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No changes in levels of bone formation and resorption markers following a broad-spectrum antibiotic course
BACKGROUND: Intestinal bacteria influence bone remodeling in rodents, and antibiotic manipulation of the rodent gut microbiota increases bone formation and prevents ovariectomy-induced bone loss. In theory, these effects may be mediated by changes in sex hormone biotransformation in the gut, gut ser...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122218/ https://www.ncbi.nlm.nih.gov/pubmed/30180841 http://dx.doi.org/10.1186/s12902-018-0291-x |
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author | Mikkelsen, Kristian H. Vilsbøll, Tina Holst, Jens J. Hartmann, Bolette Knop, Filip K. Frost, Morten |
author_facet | Mikkelsen, Kristian H. Vilsbøll, Tina Holst, Jens J. Hartmann, Bolette Knop, Filip K. Frost, Morten |
author_sort | Mikkelsen, Kristian H. |
collection | PubMed |
description | BACKGROUND: Intestinal bacteria influence bone remodeling in rodents, and antibiotic manipulation of the rodent gut microbiota increases bone formation and prevents ovariectomy-induced bone loss. In theory, these effects may be mediated by changes in sex hormone biotransformation in the gut, gut serotonin secretion or nutrition-induced secretion of glucagon-like peptide 2 (GLP-2) and glucose-dependent insulinotropic hormone (GIP). Antibiotics change the human gut microbiota, but the effect of antibiotic treatment on human bone turnover is unknown. METHODS: We analyzed serum levels of bone turnover markers, serotonin, GLP-2 and sex hormones before, immediately after, and eight, 42 and 180 days after a 4-day per oral antibiotic cocktail (vancomycin 500 mg, gentamycin 40 mg and meropenem 500 mg once-daily) in twelve healthy adult males. Fasting and meal-stimulated procollagen type I amino-terminal propeptide (P1NP), C-telopeptide of type I collagen (CTX) and osteocalcin levels were measured. RESULTS: While the antibiotic course reduced the stool abundance and composition of anaerobic bacteria as confirmed by cultivation studies, neither short nor long-term alterations in serum P1NP, CTX and osteocalcin were observed. Furthermore, we did not observe any changes in levels of serum GLP-2, serotonin or sex hormones. CONCLUSION: Eradication of anaerobic bacteria from healthy adult males had no effect on serum bone turnover markers. |
format | Online Article Text |
id | pubmed-6122218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61222182018-09-05 No changes in levels of bone formation and resorption markers following a broad-spectrum antibiotic course Mikkelsen, Kristian H. Vilsbøll, Tina Holst, Jens J. Hartmann, Bolette Knop, Filip K. Frost, Morten BMC Endocr Disord Research Article BACKGROUND: Intestinal bacteria influence bone remodeling in rodents, and antibiotic manipulation of the rodent gut microbiota increases bone formation and prevents ovariectomy-induced bone loss. In theory, these effects may be mediated by changes in sex hormone biotransformation in the gut, gut serotonin secretion or nutrition-induced secretion of glucagon-like peptide 2 (GLP-2) and glucose-dependent insulinotropic hormone (GIP). Antibiotics change the human gut microbiota, but the effect of antibiotic treatment on human bone turnover is unknown. METHODS: We analyzed serum levels of bone turnover markers, serotonin, GLP-2 and sex hormones before, immediately after, and eight, 42 and 180 days after a 4-day per oral antibiotic cocktail (vancomycin 500 mg, gentamycin 40 mg and meropenem 500 mg once-daily) in twelve healthy adult males. Fasting and meal-stimulated procollagen type I amino-terminal propeptide (P1NP), C-telopeptide of type I collagen (CTX) and osteocalcin levels were measured. RESULTS: While the antibiotic course reduced the stool abundance and composition of anaerobic bacteria as confirmed by cultivation studies, neither short nor long-term alterations in serum P1NP, CTX and osteocalcin were observed. Furthermore, we did not observe any changes in levels of serum GLP-2, serotonin or sex hormones. CONCLUSION: Eradication of anaerobic bacteria from healthy adult males had no effect on serum bone turnover markers. BioMed Central 2018-09-04 /pmc/articles/PMC6122218/ /pubmed/30180841 http://dx.doi.org/10.1186/s12902-018-0291-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Mikkelsen, Kristian H. Vilsbøll, Tina Holst, Jens J. Hartmann, Bolette Knop, Filip K. Frost, Morten No changes in levels of bone formation and resorption markers following a broad-spectrum antibiotic course |
title | No changes in levels of bone formation and resorption markers following a broad-spectrum antibiotic course |
title_full | No changes in levels of bone formation and resorption markers following a broad-spectrum antibiotic course |
title_fullStr | No changes in levels of bone formation and resorption markers following a broad-spectrum antibiotic course |
title_full_unstemmed | No changes in levels of bone formation and resorption markers following a broad-spectrum antibiotic course |
title_short | No changes in levels of bone formation and resorption markers following a broad-spectrum antibiotic course |
title_sort | no changes in levels of bone formation and resorption markers following a broad-spectrum antibiotic course |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122218/ https://www.ncbi.nlm.nih.gov/pubmed/30180841 http://dx.doi.org/10.1186/s12902-018-0291-x |
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