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Plasma levels of the pro-inflammatory protein S100A12 (EN-RAGE) are associated with muscle and fat mass in hemodialysis patients: a cross-sectional study

BACKGROUND: Malnutrition is highly prevalent and contributes to mortality in hemodialysis (HD) patients. Although the receptor for advanced glycation end products (RAGE) system also contributes to the morbidity and mortality of these patients, the role that the RAGE system plays in determining nutri...

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Autores principales: Fukasawa, Hirotaka, Ishigaki, Sayaka, Kinoshita-Katahashi, Naoko, Yasuda, Hideo, Kumagai, Hiromichi, Furuya, Ryuichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048598/
https://www.ncbi.nlm.nih.gov/pubmed/24884769
http://dx.doi.org/10.1186/1475-2891-13-48
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author Fukasawa, Hirotaka
Ishigaki, Sayaka
Kinoshita-Katahashi, Naoko
Yasuda, Hideo
Kumagai, Hiromichi
Furuya, Ryuichi
author_facet Fukasawa, Hirotaka
Ishigaki, Sayaka
Kinoshita-Katahashi, Naoko
Yasuda, Hideo
Kumagai, Hiromichi
Furuya, Ryuichi
author_sort Fukasawa, Hirotaka
collection PubMed
description BACKGROUND: Malnutrition is highly prevalent and contributes to mortality in hemodialysis (HD) patients. Although the receptor for advanced glycation end products (RAGE) system also contributes to the morbidity and mortality of these patients, the role that the RAGE system plays in determining nutritional status is currently unknown. METHODS: A cross-sectional study examining 79 HD patients was performed. The plasma concentrations of the soluble RAGE (sRAGE) and S100A12 (also known as EN-RAGE) were studied to evaluate their association with nutritional status, which was assessed by measuring the mid-thigh muscle mass and subcutaneous fat mass with computed tomography. RESULTS: Plasma S100A12 concentrations were shown to be significantly and negatively correlated with muscle mass and with fat mass (r = −0.237, P < 0.05 and r = −0.261, P < 0.05, respectively). In contrast, sRAGE was not shown to significantly correlate with either of these factors. Multiple regression analyses demonstrated that S100A12 is a significant independent predictor of both muscle mass and fat mass (P < 0.01 and P < 0.05, respectively). CONCLUSIONS: Our findings suggest that plasma S100A12 levels could play an important role in determining muscle mass and fat mass in HD patients. TRIAL REGISTRATION: Study number; UMIN000012341.
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spelling pubmed-40485982014-06-08 Plasma levels of the pro-inflammatory protein S100A12 (EN-RAGE) are associated with muscle and fat mass in hemodialysis patients: a cross-sectional study Fukasawa, Hirotaka Ishigaki, Sayaka Kinoshita-Katahashi, Naoko Yasuda, Hideo Kumagai, Hiromichi Furuya, Ryuichi Nutr J Research BACKGROUND: Malnutrition is highly prevalent and contributes to mortality in hemodialysis (HD) patients. Although the receptor for advanced glycation end products (RAGE) system also contributes to the morbidity and mortality of these patients, the role that the RAGE system plays in determining nutritional status is currently unknown. METHODS: A cross-sectional study examining 79 HD patients was performed. The plasma concentrations of the soluble RAGE (sRAGE) and S100A12 (also known as EN-RAGE) were studied to evaluate their association with nutritional status, which was assessed by measuring the mid-thigh muscle mass and subcutaneous fat mass with computed tomography. RESULTS: Plasma S100A12 concentrations were shown to be significantly and negatively correlated with muscle mass and with fat mass (r = −0.237, P < 0.05 and r = −0.261, P < 0.05, respectively). In contrast, sRAGE was not shown to significantly correlate with either of these factors. Multiple regression analyses demonstrated that S100A12 is a significant independent predictor of both muscle mass and fat mass (P < 0.01 and P < 0.05, respectively). CONCLUSIONS: Our findings suggest that plasma S100A12 levels could play an important role in determining muscle mass and fat mass in HD patients. TRIAL REGISTRATION: Study number; UMIN000012341. BioMed Central 2014-05-27 /pmc/articles/PMC4048598/ /pubmed/24884769 http://dx.doi.org/10.1186/1475-2891-13-48 Text en Copyright © 2014 Fukasawa et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Fukasawa, Hirotaka
Ishigaki, Sayaka
Kinoshita-Katahashi, Naoko
Yasuda, Hideo
Kumagai, Hiromichi
Furuya, Ryuichi
Plasma levels of the pro-inflammatory protein S100A12 (EN-RAGE) are associated with muscle and fat mass in hemodialysis patients: a cross-sectional study
title Plasma levels of the pro-inflammatory protein S100A12 (EN-RAGE) are associated with muscle and fat mass in hemodialysis patients: a cross-sectional study
title_full Plasma levels of the pro-inflammatory protein S100A12 (EN-RAGE) are associated with muscle and fat mass in hemodialysis patients: a cross-sectional study
title_fullStr Plasma levels of the pro-inflammatory protein S100A12 (EN-RAGE) are associated with muscle and fat mass in hemodialysis patients: a cross-sectional study
title_full_unstemmed Plasma levels of the pro-inflammatory protein S100A12 (EN-RAGE) are associated with muscle and fat mass in hemodialysis patients: a cross-sectional study
title_short Plasma levels of the pro-inflammatory protein S100A12 (EN-RAGE) are associated with muscle and fat mass in hemodialysis patients: a cross-sectional study
title_sort plasma levels of the pro-inflammatory protein s100a12 (en-rage) are associated with muscle and fat mass in hemodialysis patients: a cross-sectional study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048598/
https://www.ncbi.nlm.nih.gov/pubmed/24884769
http://dx.doi.org/10.1186/1475-2891-13-48
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