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Evaluation of atorvastatin efficacy and toxicity on spermatozoa, accessory glands and gonadal hormones of healthy men: a pilot prospective clinical trial

BACKGROUND: Recommendations for cardiovascular disease prevention advocate lowering both cholesterol and low-density lipoprotein cholesterol systemic levels, notably by statin intake. However, statins are the subject of questions concerning their impact on male fertility. This study aimed to evaluat...

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Autores principales: Pons-Rejraji, Hanae, Brugnon, Florence, Sion, Benoit, Maqdasy, Salwan, Gouby, Gerald, Pereira, Bruno, Marceau, Geoffroy, Gremeau, Anne-Sophie, Drevet, Joel, Grizard, Genevieve, Janny, Laurent, Tauveron, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4114109/
https://www.ncbi.nlm.nih.gov/pubmed/25016482
http://dx.doi.org/10.1186/1477-7827-12-65
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author Pons-Rejraji, Hanae
Brugnon, Florence
Sion, Benoit
Maqdasy, Salwan
Gouby, Gerald
Pereira, Bruno
Marceau, Geoffroy
Gremeau, Anne-Sophie
Drevet, Joel
Grizard, Genevieve
Janny, Laurent
Tauveron, Igor
author_facet Pons-Rejraji, Hanae
Brugnon, Florence
Sion, Benoit
Maqdasy, Salwan
Gouby, Gerald
Pereira, Bruno
Marceau, Geoffroy
Gremeau, Anne-Sophie
Drevet, Joel
Grizard, Genevieve
Janny, Laurent
Tauveron, Igor
author_sort Pons-Rejraji, Hanae
collection PubMed
description BACKGROUND: Recommendations for cardiovascular disease prevention advocate lowering both cholesterol and low-density lipoprotein cholesterol systemic levels, notably by statin intake. However, statins are the subject of questions concerning their impact on male fertility. This study aimed to evaluate, by a prospective pilot assay, the efficacy and the toxicity of a decrease of cholesterol blood levels, induced by atorvastatin on semen quality and sexual hormone levels of healthy, normocholesterolaemic and normozoospermic men. METHODS: Atorvastatin (10 mg daily) was administrated orally during 5 months to 17 men with normal plasma lipid and standard semen parameters. Spermatozoa parameters, accessory gland markers, semen lipid levels and blood levels of gonadal hormones were assayed before statin intake, during the treatment, and 3 months after its withdrawal. RESULTS: Atorvastatin treatment significantly decreased circulating low-density lipoprotein cholesterol (LDL-C) and total cholesterol concentrations by 42% and 24% (p < 0.0001) respectively, and reached the efficacy objective of the protocol. During atorvastatin therapy and/or 3 months after its withdrawal numerous semen parameters were significantly modified, such as total number of spermatozoa (-31%, p < 0.05), vitality (-9.5%, p < 0.05), total motility (+7.5%, p < 0.05), morphology (head, neck and midpiece abnormalities, p < 0.05), and the kinetics of acrosome reaction (p < 0.05). Seminal concentrations of acid phosphatases (p < 0.01), α-glucosidase (p < 0.05) and L-carnitine (p < 0.05) were also decreased during the therapy, indicating an alteration of prostatic and epididymal functions. Moreover, we measured at least one altered semen parameter in 35% of the subjects during atorvastatin treatment, and in 65% of the subjects after withdrawal, which led us to consider that atorvastatin is unsafe in the context of our study. CONCLUSIONS: Our results show for the first time that atorvastatin significantly affects the sperm parameters and the seminal fluid composition of healthy men. TRIAL REGISTRATION: ClinicalTrials.gov: NCT02094313.
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spelling pubmed-41141092014-07-30 Evaluation of atorvastatin efficacy and toxicity on spermatozoa, accessory glands and gonadal hormones of healthy men: a pilot prospective clinical trial Pons-Rejraji, Hanae Brugnon, Florence Sion, Benoit Maqdasy, Salwan Gouby, Gerald Pereira, Bruno Marceau, Geoffroy Gremeau, Anne-Sophie Drevet, Joel Grizard, Genevieve Janny, Laurent Tauveron, Igor Reprod Biol Endocrinol Research BACKGROUND: Recommendations for cardiovascular disease prevention advocate lowering both cholesterol and low-density lipoprotein cholesterol systemic levels, notably by statin intake. However, statins are the subject of questions concerning their impact on male fertility. This study aimed to evaluate, by a prospective pilot assay, the efficacy and the toxicity of a decrease of cholesterol blood levels, induced by atorvastatin on semen quality and sexual hormone levels of healthy, normocholesterolaemic and normozoospermic men. METHODS: Atorvastatin (10 mg daily) was administrated orally during 5 months to 17 men with normal plasma lipid and standard semen parameters. Spermatozoa parameters, accessory gland markers, semen lipid levels and blood levels of gonadal hormones were assayed before statin intake, during the treatment, and 3 months after its withdrawal. RESULTS: Atorvastatin treatment significantly decreased circulating low-density lipoprotein cholesterol (LDL-C) and total cholesterol concentrations by 42% and 24% (p < 0.0001) respectively, and reached the efficacy objective of the protocol. During atorvastatin therapy and/or 3 months after its withdrawal numerous semen parameters were significantly modified, such as total number of spermatozoa (-31%, p < 0.05), vitality (-9.5%, p < 0.05), total motility (+7.5%, p < 0.05), morphology (head, neck and midpiece abnormalities, p < 0.05), and the kinetics of acrosome reaction (p < 0.05). Seminal concentrations of acid phosphatases (p < 0.01), α-glucosidase (p < 0.05) and L-carnitine (p < 0.05) were also decreased during the therapy, indicating an alteration of prostatic and epididymal functions. Moreover, we measured at least one altered semen parameter in 35% of the subjects during atorvastatin treatment, and in 65% of the subjects after withdrawal, which led us to consider that atorvastatin is unsafe in the context of our study. CONCLUSIONS: Our results show for the first time that atorvastatin significantly affects the sperm parameters and the seminal fluid composition of healthy men. TRIAL REGISTRATION: ClinicalTrials.gov: NCT02094313. BioMed Central 2014-07-12 /pmc/articles/PMC4114109/ /pubmed/25016482 http://dx.doi.org/10.1186/1477-7827-12-65 Text en Copyright © 2014 Pons-Rejraji et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 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
Pons-Rejraji, Hanae
Brugnon, Florence
Sion, Benoit
Maqdasy, Salwan
Gouby, Gerald
Pereira, Bruno
Marceau, Geoffroy
Gremeau, Anne-Sophie
Drevet, Joel
Grizard, Genevieve
Janny, Laurent
Tauveron, Igor
Evaluation of atorvastatin efficacy and toxicity on spermatozoa, accessory glands and gonadal hormones of healthy men: a pilot prospective clinical trial
title Evaluation of atorvastatin efficacy and toxicity on spermatozoa, accessory glands and gonadal hormones of healthy men: a pilot prospective clinical trial
title_full Evaluation of atorvastatin efficacy and toxicity on spermatozoa, accessory glands and gonadal hormones of healthy men: a pilot prospective clinical trial
title_fullStr Evaluation of atorvastatin efficacy and toxicity on spermatozoa, accessory glands and gonadal hormones of healthy men: a pilot prospective clinical trial
title_full_unstemmed Evaluation of atorvastatin efficacy and toxicity on spermatozoa, accessory glands and gonadal hormones of healthy men: a pilot prospective clinical trial
title_short Evaluation of atorvastatin efficacy and toxicity on spermatozoa, accessory glands and gonadal hormones of healthy men: a pilot prospective clinical trial
title_sort evaluation of atorvastatin efficacy and toxicity on spermatozoa, accessory glands and gonadal hormones of healthy men: a pilot prospective clinical trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4114109/
https://www.ncbi.nlm.nih.gov/pubmed/25016482
http://dx.doi.org/10.1186/1477-7827-12-65
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