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Prediction of sarcopenia using a combination of multiple serum biomarkers
Sarcopenia is a gradual loss of skeletal muscle mass and function with aging. Given that sarcopenia has been recognized as a disease entity, effective molecular biomarkers for early diagnosis are required. We recruited 46 normal subjects and 50 patients with moderate sarcopenia aged 60 years and old...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988732/ https://www.ncbi.nlm.nih.gov/pubmed/29872072 http://dx.doi.org/10.1038/s41598-018-26617-9 |
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author | Kwak, Ju Yeon Hwang, Hyeoncheol Kim, Seon-Kyu Choi, Jeong Yi Lee, Seung-Min Bang, Hyun Kwon, Eun-Soo Lee, Kwang-Pyo Chung, Sun Gun Kwon, Ki-Sun |
author_facet | Kwak, Ju Yeon Hwang, Hyeoncheol Kim, Seon-Kyu Choi, Jeong Yi Lee, Seung-Min Bang, Hyun Kwon, Eun-Soo Lee, Kwang-Pyo Chung, Sun Gun Kwon, Ki-Sun |
author_sort | Kwak, Ju Yeon |
collection | PubMed |
description | Sarcopenia is a gradual loss of skeletal muscle mass and function with aging. Given that sarcopenia has been recognized as a disease entity, effective molecular biomarkers for early diagnosis are required. We recruited 46 normal subjects and 50 patients with moderate sarcopenia aged 60 years and older. Sarcopenia was clinically identified on the basis of the appendicular skeletal muscle index by applying cutoff values derived from the Asian Working Group for Sarcopenia. The serum levels of 21 potential biomarkers were analyzed and statistically examined. Interleukin 6, secreted protein acidic and rich in cysteine, macrophage migration inhibitory factor, and insulin-like growth factor 1 levels differed significantly between the normal and sarcopenia groups. However, in each case, the area under the receiver operating characteristics curve (AUC) was <0.7. Subsequent combination of the measurements of these biomarkers into a single risk score based on logistic regression coefficients enhanced the accuracy of diagnosis, yielding an AUC value of 0.763. The best cutoff value of 1.529 had 70.0% sensitivity and 78.3% specificity (95% CI = 2.80–21.69, p < 0.0001). Combined use of the selected biomarkers provides higher diagnostic accuracy than individual biomarkers, and may be effectively utilized for early diagnosis and prognosis of sarcopenia. |
format | Online Article Text |
id | pubmed-5988732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59887322018-06-20 Prediction of sarcopenia using a combination of multiple serum biomarkers Kwak, Ju Yeon Hwang, Hyeoncheol Kim, Seon-Kyu Choi, Jeong Yi Lee, Seung-Min Bang, Hyun Kwon, Eun-Soo Lee, Kwang-Pyo Chung, Sun Gun Kwon, Ki-Sun Sci Rep Article Sarcopenia is a gradual loss of skeletal muscle mass and function with aging. Given that sarcopenia has been recognized as a disease entity, effective molecular biomarkers for early diagnosis are required. We recruited 46 normal subjects and 50 patients with moderate sarcopenia aged 60 years and older. Sarcopenia was clinically identified on the basis of the appendicular skeletal muscle index by applying cutoff values derived from the Asian Working Group for Sarcopenia. The serum levels of 21 potential biomarkers were analyzed and statistically examined. Interleukin 6, secreted protein acidic and rich in cysteine, macrophage migration inhibitory factor, and insulin-like growth factor 1 levels differed significantly between the normal and sarcopenia groups. However, in each case, the area under the receiver operating characteristics curve (AUC) was <0.7. Subsequent combination of the measurements of these biomarkers into a single risk score based on logistic regression coefficients enhanced the accuracy of diagnosis, yielding an AUC value of 0.763. The best cutoff value of 1.529 had 70.0% sensitivity and 78.3% specificity (95% CI = 2.80–21.69, p < 0.0001). Combined use of the selected biomarkers provides higher diagnostic accuracy than individual biomarkers, and may be effectively utilized for early diagnosis and prognosis of sarcopenia. Nature Publishing Group UK 2018-06-05 /pmc/articles/PMC5988732/ /pubmed/29872072 http://dx.doi.org/10.1038/s41598-018-26617-9 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kwak, Ju Yeon Hwang, Hyeoncheol Kim, Seon-Kyu Choi, Jeong Yi Lee, Seung-Min Bang, Hyun Kwon, Eun-Soo Lee, Kwang-Pyo Chung, Sun Gun Kwon, Ki-Sun Prediction of sarcopenia using a combination of multiple serum biomarkers |
title | Prediction of sarcopenia using a combination of multiple serum biomarkers |
title_full | Prediction of sarcopenia using a combination of multiple serum biomarkers |
title_fullStr | Prediction of sarcopenia using a combination of multiple serum biomarkers |
title_full_unstemmed | Prediction of sarcopenia using a combination of multiple serum biomarkers |
title_short | Prediction of sarcopenia using a combination of multiple serum biomarkers |
title_sort | prediction of sarcopenia using a combination of multiple serum biomarkers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988732/ https://www.ncbi.nlm.nih.gov/pubmed/29872072 http://dx.doi.org/10.1038/s41598-018-26617-9 |
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