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Prognostic Value of Terminal Ileal Inflammation in Patients with Ulcerative Colitis

BACKGROUND/AIMS: Few studies have investigated terminal ileal lesions and their prognostic value in patients with ulcerative colitis (UC). We evaluated the clinical significance of these lesions as a prognostic factor in patients with UC who were in clinical remission. METHODS: We retrospectively se...

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Autores principales: Yu, Jongwook, Park, Jihye, Kang, Eun Ae, Park, Soo Jung, Park, Jae Jun, Kim, Tae Il, Kim, Won Ho, Cheon, Jae Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Office of Gut and Liver 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593494/
https://www.ncbi.nlm.nih.gov/pubmed/33767032
http://dx.doi.org/10.5009/gnl20294
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author Yu, Jongwook
Park, Jihye
Kang, Eun Ae
Park, Soo Jung
Park, Jae Jun
Kim, Tae Il
Kim, Won Ho
Cheon, Jae Hee
author_facet Yu, Jongwook
Park, Jihye
Kang, Eun Ae
Park, Soo Jung
Park, Jae Jun
Kim, Tae Il
Kim, Won Ho
Cheon, Jae Hee
author_sort Yu, Jongwook
collection PubMed
description BACKGROUND/AIMS: Few studies have investigated terminal ileal lesions and their prognostic value in patients with ulcerative colitis (UC). We evaluated the clinical significance of these lesions as a prognostic factor in patients with UC who were in clinical remission. METHODS: We retrospectively selected 567 of 4,066 colonoscopy reports that included positive findings from orificial observations of the terminal ileum (TI) and appendix in patients with UC. We finally recruited patients who were in clinical remission (n=204). We compared the clinical courses, including relapse and other prognostic parameters associated with UC, between the groups. RESULTS: The baseline patient characteristics were not significantly different between patients with (n=69, TI+ group) and without TI lesions (n=135, TI– group), although there were more never-smokers in the TI+ group (n=57 [82.6%] in the TI+ group; n=86 [63.7%] in the TI– group; p=0.005). Of note, appendiceal orifice inflammation (AOI) was less frequently found in the TI+ group (14.5%) than in the TI– group (71.9%, p<0.001). The cumulative relapse rate was numerically higher in the TI– group, but it was not significantly different according to the Kaplan-Meier analysis (p=0.116). Multivariate Cox regression analysis also revealed advanced age at diagnosis as the most significant factor (adjusted hazard ratio, 0.964; 95% confidence interval, 0.932 to 0.998; p=0.037), but neither TI inflammation nor AOI were significantly associated with the cumulative relapse rate in patients with UC in clinical remission. CONCLUSIONS: For patients with UC in clinical remission, neither terminal ileal lesions nor AOI had significant clinical or predictive value for future relapse.
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spelling pubmed-85934942021-12-01 Prognostic Value of Terminal Ileal Inflammation in Patients with Ulcerative Colitis Yu, Jongwook Park, Jihye Kang, Eun Ae Park, Soo Jung Park, Jae Jun Kim, Tae Il Kim, Won Ho Cheon, Jae Hee Gut Liver Original Article BACKGROUND/AIMS: Few studies have investigated terminal ileal lesions and their prognostic value in patients with ulcerative colitis (UC). We evaluated the clinical significance of these lesions as a prognostic factor in patients with UC who were in clinical remission. METHODS: We retrospectively selected 567 of 4,066 colonoscopy reports that included positive findings from orificial observations of the terminal ileum (TI) and appendix in patients with UC. We finally recruited patients who were in clinical remission (n=204). We compared the clinical courses, including relapse and other prognostic parameters associated with UC, between the groups. RESULTS: The baseline patient characteristics were not significantly different between patients with (n=69, TI+ group) and without TI lesions (n=135, TI– group), although there were more never-smokers in the TI+ group (n=57 [82.6%] in the TI+ group; n=86 [63.7%] in the TI– group; p=0.005). Of note, appendiceal orifice inflammation (AOI) was less frequently found in the TI+ group (14.5%) than in the TI– group (71.9%, p<0.001). The cumulative relapse rate was numerically higher in the TI– group, but it was not significantly different according to the Kaplan-Meier analysis (p=0.116). Multivariate Cox regression analysis also revealed advanced age at diagnosis as the most significant factor (adjusted hazard ratio, 0.964; 95% confidence interval, 0.932 to 0.998; p=0.037), but neither TI inflammation nor AOI were significantly associated with the cumulative relapse rate in patients with UC in clinical remission. CONCLUSIONS: For patients with UC in clinical remission, neither terminal ileal lesions nor AOI had significant clinical or predictive value for future relapse. Editorial Office of Gut and Liver 2021-11-15 2021-11-15 /pmc/articles/PMC8593494/ /pubmed/33767032 http://dx.doi.org/10.5009/gnl20294 Text en Copyright © Gut and Liver. https://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 (https://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
Yu, Jongwook
Park, Jihye
Kang, Eun Ae
Park, Soo Jung
Park, Jae Jun
Kim, Tae Il
Kim, Won Ho
Cheon, Jae Hee
Prognostic Value of Terminal Ileal Inflammation in Patients with Ulcerative Colitis
title Prognostic Value of Terminal Ileal Inflammation in Patients with Ulcerative Colitis
title_full Prognostic Value of Terminal Ileal Inflammation in Patients with Ulcerative Colitis
title_fullStr Prognostic Value of Terminal Ileal Inflammation in Patients with Ulcerative Colitis
title_full_unstemmed Prognostic Value of Terminal Ileal Inflammation in Patients with Ulcerative Colitis
title_short Prognostic Value of Terminal Ileal Inflammation in Patients with Ulcerative Colitis
title_sort prognostic value of terminal ileal inflammation in patients with ulcerative colitis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593494/
https://www.ncbi.nlm.nih.gov/pubmed/33767032
http://dx.doi.org/10.5009/gnl20294
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