Cargando…
Use of fertility drugs and risk of ovarian cancer: Danish population based cohort study
Objective To examine the effects of fertility drugs on overall risk of ovarian cancer using data from a large cohort of infertile women. Design Population based cohort study. Setting Danish hospitals and private fertility clinics. Participants 54 362 women with infertility problems referred to all D...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group Ltd.
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2640154/ https://www.ncbi.nlm.nih.gov/pubmed/19196744 http://dx.doi.org/10.1136/bmj.b249 |
_version_ | 1782164534658596864 |
---|---|
author | Jensen, Allan Sharif, Heidi Frederiksen, Kirsten Kjær, Susanne Krüger |
author_facet | Jensen, Allan Sharif, Heidi Frederiksen, Kirsten Kjær, Susanne Krüger |
author_sort | Jensen, Allan |
collection | PubMed |
description | Objective To examine the effects of fertility drugs on overall risk of ovarian cancer using data from a large cohort of infertile women. Design Population based cohort study. Setting Danish hospitals and private fertility clinics. Participants 54 362 women with infertility problems referred to all Danish fertility clinics during 1963-98. The median age at first evaluation of infertility was 30 years (range 16-55 years), and the median age at the end of follow-up was 47 (range 18-81) years. Included in the analysis were 156 women with invasive epithelial ovarian cancer (cases) and 1241 subcohort members identified in the cohort during follow-up in 2006. Main outcome measure Effect of four groups of fertility drugs (gonadotrophins, clomifene citrate, human chorionic gonadotrophin, and gonadotrophin releasing hormone) on overall risk of ovarian cancer after adjustment for potential confounding factors. Results Analyses within cohort showed no overall increased risk of ovarian cancer after any use of gonadotrophins (rate ratio 0.83, 95% confidence interval 0.50 to 1.37), clomifene (1.14, 0.79 to 1.64), human chorionic gonadotrophin (0.89, 0.62 to 1.29), or gonadotrophin releasing hormone (0.80, 0.42 to 1.51). Furthermore, no associations were found between all four groups of fertility drugs and number of cycles of use, length of follow-up, or parity. Conclusion No convincing association was found between use of fertility drugs and risk of ovarian cancer. |
format | Text |
id | pubmed-2640154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BMJ Publishing Group Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-26401542009-02-12 Use of fertility drugs and risk of ovarian cancer: Danish population based cohort study Jensen, Allan Sharif, Heidi Frederiksen, Kirsten Kjær, Susanne Krüger BMJ Research Objective To examine the effects of fertility drugs on overall risk of ovarian cancer using data from a large cohort of infertile women. Design Population based cohort study. Setting Danish hospitals and private fertility clinics. Participants 54 362 women with infertility problems referred to all Danish fertility clinics during 1963-98. The median age at first evaluation of infertility was 30 years (range 16-55 years), and the median age at the end of follow-up was 47 (range 18-81) years. Included in the analysis were 156 women with invasive epithelial ovarian cancer (cases) and 1241 subcohort members identified in the cohort during follow-up in 2006. Main outcome measure Effect of four groups of fertility drugs (gonadotrophins, clomifene citrate, human chorionic gonadotrophin, and gonadotrophin releasing hormone) on overall risk of ovarian cancer after adjustment for potential confounding factors. Results Analyses within cohort showed no overall increased risk of ovarian cancer after any use of gonadotrophins (rate ratio 0.83, 95% confidence interval 0.50 to 1.37), clomifene (1.14, 0.79 to 1.64), human chorionic gonadotrophin (0.89, 0.62 to 1.29), or gonadotrophin releasing hormone (0.80, 0.42 to 1.51). Furthermore, no associations were found between all four groups of fertility drugs and number of cycles of use, length of follow-up, or parity. Conclusion No convincing association was found between use of fertility drugs and risk of ovarian cancer. BMJ Publishing Group Ltd. 2009-02-05 /pmc/articles/PMC2640154/ /pubmed/19196744 http://dx.doi.org/10.1136/bmj.b249 Text en © Jensen et al 2009 http://creativecommons.org/licenses/by-nc/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Jensen, Allan Sharif, Heidi Frederiksen, Kirsten Kjær, Susanne Krüger Use of fertility drugs and risk of ovarian cancer: Danish population based cohort study |
title | Use of fertility drugs and risk of ovarian cancer: Danish population based cohort study |
title_full | Use of fertility drugs and risk of ovarian cancer: Danish population based cohort study |
title_fullStr | Use of fertility drugs and risk of ovarian cancer: Danish population based cohort study |
title_full_unstemmed | Use of fertility drugs and risk of ovarian cancer: Danish population based cohort study |
title_short | Use of fertility drugs and risk of ovarian cancer: Danish population based cohort study |
title_sort | use of fertility drugs and risk of ovarian cancer: danish population based cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2640154/ https://www.ncbi.nlm.nih.gov/pubmed/19196744 http://dx.doi.org/10.1136/bmj.b249 |
work_keys_str_mv | AT jensenallan useoffertilitydrugsandriskofovariancancerdanishpopulationbasedcohortstudy AT sharifheidi useoffertilitydrugsandriskofovariancancerdanishpopulationbasedcohortstudy AT frederiksenkirsten useoffertilitydrugsandriskofovariancancerdanishpopulationbasedcohortstudy AT kjærsusannekruger useoffertilitydrugsandriskofovariancancerdanishpopulationbasedcohortstudy |