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Ibuprofen reduces energy expenditure and acute-phase protein production compared with placebo in pancreatic cancer patients.
The aim of this study was to investigate the effect of the cyclo-oxygenase inhibitor ibuprofen on the acute-phase protein response and resting energy expenditure (REE) of weight-losing patients with pancreatic cancer. Patients with irresectable pancreatic cancer (n = 16) were treated with either ibu...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1995
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034153/ https://www.ncbi.nlm.nih.gov/pubmed/7541236 |
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author | Wigmore, S. J. Falconer, J. S. Plester, C. E. Ross, J. A. Maingay, J. P. Carter, D. C. Fearon, K. C. |
author_facet | Wigmore, S. J. Falconer, J. S. Plester, C. E. Ross, J. A. Maingay, J. P. Carter, D. C. Fearon, K. C. |
author_sort | Wigmore, S. J. |
collection | PubMed |
description | The aim of this study was to investigate the effect of the cyclo-oxygenase inhibitor ibuprofen on the acute-phase protein response and resting energy expenditure (REE) of weight-losing patients with pancreatic cancer. Patients with irresectable pancreatic cancer (n = 16) were treated with either ibuprofen (1200 mg day-1 for 7 days (n = 10) or placebo (n = 6). A group of 17 age-related non-cancer subjects were also studied. Indirect calorimetry, anthropometry, multifrequency bioelectrical impedence analysis and serum C-reactive protein (CRP) estimation were performed immediately before and after treatment. Before treatment, total REE was significantly elevated in the pancreatic cancer patients compared with healthy controls (1499 +/- 71 vs 1377 +/- 58 kcal) (P < 0.02). Following treatment the mean REE of the ibuprofen group fell significantly (1386 +/- 89 kcal) compared with pretreatment values (1468 +/- 99 kcal) (P < 0.02), whereas no change was observed in the placebo group. Serum CRP concentration was also reduced in the ibuprofen-treated group (pre-ibuprofen, 51 mg l-1; post-ibuprofen, 29 mg l-1; P < 0.05). These results suggest that ibuprofen may have a role in abrogating the catabolic processes which contribute to weight loss in patients with pancreatic cancer. |
format | Text |
id | pubmed-2034153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20341532009-09-10 Ibuprofen reduces energy expenditure and acute-phase protein production compared with placebo in pancreatic cancer patients. Wigmore, S. J. Falconer, J. S. Plester, C. E. Ross, J. A. Maingay, J. P. Carter, D. C. Fearon, K. C. Br J Cancer Research Article The aim of this study was to investigate the effect of the cyclo-oxygenase inhibitor ibuprofen on the acute-phase protein response and resting energy expenditure (REE) of weight-losing patients with pancreatic cancer. Patients with irresectable pancreatic cancer (n = 16) were treated with either ibuprofen (1200 mg day-1 for 7 days (n = 10) or placebo (n = 6). A group of 17 age-related non-cancer subjects were also studied. Indirect calorimetry, anthropometry, multifrequency bioelectrical impedence analysis and serum C-reactive protein (CRP) estimation were performed immediately before and after treatment. Before treatment, total REE was significantly elevated in the pancreatic cancer patients compared with healthy controls (1499 +/- 71 vs 1377 +/- 58 kcal) (P < 0.02). Following treatment the mean REE of the ibuprofen group fell significantly (1386 +/- 89 kcal) compared with pretreatment values (1468 +/- 99 kcal) (P < 0.02), whereas no change was observed in the placebo group. Serum CRP concentration was also reduced in the ibuprofen-treated group (pre-ibuprofen, 51 mg l-1; post-ibuprofen, 29 mg l-1; P < 0.05). These results suggest that ibuprofen may have a role in abrogating the catabolic processes which contribute to weight loss in patients with pancreatic cancer. Nature Publishing Group 1995-07 /pmc/articles/PMC2034153/ /pubmed/7541236 Text en https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Wigmore, S. J. Falconer, J. S. Plester, C. E. Ross, J. A. Maingay, J. P. Carter, D. C. Fearon, K. C. Ibuprofen reduces energy expenditure and acute-phase protein production compared with placebo in pancreatic cancer patients. |
title | Ibuprofen reduces energy expenditure and acute-phase protein production compared with placebo in pancreatic cancer patients. |
title_full | Ibuprofen reduces energy expenditure and acute-phase protein production compared with placebo in pancreatic cancer patients. |
title_fullStr | Ibuprofen reduces energy expenditure and acute-phase protein production compared with placebo in pancreatic cancer patients. |
title_full_unstemmed | Ibuprofen reduces energy expenditure and acute-phase protein production compared with placebo in pancreatic cancer patients. |
title_short | Ibuprofen reduces energy expenditure and acute-phase protein production compared with placebo in pancreatic cancer patients. |
title_sort | ibuprofen reduces energy expenditure and acute-phase protein production compared with placebo in pancreatic cancer patients. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034153/ https://www.ncbi.nlm.nih.gov/pubmed/7541236 |
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