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Recombinant FSH Improves Sperm DNA Damage in Male Infertility: A Phase II Clinical Trial

Background and objectives: Male infertility is a global health dilemma and Follicle-Stimulating Hormone (FSH) administration has shown promising results. Several studies showed that infertile men with normal semen parameters have low levels of DNA damage while infertile men with abnormal semen param...

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Autores principales: Colacurci, Nicola, De Leo, Vincenzo, Ruvolo, Giovanni, Piomboni, Paola, Caprio, Francesca, Pivonello, Rosario, Papaleo, Enrico, La Verde, Eugenio, Depalo, Raffaella, Lispi, Monica, Longobardi, Salvatore, Paoli, Donatella, Pallotti, Francesco, Lombardo, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048873/
https://www.ncbi.nlm.nih.gov/pubmed/30042737
http://dx.doi.org/10.3389/fendo.2018.00383
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author Colacurci, Nicola
De Leo, Vincenzo
Ruvolo, Giovanni
Piomboni, Paola
Caprio, Francesca
Pivonello, Rosario
Papaleo, Enrico
La Verde, Eugenio
Depalo, Raffaella
Lispi, Monica
Longobardi, Salvatore
Paoli, Donatella
Pallotti, Francesco
Lombardo, Francesco
author_facet Colacurci, Nicola
De Leo, Vincenzo
Ruvolo, Giovanni
Piomboni, Paola
Caprio, Francesca
Pivonello, Rosario
Papaleo, Enrico
La Verde, Eugenio
Depalo, Raffaella
Lispi, Monica
Longobardi, Salvatore
Paoli, Donatella
Pallotti, Francesco
Lombardo, Francesco
author_sort Colacurci, Nicola
collection PubMed
description Background and objectives: Male infertility is a global health dilemma and Follicle-Stimulating Hormone (FSH) administration has shown promising results. Several studies showed that infertile men with normal semen parameters have low levels of DNA damage while infertile men with abnormal semen parameters have more damage at the DNA level. Sperm DNA damage may affect the reproductive outcome and has been associated with failure in the achievement of competent embryos and pregnancy fulfillment. The aim of this study was to evaluate whether the administration of recombinant FSH (Gonal-f® PEN 900 IU) could improve sperm DNA fragmentation in men with infertility. The secondary endpoints of this study were to evaluate the FSH effects on sperm parameters and hormonal assets. Methods: A longitudinal, prospective, multicenter, open-label clinical trial was carried out. Infertile couples were recruited from six Italian Reproductive Medical Centers and 115 infertile men were enrolled for this study. All participants were treated with subcutaneous injections of Gonal-f® 150 IU every other day, within a 3 month-time frame. The semen samples were examined in accordance to the 2010 World Health Organization criteria. Sperm DNA Fragmentation (DFI) was determined by fluorescence microscopy using terminal deoxynucleotidyl transferase-mediated d-UTP Nick-end Labeling (TUNEL) assay. Statistical analysis was performed using both the t-test for paired samples and the Wilcoxon signed-rank test. Results: FSH administration improved DFI in 67% of patients, with an average decrease of 35.4% compared to the baseline. This improvement is more evident in men with basal DFI lower than 17% and in those with FSH basal levels between 2.16 and 4.27 IU/L. In addition, FSH enhanced the gonadal function, increasing the hormones AMH and Inhibin B and semen parameters. Limitation of these results are represented by the absence of a placebo group and of FSHR genotype stratification sub-analysis. Conclusion: Recombinant FSH 150 IU is well tolerated and effective in eliciting a significant DFI reduction as well as in improving gonadal function. Trial Registration: EUDRACT Number 2010-020196-23. Registred 14 April 2011.
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spelling pubmed-60488732018-07-24 Recombinant FSH Improves Sperm DNA Damage in Male Infertility: A Phase II Clinical Trial Colacurci, Nicola De Leo, Vincenzo Ruvolo, Giovanni Piomboni, Paola Caprio, Francesca Pivonello, Rosario Papaleo, Enrico La Verde, Eugenio Depalo, Raffaella Lispi, Monica Longobardi, Salvatore Paoli, Donatella Pallotti, Francesco Lombardo, Francesco Front Endocrinol (Lausanne) Endocrinology Background and objectives: Male infertility is a global health dilemma and Follicle-Stimulating Hormone (FSH) administration has shown promising results. Several studies showed that infertile men with normal semen parameters have low levels of DNA damage while infertile men with abnormal semen parameters have more damage at the DNA level. Sperm DNA damage may affect the reproductive outcome and has been associated with failure in the achievement of competent embryos and pregnancy fulfillment. The aim of this study was to evaluate whether the administration of recombinant FSH (Gonal-f® PEN 900 IU) could improve sperm DNA fragmentation in men with infertility. The secondary endpoints of this study were to evaluate the FSH effects on sperm parameters and hormonal assets. Methods: A longitudinal, prospective, multicenter, open-label clinical trial was carried out. Infertile couples were recruited from six Italian Reproductive Medical Centers and 115 infertile men were enrolled for this study. All participants were treated with subcutaneous injections of Gonal-f® 150 IU every other day, within a 3 month-time frame. The semen samples were examined in accordance to the 2010 World Health Organization criteria. Sperm DNA Fragmentation (DFI) was determined by fluorescence microscopy using terminal deoxynucleotidyl transferase-mediated d-UTP Nick-end Labeling (TUNEL) assay. Statistical analysis was performed using both the t-test for paired samples and the Wilcoxon signed-rank test. Results: FSH administration improved DFI in 67% of patients, with an average decrease of 35.4% compared to the baseline. This improvement is more evident in men with basal DFI lower than 17% and in those with FSH basal levels between 2.16 and 4.27 IU/L. In addition, FSH enhanced the gonadal function, increasing the hormones AMH and Inhibin B and semen parameters. Limitation of these results are represented by the absence of a placebo group and of FSHR genotype stratification sub-analysis. Conclusion: Recombinant FSH 150 IU is well tolerated and effective in eliciting a significant DFI reduction as well as in improving gonadal function. Trial Registration: EUDRACT Number 2010-020196-23. Registred 14 April 2011. Frontiers Media S.A. 2018-07-10 /pmc/articles/PMC6048873/ /pubmed/30042737 http://dx.doi.org/10.3389/fendo.2018.00383 Text en Copyright © 2018 Colacurci, De Leo, Ruvolo, Piomboni, Caprio, Pivonello, Papaleo, La Verde, Depalo, Lispi, Longobardi, Paoli, Pallotti and Lombardo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Colacurci, Nicola
De Leo, Vincenzo
Ruvolo, Giovanni
Piomboni, Paola
Caprio, Francesca
Pivonello, Rosario
Papaleo, Enrico
La Verde, Eugenio
Depalo, Raffaella
Lispi, Monica
Longobardi, Salvatore
Paoli, Donatella
Pallotti, Francesco
Lombardo, Francesco
Recombinant FSH Improves Sperm DNA Damage in Male Infertility: A Phase II Clinical Trial
title Recombinant FSH Improves Sperm DNA Damage in Male Infertility: A Phase II Clinical Trial
title_full Recombinant FSH Improves Sperm DNA Damage in Male Infertility: A Phase II Clinical Trial
title_fullStr Recombinant FSH Improves Sperm DNA Damage in Male Infertility: A Phase II Clinical Trial
title_full_unstemmed Recombinant FSH Improves Sperm DNA Damage in Male Infertility: A Phase II Clinical Trial
title_short Recombinant FSH Improves Sperm DNA Damage in Male Infertility: A Phase II Clinical Trial
title_sort recombinant fsh improves sperm dna damage in male infertility: a phase ii clinical trial
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048873/
https://www.ncbi.nlm.nih.gov/pubmed/30042737
http://dx.doi.org/10.3389/fendo.2018.00383
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