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Fetal Programming of Semen Quality (FEPOS) Cohort – A DNBC Male-Offspring Cohort

BACKGROUND: Prenatal exposures may contribute to male infertility in adult life, but large-scale epidemiological evidence is still lacking. The Fetal Programming of Semen quality (FEPOS) cohort was founded to provide means to examine if fetal exposures can interfere with fetal reproductive developme...

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Autores principales: Keglberg Hærvig, Katia, Bonde, Jens Peter, Ramlau-Hansen, Cecilia Høst, Toft, Gunnar, Hougaard, Karin Sørig, Specht, Ina Olmer, Giwercman, Aleksander, Nybo Andersen, Anne-Marie, Olsen, Jørn, Lindh, Christian, Bjerre Høyer, Birgit, Tøttenborg, Sandra Søgaard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373412/
https://www.ncbi.nlm.nih.gov/pubmed/32765110
http://dx.doi.org/10.2147/CLEP.S242631
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author Keglberg Hærvig, Katia
Bonde, Jens Peter
Ramlau-Hansen, Cecilia Høst
Toft, Gunnar
Hougaard, Karin Sørig
Specht, Ina Olmer
Giwercman, Aleksander
Nybo Andersen, Anne-Marie
Olsen, Jørn
Lindh, Christian
Bjerre Høyer, Birgit
Tøttenborg, Sandra Søgaard
author_facet Keglberg Hærvig, Katia
Bonde, Jens Peter
Ramlau-Hansen, Cecilia Høst
Toft, Gunnar
Hougaard, Karin Sørig
Specht, Ina Olmer
Giwercman, Aleksander
Nybo Andersen, Anne-Marie
Olsen, Jørn
Lindh, Christian
Bjerre Høyer, Birgit
Tøttenborg, Sandra Søgaard
author_sort Keglberg Hærvig, Katia
collection PubMed
description BACKGROUND: Prenatal exposures may contribute to male infertility in adult life, but large-scale epidemiological evidence is still lacking. The Fetal Programming of Semen quality (FEPOS) cohort was founded to provide means to examine if fetal exposures can interfere with fetal reproductive development and ultimately lead to reduced semen quality and reproductive hormone imbalances in young adult men. METHODS: Young adult men at least 18 years and 9 months of age born to women in the Danish National Birth Cohort living in relative proximity to Copenhagen or Aarhus and for whom a maternal blood sample and two maternal interviews during pregnancy were available were invited to FEPOS. Recruitment began in March 2017 and ended in December 2019. The participants answered a comprehensive questionnaire and underwent a physical examination where they delivered a semen, urine, and hair sample, measured their own testicular volume, and had blood drawn. RESULTS: In total 21,623 sons fulfilled eligibility criteria of whom 5697 were invited and 1058 participated making the response rate 19%. Semen characteristics did not differ between sons from the Copenhagen and Aarhus clinics. When comparing the FEPOS semen parameters to similar cohorts, the median across all semen characteristics was slightly lower for FEPOS participants, although with smaller variation. CONCLUSION: With its 1058 young adult men, the FEPOS cohort is the largest population-based male-offspring cohort worldwide specifically designed to investigate prenatal determinants of semen quality. Wide-ranging information on maternal health, lifestyle, socioeconomic status, occupation, and serum concentrations of potential reproductive toxicants during pregnancy combined with biological markers of fertility in their sons collected after puberty allow for in-depth investigations of the ‘fetal origins of adult disease hypothesis’.
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spelling pubmed-73734122020-08-05 Fetal Programming of Semen Quality (FEPOS) Cohort – A DNBC Male-Offspring Cohort Keglberg Hærvig, Katia Bonde, Jens Peter Ramlau-Hansen, Cecilia Høst Toft, Gunnar Hougaard, Karin Sørig Specht, Ina Olmer Giwercman, Aleksander Nybo Andersen, Anne-Marie Olsen, Jørn Lindh, Christian Bjerre Høyer, Birgit Tøttenborg, Sandra Søgaard Clin Epidemiol Original Research BACKGROUND: Prenatal exposures may contribute to male infertility in adult life, but large-scale epidemiological evidence is still lacking. The Fetal Programming of Semen quality (FEPOS) cohort was founded to provide means to examine if fetal exposures can interfere with fetal reproductive development and ultimately lead to reduced semen quality and reproductive hormone imbalances in young adult men. METHODS: Young adult men at least 18 years and 9 months of age born to women in the Danish National Birth Cohort living in relative proximity to Copenhagen or Aarhus and for whom a maternal blood sample and two maternal interviews during pregnancy were available were invited to FEPOS. Recruitment began in March 2017 and ended in December 2019. The participants answered a comprehensive questionnaire and underwent a physical examination where they delivered a semen, urine, and hair sample, measured their own testicular volume, and had blood drawn. RESULTS: In total 21,623 sons fulfilled eligibility criteria of whom 5697 were invited and 1058 participated making the response rate 19%. Semen characteristics did not differ between sons from the Copenhagen and Aarhus clinics. When comparing the FEPOS semen parameters to similar cohorts, the median across all semen characteristics was slightly lower for FEPOS participants, although with smaller variation. CONCLUSION: With its 1058 young adult men, the FEPOS cohort is the largest population-based male-offspring cohort worldwide specifically designed to investigate prenatal determinants of semen quality. Wide-ranging information on maternal health, lifestyle, socioeconomic status, occupation, and serum concentrations of potential reproductive toxicants during pregnancy combined with biological markers of fertility in their sons collected after puberty allow for in-depth investigations of the ‘fetal origins of adult disease hypothesis’. Dove 2020-07-17 /pmc/articles/PMC7373412/ /pubmed/32765110 http://dx.doi.org/10.2147/CLEP.S242631 Text en © 2020 Keglberg Hærvig et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Keglberg Hærvig, Katia
Bonde, Jens Peter
Ramlau-Hansen, Cecilia Høst
Toft, Gunnar
Hougaard, Karin Sørig
Specht, Ina Olmer
Giwercman, Aleksander
Nybo Andersen, Anne-Marie
Olsen, Jørn
Lindh, Christian
Bjerre Høyer, Birgit
Tøttenborg, Sandra Søgaard
Fetal Programming of Semen Quality (FEPOS) Cohort – A DNBC Male-Offspring Cohort
title Fetal Programming of Semen Quality (FEPOS) Cohort – A DNBC Male-Offspring Cohort
title_full Fetal Programming of Semen Quality (FEPOS) Cohort – A DNBC Male-Offspring Cohort
title_fullStr Fetal Programming of Semen Quality (FEPOS) Cohort – A DNBC Male-Offspring Cohort
title_full_unstemmed Fetal Programming of Semen Quality (FEPOS) Cohort – A DNBC Male-Offspring Cohort
title_short Fetal Programming of Semen Quality (FEPOS) Cohort – A DNBC Male-Offspring Cohort
title_sort fetal programming of semen quality (fepos) cohort – a dnbc male-offspring cohort
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373412/
https://www.ncbi.nlm.nih.gov/pubmed/32765110
http://dx.doi.org/10.2147/CLEP.S242631
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