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Serum vitamin D, intact parathyroid hormone, and Fetuin A concentrations were associated with geriatric sarcopenia and cardiac hypertrophy

With aging, intact parathyroid hormone (iPTH) increases. It plays a crucial role in left ventricular hypertrophy (LVH). Also, 25-hydroxy vitamin D (Vit-D) and iPTH have been observed to be determinants of muscle wasting known as sarcopenia. Fetuin A (FetA), a systemic calcification inhibitor, involv...

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Autores principales: Chang, Wei-Ting, Wu, Chih-Hsing, Hsu, Ling-Wei, Chen, Po-Wei, Yu, Jia-Rong, Chang, Chin-Sung, Tsai, Wei-Chuan, Liu, Ping-Yen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5253676/
https://www.ncbi.nlm.nih.gov/pubmed/28112206
http://dx.doi.org/10.1038/srep40996
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author Chang, Wei-Ting
Wu, Chih-Hsing
Hsu, Ling-Wei
Chen, Po-Wei
Yu, Jia-Rong
Chang, Chin-Sung
Tsai, Wei-Chuan
Liu, Ping-Yen
author_facet Chang, Wei-Ting
Wu, Chih-Hsing
Hsu, Ling-Wei
Chen, Po-Wei
Yu, Jia-Rong
Chang, Chin-Sung
Tsai, Wei-Chuan
Liu, Ping-Yen
author_sort Chang, Wei-Ting
collection PubMed
description With aging, intact parathyroid hormone (iPTH) increases. It plays a crucial role in left ventricular hypertrophy (LVH). Also, 25-hydroxy vitamin D (Vit-D) and iPTH have been observed to be determinants of muscle wasting known as sarcopenia. Fetuin A (FetA), a systemic calcification inhibitor, involves in the development of diastolic heart failure. Hence, we hypothesized that the interplay among FetA, Vit-D and iPTH may contribute to sarcopenic LVH among the elders. We analyzed a database from the Tianliao Old People study with 541 elders (≥65 years) in a Taiwan’s suburban community. After excluding patients with renal function impairment, 120/449 (26.7%) patients were diagnosed with sarcopenia. Sarcopenic patients had lower serum Vit-D levels but higher FetA as well as iPTH. Notably, sarcopenic patients with LVH had significantly lower FetA and higher iPTH levels. In multivariate logistic regression analysis, only the increase in iPTH was independently associated with sarcopenic LVH (Odds ratio: 1.05; confidence interval: 1.03–1.08, p = 0.005). Using iPTH >52.3 ng/l as a cutoff point, the sensitivity and specificity was 66% and 84%, respectively. In conclusion, FetA, Vit-D, and iPTH levels were all associated with sarcopenia in this geriatric population. Among them, iPTH specifically indicates patients with sarcopenic LVH.
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spelling pubmed-52536762017-01-24 Serum vitamin D, intact parathyroid hormone, and Fetuin A concentrations were associated with geriatric sarcopenia and cardiac hypertrophy Chang, Wei-Ting Wu, Chih-Hsing Hsu, Ling-Wei Chen, Po-Wei Yu, Jia-Rong Chang, Chin-Sung Tsai, Wei-Chuan Liu, Ping-Yen Sci Rep Article With aging, intact parathyroid hormone (iPTH) increases. It plays a crucial role in left ventricular hypertrophy (LVH). Also, 25-hydroxy vitamin D (Vit-D) and iPTH have been observed to be determinants of muscle wasting known as sarcopenia. Fetuin A (FetA), a systemic calcification inhibitor, involves in the development of diastolic heart failure. Hence, we hypothesized that the interplay among FetA, Vit-D and iPTH may contribute to sarcopenic LVH among the elders. We analyzed a database from the Tianliao Old People study with 541 elders (≥65 years) in a Taiwan’s suburban community. After excluding patients with renal function impairment, 120/449 (26.7%) patients were diagnosed with sarcopenia. Sarcopenic patients had lower serum Vit-D levels but higher FetA as well as iPTH. Notably, sarcopenic patients with LVH had significantly lower FetA and higher iPTH levels. In multivariate logistic regression analysis, only the increase in iPTH was independently associated with sarcopenic LVH (Odds ratio: 1.05; confidence interval: 1.03–1.08, p = 0.005). Using iPTH >52.3 ng/l as a cutoff point, the sensitivity and specificity was 66% and 84%, respectively. In conclusion, FetA, Vit-D, and iPTH levels were all associated with sarcopenia in this geriatric population. Among them, iPTH specifically indicates patients with sarcopenic LVH. Nature Publishing Group 2017-01-23 /pmc/articles/PMC5253676/ /pubmed/28112206 http://dx.doi.org/10.1038/srep40996 Text en Copyright © 2017, The Author(s) 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
Chang, Wei-Ting
Wu, Chih-Hsing
Hsu, Ling-Wei
Chen, Po-Wei
Yu, Jia-Rong
Chang, Chin-Sung
Tsai, Wei-Chuan
Liu, Ping-Yen
Serum vitamin D, intact parathyroid hormone, and Fetuin A concentrations were associated with geriatric sarcopenia and cardiac hypertrophy
title Serum vitamin D, intact parathyroid hormone, and Fetuin A concentrations were associated with geriatric sarcopenia and cardiac hypertrophy
title_full Serum vitamin D, intact parathyroid hormone, and Fetuin A concentrations were associated with geriatric sarcopenia and cardiac hypertrophy
title_fullStr Serum vitamin D, intact parathyroid hormone, and Fetuin A concentrations were associated with geriatric sarcopenia and cardiac hypertrophy
title_full_unstemmed Serum vitamin D, intact parathyroid hormone, and Fetuin A concentrations were associated with geriatric sarcopenia and cardiac hypertrophy
title_short Serum vitamin D, intact parathyroid hormone, and Fetuin A concentrations were associated with geriatric sarcopenia and cardiac hypertrophy
title_sort serum vitamin d, intact parathyroid hormone, and fetuin a concentrations were associated with geriatric sarcopenia and cardiac hypertrophy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5253676/
https://www.ncbi.nlm.nih.gov/pubmed/28112206
http://dx.doi.org/10.1038/srep40996
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