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High C-reactive protein level is associated with high-risk adenoma
BACKGROUND/AIMS: There is substantial evidence supporting a role of inflammation in the pathogenesis of colorectal cancer; however, little is known about the association between serum C-reactive protein (CRP) and the risk of colorectal adenoma. This study was conducted to investigate the association...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for the Study of Intestinal Diseases
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683982/ https://www.ncbi.nlm.nih.gov/pubmed/29142519 http://dx.doi.org/10.5217/ir.2017.15.4.511 |
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author | Lee, Hyae Min Cha, Jae Myung Lee, Jung Lok Jeon, Jung Won Shin, Hyun Phil Joo, Kwang Ro Yoon, Jin Young Lee, Joung Il |
author_facet | Lee, Hyae Min Cha, Jae Myung Lee, Jung Lok Jeon, Jung Won Shin, Hyun Phil Joo, Kwang Ro Yoon, Jin Young Lee, Joung Il |
author_sort | Lee, Hyae Min |
collection | PubMed |
description | BACKGROUND/AIMS: There is substantial evidence supporting a role of inflammation in the pathogenesis of colorectal cancer; however, little is known about the association between serum C-reactive protein (CRP) and the risk of colorectal adenoma. This study was conducted to investigate the association between serum CRP and colorectal adenoma risk. METHODS: A retrospective cross-sectional study was performed on first-time screening colonoscopies in asymptomatic subjects who also had their serum CRP level measured during a routine health check-up between September 2006 and September 2009 in Korea. Serum CRP level was compared between high-risk and low-risk adenoma groups and independent predictors of high-risk adenoma were analyzed using multivariate regression analysis. RESULTS: Among the 3,309 eligible patients, the high-risk adenoma group had higher serum CRP levels than the low-risk adenoma group (P=0.000). In addition, patients with a high-risk adenoma were more frequently included in the high CRP group than in the low CRP group (8.6% vs. 4.0%, P<0.001). The prevalence of high-risk adenoma was 3.5 times higher in the highest quartile of CRP level (P=0.000) compared with that in the lowest quartile. In logistic regression analysis, a higher quartile CRP level was found to be an independent risk factor for high-risk adenoma (odds ratio, 1.8; 95% confidence interval, 1.3–2.5; P=0.000). CONCLUSIONS: High CRP level is associated with high-risk adenoma in both men and women. Our data may support the association between chronic inflammation and colorectal neoplasia, which warrants further investigation. |
format | Online Article Text |
id | pubmed-5683982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Korean Association for the Study of Intestinal Diseases |
record_format | MEDLINE/PubMed |
spelling | pubmed-56839822017-11-15 High C-reactive protein level is associated with high-risk adenoma Lee, Hyae Min Cha, Jae Myung Lee, Jung Lok Jeon, Jung Won Shin, Hyun Phil Joo, Kwang Ro Yoon, Jin Young Lee, Joung Il Intest Res Original Article BACKGROUND/AIMS: There is substantial evidence supporting a role of inflammation in the pathogenesis of colorectal cancer; however, little is known about the association between serum C-reactive protein (CRP) and the risk of colorectal adenoma. This study was conducted to investigate the association between serum CRP and colorectal adenoma risk. METHODS: A retrospective cross-sectional study was performed on first-time screening colonoscopies in asymptomatic subjects who also had their serum CRP level measured during a routine health check-up between September 2006 and September 2009 in Korea. Serum CRP level was compared between high-risk and low-risk adenoma groups and independent predictors of high-risk adenoma were analyzed using multivariate regression analysis. RESULTS: Among the 3,309 eligible patients, the high-risk adenoma group had higher serum CRP levels than the low-risk adenoma group (P=0.000). In addition, patients with a high-risk adenoma were more frequently included in the high CRP group than in the low CRP group (8.6% vs. 4.0%, P<0.001). The prevalence of high-risk adenoma was 3.5 times higher in the highest quartile of CRP level (P=0.000) compared with that in the lowest quartile. In logistic regression analysis, a higher quartile CRP level was found to be an independent risk factor for high-risk adenoma (odds ratio, 1.8; 95% confidence interval, 1.3–2.5; P=0.000). CONCLUSIONS: High CRP level is associated with high-risk adenoma in both men and women. Our data may support the association between chronic inflammation and colorectal neoplasia, which warrants further investigation. Korean Association for the Study of Intestinal Diseases 2017-10 2017-10-23 /pmc/articles/PMC5683982/ /pubmed/29142519 http://dx.doi.org/10.5217/ir.2017.15.4.511 Text en © Copyright 2017. Korean Association for the Study of Intestinal Diseases. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Hyae Min Cha, Jae Myung Lee, Jung Lok Jeon, Jung Won Shin, Hyun Phil Joo, Kwang Ro Yoon, Jin Young Lee, Joung Il High C-reactive protein level is associated with high-risk adenoma |
title | High C-reactive protein level is associated with high-risk adenoma |
title_full | High C-reactive protein level is associated with high-risk adenoma |
title_fullStr | High C-reactive protein level is associated with high-risk adenoma |
title_full_unstemmed | High C-reactive protein level is associated with high-risk adenoma |
title_short | High C-reactive protein level is associated with high-risk adenoma |
title_sort | high c-reactive protein level is associated with high-risk adenoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683982/ https://www.ncbi.nlm.nih.gov/pubmed/29142519 http://dx.doi.org/10.5217/ir.2017.15.4.511 |
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