Cargando…

Reproductive Factors and Colorectal Cancer Risk: A Population-Based Case-Control Study

BACKGROUND: Hormone-replacement therapy (HRT) is associated with lower colorectal cancer (CRC) risk among postmenopausal women. However, little is known about the effects of lifetime exposure of women to varying levels of estrogen and progesterone through reproductive factors such as parity, use of...

Descripción completa

Detalles Bibliográficos
Autores principales: Amitay, Efrat L, Niedermaier, Tobias, Alwers, Elizabeth, Chang-Claude, Jenny, Hoffmeister, Michael, Brenner, Hermann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251386/
https://www.ncbi.nlm.nih.gov/pubmed/35642982
http://dx.doi.org/10.1093/jncics/pkac042
_version_ 1784740016475340800
author Amitay, Efrat L
Niedermaier, Tobias
Alwers, Elizabeth
Chang-Claude, Jenny
Hoffmeister, Michael
Brenner, Hermann
author_facet Amitay, Efrat L
Niedermaier, Tobias
Alwers, Elizabeth
Chang-Claude, Jenny
Hoffmeister, Michael
Brenner, Hermann
author_sort Amitay, Efrat L
collection PubMed
description BACKGROUND: Hormone-replacement therapy (HRT) is associated with lower colorectal cancer (CRC) risk among postmenopausal women. However, little is known about the effects of lifetime exposure of women to varying levels of estrogen and progesterone through reproductive factors such as parity, use of oral contraceptives (OC), breastfeeding, and menstruation on CRC risk. METHODS: We assessed associations between reproductive factors and CRC risk among 2650 female CRC patients aged 30+ years and 2175 matched controls in a population-based study in Germany, adjusting for potential confounders by multiple logistic regression. RESULTS: Inverse associations with CRC risk were found for numbers of pregnancies (odds ratio [OR] per pregnancy = 0.91, 95% confidence interval [CI] = 0.86 to 0.97), breastfeeding for 12 months and longer (OR = 0.74, 95% CI = 0.61 to 0.90), and use of either OC or HRT (OR = 0.75, 95% CI = 0.64 to 0.87) or both (OR = 0.58, 95% CI = 0.48 to 0.70). Similar results were found for postmenopausal women only and when adjusting for number of pregnancies and for all reproductive factors analyzed together. Breastfeeding duration of 12 months and longer was associated with lower risk of cancer only in the proximal colon (OR = 0.58, 95% CI = 0.45 to 0.74). CONCLUSIONS: Several reproductive factors were associated with lower CRC risk in women, including number of pregnancies, breastfeeding duration, and use of OC and HRT. This suggests that women’s exposure to female reproductive hormones plays a key role in the difference in CRC risk between women and men and in site-specific CRC risk.
format Online
Article
Text
id pubmed-9251386
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-92513862022-07-05 Reproductive Factors and Colorectal Cancer Risk: A Population-Based Case-Control Study Amitay, Efrat L Niedermaier, Tobias Alwers, Elizabeth Chang-Claude, Jenny Hoffmeister, Michael Brenner, Hermann JNCI Cancer Spectr Article BACKGROUND: Hormone-replacement therapy (HRT) is associated with lower colorectal cancer (CRC) risk among postmenopausal women. However, little is known about the effects of lifetime exposure of women to varying levels of estrogen and progesterone through reproductive factors such as parity, use of oral contraceptives (OC), breastfeeding, and menstruation on CRC risk. METHODS: We assessed associations between reproductive factors and CRC risk among 2650 female CRC patients aged 30+ years and 2175 matched controls in a population-based study in Germany, adjusting for potential confounders by multiple logistic regression. RESULTS: Inverse associations with CRC risk were found for numbers of pregnancies (odds ratio [OR] per pregnancy = 0.91, 95% confidence interval [CI] = 0.86 to 0.97), breastfeeding for 12 months and longer (OR = 0.74, 95% CI = 0.61 to 0.90), and use of either OC or HRT (OR = 0.75, 95% CI = 0.64 to 0.87) or both (OR = 0.58, 95% CI = 0.48 to 0.70). Similar results were found for postmenopausal women only and when adjusting for number of pregnancies and for all reproductive factors analyzed together. Breastfeeding duration of 12 months and longer was associated with lower risk of cancer only in the proximal colon (OR = 0.58, 95% CI = 0.45 to 0.74). CONCLUSIONS: Several reproductive factors were associated with lower CRC risk in women, including number of pregnancies, breastfeeding duration, and use of OC and HRT. This suggests that women’s exposure to female reproductive hormones plays a key role in the difference in CRC risk between women and men and in site-specific CRC risk. Oxford University Press 2022-06-01 /pmc/articles/PMC9251386/ /pubmed/35642982 http://dx.doi.org/10.1093/jncics/pkac042 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Amitay, Efrat L
Niedermaier, Tobias
Alwers, Elizabeth
Chang-Claude, Jenny
Hoffmeister, Michael
Brenner, Hermann
Reproductive Factors and Colorectal Cancer Risk: A Population-Based Case-Control Study
title Reproductive Factors and Colorectal Cancer Risk: A Population-Based Case-Control Study
title_full Reproductive Factors and Colorectal Cancer Risk: A Population-Based Case-Control Study
title_fullStr Reproductive Factors and Colorectal Cancer Risk: A Population-Based Case-Control Study
title_full_unstemmed Reproductive Factors and Colorectal Cancer Risk: A Population-Based Case-Control Study
title_short Reproductive Factors and Colorectal Cancer Risk: A Population-Based Case-Control Study
title_sort reproductive factors and colorectal cancer risk: a population-based case-control study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251386/
https://www.ncbi.nlm.nih.gov/pubmed/35642982
http://dx.doi.org/10.1093/jncics/pkac042
work_keys_str_mv AT amitayefratl reproductivefactorsandcolorectalcancerriskapopulationbasedcasecontrolstudy
AT niedermaiertobias reproductivefactorsandcolorectalcancerriskapopulationbasedcasecontrolstudy
AT alwerselizabeth reproductivefactorsandcolorectalcancerriskapopulationbasedcasecontrolstudy
AT changclaudejenny reproductivefactorsandcolorectalcancerriskapopulationbasedcasecontrolstudy
AT hoffmeistermichael reproductivefactorsandcolorectalcancerriskapopulationbasedcasecontrolstudy
AT brennerhermann reproductivefactorsandcolorectalcancerriskapopulationbasedcasecontrolstudy