Serveur d'exploration sur les dispositifs haptiques

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Is impaired set-shifting an endophenotype of anorexia nervosa?

Identifieur interne : 000C83 ( PascalFrancis/Corpus ); précédent : 000C82; suivant : 000C84

Is impaired set-shifting an endophenotype of anorexia nervosa?

Auteurs : Joanna Holliday ; Kate Tchanturia ; Sabine Landau ; David Collier ; Janet Treasure

Source :

RBID : Pascal:06-0356604

Descripteurs français

English descriptors

Abstract

Objective: Set-shifting difficulties have been reported in subjects with anorexia nervosa and appear to persist after recovery; therefore, they may be endophenotypic traits. The goals of this study were to investigate whether set-shifting difficulties are familial by examining discordant sister-pairs in comparison with healthy unrelated women and to replicate, with a broader battery, the lack of influence of an acute illness state on neuropsychological performance. Method: Forty-seven pairs of sisters discordant for anorexia nervosa and 47 healthy unrelated women who were comparable in age and IQ completed neuropsychological tasks selected to assess set-shifting ability. Analyses of variance with standard errors that are robust against correlations within family clusters were used to compare the groups. Results were adjusted for obsessive-compulsive, anxiety, and depression symptoms. Subjects with acute (N=24) and fully remitted (N= 23) anorexia nervosa were compared to assess state versus trait effects. Results: Sisters with and without anorexia nervosa took significantly longer than unrelated healthy women to shift their cognitive set (CatBat task) and demonstrated greater perceptual rigidity (Haptic Illusion task) but did not differ significantly from each other. Women with anorexia nervosa were slower than other groups on Trail Making tasks. Women who had fully recovered from anorexia nervosa made significantly fewer errors than those with acute anorexia nervosa on the Trail Making alphabet task, but these subgroups did not differ on other measures. Conclusions: Both affected and unaffected sisters had more set-shifting difficulties than unrelated healthy women. This finding, together with the replicated finding that set-shifting difficulties persist after recovery, suggests that set-shifting difficulties are trait characteristics and may inform the search for the endophenotype in anorexia nervosa.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0002-953X
A02 01      @0 AJPSAO
A03   1    @0 Am. j. psychiatr.
A05       @2 162
A06       @2 12
A08 01  1  ENG  @1 Is impaired set-shifting an endophenotype of anorexia nervosa?
A11 01  1    @1 HOLLIDAY (Joanna)
A11 02  1    @1 TCHANTURIA (Kate)
A11 03  1    @1 LANDAU (Sabine)
A11 04  1    @1 COLLIER (David)
A11 05  1    @1 TREASURE (Janet)
A14 01      @1 Division of Psychological Medicine, the Social, Genetic and Developmental Psychiatry Research Centre, and the Department of Biostatistics and Computing, Institute of Psychiatry, King's College London (KCL) @2 London @3 GBR
A14 02      @1 KCL Department of Academic Psychiatry, Guy's, King's and St. Thomas's Medical School @2 London @3 GBR
A20       @1 2269-2275
A21       @1 2005
A23 01      @0 ENG
A43 01      @1 INIST @2 3283 @5 354000134431150070
A44       @0 0000 @1 © 2006 INIST-CNRS. All rights reserved.
A45       @0 35 ref.
A47 01  1    @0 06-0356604
A60       @1 P
A61       @0 A
A64 01  1    @0 The American journal of psychiatry
A66 01      @0 USA
C01 01    ENG  @0 Objective: Set-shifting difficulties have been reported in subjects with anorexia nervosa and appear to persist after recovery; therefore, they may be endophenotypic traits. The goals of this study were to investigate whether set-shifting difficulties are familial by examining discordant sister-pairs in comparison with healthy unrelated women and to replicate, with a broader battery, the lack of influence of an acute illness state on neuropsychological performance. Method: Forty-seven pairs of sisters discordant for anorexia nervosa and 47 healthy unrelated women who were comparable in age and IQ completed neuropsychological tasks selected to assess set-shifting ability. Analyses of variance with standard errors that are robust against correlations within family clusters were used to compare the groups. Results were adjusted for obsessive-compulsive, anxiety, and depression symptoms. Subjects with acute (N=24) and fully remitted (N= 23) anorexia nervosa were compared to assess state versus trait effects. Results: Sisters with and without anorexia nervosa took significantly longer than unrelated healthy women to shift their cognitive set (CatBat task) and demonstrated greater perceptual rigidity (Haptic Illusion task) but did not differ significantly from each other. Women with anorexia nervosa were slower than other groups on Trail Making tasks. Women who had fully recovered from anorexia nervosa made significantly fewer errors than those with acute anorexia nervosa on the Trail Making alphabet task, but these subgroups did not differ on other measures. Conclusions: Both affected and unaffected sisters had more set-shifting difficulties than unrelated healthy women. This finding, together with the replicated finding that set-shifting difficulties persist after recovery, suggests that set-shifting difficulties are trait characteristics and may inform the search for the endophenotype in anorexia nervosa.
C02 01  X    @0 002B18C01A
C03 01  X  FRE  @0 Anorexie mentale @5 01
C03 01  X  ENG  @0 Anorexia nervosa @5 01
C03 01  X  SPA  @0 Anorexia mental @5 01
C03 02  X  FRE  @0 Aigu @5 02
C03 02  X  ENG  @0 Acute @5 02
C03 02  X  SPA  @0 Agudo @5 02
C03 03  X  FRE  @0 Rémission @5 03
C03 03  X  ENG  @0 Remission @5 03
C03 03  X  SPA  @0 Remisión @5 03
C03 04  X  FRE  @0 Etude comparative @5 04
C03 04  X  ENG  @0 Comparative study @5 04
C03 04  X  SPA  @0 Estudio comparativo @5 04
C03 05  X  FRE  @0 Fratrie @5 05
C03 05  X  ENG  @0 Sibling @5 05
C03 05  X  SPA  @0 Hermandad @5 05
C03 06  X  FRE  @0 Aptitude intellectuelle @5 06
C03 06  X  ENG  @0 Intellectual ability @5 06
C03 06  X  SPA  @0 Aptitud intelectual @5 06
C03 07  X  FRE  @0 Flexibilité intellectuelle @5 07
C03 07  X  ENG  @0 Intellectual flexibility @5 07
C03 07  X  SPA  @0 Flexibilidad intelectual @5 07
C03 08  X  FRE  @0 Traitement information @5 08
C03 08  X  ENG  @0 Information processing @5 08
C03 08  X  SPA  @0 Procesamiento información @5 08
C03 09  X  FRE  @0 Fonction exécutive @5 09
C03 09  X  ENG  @0 Executive function @5 09
C03 09  X  SPA  @0 Función ejecutiva @5 09
C03 10  X  FRE  @0 Neuropsychologie @5 10
C03 10  X  ENG  @0 Neuropsychologia @5 10
C03 10  X  SPA  @0 Neurosicología @5 10
C03 11  X  FRE  @0 Cognition @5 11
C03 11  X  ENG  @0 Cognition @5 11
C03 11  X  SPA  @0 Cognición @5 11
C03 12  X  FRE  @0 Marqueur biologique @5 12
C03 12  X  ENG  @0 Biological marker @5 12
C03 12  X  SPA  @0 Marcador biológico @5 12
C03 13  X  FRE  @0 Génétique @5 13
C03 13  X  ENG  @0 Genetics @5 13
C03 13  X  SPA  @0 Genética @5 13
C03 14  X  FRE  @0 Déterminisme génétique @5 17
C03 14  X  ENG  @0 Genetic determinism @5 17
C03 14  X  SPA  @0 Determinismo genético @5 17
C03 15  X  FRE  @0 Etude familiale @5 18
C03 15  X  ENG  @0 Family study @5 18
C03 15  X  SPA  @0 Estudio familiar @5 18
C03 16  X  FRE  @0 Etude multicentrique @5 19
C03 16  X  ENG  @0 Multicenter study @5 19
C03 16  X  SPA  @0 Estudio multicéntrico @5 19
C03 17  X  FRE  @0 Femelle @5 20
C03 17  X  ENG  @0 Female @5 20
C03 17  X  SPA  @0 Hembra @5 20
C03 18  X  FRE  @0 Homme @5 21
C03 18  X  ENG  @0 Human @5 21
C03 18  X  SPA  @0 Hombre @5 21
C03 19  X  FRE  @0 Endophénotype @4 CD @5 96
C03 19  X  ENG  @0 Endophenotype @4 CD @5 96
C03 20  X  FRE  @0 Parenté premier degré @4 CD @5 97
C03 20  X  ENG  @0 First degree relatives @4 CD @5 97
C07 01  X  FRE  @0 Trouble comportement alimentaire @5 37
C07 01  X  ENG  @0 Eating disorder @5 37
C07 01  X  SPA  @0 Trastorno conducta alimentaria @5 37
N21       @1 240
N44 01      @1 PSI
N82       @1 PSI

Format Inist (serveur)

NO : PASCAL 06-0356604 INIST
ET : Is impaired set-shifting an endophenotype of anorexia nervosa?
AU : HOLLIDAY (Joanna); TCHANTURIA (Kate); LANDAU (Sabine); COLLIER (David); TREASURE (Janet)
AF : Division of Psychological Medicine, the Social, Genetic and Developmental Psychiatry Research Centre, and the Department of Biostatistics and Computing, Institute of Psychiatry, King's College London (KCL)/London/Royaume-Uni; KCL Department of Academic Psychiatry, Guy's, King's and St. Thomas's Medical School/London/Royaume-Uni
DT : Publication en série; Niveau analytique
SO : The American journal of psychiatry; ISSN 0002-953X; Coden AJPSAO; Etats-Unis; Da. 2005; Vol. 162; No. 12; Pp. 2269-2275; Bibl. 35 ref.
LA : Anglais
EA : Objective: Set-shifting difficulties have been reported in subjects with anorexia nervosa and appear to persist after recovery; therefore, they may be endophenotypic traits. The goals of this study were to investigate whether set-shifting difficulties are familial by examining discordant sister-pairs in comparison with healthy unrelated women and to replicate, with a broader battery, the lack of influence of an acute illness state on neuropsychological performance. Method: Forty-seven pairs of sisters discordant for anorexia nervosa and 47 healthy unrelated women who were comparable in age and IQ completed neuropsychological tasks selected to assess set-shifting ability. Analyses of variance with standard errors that are robust against correlations within family clusters were used to compare the groups. Results were adjusted for obsessive-compulsive, anxiety, and depression symptoms. Subjects with acute (N=24) and fully remitted (N= 23) anorexia nervosa were compared to assess state versus trait effects. Results: Sisters with and without anorexia nervosa took significantly longer than unrelated healthy women to shift their cognitive set (CatBat task) and demonstrated greater perceptual rigidity (Haptic Illusion task) but did not differ significantly from each other. Women with anorexia nervosa were slower than other groups on Trail Making tasks. Women who had fully recovered from anorexia nervosa made significantly fewer errors than those with acute anorexia nervosa on the Trail Making alphabet task, but these subgroups did not differ on other measures. Conclusions: Both affected and unaffected sisters had more set-shifting difficulties than unrelated healthy women. This finding, together with the replicated finding that set-shifting difficulties persist after recovery, suggests that set-shifting difficulties are trait characteristics and may inform the search for the endophenotype in anorexia nervosa.
CC : 002B18C01A
FD : Anorexie mentale; Aigu; Rémission; Etude comparative; Fratrie; Aptitude intellectuelle; Flexibilité intellectuelle; Traitement information; Fonction exécutive; Neuropsychologie; Cognition; Marqueur biologique; Génétique; Déterminisme génétique; Etude familiale; Etude multicentrique; Femelle; Homme; Endophénotype; Parenté premier degré
FG : Trouble comportement alimentaire
ED : Anorexia nervosa; Acute; Remission; Comparative study; Sibling; Intellectual ability; Intellectual flexibility; Information processing; Executive function; Neuropsychologia; Cognition; Biological marker; Genetics; Genetic determinism; Family study; Multicenter study; Female; Human; Endophenotype; First degree relatives
EG : Eating disorder
SD : Anorexia mental; Agudo; Remisión; Estudio comparativo; Hermandad; Aptitud intelectual; Flexibilidad intelectual; Procesamiento información; Función ejecutiva; Neurosicología; Cognición; Marcador biológico; Genética; Determinismo genético; Estudio familiar; Estudio multicéntrico; Hembra; Hombre
LO : INIST-3283.354000134431150070
ID : 06-0356604

Links to Exploration step

Pascal:06-0356604

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en" level="a">Is impaired set-shifting an endophenotype of anorexia nervosa?</title>
<author>
<name sortKey="Holliday, Joanna" sort="Holliday, Joanna" uniqKey="Holliday J" first="Joanna" last="Holliday">Joanna Holliday</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Division of Psychological Medicine, the Social, Genetic and Developmental Psychiatry Research Centre, and the Department of Biostatistics and Computing, Institute of Psychiatry, King's College London (KCL)</s1>
<s2>London</s2>
<s3>GBR</s3>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="02">
<s1>KCL Department of Academic Psychiatry, Guy's, King's and St. Thomas's Medical School</s1>
<s2>London</s2>
<s3>GBR</s3>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Tchanturia, Kate" sort="Tchanturia, Kate" uniqKey="Tchanturia K" first="Kate" last="Tchanturia">Kate Tchanturia</name>
</author>
<author>
<name sortKey="Landau, Sabine" sort="Landau, Sabine" uniqKey="Landau S" first="Sabine" last="Landau">Sabine Landau</name>
</author>
<author>
<name sortKey="Collier, David" sort="Collier, David" uniqKey="Collier D" first="David" last="Collier">David Collier</name>
</author>
<author>
<name sortKey="Treasure, Janet" sort="Treasure, Janet" uniqKey="Treasure J" first="Janet" last="Treasure">Janet Treasure</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">INIST</idno>
<idno type="inist">06-0356604</idno>
<date when="2005">2005</date>
<idno type="stanalyst">PASCAL 06-0356604 INIST</idno>
<idno type="RBID">Pascal:06-0356604</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000C83</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a">Is impaired set-shifting an endophenotype of anorexia nervosa?</title>
<author>
<name sortKey="Holliday, Joanna" sort="Holliday, Joanna" uniqKey="Holliday J" first="Joanna" last="Holliday">Joanna Holliday</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Division of Psychological Medicine, the Social, Genetic and Developmental Psychiatry Research Centre, and the Department of Biostatistics and Computing, Institute of Psychiatry, King's College London (KCL)</s1>
<s2>London</s2>
<s3>GBR</s3>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="02">
<s1>KCL Department of Academic Psychiatry, Guy's, King's and St. Thomas's Medical School</s1>
<s2>London</s2>
<s3>GBR</s3>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Tchanturia, Kate" sort="Tchanturia, Kate" uniqKey="Tchanturia K" first="Kate" last="Tchanturia">Kate Tchanturia</name>
</author>
<author>
<name sortKey="Landau, Sabine" sort="Landau, Sabine" uniqKey="Landau S" first="Sabine" last="Landau">Sabine Landau</name>
</author>
<author>
<name sortKey="Collier, David" sort="Collier, David" uniqKey="Collier D" first="David" last="Collier">David Collier</name>
</author>
<author>
<name sortKey="Treasure, Janet" sort="Treasure, Janet" uniqKey="Treasure J" first="Janet" last="Treasure">Janet Treasure</name>
</author>
</analytic>
<series>
<title level="j" type="main">The American journal of psychiatry</title>
<title level="j" type="abbreviated">Am. j. psychiatr.</title>
<idno type="ISSN">0002-953X</idno>
<imprint>
<date when="2005">2005</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<title level="j" type="main">The American journal of psychiatry</title>
<title level="j" type="abbreviated">Am. j. psychiatr.</title>
<idno type="ISSN">0002-953X</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Acute</term>
<term>Anorexia nervosa</term>
<term>Biological marker</term>
<term>Cognition</term>
<term>Comparative study</term>
<term>Endophenotype</term>
<term>Executive function</term>
<term>Family study</term>
<term>Female</term>
<term>First degree relatives</term>
<term>Genetic determinism</term>
<term>Genetics</term>
<term>Human</term>
<term>Information processing</term>
<term>Intellectual ability</term>
<term>Intellectual flexibility</term>
<term>Multicenter study</term>
<term>Neuropsychologia</term>
<term>Remission</term>
<term>Sibling</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Anorexie mentale</term>
<term>Aigu</term>
<term>Rémission</term>
<term>Etude comparative</term>
<term>Fratrie</term>
<term>Aptitude intellectuelle</term>
<term>Flexibilité intellectuelle</term>
<term>Traitement information</term>
<term>Fonction exécutive</term>
<term>Neuropsychologie</term>
<term>Cognition</term>
<term>Marqueur biologique</term>
<term>Génétique</term>
<term>Déterminisme génétique</term>
<term>Etude familiale</term>
<term>Etude multicentrique</term>
<term>Femelle</term>
<term>Homme</term>
<term>Endophénotype</term>
<term>Parenté premier degré</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Objective: Set-shifting difficulties have been reported in subjects with anorexia nervosa and appear to persist after recovery; therefore, they may be endophenotypic traits. The goals of this study were to investigate whether set-shifting difficulties are familial by examining discordant sister-pairs in comparison with healthy unrelated women and to replicate, with a broader battery, the lack of influence of an acute illness state on neuropsychological performance. Method: Forty-seven pairs of sisters discordant for anorexia nervosa and 47 healthy unrelated women who were comparable in age and IQ completed neuropsychological tasks selected to assess set-shifting ability. Analyses of variance with standard errors that are robust against correlations within family clusters were used to compare the groups. Results were adjusted for obsessive-compulsive, anxiety, and depression symptoms. Subjects with acute (N=24) and fully remitted (N= 23) anorexia nervosa were compared to assess state versus trait effects. Results: Sisters with and without anorexia nervosa took significantly longer than unrelated healthy women to shift their cognitive set (CatBat task) and demonstrated greater perceptual rigidity (Haptic Illusion task) but did not differ significantly from each other. Women with anorexia nervosa were slower than other groups on Trail Making tasks. Women who had fully recovered from anorexia nervosa made significantly fewer errors than those with acute anorexia nervosa on the Trail Making alphabet task, but these subgroups did not differ on other measures. Conclusions: Both affected and unaffected sisters had more set-shifting difficulties than unrelated healthy women. This finding, together with the replicated finding that set-shifting difficulties persist after recovery, suggests that set-shifting difficulties are trait characteristics and may inform the search for the endophenotype in anorexia nervosa.</div>
</front>
</TEI>
<inist>
<standard h6="B">
<pA>
<fA01 i1="01" i2="1">
<s0>0002-953X</s0>
</fA01>
<fA02 i1="01">
<s0>AJPSAO</s0>
</fA02>
<fA03 i2="1">
<s0>Am. j. psychiatr.</s0>
</fA03>
<fA05>
<s2>162</s2>
</fA05>
<fA06>
<s2>12</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG">
<s1>Is impaired set-shifting an endophenotype of anorexia nervosa?</s1>
</fA08>
<fA11 i1="01" i2="1">
<s1>HOLLIDAY (Joanna)</s1>
</fA11>
<fA11 i1="02" i2="1">
<s1>TCHANTURIA (Kate)</s1>
</fA11>
<fA11 i1="03" i2="1">
<s1>LANDAU (Sabine)</s1>
</fA11>
<fA11 i1="04" i2="1">
<s1>COLLIER (David)</s1>
</fA11>
<fA11 i1="05" i2="1">
<s1>TREASURE (Janet)</s1>
</fA11>
<fA14 i1="01">
<s1>Division of Psychological Medicine, the Social, Genetic and Developmental Psychiatry Research Centre, and the Department of Biostatistics and Computing, Institute of Psychiatry, King's College London (KCL)</s1>
<s2>London</s2>
<s3>GBR</s3>
</fA14>
<fA14 i1="02">
<s1>KCL Department of Academic Psychiatry, Guy's, King's and St. Thomas's Medical School</s1>
<s2>London</s2>
<s3>GBR</s3>
</fA14>
<fA20>
<s1>2269-2275</s1>
</fA20>
<fA21>
<s1>2005</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>3283</s2>
<s5>354000134431150070</s5>
</fA43>
<fA44>
<s0>0000</s0>
<s1>© 2006 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>35 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>06-0356604</s0>
</fA47>
<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>The American journal of psychiatry</s0>
</fA64>
<fA66 i1="01">
<s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>Objective: Set-shifting difficulties have been reported in subjects with anorexia nervosa and appear to persist after recovery; therefore, they may be endophenotypic traits. The goals of this study were to investigate whether set-shifting difficulties are familial by examining discordant sister-pairs in comparison with healthy unrelated women and to replicate, with a broader battery, the lack of influence of an acute illness state on neuropsychological performance. Method: Forty-seven pairs of sisters discordant for anorexia nervosa and 47 healthy unrelated women who were comparable in age and IQ completed neuropsychological tasks selected to assess set-shifting ability. Analyses of variance with standard errors that are robust against correlations within family clusters were used to compare the groups. Results were adjusted for obsessive-compulsive, anxiety, and depression symptoms. Subjects with acute (N=24) and fully remitted (N= 23) anorexia nervosa were compared to assess state versus trait effects. Results: Sisters with and without anorexia nervosa took significantly longer than unrelated healthy women to shift their cognitive set (CatBat task) and demonstrated greater perceptual rigidity (Haptic Illusion task) but did not differ significantly from each other. Women with anorexia nervosa were slower than other groups on Trail Making tasks. Women who had fully recovered from anorexia nervosa made significantly fewer errors than those with acute anorexia nervosa on the Trail Making alphabet task, but these subgroups did not differ on other measures. Conclusions: Both affected and unaffected sisters had more set-shifting difficulties than unrelated healthy women. This finding, together with the replicated finding that set-shifting difficulties persist after recovery, suggests that set-shifting difficulties are trait characteristics and may inform the search for the endophenotype in anorexia nervosa.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002B18C01A</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Anorexie mentale</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Anorexia nervosa</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Anorexia mental</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Aigu</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Acute</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Agudo</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Rémission</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Remission</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Remisión</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Etude comparative</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Comparative study</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Estudio comparativo</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Fratrie</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Sibling</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Hermandad</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Aptitude intellectuelle</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Intellectual ability</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Aptitud intelectual</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Flexibilité intellectuelle</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Intellectual flexibility</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Flexibilidad intelectual</s0>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Traitement information</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Information processing</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Procesamiento información</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Fonction exécutive</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Executive function</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Función ejecutiva</s0>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Neuropsychologie</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Neuropsychologia</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Neurosicología</s0>
<s5>10</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Cognition</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Cognition</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Cognición</s0>
<s5>11</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Marqueur biologique</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Biological marker</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Marcador biológico</s0>
<s5>12</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE">
<s0>Génétique</s0>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG">
<s0>Genetics</s0>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA">
<s0>Genética</s0>
<s5>13</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE">
<s0>Déterminisme génétique</s0>
<s5>17</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG">
<s0>Genetic determinism</s0>
<s5>17</s5>
</fC03>
<fC03 i1="14" i2="X" l="SPA">
<s0>Determinismo genético</s0>
<s5>17</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE">
<s0>Etude familiale</s0>
<s5>18</s5>
</fC03>
<fC03 i1="15" i2="X" l="ENG">
<s0>Family study</s0>
<s5>18</s5>
</fC03>
<fC03 i1="15" i2="X" l="SPA">
<s0>Estudio familiar</s0>
<s5>18</s5>
</fC03>
<fC03 i1="16" i2="X" l="FRE">
<s0>Etude multicentrique</s0>
<s5>19</s5>
</fC03>
<fC03 i1="16" i2="X" l="ENG">
<s0>Multicenter study</s0>
<s5>19</s5>
</fC03>
<fC03 i1="16" i2="X" l="SPA">
<s0>Estudio multicéntrico</s0>
<s5>19</s5>
</fC03>
<fC03 i1="17" i2="X" l="FRE">
<s0>Femelle</s0>
<s5>20</s5>
</fC03>
<fC03 i1="17" i2="X" l="ENG">
<s0>Female</s0>
<s5>20</s5>
</fC03>
<fC03 i1="17" i2="X" l="SPA">
<s0>Hembra</s0>
<s5>20</s5>
</fC03>
<fC03 i1="18" i2="X" l="FRE">
<s0>Homme</s0>
<s5>21</s5>
</fC03>
<fC03 i1="18" i2="X" l="ENG">
<s0>Human</s0>
<s5>21</s5>
</fC03>
<fC03 i1="18" i2="X" l="SPA">
<s0>Hombre</s0>
<s5>21</s5>
</fC03>
<fC03 i1="19" i2="X" l="FRE">
<s0>Endophénotype</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="19" i2="X" l="ENG">
<s0>Endophenotype</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="20" i2="X" l="FRE">
<s0>Parenté premier degré</s0>
<s4>CD</s4>
<s5>97</s5>
</fC03>
<fC03 i1="20" i2="X" l="ENG">
<s0>First degree relatives</s0>
<s4>CD</s4>
<s5>97</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Trouble comportement alimentaire</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Eating disorder</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Trastorno conducta alimentaria</s0>
<s5>37</s5>
</fC07>
<fN21>
<s1>240</s1>
</fN21>
<fN44 i1="01">
<s1>PSI</s1>
</fN44>
<fN82>
<s1>PSI</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 06-0356604 INIST</NO>
<ET>Is impaired set-shifting an endophenotype of anorexia nervosa?</ET>
<AU>HOLLIDAY (Joanna); TCHANTURIA (Kate); LANDAU (Sabine); COLLIER (David); TREASURE (Janet)</AU>
<AF>Division of Psychological Medicine, the Social, Genetic and Developmental Psychiatry Research Centre, and the Department of Biostatistics and Computing, Institute of Psychiatry, King's College London (KCL)/London/Royaume-Uni; KCL Department of Academic Psychiatry, Guy's, King's and St. Thomas's Medical School/London/Royaume-Uni</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>The American journal of psychiatry; ISSN 0002-953X; Coden AJPSAO; Etats-Unis; Da. 2005; Vol. 162; No. 12; Pp. 2269-2275; Bibl. 35 ref.</SO>
<LA>Anglais</LA>
<EA>Objective: Set-shifting difficulties have been reported in subjects with anorexia nervosa and appear to persist after recovery; therefore, they may be endophenotypic traits. The goals of this study were to investigate whether set-shifting difficulties are familial by examining discordant sister-pairs in comparison with healthy unrelated women and to replicate, with a broader battery, the lack of influence of an acute illness state on neuropsychological performance. Method: Forty-seven pairs of sisters discordant for anorexia nervosa and 47 healthy unrelated women who were comparable in age and IQ completed neuropsychological tasks selected to assess set-shifting ability. Analyses of variance with standard errors that are robust against correlations within family clusters were used to compare the groups. Results were adjusted for obsessive-compulsive, anxiety, and depression symptoms. Subjects with acute (N=24) and fully remitted (N= 23) anorexia nervosa were compared to assess state versus trait effects. Results: Sisters with and without anorexia nervosa took significantly longer than unrelated healthy women to shift their cognitive set (CatBat task) and demonstrated greater perceptual rigidity (Haptic Illusion task) but did not differ significantly from each other. Women with anorexia nervosa were slower than other groups on Trail Making tasks. Women who had fully recovered from anorexia nervosa made significantly fewer errors than those with acute anorexia nervosa on the Trail Making alphabet task, but these subgroups did not differ on other measures. Conclusions: Both affected and unaffected sisters had more set-shifting difficulties than unrelated healthy women. This finding, together with the replicated finding that set-shifting difficulties persist after recovery, suggests that set-shifting difficulties are trait characteristics and may inform the search for the endophenotype in anorexia nervosa.</EA>
<CC>002B18C01A</CC>
<FD>Anorexie mentale; Aigu; Rémission; Etude comparative; Fratrie; Aptitude intellectuelle; Flexibilité intellectuelle; Traitement information; Fonction exécutive; Neuropsychologie; Cognition; Marqueur biologique; Génétique; Déterminisme génétique; Etude familiale; Etude multicentrique; Femelle; Homme; Endophénotype; Parenté premier degré</FD>
<FG>Trouble comportement alimentaire</FG>
<ED>Anorexia nervosa; Acute; Remission; Comparative study; Sibling; Intellectual ability; Intellectual flexibility; Information processing; Executive function; Neuropsychologia; Cognition; Biological marker; Genetics; Genetic determinism; Family study; Multicenter study; Female; Human; Endophenotype; First degree relatives</ED>
<EG>Eating disorder</EG>
<SD>Anorexia mental; Agudo; Remisión; Estudio comparativo; Hermandad; Aptitud intelectual; Flexibilidad intelectual; Procesamiento información; Función ejecutiva; Neurosicología; Cognición; Marcador biológico; Genética; Determinismo genético; Estudio familiar; Estudio multicéntrico; Hembra; Hombre</SD>
<LO>INIST-3283.354000134431150070</LO>
<ID>06-0356604</ID>
</server>
</inist>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Ticri/CIDE/explor/HapticV1/Data/PascalFrancis/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000C83 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Corpus/biblio.hfd -nk 000C83 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Ticri/CIDE
   |area=    HapticV1
   |flux=    PascalFrancis
   |étape=   Corpus
   |type=    RBID
   |clé=     Pascal:06-0356604
   |texte=   Is impaired set-shifting an endophenotype of anorexia nervosa?
}}

Wicri

This area was generated with Dilib version V0.6.23.
Data generation: Mon Jun 13 01:09:46 2016. Site generation: Wed Mar 6 09:54:07 2024