<s5>354000185030790170</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2009 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>12 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>09-0082051</s0>
</fA47>
<fA60><s1>P</s1>
<s3>PR</s3>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Neuroscience letters</s0>
</fA64>
<fA66 i1="01"><s0>IRL</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>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.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002A25</s0>
</fC02>
<fC02 i1="02" i2="X"><s0>002B17G</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Ornithine carbamoyltransferase</s0>
<s2>FE</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Ornithine carbamoyltransferase</s0>
<s2>FE</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Ornithine carbamoyltransferase</s0>
<s2>FE</s2>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Polymorphisme</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Polymorphism</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Polimorfismo</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Urée</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Urea</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Urea</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Démence d'Alzheimer</s0>
<s5>09</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Alzheimer disease</s0>
<s5>09</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Demencia Alzheimer</s0>
<s5>09</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Transferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Transferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Transferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Enzima</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>20</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>20</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>20</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Pathologie du système nerveux</s0>
<s5>21</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>21</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>21</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Pathologie de l'encéphale</s0>
<s5>22</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>22</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>22</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Pathologie du système nerveux central</s0>
<s5>23</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>23</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>23</s5>
</fC07>
<fN21><s1>061</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
<server><NO>PASCAL 09-0082051 INIST</NO>
<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>
<LA>Anglais</LA>
<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>
<CC>002A25; 002B17G</CC>
<FD>Ornithine carbamoyltransferase; Polymorphisme; Urée; Démence d'Alzheimer</FD>
<FG>Transferases; Enzyme; Maladie dégénérative; Pathologie du système nerveux; Pathologie de l'encéphale; Pathologie du système nerveux central</FG>
<ED>Ornithine carbamoyltransferase; Polymorphism; Urea; Alzheimer disease</ED>
<EG>Transferases; Enzyme; Degenerative disease; Nervous system diseases; Cerebral disorder; Central nervous system disease</EG>
<SD>Ornithine carbamoyltransferase; Polimorfismo; Urea; Demencia Alzheimer</SD>
<LO>INIST-17240.354000185030790170</LO>
<ID>09-0082051</ID>
</server>
</inist>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Asie/explor/AustralieFrV1/Data/PascalFrancis/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003027 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Corpus/biblio.hfd -nk 003027 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Asie |area= AustralieFrV1 |flux= PascalFrancis |étape= Corpus |type= RBID |clé= Pascal:09-0082051 |texte= Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease? }}
This area was generated with Dilib version V0.6.33. |