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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 |
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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. Published by BMJ. 2020 BMJ</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b507t-2b98e0e56548a121ad4616f2f8c2b29f50eb866870741d5647bced73752ce0773</citedby><cites>FETCH-LOGICAL-b507t-2b98e0e56548a121ad4616f2f8c2b29f50eb866870741d5647bced73752ce0773</cites><orcidid>0000-0002-0903-1140</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://bmj.com/content/371/bmj.m4060.full.pdf$$EPDF$$P50$$Gbmj$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://bmj.com/content/371/bmj.m4060.full$$EHTML$$P50$$Gbmj$$Hfree_for_read</linktohtml><link.rule.ids>112,113,230,314,780,784,885,3192,27923,27924,77365,77366</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33268348$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-431455$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><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><title>Cancer risk in individuals with major birth defects: large Nordic population based case-control study among children, adolescents, and adults</title><title>BMJ (Online)</title><addtitle>BMJ</addtitle><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.</description><subject>Abnormalities, Multiple - epidemiology</subject><subject>Adolescent</subject><subject>Adolescents</subject><subject>Adult</subject><subject>Adults</subject><subject>Age</subject><subject>Age Factors</subject><subject>Birth defects</subject><subject>Birth weight</subject><subject>Bone Diseases, Developmental - epidemiology</subject><subject>Bone dysplasia</subject><subject>Cancer</subject><subject>Case-Control Studies</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Chromosome Aberrations</subject><subject>Classification</subject><subject>Confidence intervals</subject><subject>Congenital Abnormalities - epidemiology</subject><subject>Congenital defects</subject><subject>Congenital diseases</subject><subject>Denmark - epidemiology</subject><subject>Dysplasia</subject><subject>Female</subject><subject>Finland - epidemiology</subject><subject>Heart Defects, Congenital - epidemiology</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Leukemia</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Medical diagnosis</subject><subject>Middle Aged</subject><subject>Molecular modelling</subject><subject>Morphology</subject><subject>Multiple births</subject><subject>Neoplasms - epidemiology</subject><subject>Nervous system</subject><subject>Nervous System Malformations - epidemiology</subject><subject>Norway - epidemiology</subject><subject>Odds Ratio</subject><subject>Population</subject><subject>Population studies</subject><subject>Population-based studies</subject><subject>Registries</subject><subject>Regression analysis</subject><subject>Risk Factors</subject><subject>Skeleton</subject><subject>Sweden - epidemiology</subject><subject>Teenagers</subject><subject>Tumors</subject><subject>Urogenital Abnormalities - epidemiology</subject><subject>Young Adult</subject><issn>1756-1833</issn><issn>0959-8138</issn><issn>1756-1833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><recordid>eNp1kttqFDEcxgdRbKm98AUkoBcKnZpzsl4IZT1C0Rv1NmSSzG7WTLImk5Y-hO9stltLKwghx9__y5fwdd1TBE8RIvz1MG1OJwo5fNAdIsF4jyQhD-_MD7rjUjYQQkyEXHD2uDsgBHNJqDzsfi91NC6D7MtP4GNr1l94W3Uo4NLPazDpTcpg8LnNrRudmcsbEHReOfAlZesN2KZtDXr2KYJBF2eBaX1vUpxzCqDM1V4BPaW4Ambtg80ungBtU3DFuDiXtoi2bdQwlyfdo7Hd7I5vxqPu-4f335af-vOvHz8vz877gUEx93hYSAcd44xKjTDSlnLERzxKgwe8GBl0g-RcCigosoxTMRhnBREMGweFIEfdyV63XLptHdQ2-0nnK5W0V-_8jzOV8krVqihBlLGGv93jjZ2c3dnOOtyrun8S_Vqt0oUSAkqJZRN4eSOQ06_qyqwm314fgo4u1aIw5Vw0v5Q09Pk_6CbVHNtvXFNIEAxho17tKZNTKdmNt2YQVLtYqBYLdR2Lxj676_6W_BuCBrzYA7ua_-v8ASp9wQY</recordid><startdate>20201202</startdate><enddate>20201202</enddate><creator>Daltveit, Dagrun Slettebø</creator><creator>Klungsøyr, Kari</creator><creator>Engeland, Anders</creator><creator>Ekbom, Anders</creator><creator>Gissler, Mika</creator><creator>Glimelius, Ingrid</creator><creator>Grotmol, Tom</creator><creator>Madanat-Harjuoja, Laura</creator><creator>Ording, Anne Gulbech</creator><creator>Sæther, Solbjørg Makalani Myrtveit</creator><creator>Sørensen, Henrik Toft</creator><creator>Troisi, Rebecca</creator><creator>Bjørge, Tone</creator><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group Ltd</general><scope>9YT</scope><scope>ACMMV</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K6X</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>ACNBI</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DF2</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0002-0903-1140</orcidid></search><sort><creationdate>20201202</creationdate><title>Cancer risk in individuals with major birth defects: large Nordic population based case-control study among children, adolescents, and adults</title><author>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</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 & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>British Nursing Index</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & 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 & 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> |
fulltext | fulltext |
identifier | ISSN: 1756-1833 |
ispartof | BMJ (Online), 2020-12, Vol.371, p.m4060-m4060 |
issn | 1756-1833 0959-8138 1756-1833 |
language | eng |
recordid | cdi_swepub_primary_oai_DiVA_org_uu_431455 |
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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