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Cardiovascular risks and elevation of serum DHT vary by route of testosterone administration: a systematic review and meta-analysis

BACKGROUND: Potential cardiovascular (CV) risks of testosterone replacement therapy (TRT) are currently a topic of intense interest. However, no studies have addressed CV risk as a function of the route of administration of TRT. METHODS: Two meta-analyses were conducted, one of CV adverse events (AE...

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Autores principales: Borst, Stephen E, Shuster, Jonathan J, Zou, Baiming, Ye, Fan, Jia, Huanguang, Wokhlu, Anita, Yarrow, Joshua F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245724/
https://www.ncbi.nlm.nih.gov/pubmed/25428524
http://dx.doi.org/10.1186/s12916-014-0211-5
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author Borst, Stephen E
Shuster, Jonathan J
Zou, Baiming
Ye, Fan
Jia, Huanguang
Wokhlu, Anita
Yarrow, Joshua F
author_facet Borst, Stephen E
Shuster, Jonathan J
Zou, Baiming
Ye, Fan
Jia, Huanguang
Wokhlu, Anita
Yarrow, Joshua F
author_sort Borst, Stephen E
collection PubMed
description BACKGROUND: Potential cardiovascular (CV) risks of testosterone replacement therapy (TRT) are currently a topic of intense interest. However, no studies have addressed CV risk as a function of the route of administration of TRT. METHODS: Two meta-analyses were conducted, one of CV adverse events (AEs) in 35 randomized controlled trials (RCTs) of TRT lasting 12 weeks or more, and one of 32 studies reporting the effect of TRT on serum testosterone and dihydrotestosterone (DHT). RESULTS: CV risks of TRT: Of 2,313 studies identified, 35 were eligible and included 3,703 mostly older men who experienced 218 CV-related AEs. No significant risk for CV AEs was present when all TRT administration routes were grouped (relative risk (RR) = 1.28, 95% confidence interval (CI): 0.76 to 2.13, P = 0.34). When analyzed separately, oral TRT produced significant CV risk (RR = 2.20, 95% CI: 1.45 to 3.55, P = 0.015), while neither intramuscular (RR = 0.66, 95% CI: 0.28 to 1.56, P = 0.32) nor transdermal (gel or patch) TRT (RR = 1.27, 95% CI: 0.62 to 2.62, P = 0.48) significantly altered CV risk. Serum testosterone/DHT following TRT: Of 419 studies identified, 32 were eligible which included 1,152 men receiving TRT. No significant difference in the elevation of serum testosterone was present between intramuscular or transdermal TRT. However, transdermal TRT elevated serum DHT (5.46-fold, 95% CI: 4.51 to 6.60) to a greater magnitude than intramuscular TRT (2.20-fold, 95% CI: 1.74 to 2.77). CONCLUSIONS: Oral TRT produces significant CV risk. While no significant effects on CV risk were observed with either injected or transdermal TRT, the point estimates suggest that further research is needed to establish whether administration by these routes is protective or detrimental, respectively. Differences in the degree to which serum DHT is elevated may underlie the varying CV risk by TRT administration route, as elevated serum dihydrotestosterone has been shown to be associated with CV risk in observational studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-014-0211-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-42457242014-11-28 Cardiovascular risks and elevation of serum DHT vary by route of testosterone administration: a systematic review and meta-analysis Borst, Stephen E Shuster, Jonathan J Zou, Baiming Ye, Fan Jia, Huanguang Wokhlu, Anita Yarrow, Joshua F BMC Med Research Article BACKGROUND: Potential cardiovascular (CV) risks of testosterone replacement therapy (TRT) are currently a topic of intense interest. However, no studies have addressed CV risk as a function of the route of administration of TRT. METHODS: Two meta-analyses were conducted, one of CV adverse events (AEs) in 35 randomized controlled trials (RCTs) of TRT lasting 12 weeks or more, and one of 32 studies reporting the effect of TRT on serum testosterone and dihydrotestosterone (DHT). RESULTS: CV risks of TRT: Of 2,313 studies identified, 35 were eligible and included 3,703 mostly older men who experienced 218 CV-related AEs. No significant risk for CV AEs was present when all TRT administration routes were grouped (relative risk (RR) = 1.28, 95% confidence interval (CI): 0.76 to 2.13, P = 0.34). When analyzed separately, oral TRT produced significant CV risk (RR = 2.20, 95% CI: 1.45 to 3.55, P = 0.015), while neither intramuscular (RR = 0.66, 95% CI: 0.28 to 1.56, P = 0.32) nor transdermal (gel or patch) TRT (RR = 1.27, 95% CI: 0.62 to 2.62, P = 0.48) significantly altered CV risk. Serum testosterone/DHT following TRT: Of 419 studies identified, 32 were eligible which included 1,152 men receiving TRT. No significant difference in the elevation of serum testosterone was present between intramuscular or transdermal TRT. However, transdermal TRT elevated serum DHT (5.46-fold, 95% CI: 4.51 to 6.60) to a greater magnitude than intramuscular TRT (2.20-fold, 95% CI: 1.74 to 2.77). CONCLUSIONS: Oral TRT produces significant CV risk. While no significant effects on CV risk were observed with either injected or transdermal TRT, the point estimates suggest that further research is needed to establish whether administration by these routes is protective or detrimental, respectively. Differences in the degree to which serum DHT is elevated may underlie the varying CV risk by TRT administration route, as elevated serum dihydrotestosterone has been shown to be associated with CV risk in observational studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-014-0211-5) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-27 /pmc/articles/PMC4245724/ /pubmed/25428524 http://dx.doi.org/10.1186/s12916-014-0211-5 Text en © Borst et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Borst, Stephen E
Shuster, Jonathan J
Zou, Baiming
Ye, Fan
Jia, Huanguang
Wokhlu, Anita
Yarrow, Joshua F
Cardiovascular risks and elevation of serum DHT vary by route of testosterone administration: a systematic review and meta-analysis
title Cardiovascular risks and elevation of serum DHT vary by route of testosterone administration: a systematic review and meta-analysis
title_full Cardiovascular risks and elevation of serum DHT vary by route of testosterone administration: a systematic review and meta-analysis
title_fullStr Cardiovascular risks and elevation of serum DHT vary by route of testosterone administration: a systematic review and meta-analysis
title_full_unstemmed Cardiovascular risks and elevation of serum DHT vary by route of testosterone administration: a systematic review and meta-analysis
title_short Cardiovascular risks and elevation of serum DHT vary by route of testosterone administration: a systematic review and meta-analysis
title_sort cardiovascular risks and elevation of serum dht vary by route of testosterone administration: a systematic review and meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245724/
https://www.ncbi.nlm.nih.gov/pubmed/25428524
http://dx.doi.org/10.1186/s12916-014-0211-5
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