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Cancer risk in individuals with major birth defects: large Nordic population based case-control study among children, adolescents, and adults

AbstractObjectiveTo examine associations between birth defects and cancer from birth into adulthood.DesignPopulation based nested case-control study.SettingNationwide health registries in Denmark, Finland, Norway, and Sweden.Participants62 295 cancer cases (0-46 years) and 724 542 frequency matched...

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Published in:BMJ (Online) 2020-12, Vol.371, p.m4060-m4060
Main Authors: Daltveit, Dagrun Slettebø, Klungsøyr, Kari, Engeland, Anders, Ekbom, Anders, Gissler, Mika, Glimelius, Ingrid, Grotmol, Tom, Madanat-Harjuoja, Laura, Ording, Anne Gulbech, Sæther, Solbjørg Makalani Myrtveit, Sørensen, Henrik Toft, Troisi, Rebecca, Bjørge, Tone
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cited_by cdi_FETCH-LOGICAL-b507t-2b98e0e56548a121ad4616f2f8c2b29f50eb866870741d5647bced73752ce0773
cites cdi_FETCH-LOGICAL-b507t-2b98e0e56548a121ad4616f2f8c2b29f50eb866870741d5647bced73752ce0773
container_end_page m4060
container_issue
container_start_page m4060
container_title BMJ (Online)
container_volume 371
creator Daltveit, Dagrun Slettebø
Klungsøyr, Kari
Engeland, Anders
Ekbom, Anders
Gissler, Mika
Glimelius, Ingrid
Grotmol, Tom
Madanat-Harjuoja, Laura
Ording, Anne Gulbech
Sæther, Solbjørg Makalani Myrtveit
Sørensen, Henrik Toft
Troisi, Rebecca
Bjørge, Tone
description AbstractObjectiveTo examine associations between birth defects and cancer from birth into adulthood.DesignPopulation based nested case-control study.SettingNationwide health registries in Denmark, Finland, Norway, and Sweden.Participants62 295 cancer cases (0-46 years) and 724 542 frequency matched controls (matched on country and birth year), born between 1967 and 2014.Main outcome measuresRelative risk of cancer in relation to major birth defects, estimated as odds ratios with 99% confidence intervals from logistic regression models.ResultsAltogether, 3.5% (2160/62 295) of cases and 2.2% (15 826/724 542) of controls were born with major birth defects. The odds ratio of cancer for people with major birth defects compared with those without was 1.74 (99% confidence interval 1.63 to 1.84). For individuals with non-chromosomal birth defects, the odds ratio of cancer was 1.54 (1.44 to 1.64); for those with chromosomal anomalies, the odds ratio was 5.53 (4.67 to 6.54). Many structural birth defects were associated with later cancer in the same organ system or anatomical location, such as defects of the eye, nervous system, and urinary organs. The odds ratio of cancer increased with number of defects and decreased with age, for both non-chromosomal and chromosomal anomalies. The odds ratio of cancer in people with any non-chromosomal birth defect was lower in adults (≥20 years: 1.21, 1.09 to 1.33) than in adolescents (15-19 years: 1.58, 1.31 to 1.90) and children (0-14 years: 2.03, 1.85 to 2.23). The relative overall cancer risk among adults with chromosomal anomalies was markedly reduced from 11.3 (9.35 to 13.8) in children to 1.50 (1.01 to 2.24). Among adults, skeletal dysplasia (odds ratio 3.54, 1.54 to 8.15), nervous system defects (1.76, 1.16 to 2.65), chromosomal anomalies (1.50, 1.01 to 2.24), genital organs defects (1.43, 1.14 to 1.78), and congenital heart defects (1.28, 1.02 to 1.59) were associated with overall cancer risk.ConclusionsThe increased risk of cancer in individuals with birth defects persisted into adulthood, both for non-chromosomal and chromosomal anomalies. Further studies on the molecular mechanisms involved are warranted.
doi_str_mv 10.1136/bmj.m4060
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The odds ratio of cancer for people with major birth defects compared with those without was 1.74 (99% confidence interval 1.63 to 1.84). For individuals with non-chromosomal birth defects, the odds ratio of cancer was 1.54 (1.44 to 1.64); for those with chromosomal anomalies, the odds ratio was 5.53 (4.67 to 6.54). Many structural birth defects were associated with later cancer in the same organ system or anatomical location, such as defects of the eye, nervous system, and urinary organs. The odds ratio of cancer increased with number of defects and decreased with age, for both non-chromosomal and chromosomal anomalies. The odds ratio of cancer in people with any non-chromosomal birth defect was lower in adults (≥20 years: 1.21, 1.09 to 1.33) than in adolescents (15-19 years: 1.58, 1.31 to 1.90) and children (0-14 years: 2.03, 1.85 to 2.23). The relative overall cancer risk among adults with chromosomal anomalies was markedly reduced from 11.3 (9.35 to 13.8) in children to 1.50 (1.01 to 2.24). Among adults, skeletal dysplasia (odds ratio 3.54, 1.54 to 8.15), nervous system defects (1.76, 1.16 to 2.65), chromosomal anomalies (1.50, 1.01 to 2.24), genital organs defects (1.43, 1.14 to 1.78), and congenital heart defects (1.28, 1.02 to 1.59) were associated with overall cancer risk.ConclusionsThe increased risk of cancer in individuals with birth defects persisted into adulthood, both for non-chromosomal and chromosomal anomalies. Further studies on the molecular mechanisms involved are warranted.</description><identifier>ISSN: 1756-1833</identifier><identifier>ISSN: 0959-8138</identifier><identifier>EISSN: 1756-1833</identifier><identifier>DOI: 10.1136/bmj.m4060</identifier><identifier>PMID: 33268348</identifier><language>eng</language><publisher>England: BMJ Publishing Group LTD</publisher><subject>Abnormalities, Multiple - epidemiology ; Adolescent ; Adolescents ; Adult ; Adults ; Age ; Age Factors ; Birth defects ; Birth weight ; Bone Diseases, Developmental - epidemiology ; Bone dysplasia ; Cancer ; Case-Control Studies ; Child ; Child, Preschool ; Children ; Chromosome Aberrations ; Classification ; Confidence intervals ; Congenital Abnormalities - epidemiology ; Congenital defects ; Congenital diseases ; Denmark - epidemiology ; Dysplasia ; Female ; Finland - epidemiology ; Heart Defects, Congenital - epidemiology ; Humans ; Infant ; Infant, Newborn ; Leukemia ; Logistic Models ; Male ; Medical diagnosis ; Middle Aged ; Molecular modelling ; Morphology ; Multiple births ; Neoplasms - epidemiology ; Nervous system ; Nervous System Malformations - epidemiology ; Norway - epidemiology ; Odds Ratio ; Population ; Population studies ; Population-based studies ; Registries ; Regression analysis ; Risk Factors ; Skeleton ; Sweden - epidemiology ; Teenagers ; Tumors ; Urogenital Abnormalities - epidemiology ; Young Adult</subject><ispartof>BMJ (Online), 2020-12, Vol.371, p.m4060-m4060</ispartof><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2020 Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. BMJ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. 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The odds ratio of cancer for people with major birth defects compared with those without was 1.74 (99% confidence interval 1.63 to 1.84). For individuals with non-chromosomal birth defects, the odds ratio of cancer was 1.54 (1.44 to 1.64); for those with chromosomal anomalies, the odds ratio was 5.53 (4.67 to 6.54). Many structural birth defects were associated with later cancer in the same organ system or anatomical location, such as defects of the eye, nervous system, and urinary organs. The odds ratio of cancer increased with number of defects and decreased with age, for both non-chromosomal and chromosomal anomalies. The odds ratio of cancer in people with any non-chromosomal birth defect was lower in adults (≥20 years: 1.21, 1.09 to 1.33) than in adolescents (15-19 years: 1.58, 1.31 to 1.90) and children (0-14 years: 2.03, 1.85 to 2.23). The relative overall cancer risk among adults with chromosomal anomalies was markedly reduced from 11.3 (9.35 to 13.8) in children to 1.50 (1.01 to 2.24). Among adults, skeletal dysplasia (odds ratio 3.54, 1.54 to 8.15), nervous system defects (1.76, 1.16 to 2.65), chromosomal anomalies (1.50, 1.01 to 2.24), genital organs defects (1.43, 1.14 to 1.78), and congenital heart defects (1.28, 1.02 to 1.59) were associated with overall cancer risk.ConclusionsThe increased risk of cancer in individuals with birth defects persisted into adulthood, both for non-chromosomal and chromosomal anomalies. 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Klungsøyr, Kari ; Engeland, Anders ; Ekbom, Anders ; Gissler, Mika ; Glimelius, Ingrid ; Grotmol, Tom ; Madanat-Harjuoja, Laura ; Ording, Anne Gulbech ; Sæther, Solbjørg Makalani Myrtveit ; Sørensen, Henrik Toft ; Troisi, Rebecca ; Bjørge, Tone</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b507t-2b98e0e56548a121ad4616f2f8c2b29f50eb866870741d5647bced73752ce0773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Abnormalities, Multiple - epidemiology</topic><topic>Adolescent</topic><topic>Adolescents</topic><topic>Adult</topic><topic>Adults</topic><topic>Age</topic><topic>Age Factors</topic><topic>Birth defects</topic><topic>Birth weight</topic><topic>Bone Diseases, Developmental - epidemiology</topic><topic>Bone dysplasia</topic><topic>Cancer</topic><topic>Case-Control Studies</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Chromosome Aberrations</topic><topic>Classification</topic><topic>Confidence intervals</topic><topic>Congenital Abnormalities - epidemiology</topic><topic>Congenital defects</topic><topic>Congenital diseases</topic><topic>Denmark - epidemiology</topic><topic>Dysplasia</topic><topic>Female</topic><topic>Finland - epidemiology</topic><topic>Heart Defects, Congenital - epidemiology</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Leukemia</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Medical diagnosis</topic><topic>Middle Aged</topic><topic>Molecular modelling</topic><topic>Morphology</topic><topic>Multiple births</topic><topic>Neoplasms - epidemiology</topic><topic>Nervous system</topic><topic>Nervous System Malformations - epidemiology</topic><topic>Norway - epidemiology</topic><topic>Odds Ratio</topic><topic>Population</topic><topic>Population studies</topic><topic>Population-based studies</topic><topic>Registries</topic><topic>Regression analysis</topic><topic>Risk Factors</topic><topic>Skeleton</topic><topic>Sweden - epidemiology</topic><topic>Teenagers</topic><topic>Tumors</topic><topic>Urogenital Abnormalities - epidemiology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Daltveit, Dagrun Slettebø</creatorcontrib><creatorcontrib>Klungsøyr, Kari</creatorcontrib><creatorcontrib>Engeland, Anders</creatorcontrib><creatorcontrib>Ekbom, Anders</creatorcontrib><creatorcontrib>Gissler, Mika</creatorcontrib><creatorcontrib>Glimelius, Ingrid</creatorcontrib><creatorcontrib>Grotmol, Tom</creatorcontrib><creatorcontrib>Madanat-Harjuoja, Laura</creatorcontrib><creatorcontrib>Ording, Anne Gulbech</creatorcontrib><creatorcontrib>Sæther, Solbjørg Makalani Myrtveit</creatorcontrib><creatorcontrib>Sørensen, Henrik Toft</creatorcontrib><creatorcontrib>Troisi, Rebecca</creatorcontrib><creatorcontrib>Bjørge, Tone</creatorcontrib><collection>BMJ Journals (Open Access)</collection><collection>BMJ Journals:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SWEPUB Uppsala universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Uppsala universitet</collection><collection>SwePub Articles full text</collection><jtitle>BMJ (Online)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Daltveit, Dagrun Slettebø</au><au>Klungsøyr, Kari</au><au>Engeland, Anders</au><au>Ekbom, Anders</au><au>Gissler, Mika</au><au>Glimelius, Ingrid</au><au>Grotmol, Tom</au><au>Madanat-Harjuoja, Laura</au><au>Ording, Anne Gulbech</au><au>Sæther, Solbjørg Makalani Myrtveit</au><au>Sørensen, Henrik Toft</au><au>Troisi, Rebecca</au><au>Bjørge, Tone</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cancer risk in individuals with major birth defects: large Nordic population based case-control study among children, adolescents, and adults</atitle><jtitle>BMJ (Online)</jtitle><addtitle>BMJ</addtitle><date>2020-12-02</date><risdate>2020</risdate><volume>371</volume><spage>m4060</spage><epage>m4060</epage><pages>m4060-m4060</pages><issn>1756-1833</issn><issn>0959-8138</issn><eissn>1756-1833</eissn><abstract>AbstractObjectiveTo examine associations between birth defects and cancer from birth into adulthood.DesignPopulation based nested case-control study.SettingNationwide health registries in Denmark, Finland, Norway, and Sweden.Participants62 295 cancer cases (0-46 years) and 724 542 frequency matched controls (matched on country and birth year), born between 1967 and 2014.Main outcome measuresRelative risk of cancer in relation to major birth defects, estimated as odds ratios with 99% confidence intervals from logistic regression models.ResultsAltogether, 3.5% (2160/62 295) of cases and 2.2% (15 826/724 542) of controls were born with major birth defects. The odds ratio of cancer for people with major birth defects compared with those without was 1.74 (99% confidence interval 1.63 to 1.84). For individuals with non-chromosomal birth defects, the odds ratio of cancer was 1.54 (1.44 to 1.64); for those with chromosomal anomalies, the odds ratio was 5.53 (4.67 to 6.54). Many structural birth defects were associated with later cancer in the same organ system or anatomical location, such as defects of the eye, nervous system, and urinary organs. The odds ratio of cancer increased with number of defects and decreased with age, for both non-chromosomal and chromosomal anomalies. The odds ratio of cancer in people with any non-chromosomal birth defect was lower in adults (≥20 years: 1.21, 1.09 to 1.33) than in adolescents (15-19 years: 1.58, 1.31 to 1.90) and children (0-14 years: 2.03, 1.85 to 2.23). The relative overall cancer risk among adults with chromosomal anomalies was markedly reduced from 11.3 (9.35 to 13.8) in children to 1.50 (1.01 to 2.24). Among adults, skeletal dysplasia (odds ratio 3.54, 1.54 to 8.15), nervous system defects (1.76, 1.16 to 2.65), chromosomal anomalies (1.50, 1.01 to 2.24), genital organs defects (1.43, 1.14 to 1.78), and congenital heart defects (1.28, 1.02 to 1.59) were associated with overall cancer risk.ConclusionsThe increased risk of cancer in individuals with birth defects persisted into adulthood, both for non-chromosomal and chromosomal anomalies. Further studies on the molecular mechanisms involved are warranted.</abstract><cop>England</cop><pub>BMJ Publishing Group LTD</pub><pmid>33268348</pmid><doi>10.1136/bmj.m4060</doi><orcidid>https://orcid.org/0000-0002-0903-1140</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1756-1833
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issn 1756-1833
0959-8138
1756-1833
language eng
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source JSTOR Archival Journals and Primary Sources Collection; BMJ Publishing
subjects Abnormalities, Multiple - epidemiology
Adolescent
Adolescents
Adult
Adults
Age
Age Factors
Birth defects
Birth weight
Bone Diseases, Developmental - epidemiology
Bone dysplasia
Cancer
Case-Control Studies
Child
Child, Preschool
Children
Chromosome Aberrations
Classification
Confidence intervals
Congenital Abnormalities - epidemiology
Congenital defects
Congenital diseases
Denmark - epidemiology
Dysplasia
Female
Finland - epidemiology
Heart Defects, Congenital - epidemiology
Humans
Infant
Infant, Newborn
Leukemia
Logistic Models
Male
Medical diagnosis
Middle Aged
Molecular modelling
Morphology
Multiple births
Neoplasms - epidemiology
Nervous system
Nervous System Malformations - epidemiology
Norway - epidemiology
Odds Ratio
Population
Population studies
Population-based studies
Registries
Regression analysis
Risk Factors
Skeleton
Sweden - epidemiology
Teenagers
Tumors
Urogenital Abnormalities - epidemiology
Young Adult
title Cancer risk in individuals with major birth defects: large Nordic population based case-control study among children, adolescents, and adults
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