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dc.contributor.authorDaltveit, Dagrun Slettebø
dc.contributor.authorKlungsøyr, Kari
dc.contributor.authorEngeland, Anders
dc.contributor.authorEkbom, Anders
dc.contributor.authorGissler, Mika
dc.contributor.authorGlimelius, Ingrid
dc.contributor.authorGrotmol, Tom
dc.contributor.authorMadanat-Harjuoja, Laura M.
dc.contributor.authorOrding, Anne Gulbech
dc.contributor.authorSæther, Solbjørg Makalani Myrtveit
dc.contributor.authorSørensen, Henrik Toft
dc.contributor.authorTroisi, Rebecca
dc.contributor.authorBjørge, Tone
dc.date.accessioned2021-06-01T08:18:34Z
dc.date.available2021-06-01T08:18:34Z
dc.date.created2021-01-12T14:03:47Z
dc.date.issued2020
dc.PublishedBMJ. British Medical Journal. 2020, .
dc.identifier.issn1756-1833
dc.identifier.urihttps://hdl.handle.net/11250/2757151
dc.description.abstractObjective To examine associations between birth defects and cancer from birth into adulthood. Design Population based nested case-control study. Setting Nationwide health registries in Denmark, Finland, Norway, and Sweden. Participants 62 295 cancer cases (0-46 years) and 724 542 frequency matched controls (matched on country and birth year), born between 1967 and 2014. Main outcome measures Relative risk of cancer in relation to major birth defects, estimated as odds ratios with 99% confidence intervals from logistic regression models. Results Altogether, 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. Conclusions The 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.en_US
dc.language.isoengen_US
dc.publisherBMJ Publishing Groupen_US
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.titleCancer risk in individuals with major birth defects: large Nordic population based case-control study among children, adolescents, and adultsen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.source.articlenumberm4060en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1136/bmj.m4060
dc.identifier.cristin1869892
dc.source.journalBMJen_US
dc.relation.projectKreftregisteret: 5703714-2014en_US
dc.identifier.citationBMJ. 2020, 371, m4060.en_US
dc.source.volume371en_US


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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