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Circulating 20S Proteasome Is Independently Associated with Abdominal Muscle Mass in Hemodialysis Patients
Protein-energy wasting is highly prevalent in hemodialysis patients, and it contributes to patient morbidity and mortality. The ubiquitin-proteasome system is the major pathway for intracellular protein degradation and it is involved in the regulation of basic cellular processes. However, the role o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372611/ https://www.ncbi.nlm.nih.gov/pubmed/25803510 http://dx.doi.org/10.1371/journal.pone.0121352 |
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author | Fukasawa, Hirotaka Kaneko, Mai Niwa, Hiroki Matsuyama, Takashi Yasuda, Hideo Kumagai, Hiromichi Furuya, Ryuichi |
author_facet | Fukasawa, Hirotaka Kaneko, Mai Niwa, Hiroki Matsuyama, Takashi Yasuda, Hideo Kumagai, Hiromichi Furuya, Ryuichi |
author_sort | Fukasawa, Hirotaka |
collection | PubMed |
description | Protein-energy wasting is highly prevalent in hemodialysis patients, and it contributes to patient morbidity and mortality. The ubiquitin-proteasome system is the major pathway for intracellular protein degradation and it is involved in the regulation of basic cellular processes. However, the role of this system in the determination of nutritional status is largely unknown. To examine a relationship between protein-energy wasting and the ubiquitin-proteasome system, a cross-sectional study of 76 hemodialysis patients was performed. Plasma concentrations of 20S proteasome were studied to evaluate its association with muscle and fat mass, which were investigated by abdominal muscle and fat areas measured using computed tomography and by creatinine production estimated using the creatinine kinetic model. Plasma 20S proteasome concentrations significantly and negatively correlated with abdominal muscle areas and creatinine production (rho = -0.263, P < 0.05 and rho = -0.241, P < 0.05, respectively), but not abdominal subcutaneous and visceral fat areas. Multiple regression analyses showed that 20S proteasome was a significant independent predictor of abdominal muscle area (P < 0.05). In conclusion, plasma 20S proteasome concentrations were independently associated with abdominal muscle mass in hemodialysis patients. Our findings indicate a relationship between circulating 20S proteasomes and muscle metabolism in these patients. TRIAL REGISTRATION: UMIN Clinical Trials Registry UMIN000012341 |
format | Online Article Text |
id | pubmed-4372611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43726112015-04-04 Circulating 20S Proteasome Is Independently Associated with Abdominal Muscle Mass in Hemodialysis Patients Fukasawa, Hirotaka Kaneko, Mai Niwa, Hiroki Matsuyama, Takashi Yasuda, Hideo Kumagai, Hiromichi Furuya, Ryuichi PLoS One Research Article Protein-energy wasting is highly prevalent in hemodialysis patients, and it contributes to patient morbidity and mortality. The ubiquitin-proteasome system is the major pathway for intracellular protein degradation and it is involved in the regulation of basic cellular processes. However, the role of this system in the determination of nutritional status is largely unknown. To examine a relationship between protein-energy wasting and the ubiquitin-proteasome system, a cross-sectional study of 76 hemodialysis patients was performed. Plasma concentrations of 20S proteasome were studied to evaluate its association with muscle and fat mass, which were investigated by abdominal muscle and fat areas measured using computed tomography and by creatinine production estimated using the creatinine kinetic model. Plasma 20S proteasome concentrations significantly and negatively correlated with abdominal muscle areas and creatinine production (rho = -0.263, P < 0.05 and rho = -0.241, P < 0.05, respectively), but not abdominal subcutaneous and visceral fat areas. Multiple regression analyses showed that 20S proteasome was a significant independent predictor of abdominal muscle area (P < 0.05). In conclusion, plasma 20S proteasome concentrations were independently associated with abdominal muscle mass in hemodialysis patients. Our findings indicate a relationship between circulating 20S proteasomes and muscle metabolism in these patients. TRIAL REGISTRATION: UMIN Clinical Trials Registry UMIN000012341 Public Library of Science 2015-03-24 /pmc/articles/PMC4372611/ /pubmed/25803510 http://dx.doi.org/10.1371/journal.pone.0121352 Text en © 2015 Fukasawa et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Fukasawa, Hirotaka Kaneko, Mai Niwa, Hiroki Matsuyama, Takashi Yasuda, Hideo Kumagai, Hiromichi Furuya, Ryuichi Circulating 20S Proteasome Is Independently Associated with Abdominal Muscle Mass in Hemodialysis Patients |
title | Circulating 20S Proteasome Is Independently Associated with Abdominal Muscle Mass in Hemodialysis Patients |
title_full | Circulating 20S Proteasome Is Independently Associated with Abdominal Muscle Mass in Hemodialysis Patients |
title_fullStr | Circulating 20S Proteasome Is Independently Associated with Abdominal Muscle Mass in Hemodialysis Patients |
title_full_unstemmed | Circulating 20S Proteasome Is Independently Associated with Abdominal Muscle Mass in Hemodialysis Patients |
title_short | Circulating 20S Proteasome Is Independently Associated with Abdominal Muscle Mass in Hemodialysis Patients |
title_sort | circulating 20s proteasome is independently associated with abdominal muscle mass in hemodialysis patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372611/ https://www.ncbi.nlm.nih.gov/pubmed/25803510 http://dx.doi.org/10.1371/journal.pone.0121352 |
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