Serveur d'exploration sur les relations entre la France et l'Australie

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.

Common Genetic Variants Associated with Breast Cancer and Mammographic Density Measures That Predict Disease

Identifieur interne : 002794 ( PascalFrancis/Corpus ); précédent : 002793; suivant : 002795

Common Genetic Variants Associated with Breast Cancer and Mammographic Density Measures That Predict Disease

Auteurs : Fabrice Odefrey ; Jennifer Stone ; Lyle C. Gurrin ; Graham B. Byrnes ; Carmel Apicella ; Gillian S. Dite ; Jennifer N. Cawson ; Graham G. Giles ; Susan A. Treloar ; Dallas R. English ; John L. Hopper ; Melissa C. Southey

Source :

RBID : Pascal:10-0157550

Descripteurs français

English descriptors

Abstract

Mammographic density for age and body mass index (BMI) is a heritable risk factor for breast cancer. We aimed to determine if recently identified common variants associated with small gradients in breast cancer risk are associated with mammographic density. We genotyped 497 monozygotic and 330 dizygotic twin pairs and 634 of their sisters from 903 families for 12 independent variants. Mammographic dense area, percent dense area, and nondense area were measured by three observers using a computer-thresholding technique. Associations with mammographic density measures adjusted for age, BMI, and other determinants were estimated (a) cross-sectionally using a multivariate normal model for pedigree analysis (Px), (b) between sibships, and (c) within sibships using orthogonal transformations of outcomes and exposures. A combined test of association (Pc) was derived using the independent estimates from b and c. We tested if the distributions of P values across variants differed from the uniform distribution (Pu). For dense area and percent dense area, the distributions of Pc values were not uniform (both Pu <0.007). Consistent with their breast cancer associations, rs3817198 (LSP1) and rs13281615 (8q) were associated with dense area and percent dense area (all Px and Pc <0.05), and rs889312 (MAP3K1), rs2107425 (H19), and rs17468277 (CASP8) were marginally associated with dense area (some Px or Pc <0.05). All associations were independent of menopausal status. At least two common breast cancer susceptibility variants are associated with mammographic density measures that predict breast cancer. These findings could help elucidate how those variants and mammographic density measures are associated with breast cancer susceptibility.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0008-5472
A02 01      @0 CNREA8
A03   1    @0 Cancer res. : (Baltimore)
A05       @2 70
A06       @2 4
A08 01  1  ENG  @1 Common Genetic Variants Associated with Breast Cancer and Mammographic Density Measures That Predict Disease
A11 01  1    @1 ODEFREY (Fabrice)
A11 02  1    @1 STONE (Jennifer)
A11 03  1    @1 GURRIN (Lyle C.)
A11 04  1    @1 BYRNES (Graham B.)
A11 05  1    @1 APICELLA (Carmel)
A11 06  1    @1 DITE (Gillian S.)
A11 07  1    @1 CAWSON (Jennifer N.)
A11 08  1    @1 GILES (Graham G.)
A11 09  1    @1 TRELOAR (Susan A.)
A11 10  1    @1 ENGLISH (Dallas R.)
A11 11  1    @1 HOPPER (John L.)
A11 12  1    @1 SOUTHEY (Melissa C.)
A14 01      @1 Department of Pathology, University of Melbourne @2 Melbourne @3 AUS @Z 1 aut. @Z 12 aut.
A14 02      @1 Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne @2 Melbourne @3 AUS @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 10 aut. @Z 11 aut.
A14 03      @1 Cancer Council Victoria @2 Melbourne @3 AUS @Z 8 aut.
A14 04      @1 International Agency for Research on Cancer @2 Lyon @3 FRA @Z 4 aut.
A14 05      @1 St. Vincent's Hospital, University of Melbourne, Fitzroy @2 Victoria @3 AUS @Z 7 aut.
A14 06      @1 Centre for Military and Veterans' Health, University of Queensland @2 Brisbane @3 AUS @Z 9 aut.
A17 01  1    @1 Australian Twins and Sisters Mammographic Density Study @3 AUS
A20       @1 1449-1458
A21       @1 2010
A23 01      @0 ENG
A43 01      @1 INIST @2 5088 @5 354000189349440190
A44       @0 0000 @1 © 2010 INIST-CNRS. All rights reserved.
A45       @0 18 ref.
A47 01  1    @0 10-0157550
A60       @1 P
A61       @0 A
A64 01  1    @0 Cancer research : (Baltimore)
A66 01      @0 USA
C01 01    ENG  @0 Mammographic density for age and body mass index (BMI) is a heritable risk factor for breast cancer. We aimed to determine if recently identified common variants associated with small gradients in breast cancer risk are associated with mammographic density. We genotyped 497 monozygotic and 330 dizygotic twin pairs and 634 of their sisters from 903 families for 12 independent variants. Mammographic dense area, percent dense area, and nondense area were measured by three observers using a computer-thresholding technique. Associations with mammographic density measures adjusted for age, BMI, and other determinants were estimated (a) cross-sectionally using a multivariate normal model for pedigree analysis (Px), (b) between sibships, and (c) within sibships using orthogonal transformations of outcomes and exposures. A combined test of association (Pc) was derived using the independent estimates from b and c. We tested if the distributions of P values across variants differed from the uniform distribution (Pu). For dense area and percent dense area, the distributions of Pc values were not uniform (both Pu <0.007). Consistent with their breast cancer associations, rs3817198 (LSP1) and rs13281615 (8q) were associated with dense area and percent dense area (all Px and Pc <0.05), and rs889312 (MAP3K1), rs2107425 (H19), and rs17468277 (CASP8) were marginally associated with dense area (some Px or Pc <0.05). All associations were independent of menopausal status. At least two common breast cancer susceptibility variants are associated with mammographic density measures that predict breast cancer. These findings could help elucidate how those variants and mammographic density measures are associated with breast cancer susceptibility.
C02 01  X    @0 002B02R
C02 02  X    @0 002B04
C02 03  X    @0 002B20E02
C03 01  X  FRE  @0 Variant génétique @5 01
C03 01  X  ENG  @0 Genetic variant @5 01
C03 01  X  SPA  @0 Variante genética @5 01
C03 02  X  FRE  @0 Cancer du sein @2 NM @5 02
C03 02  X  ENG  @0 Breast cancer @2 NM @5 02
C03 02  X  SPA  @0 Cáncer del pecho @2 NM @5 02
C03 03  X  FRE  @0 Mammographie @5 03
C03 03  X  ENG  @0 Mammography @5 03
C03 03  X  SPA  @0 Mastografía @5 03
C03 04  X  FRE  @0 Densité @5 04
C03 04  X  ENG  @0 Density @5 04
C03 04  X  SPA  @0 Densidad @5 04
C03 05  X  FRE  @0 Facteur prédictif @5 05
C03 05  X  ENG  @0 Predictive factor @5 05
C03 05  X  SPA  @0 Factor predictivo @5 05
C03 06  X  FRE  @0 Maladie @5 06
C03 06  X  ENG  @0 Disease @5 06
C03 06  X  SPA  @0 Enfermedad @5 06
C07 01  X  FRE  @0 Tumeur maligne @2 NM @5 37
C07 01  X  ENG  @0 Malignant tumor @2 NM @5 37
C07 01  X  SPA  @0 Tumor maligno @2 NM @5 37
C07 02  X  FRE  @0 Cancer @2 NM
C07 02  X  ENG  @0 Cancer @2 NM
C07 02  X  SPA  @0 Cáncer @2 NM
C07 03  X  FRE  @0 Pathologie de la glande mammaire @2 NM @5 38
C07 03  X  ENG  @0 Mammary gland diseases @2 NM @5 38
C07 03  X  SPA  @0 Glándula mamaria patología @2 NM @5 38
C07 04  X  FRE  @0 Pathologie du sein @2 NM @5 39
C07 04  X  ENG  @0 Breast disease @2 NM @5 39
C07 04  X  SPA  @0 Seno patología @2 NM @5 39
C07 05  X  FRE  @0 Radiodiagnostic @5 40
C07 05  X  ENG  @0 Radiodiagnosis @5 40
C07 05  X  SPA  @0 Radiodiagnóstico @5 40
N21       @1 102
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 10-0157550 INIST
ET : Common Genetic Variants Associated with Breast Cancer and Mammographic Density Measures That Predict Disease
AU : ODEFREY (Fabrice); STONE (Jennifer); GURRIN (Lyle C.); BYRNES (Graham B.); APICELLA (Carmel); DITE (Gillian S.); CAWSON (Jennifer N.); GILES (Graham G.); TRELOAR (Susan A.); ENGLISH (Dallas R.); HOPPER (John L.); SOUTHEY (Melissa C.)
AF : Department of Pathology, University of Melbourne/Melbourne/Australie (1 aut., 12 aut.); Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne/Melbourne/Australie (2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 10 aut., 11 aut.); Cancer Council Victoria/Melbourne/Australie (8 aut.); International Agency for Research on Cancer/Lyon/France (4 aut.); St. Vincent's Hospital, University of Melbourne, Fitzroy/Victoria/Australie (7 aut.); Centre for Military and Veterans' Health, University of Queensland/Brisbane/Australie (9 aut.)
DT : Publication en série; Niveau analytique
SO : Cancer research : (Baltimore); ISSN 0008-5472; Coden CNREA8; Etats-Unis; Da. 2010; Vol. 70; No. 4; Pp. 1449-1458; Bibl. 18 ref.
LA : Anglais
EA : Mammographic density for age and body mass index (BMI) is a heritable risk factor for breast cancer. We aimed to determine if recently identified common variants associated with small gradients in breast cancer risk are associated with mammographic density. We genotyped 497 monozygotic and 330 dizygotic twin pairs and 634 of their sisters from 903 families for 12 independent variants. Mammographic dense area, percent dense area, and nondense area were measured by three observers using a computer-thresholding technique. Associations with mammographic density measures adjusted for age, BMI, and other determinants were estimated (a) cross-sectionally using a multivariate normal model for pedigree analysis (Px), (b) between sibships, and (c) within sibships using orthogonal transformations of outcomes and exposures. A combined test of association (Pc) was derived using the independent estimates from b and c. We tested if the distributions of P values across variants differed from the uniform distribution (Pu). For dense area and percent dense area, the distributions of Pc values were not uniform (both Pu <0.007). Consistent with their breast cancer associations, rs3817198 (LSP1) and rs13281615 (8q) were associated with dense area and percent dense area (all Px and Pc <0.05), and rs889312 (MAP3K1), rs2107425 (H19), and rs17468277 (CASP8) were marginally associated with dense area (some Px or Pc <0.05). All associations were independent of menopausal status. At least two common breast cancer susceptibility variants are associated with mammographic density measures that predict breast cancer. These findings could help elucidate how those variants and mammographic density measures are associated with breast cancer susceptibility.
CC : 002B02R; 002B04; 002B20E02
FD : Variant génétique; Cancer du sein; Mammographie; Densité; Facteur prédictif; Maladie
FG : Tumeur maligne; Cancer; Pathologie de la glande mammaire; Pathologie du sein; Radiodiagnostic
ED : Genetic variant; Breast cancer; Mammography; Density; Predictive factor; Disease
EG : Malignant tumor; Cancer; Mammary gland diseases; Breast disease; Radiodiagnosis
SD : Variante genética; Cáncer del pecho; Mastografía; Densidad; Factor predictivo; Enfermedad
LO : INIST-5088.354000189349440190
ID : 10-0157550

Links to Exploration step

Pascal:10-0157550

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en" level="a">Common Genetic Variants Associated with Breast Cancer and Mammographic Density Measures That Predict Disease</title>
<author>
<name sortKey="Odefrey, Fabrice" sort="Odefrey, Fabrice" uniqKey="Odefrey F" first="Fabrice" last="Odefrey">Fabrice Odefrey</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Pathology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>1 aut.</sZ>
<sZ>12 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Stone, Jennifer" sort="Stone, Jennifer" uniqKey="Stone J" first="Jennifer" last="Stone">Jennifer Stone</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Gurrin, Lyle C" sort="Gurrin, Lyle C" uniqKey="Gurrin L" first="Lyle C." last="Gurrin">Lyle C. Gurrin</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Byrnes, Graham B" sort="Byrnes, Graham B" uniqKey="Byrnes G" first="Graham B." last="Byrnes">Graham B. Byrnes</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="04">
<s1>International Agency for Research on Cancer</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Apicella, Carmel" sort="Apicella, Carmel" uniqKey="Apicella C" first="Carmel" last="Apicella">Carmel Apicella</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Dite, Gillian S" sort="Dite, Gillian S" uniqKey="Dite G" first="Gillian S." last="Dite">Gillian S. Dite</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Cawson, Jennifer N" sort="Cawson, Jennifer N" uniqKey="Cawson J" first="Jennifer N." last="Cawson">Jennifer N. Cawson</name>
<affiliation>
<inist:fA14 i1="05">
<s1>St. Vincent's Hospital, University of Melbourne, Fitzroy</s1>
<s2>Victoria</s2>
<s3>AUS</s3>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Giles, Graham G" sort="Giles, Graham G" uniqKey="Giles G" first="Graham G." last="Giles">Graham G. Giles</name>
<affiliation>
<inist:fA14 i1="03">
<s1>Cancer Council Victoria</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Treloar, Susan A" sort="Treloar, Susan A" uniqKey="Treloar S" first="Susan A." last="Treloar">Susan A. Treloar</name>
<affiliation>
<inist:fA14 i1="06">
<s1>Centre for Military and Veterans' Health, University of Queensland</s1>
<s2>Brisbane</s2>
<s3>AUS</s3>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="English, Dallas R" sort="English, Dallas R" uniqKey="English D" first="Dallas R." last="English">Dallas R. English</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Hopper, John L" sort="Hopper, John L" uniqKey="Hopper J" first="John L." last="Hopper">John L. Hopper</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Southey, Melissa C" sort="Southey, Melissa C" uniqKey="Southey M" first="Melissa C." last="Southey">Melissa C. Southey</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Pathology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>1 aut.</sZ>
<sZ>12 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">INIST</idno>
<idno type="inist">10-0157550</idno>
<date when="2010">2010</date>
<idno type="stanalyst">PASCAL 10-0157550 INIST</idno>
<idno type="RBID">Pascal:10-0157550</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">002794</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a">Common Genetic Variants Associated with Breast Cancer and Mammographic Density Measures That Predict Disease</title>
<author>
<name sortKey="Odefrey, Fabrice" sort="Odefrey, Fabrice" uniqKey="Odefrey F" first="Fabrice" last="Odefrey">Fabrice Odefrey</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Pathology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>1 aut.</sZ>
<sZ>12 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Stone, Jennifer" sort="Stone, Jennifer" uniqKey="Stone J" first="Jennifer" last="Stone">Jennifer Stone</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Gurrin, Lyle C" sort="Gurrin, Lyle C" uniqKey="Gurrin L" first="Lyle C." last="Gurrin">Lyle C. Gurrin</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Byrnes, Graham B" sort="Byrnes, Graham B" uniqKey="Byrnes G" first="Graham B." last="Byrnes">Graham B. Byrnes</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="04">
<s1>International Agency for Research on Cancer</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Apicella, Carmel" sort="Apicella, Carmel" uniqKey="Apicella C" first="Carmel" last="Apicella">Carmel Apicella</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Dite, Gillian S" sort="Dite, Gillian S" uniqKey="Dite G" first="Gillian S." last="Dite">Gillian S. Dite</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Cawson, Jennifer N" sort="Cawson, Jennifer N" uniqKey="Cawson J" first="Jennifer N." last="Cawson">Jennifer N. Cawson</name>
<affiliation>
<inist:fA14 i1="05">
<s1>St. Vincent's Hospital, University of Melbourne, Fitzroy</s1>
<s2>Victoria</s2>
<s3>AUS</s3>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Giles, Graham G" sort="Giles, Graham G" uniqKey="Giles G" first="Graham G." last="Giles">Graham G. Giles</name>
<affiliation>
<inist:fA14 i1="03">
<s1>Cancer Council Victoria</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Treloar, Susan A" sort="Treloar, Susan A" uniqKey="Treloar S" first="Susan A." last="Treloar">Susan A. Treloar</name>
<affiliation>
<inist:fA14 i1="06">
<s1>Centre for Military and Veterans' Health, University of Queensland</s1>
<s2>Brisbane</s2>
<s3>AUS</s3>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="English, Dallas R" sort="English, Dallas R" uniqKey="English D" first="Dallas R." last="English">Dallas R. English</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Hopper, John L" sort="Hopper, John L" uniqKey="Hopper J" first="John L." last="Hopper">John L. Hopper</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Southey, Melissa C" sort="Southey, Melissa C" uniqKey="Southey M" first="Melissa C." last="Southey">Melissa C. Southey</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Pathology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>1 aut.</sZ>
<sZ>12 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Cancer research : (Baltimore)</title>
<title level="j" type="abbreviated">Cancer res. : (Baltimore)</title>
<idno type="ISSN">0008-5472</idno>
<imprint>
<date when="2010">2010</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<title level="j" type="main">Cancer research : (Baltimore)</title>
<title level="j" type="abbreviated">Cancer res. : (Baltimore)</title>
<idno type="ISSN">0008-5472</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Breast cancer</term>
<term>Density</term>
<term>Disease</term>
<term>Genetic variant</term>
<term>Mammography</term>
<term>Predictive factor</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Variant génétique</term>
<term>Cancer du sein</term>
<term>Mammographie</term>
<term>Densité</term>
<term>Facteur prédictif</term>
<term>Maladie</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Mammographic density for age and body mass index (BMI) is a heritable risk factor for breast cancer. We aimed to determine if recently identified common variants associated with small gradients in breast cancer risk are associated with mammographic density. We genotyped 497 monozygotic and 330 dizygotic twin pairs and 634 of their sisters from 903 families for 12 independent variants. Mammographic dense area, percent dense area, and nondense area were measured by three observers using a computer-thresholding technique. Associations with mammographic density measures adjusted for age, BMI, and other determinants were estimated (a) cross-sectionally using a multivariate normal model for pedigree analysis (P
<sub>x</sub>
), (b) between sibships, and (c) within sibships using orthogonal transformations of outcomes and exposures. A combined test of association (P
<sub>c</sub>
) was derived using the independent estimates from b and c. We tested if the distributions of P values across variants differed from the uniform distribution (P
<sub>u</sub>
). For dense area and percent dense area, the distributions of P
<sub>c</sub>
values were not uniform (both P
<sub>u</sub>
<0.007). Consistent with their breast cancer associations, rs3817198 (LSP1) and rs13281615 (8q) were associated with dense area and percent dense area (all P
<sub>x</sub>
and P
<sub>c</sub>
<0.05), and rs889312 (MAP3K1), rs2107425 (H19), and rs17468277 (CASP8) were marginally associated with dense area (some P
<sub>x</sub>
or P
<sub>c</sub>
<0.05). All associations were independent of menopausal status. At least two common breast cancer susceptibility variants are associated with mammographic density measures that predict breast cancer. These findings could help elucidate how those variants and mammographic density measures are associated with breast cancer susceptibility.</div>
</front>
</TEI>
<inist>
<standard h6="B">
<pA>
<fA01 i1="01" i2="1">
<s0>0008-5472</s0>
</fA01>
<fA02 i1="01">
<s0>CNREA8</s0>
</fA02>
<fA03 i2="1">
<s0>Cancer res. : (Baltimore)</s0>
</fA03>
<fA05>
<s2>70</s2>
</fA05>
<fA06>
<s2>4</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG">
<s1>Common Genetic Variants Associated with Breast Cancer and Mammographic Density Measures That Predict Disease</s1>
</fA08>
<fA11 i1="01" i2="1">
<s1>ODEFREY (Fabrice)</s1>
</fA11>
<fA11 i1="02" i2="1">
<s1>STONE (Jennifer)</s1>
</fA11>
<fA11 i1="03" i2="1">
<s1>GURRIN (Lyle C.)</s1>
</fA11>
<fA11 i1="04" i2="1">
<s1>BYRNES (Graham B.)</s1>
</fA11>
<fA11 i1="05" i2="1">
<s1>APICELLA (Carmel)</s1>
</fA11>
<fA11 i1="06" i2="1">
<s1>DITE (Gillian S.)</s1>
</fA11>
<fA11 i1="07" i2="1">
<s1>CAWSON (Jennifer N.)</s1>
</fA11>
<fA11 i1="08" i2="1">
<s1>GILES (Graham G.)</s1>
</fA11>
<fA11 i1="09" i2="1">
<s1>TRELOAR (Susan A.)</s1>
</fA11>
<fA11 i1="10" i2="1">
<s1>ENGLISH (Dallas R.)</s1>
</fA11>
<fA11 i1="11" i2="1">
<s1>HOPPER (John L.)</s1>
</fA11>
<fA11 i1="12" i2="1">
<s1>SOUTHEY (Melissa C.)</s1>
</fA11>
<fA14 i1="01">
<s1>Department of Pathology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>1 aut.</sZ>
<sZ>12 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
</fA14>
<fA14 i1="03">
<s1>Cancer Council Victoria</s1>
<s2>Melbourne</s2>
<s3>AUS</s3>
<sZ>8 aut.</sZ>
</fA14>
<fA14 i1="04">
<s1>International Agency for Research on Cancer</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="05">
<s1>St. Vincent's Hospital, University of Melbourne, Fitzroy</s1>
<s2>Victoria</s2>
<s3>AUS</s3>
<sZ>7 aut.</sZ>
</fA14>
<fA14 i1="06">
<s1>Centre for Military and Veterans' Health, University of Queensland</s1>
<s2>Brisbane</s2>
<s3>AUS</s3>
<sZ>9 aut.</sZ>
</fA14>
<fA17 i1="01" i2="1">
<s1>Australian Twins and Sisters Mammographic Density Study</s1>
<s3>AUS</s3>
</fA17>
<fA20>
<s1>1449-1458</s1>
</fA20>
<fA21>
<s1>2010</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>5088</s2>
<s5>354000189349440190</s5>
</fA43>
<fA44>
<s0>0000</s0>
<s1>© 2010 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>18 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>10-0157550</s0>
</fA47>
<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Cancer research : (Baltimore)</s0>
</fA64>
<fA66 i1="01">
<s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>Mammographic density for age and body mass index (BMI) is a heritable risk factor for breast cancer. We aimed to determine if recently identified common variants associated with small gradients in breast cancer risk are associated with mammographic density. We genotyped 497 monozygotic and 330 dizygotic twin pairs and 634 of their sisters from 903 families for 12 independent variants. Mammographic dense area, percent dense area, and nondense area were measured by three observers using a computer-thresholding technique. Associations with mammographic density measures adjusted for age, BMI, and other determinants were estimated (a) cross-sectionally using a multivariate normal model for pedigree analysis (P
<sub>x</sub>
), (b) between sibships, and (c) within sibships using orthogonal transformations of outcomes and exposures. A combined test of association (P
<sub>c</sub>
) was derived using the independent estimates from b and c. We tested if the distributions of P values across variants differed from the uniform distribution (P
<sub>u</sub>
). For dense area and percent dense area, the distributions of P
<sub>c</sub>
values were not uniform (both P
<sub>u</sub>
<0.007). Consistent with their breast cancer associations, rs3817198 (LSP1) and rs13281615 (8q) were associated with dense area and percent dense area (all P
<sub>x</sub>
and P
<sub>c</sub>
<0.05), and rs889312 (MAP3K1), rs2107425 (H19), and rs17468277 (CASP8) were marginally associated with dense area (some P
<sub>x</sub>
or P
<sub>c</sub>
<0.05). All associations were independent of menopausal status. At least two common breast cancer susceptibility variants are associated with mammographic density measures that predict breast cancer. These findings could help elucidate how those variants and mammographic density measures are associated with breast cancer susceptibility.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002B02R</s0>
</fC02>
<fC02 i1="02" i2="X">
<s0>002B04</s0>
</fC02>
<fC02 i1="03" i2="X">
<s0>002B20E02</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Variant génétique</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Genetic variant</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Variante genética</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Cancer du sein</s0>
<s2>NM</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Breast cancer</s0>
<s2>NM</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Cáncer del pecho</s0>
<s2>NM</s2>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Mammographie</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Mammography</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Mastografía</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Densité</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Density</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Densidad</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Facteur prédictif</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Predictive factor</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Factor predictivo</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Maladie</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Disease</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Enfermedad</s0>
<s5>06</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Tumeur maligne</s0>
<s2>NM</s2>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Malignant tumor</s0>
<s2>NM</s2>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Tumor maligno</s0>
<s2>NM</s2>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Cancer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Cancer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Cáncer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Pathologie de la glande mammaire</s0>
<s2>NM</s2>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Mammary gland diseases</s0>
<s2>NM</s2>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Glándula mamaria patología</s0>
<s2>NM</s2>
<s5>38</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Pathologie du sein</s0>
<s2>NM</s2>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Breast disease</s0>
<s2>NM</s2>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Seno patología</s0>
<s2>NM</s2>
<s5>39</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Radiodiagnostic</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Radiodiagnosis</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Radiodiagnóstico</s0>
<s5>40</s5>
</fC07>
<fN21>
<s1>102</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 10-0157550 INIST</NO>
<ET>Common Genetic Variants Associated with Breast Cancer and Mammographic Density Measures That Predict Disease</ET>
<AU>ODEFREY (Fabrice); STONE (Jennifer); GURRIN (Lyle C.); BYRNES (Graham B.); APICELLA (Carmel); DITE (Gillian S.); CAWSON (Jennifer N.); GILES (Graham G.); TRELOAR (Susan A.); ENGLISH (Dallas R.); HOPPER (John L.); SOUTHEY (Melissa C.)</AU>
<AF>Department of Pathology, University of Melbourne/Melbourne/Australie (1 aut., 12 aut.); Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne/Melbourne/Australie (2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 10 aut., 11 aut.); Cancer Council Victoria/Melbourne/Australie (8 aut.); International Agency for Research on Cancer/Lyon/France (4 aut.); St. Vincent's Hospital, University of Melbourne, Fitzroy/Victoria/Australie (7 aut.); Centre for Military and Veterans' Health, University of Queensland/Brisbane/Australie (9 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Cancer research : (Baltimore); ISSN 0008-5472; Coden CNREA8; Etats-Unis; Da. 2010; Vol. 70; No. 4; Pp. 1449-1458; Bibl. 18 ref.</SO>
<LA>Anglais</LA>
<EA>Mammographic density for age and body mass index (BMI) is a heritable risk factor for breast cancer. We aimed to determine if recently identified common variants associated with small gradients in breast cancer risk are associated with mammographic density. We genotyped 497 monozygotic and 330 dizygotic twin pairs and 634 of their sisters from 903 families for 12 independent variants. Mammographic dense area, percent dense area, and nondense area were measured by three observers using a computer-thresholding technique. Associations with mammographic density measures adjusted for age, BMI, and other determinants were estimated (a) cross-sectionally using a multivariate normal model for pedigree analysis (P
<sub>x</sub>
), (b) between sibships, and (c) within sibships using orthogonal transformations of outcomes and exposures. A combined test of association (P
<sub>c</sub>
) was derived using the independent estimates from b and c. We tested if the distributions of P values across variants differed from the uniform distribution (P
<sub>u</sub>
). For dense area and percent dense area, the distributions of P
<sub>c</sub>
values were not uniform (both P
<sub>u</sub>
<0.007). Consistent with their breast cancer associations, rs3817198 (LSP1) and rs13281615 (8q) were associated with dense area and percent dense area (all P
<sub>x</sub>
and P
<sub>c</sub>
<0.05), and rs889312 (MAP3K1), rs2107425 (H19), and rs17468277 (CASP8) were marginally associated with dense area (some P
<sub>x</sub>
or P
<sub>c</sub>
<0.05). All associations were independent of menopausal status. At least two common breast cancer susceptibility variants are associated with mammographic density measures that predict breast cancer. These findings could help elucidate how those variants and mammographic density measures are associated with breast cancer susceptibility.</EA>
<CC>002B02R; 002B04; 002B20E02</CC>
<FD>Variant génétique; Cancer du sein; Mammographie; Densité; Facteur prédictif; Maladie</FD>
<FG>Tumeur maligne; Cancer; Pathologie de la glande mammaire; Pathologie du sein; Radiodiagnostic</FG>
<ED>Genetic variant; Breast cancer; Mammography; Density; Predictive factor; Disease</ED>
<EG>Malignant tumor; Cancer; Mammary gland diseases; Breast disease; Radiodiagnosis</EG>
<SD>Variante genética; Cáncer del pecho; Mastografía; Densidad; Factor predictivo; Enfermedad</SD>
<LO>INIST-5088.354000189349440190</LO>
<ID>10-0157550</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 002794 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Corpus/biblio.hfd -nk 002794 | 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:10-0157550
   |texte=   Common Genetic Variants Associated with Breast Cancer and Mammographic Density Measures That Predict Disease
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Tue Dec 5 10:43:12 2017. Site generation: Tue Mar 5 14:07:20 2024