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No increased risk of dementia in patients receiving androgen deprivation therapy for prostate cancer: a 5-year follow-up study

Prior studies suggested that the use of androgen deprivation therapy (ADT) in patients with prostate cancer (PC) might cause the impairment of cognitive function which is one of the common symptoms of dementia; however, the association between ADT and cognitive impairment still remains controversial...

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Autores principales: Kao, Li-Ting, Lin, Herng-Ching, Chung, Shiu-Dong, Huang, Chao-Yuan
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/PMC5507085/
https://www.ncbi.nlm.nih.gov/pubmed/27232853
http://dx.doi.org/10.4103/1008-682X.179528
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author Kao, Li-Ting
Lin, Herng-Ching
Chung, Shiu-Dong
Huang, Chao-Yuan
author_facet Kao, Li-Ting
Lin, Herng-Ching
Chung, Shiu-Dong
Huang, Chao-Yuan
author_sort Kao, Li-Ting
collection PubMed
description Prior studies suggested that the use of androgen deprivation therapy (ADT) in patients with prostate cancer (PC) might cause the impairment of cognitive function which is one of the common symptoms of dementia; however, the association between ADT and cognitive impairment still remains controversial. This retrospective cohort study aimed to investigate the relationship between ADT and subsequent risk of dementia using a population-based dataset. Data for this study were taken from the Taiwan (China)Longitudinal Health Insurance Database 2005. We included 755 PC patients who received ADT in the study cohort and 559 PC patients who did not receive ADT in the comparison cohort. Each patient was individually tracked for a 5-year period to define those who subsequently received a diagnosis of dementia. Results show that the incidence rates of dementia per 100 person-years were 2.35 (95% confidence interval [95% CI]: 1.82–2.98) and 1.85 (95% CI: 1.35–2.48) for PC patients who received ADT and those who did not receive ADT, respectively. The adjusted hazard ratio (HR) for dementia for PC patients who received ADT was 1.21 (95% CI: 0.82–1.78, P = 0.333) compared to those who did not receive ADT. In addition, the adjusted HRs for dementia for PC patients receiving ADT with gonadotropin-releasing hormone (GnRH) agonists and without GnRH agonists were 1.39 (95% CI: 0.80–2.40, P = 0.240) and 1.13 (95% CI: 0.75–1.71, P = 0.564), respectively, compared to PC patients not receiving ADT. We concluded that there was no difference in the risk of subsequent dementia between PC patients who did and those who did not receive ADT.
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spelling pubmed-55070852017-07-17 No increased risk of dementia in patients receiving androgen deprivation therapy for prostate cancer: a 5-year follow-up study Kao, Li-Ting Lin, Herng-Ching Chung, Shiu-Dong Huang, Chao-Yuan Asian J Androl Original Article Prior studies suggested that the use of androgen deprivation therapy (ADT) in patients with prostate cancer (PC) might cause the impairment of cognitive function which is one of the common symptoms of dementia; however, the association between ADT and cognitive impairment still remains controversial. This retrospective cohort study aimed to investigate the relationship between ADT and subsequent risk of dementia using a population-based dataset. Data for this study were taken from the Taiwan (China)Longitudinal Health Insurance Database 2005. We included 755 PC patients who received ADT in the study cohort and 559 PC patients who did not receive ADT in the comparison cohort. Each patient was individually tracked for a 5-year period to define those who subsequently received a diagnosis of dementia. Results show that the incidence rates of dementia per 100 person-years were 2.35 (95% confidence interval [95% CI]: 1.82–2.98) and 1.85 (95% CI: 1.35–2.48) for PC patients who received ADT and those who did not receive ADT, respectively. The adjusted hazard ratio (HR) for dementia for PC patients who received ADT was 1.21 (95% CI: 0.82–1.78, P = 0.333) compared to those who did not receive ADT. In addition, the adjusted HRs for dementia for PC patients receiving ADT with gonadotropin-releasing hormone (GnRH) agonists and without GnRH agonists were 1.39 (95% CI: 0.80–2.40, P = 0.240) and 1.13 (95% CI: 0.75–1.71, P = 0.564), respectively, compared to PC patients not receiving ADT. We concluded that there was no difference in the risk of subsequent dementia between PC patients who did and those who did not receive ADT. Medknow Publications & Media Pvt Ltd 2017 2016-05-27 /pmc/articles/PMC5507085/ /pubmed/27232853 http://dx.doi.org/10.4103/1008-682X.179528 Text en Copyright: © The Author(s)(2017) 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
Kao, Li-Ting
Lin, Herng-Ching
Chung, Shiu-Dong
Huang, Chao-Yuan
No increased risk of dementia in patients receiving androgen deprivation therapy for prostate cancer: a 5-year follow-up study
title No increased risk of dementia in patients receiving androgen deprivation therapy for prostate cancer: a 5-year follow-up study
title_full No increased risk of dementia in patients receiving androgen deprivation therapy for prostate cancer: a 5-year follow-up study
title_fullStr No increased risk of dementia in patients receiving androgen deprivation therapy for prostate cancer: a 5-year follow-up study
title_full_unstemmed No increased risk of dementia in patients receiving androgen deprivation therapy for prostate cancer: a 5-year follow-up study
title_short No increased risk of dementia in patients receiving androgen deprivation therapy for prostate cancer: a 5-year follow-up study
title_sort no increased risk of dementia in patients receiving androgen deprivation therapy for prostate cancer: a 5-year follow-up study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507085/
https://www.ncbi.nlm.nih.gov/pubmed/27232853
http://dx.doi.org/10.4103/1008-682X.179528
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