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The Relationship between Sarcopenia and Systemic Inflammatory Response for Cancer Cachexia in Small Cell Lung Cancer

BACKGROUND: The prognostic significance of sarcopenia, an important component of cancer cachexia, has been demonstrated in oncologic patients. Catabolic drivers have been suggested to be key features of cancer cachexia. OBJECTIVE: To determine the relationship between systemic inflammatory markers a...

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Autores principales: Kim, Eun Young, Kim, Young Saing, Seo, Ja-Young, Park, Inkeun, Ahn, Hee Kyung, Jeong, Yu Mi, Kim, Jeong Ho, Kim, Nambeom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990336/
https://www.ncbi.nlm.nih.gov/pubmed/27537502
http://dx.doi.org/10.1371/journal.pone.0161125
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author Kim, Eun Young
Kim, Young Saing
Seo, Ja-Young
Park, Inkeun
Ahn, Hee Kyung
Jeong, Yu Mi
Kim, Jeong Ho
Kim, Nambeom
author_facet Kim, Eun Young
Kim, Young Saing
Seo, Ja-Young
Park, Inkeun
Ahn, Hee Kyung
Jeong, Yu Mi
Kim, Jeong Ho
Kim, Nambeom
author_sort Kim, Eun Young
collection PubMed
description BACKGROUND: The prognostic significance of sarcopenia, an important component of cancer cachexia, has been demonstrated in oncologic patients. Catabolic drivers have been suggested to be key features of cancer cachexia. OBJECTIVE: To determine the relationship between systemic inflammatory markers and CT-determined muscle mass in patients with SCLC. METHODS: Cross-sectional muscle areas were evaluated at the level of the third lumbar vertebra (L3) using baseline CT images in 186 SCLC patients. Sarcopenia was defined as a L3 muscle index (L3MI, muscle area at L3/height(2)) of < 55 cm(2)/m(2) for men and of < 39 cm(2)/m(2) for women. Systemic inflammatory markers investigated included serum white blood cell count (WBC), neutrophil: lymphocyte ratio (NLR), C-reactive protein (CRP), and albumin. RESULTS: Mean L3MI was 47.9 ± 9.7 cm(2)/m(2) for men and 41.6 ± 7.0 cm(2)/m(2) for women. Sarcopenia was present in 128 patients (68.8%), and sarcopenic patients had significant serum lymphocyte counts and albumin levels (p = 0.002 and 0.041, respectively), and higher NLRs and CRP levels (p = 0.011 and 0.026) than non-sarcopenic patients. Multivariable analysis revealed that CRP independently predicted L3MI (β = -0.208; 95% CI, -0.415 to -0.002; p = 0.048), along with gender and BMI (p values < 0.001) and performance status (p = 0.010). CONCLUSION: The present study confirms a significant linear relationship exists between CT-determined muscle mass and CRP in SCLC patients. This association might provide a better understanding of the mechanism of cancer cachexia.
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spelling pubmed-49903362016-08-29 The Relationship between Sarcopenia and Systemic Inflammatory Response for Cancer Cachexia in Small Cell Lung Cancer Kim, Eun Young Kim, Young Saing Seo, Ja-Young Park, Inkeun Ahn, Hee Kyung Jeong, Yu Mi Kim, Jeong Ho Kim, Nambeom PLoS One Research Article BACKGROUND: The prognostic significance of sarcopenia, an important component of cancer cachexia, has been demonstrated in oncologic patients. Catabolic drivers have been suggested to be key features of cancer cachexia. OBJECTIVE: To determine the relationship between systemic inflammatory markers and CT-determined muscle mass in patients with SCLC. METHODS: Cross-sectional muscle areas were evaluated at the level of the third lumbar vertebra (L3) using baseline CT images in 186 SCLC patients. Sarcopenia was defined as a L3 muscle index (L3MI, muscle area at L3/height(2)) of < 55 cm(2)/m(2) for men and of < 39 cm(2)/m(2) for women. Systemic inflammatory markers investigated included serum white blood cell count (WBC), neutrophil: lymphocyte ratio (NLR), C-reactive protein (CRP), and albumin. RESULTS: Mean L3MI was 47.9 ± 9.7 cm(2)/m(2) for men and 41.6 ± 7.0 cm(2)/m(2) for women. Sarcopenia was present in 128 patients (68.8%), and sarcopenic patients had significant serum lymphocyte counts and albumin levels (p = 0.002 and 0.041, respectively), and higher NLRs and CRP levels (p = 0.011 and 0.026) than non-sarcopenic patients. Multivariable analysis revealed that CRP independently predicted L3MI (β = -0.208; 95% CI, -0.415 to -0.002; p = 0.048), along with gender and BMI (p values < 0.001) and performance status (p = 0.010). CONCLUSION: The present study confirms a significant linear relationship exists between CT-determined muscle mass and CRP in SCLC patients. This association might provide a better understanding of the mechanism of cancer cachexia. Public Library of Science 2016-08-18 /pmc/articles/PMC4990336/ /pubmed/27537502 http://dx.doi.org/10.1371/journal.pone.0161125 Text en © 2016 Kim 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kim, Eun Young
Kim, Young Saing
Seo, Ja-Young
Park, Inkeun
Ahn, Hee Kyung
Jeong, Yu Mi
Kim, Jeong Ho
Kim, Nambeom
The Relationship between Sarcopenia and Systemic Inflammatory Response for Cancer Cachexia in Small Cell Lung Cancer
title The Relationship between Sarcopenia and Systemic Inflammatory Response for Cancer Cachexia in Small Cell Lung Cancer
title_full The Relationship between Sarcopenia and Systemic Inflammatory Response for Cancer Cachexia in Small Cell Lung Cancer
title_fullStr The Relationship between Sarcopenia and Systemic Inflammatory Response for Cancer Cachexia in Small Cell Lung Cancer
title_full_unstemmed The Relationship between Sarcopenia and Systemic Inflammatory Response for Cancer Cachexia in Small Cell Lung Cancer
title_short The Relationship between Sarcopenia and Systemic Inflammatory Response for Cancer Cachexia in Small Cell Lung Cancer
title_sort relationship between sarcopenia and systemic inflammatory response for cancer cachexia in small cell lung cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990336/
https://www.ncbi.nlm.nih.gov/pubmed/27537502
http://dx.doi.org/10.1371/journal.pone.0161125
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