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Cancer risk by combined levels of YKL-40 and C-reactive protein in the general population
BACKGROUND: YKL-40 and C-reactive protein (CRP) are biomarkers that may reflect cancer-related subclinical inflammation. We assessed elevated YKL-40 and CRP levels as combined risk predictors for cancer. METHODS: We measured plasma YKL-40 and CRP at baseline in 8706 individuals from the Danish gener...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251851/ https://www.ncbi.nlm.nih.gov/pubmed/22095223 http://dx.doi.org/10.1038/bjc.2011.501 |
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author | Allin, K H Bojesen, S E Johansen, J S Nordestgaard, B G |
author_facet | Allin, K H Bojesen, S E Johansen, J S Nordestgaard, B G |
author_sort | Allin, K H |
collection | PubMed |
description | BACKGROUND: YKL-40 and C-reactive protein (CRP) are biomarkers that may reflect cancer-related subclinical inflammation. We assessed elevated YKL-40 and CRP levels as combined risk predictors for cancer. METHODS: We measured plasma YKL-40 and CRP at baseline in 8706 individuals from the Danish general population. RESULTS: Hazard ratio (HR) of gastrointestinal cancer for a doubling of YKL-40 levels was 1.37 (95% CI: 1.17–1.61) and indifferent to adjustment for CRP levels. Hazard ratio of lung cancer for a doubling of CRP levels was 1.35 (1.17–1.56) and indifferent to adjustment for YKL-40 levels. Compared to individuals with both low CRP (<1.7 mg l(−1)) and YKL-40 (<154 μg l(−1)), individuals with high YKL-40 but low CRP had an HR of gastrointestinal cancer of 3.36 (1.70–6.64), whereas individuals with high CRP but low YKL-40 had an HR of lung cancer of 2.19 (1.24–3.87). The area under the receiver operating characteristic (ROC) curve was 0.68 for the ability of YKL-40 to predict gastrointestinal cancer and 0.67 for the ability of CRP to predict lung cancer. CONCLUSION: Elevated YKL-40 levels are associated with increased risk of gastrointestinal cancer, independently of CRP levels, whereas elevated CRP levels are associated with increased risk of lung cancer, independently of YKL-40 levels. |
format | Online Article Text |
id | pubmed-3251851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-32518512013-01-03 Cancer risk by combined levels of YKL-40 and C-reactive protein in the general population Allin, K H Bojesen, S E Johansen, J S Nordestgaard, B G Br J Cancer Molecular Diagnostics BACKGROUND: YKL-40 and C-reactive protein (CRP) are biomarkers that may reflect cancer-related subclinical inflammation. We assessed elevated YKL-40 and CRP levels as combined risk predictors for cancer. METHODS: We measured plasma YKL-40 and CRP at baseline in 8706 individuals from the Danish general population. RESULTS: Hazard ratio (HR) of gastrointestinal cancer for a doubling of YKL-40 levels was 1.37 (95% CI: 1.17–1.61) and indifferent to adjustment for CRP levels. Hazard ratio of lung cancer for a doubling of CRP levels was 1.35 (1.17–1.56) and indifferent to adjustment for YKL-40 levels. Compared to individuals with both low CRP (<1.7 mg l(−1)) and YKL-40 (<154 μg l(−1)), individuals with high YKL-40 but low CRP had an HR of gastrointestinal cancer of 3.36 (1.70–6.64), whereas individuals with high CRP but low YKL-40 had an HR of lung cancer of 2.19 (1.24–3.87). The area under the receiver operating characteristic (ROC) curve was 0.68 for the ability of YKL-40 to predict gastrointestinal cancer and 0.67 for the ability of CRP to predict lung cancer. CONCLUSION: Elevated YKL-40 levels are associated with increased risk of gastrointestinal cancer, independently of CRP levels, whereas elevated CRP levels are associated with increased risk of lung cancer, independently of YKL-40 levels. Nature Publishing Group 2012-01-03 2011-11-17 /pmc/articles/PMC3251851/ /pubmed/22095223 http://dx.doi.org/10.1038/bjc.2011.501 Text en Copyright © 2012 Cancer Research UK 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 | Molecular Diagnostics Allin, K H Bojesen, S E Johansen, J S Nordestgaard, B G Cancer risk by combined levels of YKL-40 and C-reactive protein in the general population |
title | Cancer risk by combined levels of YKL-40 and C-reactive protein in the general population |
title_full | Cancer risk by combined levels of YKL-40 and C-reactive protein in the general population |
title_fullStr | Cancer risk by combined levels of YKL-40 and C-reactive protein in the general population |
title_full_unstemmed | Cancer risk by combined levels of YKL-40 and C-reactive protein in the general population |
title_short | Cancer risk by combined levels of YKL-40 and C-reactive protein in the general population |
title_sort | cancer risk by combined levels of ykl-40 and c-reactive protein in the general population |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251851/ https://www.ncbi.nlm.nih.gov/pubmed/22095223 http://dx.doi.org/10.1038/bjc.2011.501 |
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