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Emerging markers of cachexia predict survival in cancer patients
BACKGROUND: Cachexia may occur in 40% of cancer patients, representing the major cause of death in more than 20% of them. The aim of this study was to investigate the role of leptin, ghrelin and obestatin as diagnostic and predictive markers of cachexia in oncologic patients. Their impact on patient...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239407/ https://www.ncbi.nlm.nih.gov/pubmed/25400234 http://dx.doi.org/10.1186/1471-2407-14-828 |
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author | Mondello, Patrizia Lacquaniti, Antonio Mondello, Stefania Bolignano, Davide Pitini, Vincenzo Aloisi, Carmela Buemi, Michele |
author_facet | Mondello, Patrizia Lacquaniti, Antonio Mondello, Stefania Bolignano, Davide Pitini, Vincenzo Aloisi, Carmela Buemi, Michele |
author_sort | Mondello, Patrizia |
collection | PubMed |
description | BACKGROUND: Cachexia may occur in 40% of cancer patients, representing the major cause of death in more than 20% of them. The aim of this study was to investigate the role of leptin, ghrelin and obestatin as diagnostic and predictive markers of cachexia in oncologic patients. Their impact on patient survival was also evaluated. METHODS: 140 adults with different cancer diagnoses were recruited. Thirty healthy volunteers served as control. Serum ghrelin, obestatin and leptin were tested at baseline and after a follow-up period of 18 months. RESULTS: Ghrelin levels were significantly higher in cancer patients than in healthy subjects (573.31 ± 130 vs 320.20 ± 66.48 ng/ml, p < 0.0001), while obestatin (17.42 ± 7.12 vs 24.89 ± 5.54 ng/ml, p < 0.0001) and leptin (38.4 ± 21.2 vs 76.28 ± 17.48 ng/ml, p < 0.0001) values were lower. At ROC analyses the diagnostic profile of ghrelin (AUC 0.962; sensitivity 83%; specificity 98%), obestatin (AUC 0.798; sensitivity 74.5%; specificity 81.5%) and leptin (AUC 0.828; sensitivity 79%; specificity 73%) was superior to that of albumin (AUC 0.547; sensitivity 63%, specificity 69.4%) for detecting cachexia among cancer patients. On Cox multivariate analyses ghrelin (HR 1.02; 95% CI 1.01 – 1.03; p < 0.0001) and leptin (HR 0.94; 95% CI 0.92 – 0.96; p < 0.0001) were significant predictors of death even after correction for other known risk factors such as presence of metastasis and chronic kidney disease. CONCLUSION: Ghrelin and leptin are promising biomarkers to diagnose cachexia and to predict survival in cancer patients. |
format | Online Article Text |
id | pubmed-4239407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42394072014-11-21 Emerging markers of cachexia predict survival in cancer patients Mondello, Patrizia Lacquaniti, Antonio Mondello, Stefania Bolignano, Davide Pitini, Vincenzo Aloisi, Carmela Buemi, Michele BMC Cancer Research Article BACKGROUND: Cachexia may occur in 40% of cancer patients, representing the major cause of death in more than 20% of them. The aim of this study was to investigate the role of leptin, ghrelin and obestatin as diagnostic and predictive markers of cachexia in oncologic patients. Their impact on patient survival was also evaluated. METHODS: 140 adults with different cancer diagnoses were recruited. Thirty healthy volunteers served as control. Serum ghrelin, obestatin and leptin were tested at baseline and after a follow-up period of 18 months. RESULTS: Ghrelin levels were significantly higher in cancer patients than in healthy subjects (573.31 ± 130 vs 320.20 ± 66.48 ng/ml, p < 0.0001), while obestatin (17.42 ± 7.12 vs 24.89 ± 5.54 ng/ml, p < 0.0001) and leptin (38.4 ± 21.2 vs 76.28 ± 17.48 ng/ml, p < 0.0001) values were lower. At ROC analyses the diagnostic profile of ghrelin (AUC 0.962; sensitivity 83%; specificity 98%), obestatin (AUC 0.798; sensitivity 74.5%; specificity 81.5%) and leptin (AUC 0.828; sensitivity 79%; specificity 73%) was superior to that of albumin (AUC 0.547; sensitivity 63%, specificity 69.4%) for detecting cachexia among cancer patients. On Cox multivariate analyses ghrelin (HR 1.02; 95% CI 1.01 – 1.03; p < 0.0001) and leptin (HR 0.94; 95% CI 0.92 – 0.96; p < 0.0001) were significant predictors of death even after correction for other known risk factors such as presence of metastasis and chronic kidney disease. CONCLUSION: Ghrelin and leptin are promising biomarkers to diagnose cachexia and to predict survival in cancer patients. BioMed Central 2014-11-16 /pmc/articles/PMC4239407/ /pubmed/25400234 http://dx.doi.org/10.1186/1471-2407-14-828 Text en © Mondello et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 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 Article Mondello, Patrizia Lacquaniti, Antonio Mondello, Stefania Bolignano, Davide Pitini, Vincenzo Aloisi, Carmela Buemi, Michele Emerging markers of cachexia predict survival in cancer patients |
title | Emerging markers of cachexia predict survival in cancer patients |
title_full | Emerging markers of cachexia predict survival in cancer patients |
title_fullStr | Emerging markers of cachexia predict survival in cancer patients |
title_full_unstemmed | Emerging markers of cachexia predict survival in cancer patients |
title_short | Emerging markers of cachexia predict survival in cancer patients |
title_sort | emerging markers of cachexia predict survival in cancer patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239407/ https://www.ncbi.nlm.nih.gov/pubmed/25400234 http://dx.doi.org/10.1186/1471-2407-14-828 |
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