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The association between sexual function and prostate cancer risk in US veterans

Sexual dysfunction and prostate cancer are common among older men. Few studies explored the association between these two illnesses. We examined whether sexual function is associated with prostate cancer risk among older men. Among 448 men undergoing prostate biopsy at the Durham Veterans Affairs Ho...

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Autores principales: Zapata, Daniel F, Howard, Lauren E, Frank, Jennifer, Simon, Ross M, Hoyo, Cathrine, Grant, Delores J, Freedland, Stephen J, Vidal, Adriana C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312217/
https://www.ncbi.nlm.nih.gov/pubmed/27586025
http://dx.doi.org/10.4103/1008-682X.184869
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author Zapata, Daniel F
Howard, Lauren E
Frank, Jennifer
Simon, Ross M
Hoyo, Cathrine
Grant, Delores J
Freedland, Stephen J
Vidal, Adriana C
author_facet Zapata, Daniel F
Howard, Lauren E
Frank, Jennifer
Simon, Ross M
Hoyo, Cathrine
Grant, Delores J
Freedland, Stephen J
Vidal, Adriana C
author_sort Zapata, Daniel F
collection PubMed
description Sexual dysfunction and prostate cancer are common among older men. Few studies explored the association between these two illnesses. We examined whether sexual function is associated with prostate cancer risk among older men. Among 448 men undergoing prostate biopsy at the Durham Veterans Affairs Hospital, sexual function was ascertained from the Expanded Prostate Cancer Index Composite sexual assessment. We tested the link between sexual function and prostate cancer risk adjusting for multiple demographic and clinical characteristics using logistic regression. Multinomial logistic regression was used to test the associations with risk of low-grade (Gleason ≤6) and high-grade (Gleason ≥7 or ≥4 + 3) disease versus no cancer. Of 448 men, 209 (47%) had a positive biopsy; these men were less likely to be white (43% vs 55%, P = 0.013), had higher prostate-specific antigen (PSA) (6.0 vs 5.4 ng ml(−1), P < 0.001), but with lower mean sexual function score (47 vs 54, P = 0.007). There was no difference in age, BMI, pack years smoked, history of heart disease and/or diabetes. After adjusting for baseline differences, sexual function was linked with a decreased risk of overall prostate cancer risk (OR: 0.91 per 10-point change in sexual function, P = 0.004) and high-grade disease whether defined as Gleason ≥7 (OR: 0.86, P = 0.001) or ≥4 + 3 (OR: 0.85, P = 0.009). Sexual function was unrelated to low-grade prostate cancer (OR: 0.94, P = 0.13). Thus, among men undergoing prostate biopsy, higher sexual function was associated with a decreased risk of overall and high-grade prostate cancer. Confirmatory studies are needed.
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spelling pubmed-53122172017-03-01 The association between sexual function and prostate cancer risk in US veterans Zapata, Daniel F Howard, Lauren E Frank, Jennifer Simon, Ross M Hoyo, Cathrine Grant, Delores J Freedland, Stephen J Vidal, Adriana C Asian J Androl Original Article Sexual dysfunction and prostate cancer are common among older men. Few studies explored the association between these two illnesses. We examined whether sexual function is associated with prostate cancer risk among older men. Among 448 men undergoing prostate biopsy at the Durham Veterans Affairs Hospital, sexual function was ascertained from the Expanded Prostate Cancer Index Composite sexual assessment. We tested the link between sexual function and prostate cancer risk adjusting for multiple demographic and clinical characteristics using logistic regression. Multinomial logistic regression was used to test the associations with risk of low-grade (Gleason ≤6) and high-grade (Gleason ≥7 or ≥4 + 3) disease versus no cancer. Of 448 men, 209 (47%) had a positive biopsy; these men were less likely to be white (43% vs 55%, P = 0.013), had higher prostate-specific antigen (PSA) (6.0 vs 5.4 ng ml(−1), P < 0.001), but with lower mean sexual function score (47 vs 54, P = 0.007). There was no difference in age, BMI, pack years smoked, history of heart disease and/or diabetes. After adjusting for baseline differences, sexual function was linked with a decreased risk of overall prostate cancer risk (OR: 0.91 per 10-point change in sexual function, P = 0.004) and high-grade disease whether defined as Gleason ≥7 (OR: 0.86, P = 0.001) or ≥4 + 3 (OR: 0.85, P = 0.009). Sexual function was unrelated to low-grade prostate cancer (OR: 0.94, P = 0.13). Thus, among men undergoing prostate biopsy, higher sexual function was associated with a decreased risk of overall and high-grade prostate cancer. Confirmatory studies are needed. Medknow Publications & Media Pvt Ltd 2017 2016-08-30 /pmc/articles/PMC5312217/ /pubmed/27586025 http://dx.doi.org/10.4103/1008-682X.184869 Text en Copyright: © 2017 Asian Journal of Andrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Zapata, Daniel F
Howard, Lauren E
Frank, Jennifer
Simon, Ross M
Hoyo, Cathrine
Grant, Delores J
Freedland, Stephen J
Vidal, Adriana C
The association between sexual function and prostate cancer risk in US veterans
title The association between sexual function and prostate cancer risk in US veterans
title_full The association between sexual function and prostate cancer risk in US veterans
title_fullStr The association between sexual function and prostate cancer risk in US veterans
title_full_unstemmed The association between sexual function and prostate cancer risk in US veterans
title_short The association between sexual function and prostate cancer risk in US veterans
title_sort association between sexual function and prostate cancer risk in us veterans
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312217/
https://www.ncbi.nlm.nih.gov/pubmed/27586025
http://dx.doi.org/10.4103/1008-682X.184869
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