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Correlation between Histological Activity and Endoscopic, Clinical, and Serologic Activities in Patients with Ulcerative Colitis

Objectives. Recent studies suggest that histological healing is a treatment goal in ulcerative colitis (UC). We aimed to evaluate the correlation between histological activity and clinical, endoscopic, and serologic activities in patients with UC. Methods. We retrospectively reviewed medical records...

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Autores principales: Kim, Dae Bum, Lee, Kang-Moon, Lee, Ji Min, Chung, Yoon Yung, Sung, Hea Jung, Paik, Chang Nyol, Chung, Woo Chul, Jung, Ji-Han, Choi, Hyun Joo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709652/
https://www.ncbi.nlm.nih.gov/pubmed/26839541
http://dx.doi.org/10.1155/2016/5832051
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author Kim, Dae Bum
Lee, Kang-Moon
Lee, Ji Min
Chung, Yoon Yung
Sung, Hea Jung
Paik, Chang Nyol
Chung, Woo Chul
Jung, Ji-Han
Choi, Hyun Joo
author_facet Kim, Dae Bum
Lee, Kang-Moon
Lee, Ji Min
Chung, Yoon Yung
Sung, Hea Jung
Paik, Chang Nyol
Chung, Woo Chul
Jung, Ji-Han
Choi, Hyun Joo
author_sort Kim, Dae Bum
collection PubMed
description Objectives. Recent studies suggest that histological healing is a treatment goal in ulcerative colitis (UC). We aimed to evaluate the correlation between histological activity and clinical, endoscopic, and serologic activities in patients with UC. Methods. We retrospectively reviewed medical records from patients with UC who underwent colonoscopy or sigmoidoscopy with biopsies. The Mayo endoscopic subscore was used to assess endoscopic activity. Biopsy specimens were reviewed by two blinded pathologists and scored using the Geboes scoring system. Results. We analyzed 154 biopsy specimens from 82 patients with UC. Histological scores exhibited strong correlation with endoscopic subscores (Spearman's rank correlation coefficient r = 0.774, p < 0.001) and moderate correlation with C-reactive protein levels (r = 0.422, p < 0.001) and partial Mayo scores (r = 0.403, p < 0.001). Active histological inflammation (Geboes score ≥ 3.1) was observed in 6% (2 of 33) of the endoscopically normal mucosa samples, 66% (19 of 29) of mild disease samples, and 98% (90 of 92) of moderate-to-severe disease samples. Conclusions. Histological activity was closely correlated with the endoscopic, clinical, and serologic UC activities. However, several patients with mild or normal endoscopic findings exhibited histological evidence of inflammation. Therefore, histological assessment may be helpful in evaluating treatment outcomes and determining follow-up strategies.
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spelling pubmed-47096522016-02-02 Correlation between Histological Activity and Endoscopic, Clinical, and Serologic Activities in Patients with Ulcerative Colitis Kim, Dae Bum Lee, Kang-Moon Lee, Ji Min Chung, Yoon Yung Sung, Hea Jung Paik, Chang Nyol Chung, Woo Chul Jung, Ji-Han Choi, Hyun Joo Gastroenterol Res Pract Research Article Objectives. Recent studies suggest that histological healing is a treatment goal in ulcerative colitis (UC). We aimed to evaluate the correlation between histological activity and clinical, endoscopic, and serologic activities in patients with UC. Methods. We retrospectively reviewed medical records from patients with UC who underwent colonoscopy or sigmoidoscopy with biopsies. The Mayo endoscopic subscore was used to assess endoscopic activity. Biopsy specimens were reviewed by two blinded pathologists and scored using the Geboes scoring system. Results. We analyzed 154 biopsy specimens from 82 patients with UC. Histological scores exhibited strong correlation with endoscopic subscores (Spearman's rank correlation coefficient r = 0.774, p < 0.001) and moderate correlation with C-reactive protein levels (r = 0.422, p < 0.001) and partial Mayo scores (r = 0.403, p < 0.001). Active histological inflammation (Geboes score ≥ 3.1) was observed in 6% (2 of 33) of the endoscopically normal mucosa samples, 66% (19 of 29) of mild disease samples, and 98% (90 of 92) of moderate-to-severe disease samples. Conclusions. Histological activity was closely correlated with the endoscopic, clinical, and serologic UC activities. However, several patients with mild or normal endoscopic findings exhibited histological evidence of inflammation. Therefore, histological assessment may be helpful in evaluating treatment outcomes and determining follow-up strategies. Hindawi Publishing Corporation 2016 2015-12-29 /pmc/articles/PMC4709652/ /pubmed/26839541 http://dx.doi.org/10.1155/2016/5832051 Text en Copyright © 2016 Dae Bum Kim et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kim, Dae Bum
Lee, Kang-Moon
Lee, Ji Min
Chung, Yoon Yung
Sung, Hea Jung
Paik, Chang Nyol
Chung, Woo Chul
Jung, Ji-Han
Choi, Hyun Joo
Correlation between Histological Activity and Endoscopic, Clinical, and Serologic Activities in Patients with Ulcerative Colitis
title Correlation between Histological Activity and Endoscopic, Clinical, and Serologic Activities in Patients with Ulcerative Colitis
title_full Correlation between Histological Activity and Endoscopic, Clinical, and Serologic Activities in Patients with Ulcerative Colitis
title_fullStr Correlation between Histological Activity and Endoscopic, Clinical, and Serologic Activities in Patients with Ulcerative Colitis
title_full_unstemmed Correlation between Histological Activity and Endoscopic, Clinical, and Serologic Activities in Patients with Ulcerative Colitis
title_short Correlation between Histological Activity and Endoscopic, Clinical, and Serologic Activities in Patients with Ulcerative Colitis
title_sort correlation between histological activity and endoscopic, clinical, and serologic activities in patients with ulcerative colitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709652/
https://www.ncbi.nlm.nih.gov/pubmed/26839541
http://dx.doi.org/10.1155/2016/5832051
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