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Primary sclerosing cholangitis and the risk of colon neoplasia in patients with Crohn’s colitis
Background and aim: Crohn’s colitis (CC) is associated with primary sclerosing cholangitis (PSC). However the risk of colon cancer or dysplasia in CC and PSC is unclear. Our aim was to study the risk of colon neoplasia in CC in patients with and without PSC. Methods: This is a nested, case-control c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976675/ https://www.ncbi.nlm.nih.gov/pubmed/25725040 http://dx.doi.org/10.1093/gastro/gov007 |
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author | Navaneethan, Udayakumar Rai, Tarun Venkatesh, Preethi GK Kiran, Ravi P |
author_facet | Navaneethan, Udayakumar Rai, Tarun Venkatesh, Preethi GK Kiran, Ravi P |
author_sort | Navaneethan, Udayakumar |
collection | PubMed |
description | Background and aim: Crohn’s colitis (CC) is associated with primary sclerosing cholangitis (PSC). However the risk of colon cancer or dysplasia in CC and PSC is unclear. Our aim was to study the risk of colon neoplasia in CC in patients with and without PSC. Methods: This is a nested, case-control cohort study of all patients diagnosed with concurrent CC and PSC, seen at the Cleveland Clinic between 1985 and 2012. Forty-three patients with both CC and PSC were compared with a random sample of 159 CC controls without PSC during the same period. Results: Seven (16.3%) of 43 CC patients with PSC developed colon cancer or dysplasia, compared with 22 (13.8%) of 159 controls (P = 0.98). Of seven colon neoplasia cases in the PSC group, 100% occurred proximal to the splenic flexure, compared with 50% (11/22) cases of colon neoplasia in controls occurring in the proximal colon (P = 0.001). Based on Cox regression analysis, male gender independently increased the risk of neoplasia [hazard ratio (HR) = 2.68; 95% confidence interval (CI) 1.30–5.54; P = 0.008], as did age at CC diagnosis (HR = 1.29; 95% CI 1.14–1.47; P < 0.001), while the use of azathioprine/6-mercaptopurine was protective (HR = 0.30; 95% CI 0.13–0.70; P = 0.005). The presence of PSC did not increase the risk for colon neoplasia (HR = 0.45; 95% CI 0.18–1.13; P = 0.09). Conclusions: CC patients with PSC appear not to be at increased risk of developing colon neoplasia. Among patients in our cohort with colon neoplasia and concurrent PSC, the neoplasia occurred in the proximal colon in all cases. |
format | Online Article Text |
id | pubmed-4976675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49766752016-08-09 Primary sclerosing cholangitis and the risk of colon neoplasia in patients with Crohn’s colitis Navaneethan, Udayakumar Rai, Tarun Venkatesh, Preethi GK Kiran, Ravi P Gastroenterol Rep (Oxf) Original Articles Background and aim: Crohn’s colitis (CC) is associated with primary sclerosing cholangitis (PSC). However the risk of colon cancer or dysplasia in CC and PSC is unclear. Our aim was to study the risk of colon neoplasia in CC in patients with and without PSC. Methods: This is a nested, case-control cohort study of all patients diagnosed with concurrent CC and PSC, seen at the Cleveland Clinic between 1985 and 2012. Forty-three patients with both CC and PSC were compared with a random sample of 159 CC controls without PSC during the same period. Results: Seven (16.3%) of 43 CC patients with PSC developed colon cancer or dysplasia, compared with 22 (13.8%) of 159 controls (P = 0.98). Of seven colon neoplasia cases in the PSC group, 100% occurred proximal to the splenic flexure, compared with 50% (11/22) cases of colon neoplasia in controls occurring in the proximal colon (P = 0.001). Based on Cox regression analysis, male gender independently increased the risk of neoplasia [hazard ratio (HR) = 2.68; 95% confidence interval (CI) 1.30–5.54; P = 0.008], as did age at CC diagnosis (HR = 1.29; 95% CI 1.14–1.47; P < 0.001), while the use of azathioprine/6-mercaptopurine was protective (HR = 0.30; 95% CI 0.13–0.70; P = 0.005). The presence of PSC did not increase the risk for colon neoplasia (HR = 0.45; 95% CI 0.18–1.13; P = 0.09). Conclusions: CC patients with PSC appear not to be at increased risk of developing colon neoplasia. Among patients in our cohort with colon neoplasia and concurrent PSC, the neoplasia occurred in the proximal colon in all cases. Oxford University Press 2016-08 2015-02-26 /pmc/articles/PMC4976675/ /pubmed/25725040 http://dx.doi.org/10.1093/gastro/gov007 Text en © The Author(s) 2015. Published by Oxford University Press and the Digestive Science Publishing Co. Limited. http://creativecommons.org/licenses/by/4.0/ 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Navaneethan, Udayakumar Rai, Tarun Venkatesh, Preethi GK Kiran, Ravi P Primary sclerosing cholangitis and the risk of colon neoplasia in patients with Crohn’s colitis |
title | Primary sclerosing cholangitis and the risk of colon neoplasia in patients with Crohn’s colitis |
title_full | Primary sclerosing cholangitis and the risk of colon neoplasia in patients with Crohn’s colitis |
title_fullStr | Primary sclerosing cholangitis and the risk of colon neoplasia in patients with Crohn’s colitis |
title_full_unstemmed | Primary sclerosing cholangitis and the risk of colon neoplasia in patients with Crohn’s colitis |
title_short | Primary sclerosing cholangitis and the risk of colon neoplasia in patients with Crohn’s colitis |
title_sort | primary sclerosing cholangitis and the risk of colon neoplasia in patients with crohn’s colitis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976675/ https://www.ncbi.nlm.nih.gov/pubmed/25725040 http://dx.doi.org/10.1093/gastro/gov007 |
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