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Association between duration of gonadotrophin‐releasing hormone agonist use and cardiovascular risks: A population‐based competing‐risk analysis

BACKGROUND: Although androgen deprivation therapy has known cardiovascular risks, it is unclear if its duration is related to cardiovascular risks. This study thus aimed to investigate the associations between gonadotrophin‐releasing hormone (GnRH) agonist use duration and cardiovascular risks. METH...

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Autores principales: Chan, Jeffrey S. K., Tang, Pias, Hui, Jeremy M. Ho, Lee, Yan H. A., Dee, Edward C., Ng, Kenrick, Liu, Kang, Tse, Gary, Ng, Chi Fai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804360/
https://www.ncbi.nlm.nih.gov/pubmed/35915869
http://dx.doi.org/10.1002/pros.24423
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author Chan, Jeffrey S. K.
Tang, Pias
Hui, Jeremy M. Ho
Lee, Yan H. A.
Dee, Edward C.
Ng, Kenrick
Liu, Kang
Tse, Gary
Ng, Chi Fai
author_facet Chan, Jeffrey S. K.
Tang, Pias
Hui, Jeremy M. Ho
Lee, Yan H. A.
Dee, Edward C.
Ng, Kenrick
Liu, Kang
Tse, Gary
Ng, Chi Fai
author_sort Chan, Jeffrey S. K.
collection PubMed
description BACKGROUND: Although androgen deprivation therapy has known cardiovascular risks, it is unclear if its duration is related to cardiovascular risks. This study thus aimed to investigate the associations between gonadotrophin‐releasing hormone (GnRH) agonist use duration and cardiovascular risks. METHODS: This retrospective cohort study included adult patients with prostate cancer receiving GnRH agonists in Hong Kong during 1999–2021. Patients who switched to GnRH antagonists, underwent bilateral orchidectomy, had <6 months of GnRH agonist, prior myocardial infarction (MI), or prior stroke was excluded. All patients were followed up until September 2021 for a composite endpoint of MI and stroke. Multivariable competing‐risk regression using the Fine‐Gray subdistribution model was used, with mortality from any cause as the competing event. RESULTS: In total, 4038 patients were analyzed (median age 74.9 years old, interquartile range (IQR) 68.7–80.8 years old). Over a median follow‐up of 4.1 years (IQR 2.1–7.5 years), longer GnRH agonists use was associated with higher risk of the endpoint (sub‐hazard ratio per year 1.04 [1.01–1.06], p = 0.001), with those using GnRH agonists for ≥2 years having an estimated 23% increase in the sub‐hazard of the endpoint (sub‐hazard ratio 1.23 [1.04–1.46], p = 0.017). CONCLUSION: Longer GnRH agonist use may be associated with greater cardiovascular risks.
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spelling pubmed-98043602023-01-03 Association between duration of gonadotrophin‐releasing hormone agonist use and cardiovascular risks: A population‐based competing‐risk analysis Chan, Jeffrey S. K. Tang, Pias Hui, Jeremy M. Ho Lee, Yan H. A. Dee, Edward C. Ng, Kenrick Liu, Kang Tse, Gary Ng, Chi Fai Prostate Rapid Communication BACKGROUND: Although androgen deprivation therapy has known cardiovascular risks, it is unclear if its duration is related to cardiovascular risks. This study thus aimed to investigate the associations between gonadotrophin‐releasing hormone (GnRH) agonist use duration and cardiovascular risks. METHODS: This retrospective cohort study included adult patients with prostate cancer receiving GnRH agonists in Hong Kong during 1999–2021. Patients who switched to GnRH antagonists, underwent bilateral orchidectomy, had <6 months of GnRH agonist, prior myocardial infarction (MI), or prior stroke was excluded. All patients were followed up until September 2021 for a composite endpoint of MI and stroke. Multivariable competing‐risk regression using the Fine‐Gray subdistribution model was used, with mortality from any cause as the competing event. RESULTS: In total, 4038 patients were analyzed (median age 74.9 years old, interquartile range (IQR) 68.7–80.8 years old). Over a median follow‐up of 4.1 years (IQR 2.1–7.5 years), longer GnRH agonists use was associated with higher risk of the endpoint (sub‐hazard ratio per year 1.04 [1.01–1.06], p = 0.001), with those using GnRH agonists for ≥2 years having an estimated 23% increase in the sub‐hazard of the endpoint (sub‐hazard ratio 1.23 [1.04–1.46], p = 0.017). CONCLUSION: Longer GnRH agonist use may be associated with greater cardiovascular risks. John Wiley and Sons Inc. 2022-08-01 2022-11-01 /pmc/articles/PMC9804360/ /pubmed/35915869 http://dx.doi.org/10.1002/pros.24423 Text en © 2022 The Authors. The Prostate published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Rapid Communication
Chan, Jeffrey S. K.
Tang, Pias
Hui, Jeremy M. Ho
Lee, Yan H. A.
Dee, Edward C.
Ng, Kenrick
Liu, Kang
Tse, Gary
Ng, Chi Fai
Association between duration of gonadotrophin‐releasing hormone agonist use and cardiovascular risks: A population‐based competing‐risk analysis
title Association between duration of gonadotrophin‐releasing hormone agonist use and cardiovascular risks: A population‐based competing‐risk analysis
title_full Association between duration of gonadotrophin‐releasing hormone agonist use and cardiovascular risks: A population‐based competing‐risk analysis
title_fullStr Association between duration of gonadotrophin‐releasing hormone agonist use and cardiovascular risks: A population‐based competing‐risk analysis
title_full_unstemmed Association between duration of gonadotrophin‐releasing hormone agonist use and cardiovascular risks: A population‐based competing‐risk analysis
title_short Association between duration of gonadotrophin‐releasing hormone agonist use and cardiovascular risks: A population‐based competing‐risk analysis
title_sort association between duration of gonadotrophin‐releasing hormone agonist use and cardiovascular risks: a population‐based competing‐risk analysis
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804360/
https://www.ncbi.nlm.nih.gov/pubmed/35915869
http://dx.doi.org/10.1002/pros.24423
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