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Low serum anti-Müllerian hormone is associated with semen quality in infertile men and not influenced by vitamin D supplementation
BACKGROUND: Anti-Müllerian hormone (AMH) is released by testicular Sertoli cells and of great importance during fetal male sexual development, but less is known about the role of circulating AMH during adulthood. In vitro studies have shown that vitamin D may induce AMH transcription, but a controll...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9976369/ https://www.ncbi.nlm.nih.gov/pubmed/36855109 http://dx.doi.org/10.1186/s12916-023-02782-1 |
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author | Holt, Rune Yahyavi, Sam Kafai Kooij, Ireen Andreassen, Christine Hjorth Andersson, Anna-Maria Juul, Anders Jørgensen, Niels Blomberg Jensen, Martin |
author_facet | Holt, Rune Yahyavi, Sam Kafai Kooij, Ireen Andreassen, Christine Hjorth Andersson, Anna-Maria Juul, Anders Jørgensen, Niels Blomberg Jensen, Martin |
author_sort | Holt, Rune |
collection | PubMed |
description | BACKGROUND: Anti-Müllerian hormone (AMH) is released by testicular Sertoli cells and of great importance during fetal male sexual development, but less is known about the role of circulating AMH during adulthood. In vitro studies have shown that vitamin D may induce AMH transcription, but a controlled trial investigating the possible effect of vitamin D on serum AMH has not been conducted in men. METHODS: A single-center, double-blinded, randomized placebo-controlled clinical trial (NCT01304927) conducted in Copenhagen, Denmark. A total of 307 infertile men were included and randomly assigned (1:1) to a single dose of 300,000 IU cholecalciferol followed by 1400 IU cholecalciferol + 500 mg of calcium daily (n = 151) or placebo (n = 156) for 150 days. Difference in serum AMH was a predefined secondary endpoint. Explorative outcomes were associations between serum AMH and gonadal function in infertile men. The primary endpoint was difference in semen quality and has previously been published. RESULTS: Infertile men in the lowest AMH tertile had significantly lower sperm concentration (∆(T3-1) 16 mill/mL (228%); P < 0.001), sperm count (∆(T3-1) 55 million (262%); P < 0.001), motile sperm count (∆(T3-1) 28 million (255%); P < 0.001), progressive motile sperm count (∆(T3-1) 18 million (300%); P < 0.001), testis size (∆(T3-1) 2.7 mL (16%); P < 0.001), serum inhibin B (∆(T3-1) 72 pg/mL (59%); P < 0.001), inhibin B/FSH ratio (∆(T3-1) 48 (145%); P < 0.001), and higher FSH (∆(T3-1) 2.6 (38%); P < 0.001) than the tertile of infertile men with highest serum AMH. Vitamin D supplementation had no effect on serum AMH compared with placebo treatment. CONCLUSIONS: In infertile men, low serum AMH is associated with severely impaired gonadal function illustrated by poor semen quality and lower testosterone/LH ratio. Serum AMH in infertile men was not influenced by vitamin D supplementation. |
format | Online Article Text |
id | pubmed-9976369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99763692023-03-02 Low serum anti-Müllerian hormone is associated with semen quality in infertile men and not influenced by vitamin D supplementation Holt, Rune Yahyavi, Sam Kafai Kooij, Ireen Andreassen, Christine Hjorth Andersson, Anna-Maria Juul, Anders Jørgensen, Niels Blomberg Jensen, Martin BMC Med Research Article BACKGROUND: Anti-Müllerian hormone (AMH) is released by testicular Sertoli cells and of great importance during fetal male sexual development, but less is known about the role of circulating AMH during adulthood. In vitro studies have shown that vitamin D may induce AMH transcription, but a controlled trial investigating the possible effect of vitamin D on serum AMH has not been conducted in men. METHODS: A single-center, double-blinded, randomized placebo-controlled clinical trial (NCT01304927) conducted in Copenhagen, Denmark. A total of 307 infertile men were included and randomly assigned (1:1) to a single dose of 300,000 IU cholecalciferol followed by 1400 IU cholecalciferol + 500 mg of calcium daily (n = 151) or placebo (n = 156) for 150 days. Difference in serum AMH was a predefined secondary endpoint. Explorative outcomes were associations between serum AMH and gonadal function in infertile men. The primary endpoint was difference in semen quality and has previously been published. RESULTS: Infertile men in the lowest AMH tertile had significantly lower sperm concentration (∆(T3-1) 16 mill/mL (228%); P < 0.001), sperm count (∆(T3-1) 55 million (262%); P < 0.001), motile sperm count (∆(T3-1) 28 million (255%); P < 0.001), progressive motile sperm count (∆(T3-1) 18 million (300%); P < 0.001), testis size (∆(T3-1) 2.7 mL (16%); P < 0.001), serum inhibin B (∆(T3-1) 72 pg/mL (59%); P < 0.001), inhibin B/FSH ratio (∆(T3-1) 48 (145%); P < 0.001), and higher FSH (∆(T3-1) 2.6 (38%); P < 0.001) than the tertile of infertile men with highest serum AMH. Vitamin D supplementation had no effect on serum AMH compared with placebo treatment. CONCLUSIONS: In infertile men, low serum AMH is associated with severely impaired gonadal function illustrated by poor semen quality and lower testosterone/LH ratio. Serum AMH in infertile men was not influenced by vitamin D supplementation. BioMed Central 2023-02-28 /pmc/articles/PMC9976369/ /pubmed/36855109 http://dx.doi.org/10.1186/s12916-023-02782-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Holt, Rune Yahyavi, Sam Kafai Kooij, Ireen Andreassen, Christine Hjorth Andersson, Anna-Maria Juul, Anders Jørgensen, Niels Blomberg Jensen, Martin Low serum anti-Müllerian hormone is associated with semen quality in infertile men and not influenced by vitamin D supplementation |
title | Low serum anti-Müllerian hormone is associated with semen quality in infertile men and not influenced by vitamin D supplementation |
title_full | Low serum anti-Müllerian hormone is associated with semen quality in infertile men and not influenced by vitamin D supplementation |
title_fullStr | Low serum anti-Müllerian hormone is associated with semen quality in infertile men and not influenced by vitamin D supplementation |
title_full_unstemmed | Low serum anti-Müllerian hormone is associated with semen quality in infertile men and not influenced by vitamin D supplementation |
title_short | Low serum anti-Müllerian hormone is associated with semen quality in infertile men and not influenced by vitamin D supplementation |
title_sort | low serum anti-müllerian hormone is associated with semen quality in infertile men and not influenced by vitamin d supplementation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9976369/ https://www.ncbi.nlm.nih.gov/pubmed/36855109 http://dx.doi.org/10.1186/s12916-023-02782-1 |
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