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dc.contributor.authorBotteri, Edoardo
dc.contributor.authorStøer, Nathalie Charlotte
dc.contributor.authorSakshaug, Solveig
dc.contributor.authorGraff-Iversen, Sidsel
dc.contributor.authorVangen, Siri
dc.contributor.authorHofvind, Solveig
dc.contributor.authorde Lange, Thomas
dc.contributor.authorBagnardi, Vincenzo
dc.contributor.authorUrsin, Giske
dc.contributor.authorWeiderpass, Elisabete
dc.date.accessioned2018-02-16T11:24:42Z
dc.date.accessioned2018-06-22T06:47:22Z
dc.date.available2018-02-16T11:24:42Z
dc.date.available2018-06-22T06:47:22Z
dc.date.issued2017-11-15
dc.identifier.citationBotteri E, Støer N, Sakshaug S, Graff-Iversen S, Vangen S, Hofvind S, de Lange T, Bagnardi, Ursin G, Weiderpass E. Menopausal hormone therapy and colorectal cancer: a linkage between nationwide registries in Norway.. BMJ Open. 2017;7(11)en
dc.identifier.issn2044-6055
dc.identifier.issn2044-6055
dc.identifier.urihttps://hdl.handle.net/10642/5980
dc.description.abstractObjectives: With the present study, we aimed to investigate the association between menopausal hormone therapy (HT) and risk of colorectal cancer (CRC). Setting: Cohort study based on the linkage of Norwegian population-based registries. Participants: We selected 466822 Norwegian women, aged 55–79, alive and residing in Norway as of 1 January 2004, and we followed them from 2004 to 2008. Each woman contributed person-years at risk as non-user, current user and/or past HT user. Outcome measures: The outcome of interest was adenocarcinoma of the colorectal tract, overall, by anatomic site and stage at diagnosis. Incidence rate ratios (RRs) with 95% CIs were estimated by Poisson regression and were used to evaluate the association between HT and CRC incidence. Results: During the median follow-up of 4.8 years, 138 655 (30%) women received HT and 3799 (0.8%) incident CRCs occurred. Current, but not past, use of HT was associated with a lower risk of CRC (RR 0.88; 95% CI 0.80 to 0.98). RRs for localised, regionally advanced and metastatic CRC were 1.13 (95% CI 0.91 to 1.41), 0.81 (95% CI 0.70 to 0.94) and 0.79 (95% CI 0.62 to 1.00), respectively. RRs for current use of oestrogen therapy (ET) were 0.91 (95% CI 0.80 to 1.04) while RR for current use of combined oestrogen–progestin therapy (EPT) was 0.85 (95% CI 0.70 to 1.03), as compared with no use of HT. The same figures for ET and EPT in oral formulations were 0.83 (95% CI 0.68 to 1.03) and 0.86 (95% CI 0.71 to 1.05), respectively. Conclusions: In our nationwide cohort study, HT use lowered the risk of CRC, specifically the most advanced CRC.en
dc.language.isoenen
dc.publisherBMJ Publishing Groupen
dc.relation.ispartofseriesBMJ Open;Volume 7, Issue 11
dc.relation.urihttp://bmjopen.bmj.com/content/bmjopen/7/11/e017639.full.pdf
dc.rightsOpen Access: 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/ © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.en
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectMenopausal hormone therapiesen
dc.subjectColorectal canceren
dc.subjectNationwide registriesen
dc.subjectNorwayen
dc.titleMenopausal hormone therapy and colorectal cancer: a linkage between nationwide registries in Norway.en
dc.typeJournal articleen
dc.typePeer revieweden
dc.date.updated2018-02-16T11:24:42Z
dc.description.versionpublishedVersionen
dc.identifier.doihttp://dx.doi.org/10.1136/bmjopen-2017-017639
dc.identifier.cristin1560485
dc.source.journalBMJ Open


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Open Access: 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/ © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.
Med mindre annet er angitt, så er denne innførselen lisensiert som Open Access: 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/ © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.