Fetal growth and childhood acute lymphoblastic leukemia: Findings from the childhood leukemia international consortium
Identifieur interne : 000758 ( PascalFrancis/Corpus ); précédent : 000757; suivant : 000759Fetal growth and childhood acute lymphoblastic leukemia: Findings from the childhood leukemia international consortium
Auteurs : Elizabeth Milne ; Kathryn R. Greenop ; Catherine Metayer ; Joachim Schüz ; Eleni Petridou ; Maria S. Pombo-De-Oliveira ; Claire Infante-Rivard ; Eve Roman ; John D. Dockerty ; Logan G. Spector ; Sérgio Koifman ; Laurent Orsi ; Jérémie Rudant ; Nick Dessypris ; Jill Simpson ; Tracy Lightfoot ; Peter Kaatsch ; Margarita Baka ; Alessandra Faro ; Bruce K. Armstrong ; Jacqueline Clavel ; Patricia A. BufflerSource :
- International journal of cancer : (Print) [ 0020-7136 ] ; 2013.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Positive associations have been reported between the measures of accelerated fetal growth and risk of childhood acute lymphoblastic leukemia (ALL). We investigated this association by pooling individual-level data from 12 case-control studies participating in the Childhood Leukemia International Consortium. Two measures of fetal growth-weight-for-gestational-age and proportion of optimal birth weight (POBW)-were analysed. Study-specific odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using multivariable logistic regression, and combined in fixed effects meta-analyses. Pooled analyses of all data were also undertaken using multivariable logistic regression. Subgroup analyses were undertaken when possible. Data on weight for gestational age were available for 7,348 cases and 12,489 controls from all 12 studies and POBW data were available for 1,680 cases and 3,139 controls from three studies. The summary ORs from the meta-analyses were 1.24 (95% CI: 1.13, 1.36) for children who were large for gestational age relative to appropriate for gestational age, and 1.16 (95% CI: 1.09, 1.24) for a one-standard deviation increase in POBW. The pooled analyses produced similar results. The summary and pooled ORs for small-for-gestational-age children were 0.83 (95% CI: 0.75, 0.92) and 0.86 (95% CI: 0.77, 0.95), respectively. Results were consistent across subgroups defined by sex, ethnicity and immunophenotype, and when the analysis was restricted to children who did not have high birth weight. The evidence that accelerated fetal growth is associated with a modest increased risk of childhood ALL is strong and consistent with known biological mechanisms involving insulin-like growth factors.
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Format Inist (serveur)
NO : | PASCAL 13-0338338 INIST |
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ET : | Fetal growth and childhood acute lymphoblastic leukemia: Findings from the childhood leukemia international consortium |
AU : | MILNE (Elizabeth); GREENOP (Kathryn R.); METAYER (Catherine); SCHÜZ (Joachim); PETRIDOU (Eleni); POMBO-DE-OLIVEIRA (Maria S.); INFANTE-RIVARD (Claire); ROMAN (Eve); DOCKERTY (John D.); SPECTOR (Logan G.); KOIFMAN (Sérgio); ORSI (Laurent); RUDANT (Jérémie); DESSYPRIS (Nick); SIMPSON (Jill); LIGHTFOOT (Tracy); KAATSCH (Peter); BAKA (Margarita); FARO (Alessandra); ARMSTRONG (Bruce K.); CLAVEL (Jacqueline); BUFFLER (Patricia A.) |
AF : | Telethon Institute for Child Health Research, Centre for Child Health Research, University of Western Australia/WA/Australie (1 aut., 2 aut.); School of Public Health, University of California, Berkeley/Berkeley, CA/Etats-Unis (3 aut., 22 aut.); Section of Environment and Radiation, International Agency for Research on Cancer (IARC)/Lyon/France (4 aut.); Department of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens/Athens/Grèce (5 aut., 14 aut.); Pediatric Hematology-Oncology Program, Research Program, Instituto Nacional de Cancer/Rio de Janeiro/Brésil (6 aut., 19 aut.); Department of Epidemiology, Biostatistics and Occupational Health, Faculty of Medicine, McGill University/Montréal, QC/Canada (7 aut.); Department of Health Science, University of York/York/Royaume-Uni (8 aut., 15 aut., 16 aut.); Dean's Department, Dunedin School of Medicine, University of Otago/Dunedin/Nouvelle-Zélande (9 aut.); Department of Preventive and Social Medicine, Dunedin School of Medicine, University of Otago/Dunedin/Nouvelle-Zélande (9 aut.); Division of Epidemiology/Clinical Research, Masonic Cancer Center, University of Minnesota/Minneapolis, MN/Etats-Unis (10 aut.); Department of Pediatrics, Masonic Cancer Center, University of Minnesota/Minneapolis, MN/Etats-Unis (10 aut.); National School of Public Health, Oswaldo Cruz Foundation (FIOCRUZ), Ministry of Health/Rio de Janeiro/Brésil (11 aut.); INSERM U1018, CESP Villejuif/France (12 aut., 13 aut., 21 aut.); Université Paris-Sud, UMRS 1018/Villejuif/France (12 aut., 13 aut., 21 aut.); National Registry of Childhood Hematopoietic Malignancies/Villejuif/France (13 aut., 21 aut.); German Childhood Cancer Registry at the Institute for Medical Biostatistics, Epidemiology and Informatics, University Medical Centre, Johannes Gutenberg-University Mainz/Mainz/Allemagne (17 aut.); Department of Pediatric Hematology-Oncology, "Pan.&Agl. Kyriakou" Children's Hospital/Athens/Grèce (18 aut.); Sydney School of Public Health, University of Sydney/NSW/Australie (20 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | International journal of cancer : (Print); ISSN 0020-7136; Coden IJCNAW; Etats-Unis; Da. 2013; Vol. 133; No. 12; Pp. 2968-2979; Bibl. 35 ref. |
LA : | Anglais |
EA : | Positive associations have been reported between the measures of accelerated fetal growth and risk of childhood acute lymphoblastic leukemia (ALL). We investigated this association by pooling individual-level data from 12 case-control studies participating in the Childhood Leukemia International Consortium. Two measures of fetal growth-weight-for-gestational-age and proportion of optimal birth weight (POBW)-were analysed. Study-specific odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using multivariable logistic regression, and combined in fixed effects meta-analyses. Pooled analyses of all data were also undertaken using multivariable logistic regression. Subgroup analyses were undertaken when possible. Data on weight for gestational age were available for 7,348 cases and 12,489 controls from all 12 studies and POBW data were available for 1,680 cases and 3,139 controls from three studies. The summary ORs from the meta-analyses were 1.24 (95% CI: 1.13, 1.36) for children who were large for gestational age relative to appropriate for gestational age, and 1.16 (95% CI: 1.09, 1.24) for a one-standard deviation increase in POBW. The pooled analyses produced similar results. The summary and pooled ORs for small-for-gestational-age children were 0.83 (95% CI: 0.75, 0.92) and 0.86 (95% CI: 0.77, 0.95), respectively. Results were consistent across subgroups defined by sex, ethnicity and immunophenotype, and when the analysis was restricted to children who did not have high birth weight. The evidence that accelerated fetal growth is associated with a modest increased risk of childhood ALL is strong and consistent with known biological mechanisms involving insulin-like growth factors. |
CC : | 002B04; 002B19B |
FD : | Foetus; Croissance; Enfant; Leucémie aiguë lymphoblastique; Poids naissance; Métaanalyse; Cancérologie |
FG : | Homme; Hémopathie maligne; Cancer; Syndrome lymphoprolifératif |
ED : | Fetus; Growth; Child; Acute lymphocytic leukemia; Birth weight; Metaanalysis; Cancerology |
EG : | Human; Malignant hemopathy; Cancer; Lymphoproliferative syndrome |
SD : | Feto; Crecimiento; Niño; Leucemia aguda linfoblástica; Peso nacimiento; Meta-análisis; Cancerología |
LO : | INIST-13027.354000501579740220 |
ID : | 13-0338338 |
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Pascal:13-0338338Le document en format XML
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<author><name sortKey="Faro, Alessandra" sort="Faro, Alessandra" uniqKey="Faro A" first="Alessandra" last="Faro">Alessandra Faro</name>
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<author><name sortKey="Buffler, Patricia A" sort="Buffler, Patricia A" uniqKey="Buffler P" first="Patricia A." last="Buffler">Patricia A. Buffler</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Fetal growth and childhood acute lymphoblastic leukemia: Findings from the childhood leukemia international consortium</title>
<author><name sortKey="Milne, Elizabeth" sort="Milne, Elizabeth" uniqKey="Milne E" first="Elizabeth" last="Milne">Elizabeth Milne</name>
<affiliation><inist:fA14 i1="01"><s1>Telethon Institute for Child Health Research, Centre for Child Health Research, University of Western Australia</s1>
<s2>WA</s2>
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<author><name sortKey="Greenop, Kathryn R" sort="Greenop, Kathryn R" uniqKey="Greenop K" first="Kathryn R." last="Greenop">Kathryn R. Greenop</name>
<affiliation><inist:fA14 i1="01"><s1>Telethon Institute for Child Health Research, Centre for Child Health Research, University of Western Australia</s1>
<s2>WA</s2>
<s3>AUS</s3>
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<author><name sortKey="Metayer, Catherine" sort="Metayer, Catherine" uniqKey="Metayer C" first="Catherine" last="Metayer">Catherine Metayer</name>
<affiliation><inist:fA14 i1="02"><s1>School of Public Health, University of California, Berkeley</s1>
<s2>Berkeley, CA</s2>
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<author><name sortKey="Schuz, Joachim" sort="Schuz, Joachim" uniqKey="Schuz J" first="Joachim" last="Schüz">Joachim Schüz</name>
<affiliation><inist:fA14 i1="03"><s1>Section of Environment and Radiation, International Agency for Research on Cancer (IARC)</s1>
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<author><name sortKey="Petridou, Eleni" sort="Petridou, Eleni" uniqKey="Petridou E" first="Eleni" last="Petridou">Eleni Petridou</name>
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<author><name sortKey="Pombo De Oliveira, Maria S" sort="Pombo De Oliveira, Maria S" uniqKey="Pombo De Oliveira M" first="Maria S." last="Pombo-De-Oliveira">Maria S. Pombo-De-Oliveira</name>
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<author><name sortKey="Infante Rivard, Claire" sort="Infante Rivard, Claire" uniqKey="Infante Rivard C" first="Claire" last="Infante-Rivard">Claire Infante-Rivard</name>
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<author><name sortKey="Roman, Eve" sort="Roman, Eve" uniqKey="Roman E" first="Eve" last="Roman">Eve Roman</name>
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<author><name sortKey="Simpson, Jill" sort="Simpson, Jill" uniqKey="Simpson J" first="Jill" last="Simpson">Jill Simpson</name>
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<author><name sortKey="Buffler, Patricia A" sort="Buffler, Patricia A" uniqKey="Buffler P" first="Patricia A." last="Buffler">Patricia A. Buffler</name>
<affiliation><inist:fA14 i1="02"><s1>School of Public Health, University of California, Berkeley</s1>
<s2>Berkeley, CA</s2>
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<series><title level="j" type="main">International journal of cancer : (Print)</title>
<title level="j" type="abbreviated">Int. j. cancer : (Print)</title>
<idno type="ISSN">0020-7136</idno>
<imprint><date when="2013">2013</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acute lymphocytic leukemia</term>
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<term>Cancerology</term>
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<term>Fetus</term>
<term>Growth</term>
<term>Metaanalysis</term>
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<term>Croissance</term>
<term>Enfant</term>
<term>Leucémie aiguë lymphoblastique</term>
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<front><div type="abstract" xml:lang="en">Positive associations have been reported between the measures of accelerated fetal growth and risk of childhood acute lymphoblastic leukemia (ALL). We investigated this association by pooling individual-level data from 12 case-control studies participating in the Childhood Leukemia International Consortium. Two measures of fetal growth-weight-for-gestational-age and proportion of optimal birth weight (POBW)-were analysed. Study-specific odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using multivariable logistic regression, and combined in fixed effects meta-analyses. Pooled analyses of all data were also undertaken using multivariable logistic regression. Subgroup analyses were undertaken when possible. Data on weight for gestational age were available for 7,348 cases and 12,489 controls from all 12 studies and POBW data were available for 1,680 cases and 3,139 controls from three studies. The summary ORs from the meta-analyses were 1.24 (95% CI: 1.13, 1.36) for children who were large for gestational age relative to appropriate for gestational age, and 1.16 (95% CI: 1.09, 1.24) for a one-standard deviation increase in POBW. The pooled analyses produced similar results. The summary and pooled ORs for small-for-gestational-age children were 0.83 (95% CI: 0.75, 0.92) and 0.86 (95% CI: 0.77, 0.95), respectively. Results were consistent across subgroups defined by sex, ethnicity and immunophenotype, and when the analysis was restricted to children who did not have high birth weight. The evidence that accelerated fetal growth is associated with a modest increased risk of childhood ALL is strong and consistent with known biological mechanisms involving insulin-like growth factors.</div>
</front>
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<fA08 i1="01" i2="1" l="ENG"><s1>Fetal growth and childhood acute lymphoblastic leukemia: Findings from the childhood leukemia international consortium</s1>
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<fA14 i1="07"><s1>Department of Health Science, University of York</s1>
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<fA14 i1="12"><s1>National School of Public Health, Oswaldo Cruz Foundation (FIOCRUZ), Ministry of Health</s1>
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<fA14 i1="15"><s1>National Registry of Childhood Hematopoietic Malignancies</s1>
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<fC07 i1="02" i2="X" l="SPA"><s0>Hemopatía maligna</s0>
<s2>NM</s2>
<s5>37</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Cancer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Cancer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Cáncer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Syndrome lymphoprolifératif</s0>
<s2>NM</s2>
<s5>38</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Lymphoproliferative syndrome</s0>
<s2>NM</s2>
<s5>38</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Linfoproliferativo síndrome</s0>
<s2>NM</s2>
<s5>38</s5>
</fC07>
<fN21><s1>322</s1>
</fN21>
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<server><NO>PASCAL 13-0338338 INIST</NO>
<ET>Fetal growth and childhood acute lymphoblastic leukemia: Findings from the childhood leukemia international consortium</ET>
<AU>MILNE (Elizabeth); GREENOP (Kathryn R.); METAYER (Catherine); SCHÜZ (Joachim); PETRIDOU (Eleni); POMBO-DE-OLIVEIRA (Maria S.); INFANTE-RIVARD (Claire); ROMAN (Eve); DOCKERTY (John D.); SPECTOR (Logan G.); KOIFMAN (Sérgio); ORSI (Laurent); RUDANT (Jérémie); DESSYPRIS (Nick); SIMPSON (Jill); LIGHTFOOT (Tracy); KAATSCH (Peter); BAKA (Margarita); FARO (Alessandra); ARMSTRONG (Bruce K.); CLAVEL (Jacqueline); BUFFLER (Patricia A.)</AU>
<AF>Telethon Institute for Child Health Research, Centre for Child Health Research, University of Western Australia/WA/Australie (1 aut., 2 aut.); School of Public Health, University of California, Berkeley/Berkeley, CA/Etats-Unis (3 aut., 22 aut.); Section of Environment and Radiation, International Agency for Research on Cancer (IARC)/Lyon/France (4 aut.); Department of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens/Athens/Grèce (5 aut., 14 aut.); Pediatric Hematology-Oncology Program, Research Program, Instituto Nacional de Cancer/Rio de Janeiro/Brésil (6 aut., 19 aut.); Department of Epidemiology, Biostatistics and Occupational Health, Faculty of Medicine, McGill University/Montréal, QC/Canada (7 aut.); Department of Health Science, University of York/York/Royaume-Uni (8 aut., 15 aut., 16 aut.); Dean's Department, Dunedin School of Medicine, University of Otago/Dunedin/Nouvelle-Zélande (9 aut.); Department of Preventive and Social Medicine, Dunedin School of Medicine, University of Otago/Dunedin/Nouvelle-Zélande (9 aut.); Division of Epidemiology/Clinical Research, Masonic Cancer Center, University of Minnesota/Minneapolis, MN/Etats-Unis (10 aut.); Department of Pediatrics, Masonic Cancer Center, University of Minnesota/Minneapolis, MN/Etats-Unis (10 aut.); National School of Public Health, Oswaldo Cruz Foundation (FIOCRUZ), Ministry of Health/Rio de Janeiro/Brésil (11 aut.); INSERM U1018, CESP Villejuif/France (12 aut., 13 aut., 21 aut.); Université Paris-Sud, UMRS 1018/Villejuif/France (12 aut., 13 aut., 21 aut.); National Registry of Childhood Hematopoietic Malignancies/Villejuif/France (13 aut., 21 aut.); German Childhood Cancer Registry at the Institute for Medical Biostatistics, Epidemiology and Informatics, University Medical Centre, Johannes Gutenberg-University Mainz/Mainz/Allemagne (17 aut.); Department of Pediatric Hematology-Oncology, "Pan.&Agl. Kyriakou" Children's Hospital/Athens/Grèce (18 aut.); Sydney School of Public Health, University of Sydney/NSW/Australie (20 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>International journal of cancer : (Print); ISSN 0020-7136; Coden IJCNAW; Etats-Unis; Da. 2013; Vol. 133; No. 12; Pp. 2968-2979; Bibl. 35 ref.</SO>
<LA>Anglais</LA>
<EA>Positive associations have been reported between the measures of accelerated fetal growth and risk of childhood acute lymphoblastic leukemia (ALL). We investigated this association by pooling individual-level data from 12 case-control studies participating in the Childhood Leukemia International Consortium. Two measures of fetal growth-weight-for-gestational-age and proportion of optimal birth weight (POBW)-were analysed. Study-specific odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using multivariable logistic regression, and combined in fixed effects meta-analyses. Pooled analyses of all data were also undertaken using multivariable logistic regression. Subgroup analyses were undertaken when possible. Data on weight for gestational age were available for 7,348 cases and 12,489 controls from all 12 studies and POBW data were available for 1,680 cases and 3,139 controls from three studies. The summary ORs from the meta-analyses were 1.24 (95% CI: 1.13, 1.36) for children who were large for gestational age relative to appropriate for gestational age, and 1.16 (95% CI: 1.09, 1.24) for a one-standard deviation increase in POBW. The pooled analyses produced similar results. The summary and pooled ORs for small-for-gestational-age children were 0.83 (95% CI: 0.75, 0.92) and 0.86 (95% CI: 0.77, 0.95), respectively. Results were consistent across subgroups defined by sex, ethnicity and immunophenotype, and when the analysis was restricted to children who did not have high birth weight. The evidence that accelerated fetal growth is associated with a modest increased risk of childhood ALL is strong and consistent with known biological mechanisms involving insulin-like growth factors.</EA>
<CC>002B04; 002B19B</CC>
<FD>Foetus; Croissance; Enfant; Leucémie aiguë lymphoblastique; Poids naissance; Métaanalyse; Cancérologie</FD>
<FG>Homme; Hémopathie maligne; Cancer; Syndrome lymphoprolifératif</FG>
<ED>Fetus; Growth; Child; Acute lymphocytic leukemia; Birth weight; Metaanalysis; Cancerology</ED>
<EG>Human; Malignant hemopathy; Cancer; Lymphoproliferative syndrome</EG>
<SD>Feto; Crecimiento; Niño; Leucemia aguda linfoblástica; Peso nacimiento; Meta-análisis; Cancerología</SD>
<LO>INIST-13027.354000501579740220</LO>
<ID>13-0338338</ID>
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