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Digoxin and prostate cancer survival in the Finnish Randomized Study of Screening for Prostate Cancer

BACKGROUND: Protective effects have been suggested for digoxin against prostate cancer risk. However, few studies have evaluated the possible effects on prostate cancer-specific survival. We studied the association between use of digoxin or beta-blocker sotalol and prostate cancer-specific survival...

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Autores principales: Kaapu, Kalle J, Murtola, Teemu J, Talala, Kirsi, Taari, Kimmo, Tammela, Teuvo LJ, Auvinen, Anssi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129833/
https://www.ncbi.nlm.nih.gov/pubmed/27755533
http://dx.doi.org/10.1038/bjc.2016.328
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author Kaapu, Kalle J
Murtola, Teemu J
Talala, Kirsi
Taari, Kimmo
Tammela, Teuvo LJ
Auvinen, Anssi
author_facet Kaapu, Kalle J
Murtola, Teemu J
Talala, Kirsi
Taari, Kimmo
Tammela, Teuvo LJ
Auvinen, Anssi
author_sort Kaapu, Kalle J
collection PubMed
description BACKGROUND: Protective effects have been suggested for digoxin against prostate cancer risk. However, few studies have evaluated the possible effects on prostate cancer-specific survival. We studied the association between use of digoxin or beta-blocker sotalol and prostate cancer-specific survival as compared with users of other antiarrhythmic drugs in a retrospective cohort study. METHODS: Our study population consisted of 6537 prostate cancer cases from the Finnish Randomized Study of Screening for Prostate Cancer diagnosed during 1996–2009 (485 digoxin users). The median exposure for digoxin was 480 DDDs (interquartile range 100–1400 DDDs). During a median follow-up of 7.5 years after diagnosis, 617 men (48 digoxin users) died of prostate cancer. We collected information on antiarrhythmic drug purchases from the national prescription database. Both prediagnostic and postdiagnostic drug usages were analysed using the Cox regression method. RESULTS: No association was found for prostate cancer death with digoxin usage before (HR 1.00, 95% CI 0.56–1.80) or after (HR 0.81, 95% CI 0.43–1.51) prostate cancer diagnosis. The results were also comparable for sotalol and antiarrhythmic drugs in general. Among men not receiving hormonal therapy, prediagnostic digoxin usage was associated with prolonged prostate cancer survival (HR 0.20, 95% CI 0.05–0.86). CONCLUSIONS: No general protective effects against prostate cancer were observed for digoxin or sotalol usage.
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spelling pubmed-51298332017-11-22 Digoxin and prostate cancer survival in the Finnish Randomized Study of Screening for Prostate Cancer Kaapu, Kalle J Murtola, Teemu J Talala, Kirsi Taari, Kimmo Tammela, Teuvo LJ Auvinen, Anssi Br J Cancer Clinical Study BACKGROUND: Protective effects have been suggested for digoxin against prostate cancer risk. However, few studies have evaluated the possible effects on prostate cancer-specific survival. We studied the association between use of digoxin or beta-blocker sotalol and prostate cancer-specific survival as compared with users of other antiarrhythmic drugs in a retrospective cohort study. METHODS: Our study population consisted of 6537 prostate cancer cases from the Finnish Randomized Study of Screening for Prostate Cancer diagnosed during 1996–2009 (485 digoxin users). The median exposure for digoxin was 480 DDDs (interquartile range 100–1400 DDDs). During a median follow-up of 7.5 years after diagnosis, 617 men (48 digoxin users) died of prostate cancer. We collected information on antiarrhythmic drug purchases from the national prescription database. Both prediagnostic and postdiagnostic drug usages were analysed using the Cox regression method. RESULTS: No association was found for prostate cancer death with digoxin usage before (HR 1.00, 95% CI 0.56–1.80) or after (HR 0.81, 95% CI 0.43–1.51) prostate cancer diagnosis. The results were also comparable for sotalol and antiarrhythmic drugs in general. Among men not receiving hormonal therapy, prediagnostic digoxin usage was associated with prolonged prostate cancer survival (HR 0.20, 95% CI 0.05–0.86). CONCLUSIONS: No general protective effects against prostate cancer were observed for digoxin or sotalol usage. Nature Publishing Group 2016-11-22 2016-10-18 /pmc/articles/PMC5129833/ /pubmed/27755533 http://dx.doi.org/10.1038/bjc.2016.328 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Clinical Study
Kaapu, Kalle J
Murtola, Teemu J
Talala, Kirsi
Taari, Kimmo
Tammela, Teuvo LJ
Auvinen, Anssi
Digoxin and prostate cancer survival in the Finnish Randomized Study of Screening for Prostate Cancer
title Digoxin and prostate cancer survival in the Finnish Randomized Study of Screening for Prostate Cancer
title_full Digoxin and prostate cancer survival in the Finnish Randomized Study of Screening for Prostate Cancer
title_fullStr Digoxin and prostate cancer survival in the Finnish Randomized Study of Screening for Prostate Cancer
title_full_unstemmed Digoxin and prostate cancer survival in the Finnish Randomized Study of Screening for Prostate Cancer
title_short Digoxin and prostate cancer survival in the Finnish Randomized Study of Screening for Prostate Cancer
title_sort digoxin and prostate cancer survival in the finnish randomized study of screening for prostate cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129833/
https://www.ncbi.nlm.nih.gov/pubmed/27755533
http://dx.doi.org/10.1038/bjc.2016.328
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