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Reproductive history and risk of colorectal adenocarcinoma in parous women: a Nordic population-based case–control study

BACKGROUND: Data are conflicting regarding the role of endogenous sex hormones in colorectal carcinogenesis. In this large population-based study, we pooled data from birth and cancer registries in four Nordic countries, to evaluate the risk of colorectal adenocarcinoma in relation to women's r...

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Autores principales: Bjørge, Tone, Gissler, Mika, Ording, Anne Gulbech, Engeland, Anders, Glimelius, Ingrid, Leinonen, Maarit, Sørensen, Henrik Toft, Tretli, Steinar, Ekbom, Anders, Troisi, Rebecca, Grotmol, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129816/
https://www.ncbi.nlm.nih.gov/pubmed/27701386
http://dx.doi.org/10.1038/bjc.2016.315
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author Bjørge, Tone
Gissler, Mika
Ording, Anne Gulbech
Engeland, Anders
Glimelius, Ingrid
Leinonen, Maarit
Sørensen, Henrik Toft
Tretli, Steinar
Ekbom, Anders
Troisi, Rebecca
Grotmol, Tom
author_facet Bjørge, Tone
Gissler, Mika
Ording, Anne Gulbech
Engeland, Anders
Glimelius, Ingrid
Leinonen, Maarit
Sørensen, Henrik Toft
Tretli, Steinar
Ekbom, Anders
Troisi, Rebecca
Grotmol, Tom
author_sort Bjørge, Tone
collection PubMed
description BACKGROUND: Data are conflicting regarding the role of endogenous sex hormones in colorectal carcinogenesis. In this large population-based study, we pooled data from birth and cancer registries in four Nordic countries, to evaluate the risk of colorectal adenocarcinoma in relation to women's reproductive history. METHODS: We conducted a population-based case–control study among women registered in Nordic birth registries. The study included colorectal adenocarcinoma cases diagnosed in Denmark, Finland, Norway, and Sweden during 1967–2013 and up to 10 matched controls per case, in total 22 185 cases and 220 246 controls. Odds ratios (ORs) with 95% confidence intervals (95% CIs) were derived from conditional logistic regression models. We had limited information available on possible confounders. RESULTS: We found no evidence for associations between colorectal adenocarcinoma and parity, age at first and last birth, and time since first and last birth. The risk estimates were also close to unity for specific cancer subsites (proximal and distal colon and rectum). As well, when the analyses were stratified on menopausal status, parity, and mother's year of birth, no indication of associations was found. CONCLUSIONS: In this large, Nordic population-based study, no evidence for associations was found between women's reproductive history and colorectal adenocarcinoma in parous women.
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spelling pubmed-51298162016-12-16 Reproductive history and risk of colorectal adenocarcinoma in parous women: a Nordic population-based case–control study Bjørge, Tone Gissler, Mika Ording, Anne Gulbech Engeland, Anders Glimelius, Ingrid Leinonen, Maarit Sørensen, Henrik Toft Tretli, Steinar Ekbom, Anders Troisi, Rebecca Grotmol, Tom Br J Cancer Epidemiology BACKGROUND: Data are conflicting regarding the role of endogenous sex hormones in colorectal carcinogenesis. In this large population-based study, we pooled data from birth and cancer registries in four Nordic countries, to evaluate the risk of colorectal adenocarcinoma in relation to women's reproductive history. METHODS: We conducted a population-based case–control study among women registered in Nordic birth registries. The study included colorectal adenocarcinoma cases diagnosed in Denmark, Finland, Norway, and Sweden during 1967–2013 and up to 10 matched controls per case, in total 22 185 cases and 220 246 controls. Odds ratios (ORs) with 95% confidence intervals (95% CIs) were derived from conditional logistic regression models. We had limited information available on possible confounders. RESULTS: We found no evidence for associations between colorectal adenocarcinoma and parity, age at first and last birth, and time since first and last birth. The risk estimates were also close to unity for specific cancer subsites (proximal and distal colon and rectum). As well, when the analyses were stratified on menopausal status, parity, and mother's year of birth, no indication of associations was found. CONCLUSIONS: In this large, Nordic population-based study, no evidence for associations was found between women's reproductive history and colorectal adenocarcinoma in parous women. Nature Publishing Group 2016-11-22 2016-10-04 /pmc/articles/PMC5129816/ /pubmed/27701386 http://dx.doi.org/10.1038/bjc.2016.315 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Epidemiology
Bjørge, Tone
Gissler, Mika
Ording, Anne Gulbech
Engeland, Anders
Glimelius, Ingrid
Leinonen, Maarit
Sørensen, Henrik Toft
Tretli, Steinar
Ekbom, Anders
Troisi, Rebecca
Grotmol, Tom
Reproductive history and risk of colorectal adenocarcinoma in parous women: a Nordic population-based case–control study
title Reproductive history and risk of colorectal adenocarcinoma in parous women: a Nordic population-based case–control study
title_full Reproductive history and risk of colorectal adenocarcinoma in parous women: a Nordic population-based case–control study
title_fullStr Reproductive history and risk of colorectal adenocarcinoma in parous women: a Nordic population-based case–control study
title_full_unstemmed Reproductive history and risk of colorectal adenocarcinoma in parous women: a Nordic population-based case–control study
title_short Reproductive history and risk of colorectal adenocarcinoma in parous women: a Nordic population-based case–control study
title_sort reproductive history and risk of colorectal adenocarcinoma in parous women: a nordic population-based case–control study
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129816/
https://www.ncbi.nlm.nih.gov/pubmed/27701386
http://dx.doi.org/10.1038/bjc.2016.315
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