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Serum inflammatory markers and colorectal cancer risk and survival
BACKGROUND: Inflammation has been linked with development of some cancers. We investigated systemic inflammation in relation to colorectal cancer incidence and subsequent survival using common serum inflammatory markers DESIGN: A cohort of men and women aged 20 years and older in greater Stockholm a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5482738/ https://www.ncbi.nlm.nih.gov/pubmed/28376082 http://dx.doi.org/10.1038/bjc.2017.96 |
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author | Ghuman, Sundeep Van Hemelrijck, Mieke Garmo, Hans Holmberg, Lars Malmström, Håkan Lambe, Mats Hammar, Niklas Walldius, Göran Jungner, Ingmar Wulaningsih, Wahyu |
author_facet | Ghuman, Sundeep Van Hemelrijck, Mieke Garmo, Hans Holmberg, Lars Malmström, Håkan Lambe, Mats Hammar, Niklas Walldius, Göran Jungner, Ingmar Wulaningsih, Wahyu |
author_sort | Ghuman, Sundeep |
collection | PubMed |
description | BACKGROUND: Inflammation has been linked with development of some cancers. We investigated systemic inflammation in relation to colorectal cancer incidence and subsequent survival using common serum inflammatory markers DESIGN: A cohort of men and women aged 20 years and older in greater Stockholm area with serum C-reactive protein (CRP) and albumin measured between 1986 and 1999 were included (n=325 599). A subset of these had baseline measurements of haptoglobin and leukocytes. Multivariable Cox regression was performed to assess risk of colorectal cancer by levels of inflammatory markers, adjusting for potential confounders. Analyses were stratified by circulating glucose, total cholesterol and triglycerides. Overall and CRC-specific death following diagnosis were assessed as secondary outcomes. RESULTS: A total of 4764 individuals were diagnosed with colorectal cancer. A positive association between haptoglobin and colorectal cancer incidence was found (hazard ratio (HR): 1.17; 95% CI: 1.06–1.28). A positive association was also observed with leukocytes (HR: 1.21; 95% CI: 1.03–1.42). No evidence of association was noted between CRP and colorectal cancer risk. Higher risks of all-cause death were seen with haptoglobin and leukocytes levels. Higher haptoglobin levels were linked with an increased risk of colorectal cancer death (HR: 1.19; 95% CI: 1.01–1.41). CONCLUSIONS: Prediagnostic systemic inflammation may impact colorectal cancer incidence and survival; therefore, prompting investigations linking inflammatory pathways preceding colorectal cancer with disease severity and progression. |
format | Online Article Text |
id | pubmed-5482738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54827382018-05-09 Serum inflammatory markers and colorectal cancer risk and survival Ghuman, Sundeep Van Hemelrijck, Mieke Garmo, Hans Holmberg, Lars Malmström, Håkan Lambe, Mats Hammar, Niklas Walldius, Göran Jungner, Ingmar Wulaningsih, Wahyu Br J Cancer Epidemiology BACKGROUND: Inflammation has been linked with development of some cancers. We investigated systemic inflammation in relation to colorectal cancer incidence and subsequent survival using common serum inflammatory markers DESIGN: A cohort of men and women aged 20 years and older in greater Stockholm area with serum C-reactive protein (CRP) and albumin measured between 1986 and 1999 were included (n=325 599). A subset of these had baseline measurements of haptoglobin and leukocytes. Multivariable Cox regression was performed to assess risk of colorectal cancer by levels of inflammatory markers, adjusting for potential confounders. Analyses were stratified by circulating glucose, total cholesterol and triglycerides. Overall and CRC-specific death following diagnosis were assessed as secondary outcomes. RESULTS: A total of 4764 individuals were diagnosed with colorectal cancer. A positive association between haptoglobin and colorectal cancer incidence was found (hazard ratio (HR): 1.17; 95% CI: 1.06–1.28). A positive association was also observed with leukocytes (HR: 1.21; 95% CI: 1.03–1.42). No evidence of association was noted between CRP and colorectal cancer risk. Higher risks of all-cause death were seen with haptoglobin and leukocytes levels. Higher haptoglobin levels were linked with an increased risk of colorectal cancer death (HR: 1.19; 95% CI: 1.01–1.41). CONCLUSIONS: Prediagnostic systemic inflammation may impact colorectal cancer incidence and survival; therefore, prompting investigations linking inflammatory pathways preceding colorectal cancer with disease severity and progression. Nature Publishing Group 2017-05-09 2017-04-04 /pmc/articles/PMC5482738/ /pubmed/28376082 http://dx.doi.org/10.1038/bjc.2017.96 Text en Copyright © 2017 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Epidemiology Ghuman, Sundeep Van Hemelrijck, Mieke Garmo, Hans Holmberg, Lars Malmström, Håkan Lambe, Mats Hammar, Niklas Walldius, Göran Jungner, Ingmar Wulaningsih, Wahyu Serum inflammatory markers and colorectal cancer risk and survival |
title | Serum inflammatory markers and colorectal cancer risk and survival |
title_full | Serum inflammatory markers and colorectal cancer risk and survival |
title_fullStr | Serum inflammatory markers and colorectal cancer risk and survival |
title_full_unstemmed | Serum inflammatory markers and colorectal cancer risk and survival |
title_short | Serum inflammatory markers and colorectal cancer risk and survival |
title_sort | serum inflammatory markers and colorectal cancer risk and survival |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5482738/ https://www.ncbi.nlm.nih.gov/pubmed/28376082 http://dx.doi.org/10.1038/bjc.2017.96 |
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