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dc.contributor.authorSun, Yi-Qian
dc.contributor.authorBrumpton, Ben Michael
dc.contributor.authorBonilla, Carolina
dc.contributor.authorLewis, Sarah J.
dc.contributor.authorBurgess, Stephen
dc.contributor.authorSkorpen, Frank
dc.contributor.authorChen, Yue
dc.contributor.authorNilsen, Tom Ivar Lund
dc.contributor.authorRomundstad, Pål Richard
dc.contributor.authorMai, Xiao-Mei
dc.date.accessioned2019-07-01T12:00:53Z
dc.date.available2019-07-01T12:00:53Z
dc.date.created2018-05-16T15:32:47Z
dc.date.issued2018
dc.identifier.issn0903-1936
dc.identifier.urihttp://hdl.handle.net/11250/2603040
dc.description.abstractWe aimed to investigate potential causal associations between serum 25-hydroxyvitamin D [25(OH)D] levels and incidence of lung cancer overall and histologic types. We performed a Mendelian randomization (MR) analysis using a prospective cohort study in Norway, including 54580 individuals and 676 incident lung cancer cases. A 25(OH)D allele score was generated based on vitamin D-increasing alleles of rs2282679, rs12785878 and rs10741657. Hazard ratios (HRs) with 95% confidence intervals (CIs) for incidence of lung cancer and histologic types were estimated in relation to the allele score. Inverse-variance weighted method using summarized data of individual single-nucleotide polymorphisms was applied to calculate the MR estimates. The allele score accounted for 3.4% of the variation in serum 25(OH)D levels. There was no association between the allele score and lung cancer incidence overall, with HR being 0.99 (95% CI 0.93 to 1.06) per allele score. A 25 nmol/L increase in genetically determined 25(OH)D level was not associated with the incidence of lung cancer overall (MR estimate HR 0.96, 95% CI 0.54 to 1.69) or any histologic type. MR analysis did not suggest causal association between 25(OH)D levels and risk of lung cancer overall or histologic types in this population-based cohort study.nb_NO
dc.language.isoengnb_NO
dc.publisherEuropean Respiratory Society: ERJnb_NO
dc.titleSerum 25-hydroxyvitamin D levels and risk of lung cancer and histologic types: a Mendelian randomization analysis of the HUNT studynb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.volume51nb_NO
dc.source.journalEuropean Respiratory Journalnb_NO
dc.source.issue6nb_NO
dc.identifier.doi10.1183/13993003.00329-2018
dc.identifier.cristin1585461
dc.relation.projectKreftforeningen: 5769155- 2015nb_NO
dc.relation.projectSamarbeidsorganet mellom Helse Midt-Norge og NTNU: #46055500-10nb_NO
dc.description.localcode© 2018. This is the authors' accepted and refereed manuscript to the article. The final authenticated version is available online at: 10.1183/13993003.00329-2018nb_NO
cristin.unitcode194,65,15,0
cristin.unitcode194,65,20,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.unitnameInstitutt for samfunnsmedisin og sykepleie
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.fulltextpostprint
cristin.qualitycode2


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