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Relationship of serum GDF11 levels with bone mineral density and bone turnover markers in postmenopausal Chinese women
Growth differentiation factor 11 (GDF11) is an important circulating factor that regulates aging. However, the role of GDF11 in bone metabolism remains unclear. The present study was undertaken to investigate the relationship between serum GDF11 level, bone mass, and bone turnover markers in postmen...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923943/ https://www.ncbi.nlm.nih.gov/pubmed/27408764 http://dx.doi.org/10.1038/boneres.2016.12 |
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author | Chen, Yusi Guo, Qi Zhang, Min Song, Shumin Quan, Tonggui Zhao, Tiepeng Li, Hongliang Guo, Lijuan Jiang, Tiejian Wang, Guangwei |
author_facet | Chen, Yusi Guo, Qi Zhang, Min Song, Shumin Quan, Tonggui Zhao, Tiepeng Li, Hongliang Guo, Lijuan Jiang, Tiejian Wang, Guangwei |
author_sort | Chen, Yusi |
collection | PubMed |
description | Growth differentiation factor 11 (GDF11) is an important circulating factor that regulates aging. However, the role of GDF11 in bone metabolism remains unclear. The present study was undertaken to investigate the relationship between serum GDF11 level, bone mass, and bone turnover markers in postmenopausal Chinese women. Serum GDF11 level, bone turnover biochemical markers, and bone mineral density (BMD) were determined in 169 postmenopausal Chinese women (47–78 years old). GDF11 serum levels increased with aging. There were negative correlations between GDF11 and BMD at the various skeletal sites. After adjusting for age and body mass index (BMI), the correlations remained statistically significant. In the multiple linear stepwise regression analysis, age or years since menopause, BMI, GDF11, and estradiol were independent predictors of BMD. A significant negative correlation between GDF11 and bone alkaline phosphatase (BAP) was identified and remained significant after adjusting for age and BMI. No significant correlation was noted between cross-linked N-telopeptides of type I collagen (NTX) and GDF11. In conclusion, GDF11 is an independent negative predictor of BMD and correlates with a biomarker of bone formation, BAP, in postmenopausal Chinese women. GDF11 potentially exerts a negative effect on bone mass by regulating bone formation. |
format | Online Article Text |
id | pubmed-4923943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49239432016-07-12 Relationship of serum GDF11 levels with bone mineral density and bone turnover markers in postmenopausal Chinese women Chen, Yusi Guo, Qi Zhang, Min Song, Shumin Quan, Tonggui Zhao, Tiepeng Li, Hongliang Guo, Lijuan Jiang, Tiejian Wang, Guangwei Bone Res Article Growth differentiation factor 11 (GDF11) is an important circulating factor that regulates aging. However, the role of GDF11 in bone metabolism remains unclear. The present study was undertaken to investigate the relationship between serum GDF11 level, bone mass, and bone turnover markers in postmenopausal Chinese women. Serum GDF11 level, bone turnover biochemical markers, and bone mineral density (BMD) were determined in 169 postmenopausal Chinese women (47–78 years old). GDF11 serum levels increased with aging. There were negative correlations between GDF11 and BMD at the various skeletal sites. After adjusting for age and body mass index (BMI), the correlations remained statistically significant. In the multiple linear stepwise regression analysis, age or years since menopause, BMI, GDF11, and estradiol were independent predictors of BMD. A significant negative correlation between GDF11 and bone alkaline phosphatase (BAP) was identified and remained significant after adjusting for age and BMI. No significant correlation was noted between cross-linked N-telopeptides of type I collagen (NTX) and GDF11. In conclusion, GDF11 is an independent negative predictor of BMD and correlates with a biomarker of bone formation, BAP, in postmenopausal Chinese women. GDF11 potentially exerts a negative effect on bone mass by regulating bone formation. Nature Publishing Group 2016-06-21 /pmc/articles/PMC4923943/ /pubmed/27408764 http://dx.doi.org/10.1038/boneres.2016.12 Text en Copyright © 2016 Sichuan University http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chen, Yusi Guo, Qi Zhang, Min Song, Shumin Quan, Tonggui Zhao, Tiepeng Li, Hongliang Guo, Lijuan Jiang, Tiejian Wang, Guangwei Relationship of serum GDF11 levels with bone mineral density and bone turnover markers in postmenopausal Chinese women |
title | Relationship of serum GDF11 levels with bone mineral density and bone turnover markers in postmenopausal Chinese women |
title_full | Relationship of serum GDF11 levels with bone mineral density and bone turnover markers in postmenopausal Chinese women |
title_fullStr | Relationship of serum GDF11 levels with bone mineral density and bone turnover markers in postmenopausal Chinese women |
title_full_unstemmed | Relationship of serum GDF11 levels with bone mineral density and bone turnover markers in postmenopausal Chinese women |
title_short | Relationship of serum GDF11 levels with bone mineral density and bone turnover markers in postmenopausal Chinese women |
title_sort | relationship of serum gdf11 levels with bone mineral density and bone turnover markers in postmenopausal chinese women |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923943/ https://www.ncbi.nlm.nih.gov/pubmed/27408764 http://dx.doi.org/10.1038/boneres.2016.12 |
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