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Inflammation and fibrosis in Crohn’s disease: location-matched histological correlation of small bowel ultrasound features

PURPOSE: To evaluate the utility of mural and extramural sonographic features of Crohn’s Disease as potential imaging biomarkers of inflammation and fibrosis against whole-mount histological sections. METHODS: Twelve Crohn’s disease patients (Mean age 35(25–69), 7 males) underwent small bowel ultras...

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Autores principales: Bhatnagar, Gauraang, Rodriguez-Justo, Manuel, Higginson, Antony, Bassett, Paul, Windsor, Alastair, Cohen, Richard, Halligan, Steve, Taylor, Stuart A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864849/
https://www.ncbi.nlm.nih.gov/pubmed/32564208
http://dx.doi.org/10.1007/s00261-020-02603-6
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author Bhatnagar, Gauraang
Rodriguez-Justo, Manuel
Higginson, Antony
Bassett, Paul
Windsor, Alastair
Cohen, Richard
Halligan, Steve
Taylor, Stuart A.
author_facet Bhatnagar, Gauraang
Rodriguez-Justo, Manuel
Higginson, Antony
Bassett, Paul
Windsor, Alastair
Cohen, Richard
Halligan, Steve
Taylor, Stuart A.
author_sort Bhatnagar, Gauraang
collection PubMed
description PURPOSE: To evaluate the utility of mural and extramural sonographic features of Crohn’s Disease as potential imaging biomarkers of inflammation and fibrosis against whole-mount histological sections. METHODS: Twelve Crohn’s disease patients (Mean age 35(25–69), 7 males) underwent small bowel ultrasound prior to small bowel resection. Two radiologists in consensus graded multiple parameters including mural, mucosal and submucosal thickness, submucosal/mesenteric echogenicity and clarity and mural Doppler signal in 50 selected bowel cross-sections. Matching with histological sampling sites was facilitated via scanning of the resected specimen. A histopathologist scored acute and chronic inflammation, and fibrosis (using histological scoring systems) following analysis of whole mount block sections. The association between sonographic observations and histopathological scores was examined via univariable and multivariable analysis. RESULTS: In univariate analyses, bowel wall thickness (regression co-efficient and 95% CI 0.8 (0.3, 1.3) p = 0.001), mesenteric fat echogenicity (8.7(3.0, 14.5) p = 0.005), submucosal layer thickness (7.4(1.2, 13.5) p = 0.02), submucosal layer clarity (4.4(0.6, 8.2) p = 0.02) and mucosal layer thickness (4.6(1.8, 7.4) p = 0.001) were all significantly associated with acute inflammation. Mesenteric fat echogenicity (674(8.67, 52404) p = 0.009), submucosal layer thickness (79.9(2.16, 2951) p = 0.02) and mucosal layer thickness (13.6(1.54, 121) p = 0.02) were significantly associated with chronic inflammation. Submucosal layer echogenicity (p = 0.03), clarity (25.0(1.76, 356) p = 0.02) and mucosal layer thickness (53.8(3.19, 908) p = 0.006) were significantly associated with fibrosis. In multivariate analyses, wall and mucosal thickness remained significantly associated with acute inflammation (p = 0.02), mesenteric fat echogenicity with chronic inflammation (p = 0.009) and mucosal thickness (p = 0.006) with fibrosis. CONCLUSION: Multiple sonographic parameters are associated with histological phenotypes in Crohn’s disease although there is overlap between ultrasonic stigmata of acute inflammation, chronic inflammation and fibrosis. GRAPHIC ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00261-020-02603-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-78648492021-02-16 Inflammation and fibrosis in Crohn’s disease: location-matched histological correlation of small bowel ultrasound features Bhatnagar, Gauraang Rodriguez-Justo, Manuel Higginson, Antony Bassett, Paul Windsor, Alastair Cohen, Richard Halligan, Steve Taylor, Stuart A. Abdom Radiol (NY) Hollow Organ GI PURPOSE: To evaluate the utility of mural and extramural sonographic features of Crohn’s Disease as potential imaging biomarkers of inflammation and fibrosis against whole-mount histological sections. METHODS: Twelve Crohn’s disease patients (Mean age 35(25–69), 7 males) underwent small bowel ultrasound prior to small bowel resection. Two radiologists in consensus graded multiple parameters including mural, mucosal and submucosal thickness, submucosal/mesenteric echogenicity and clarity and mural Doppler signal in 50 selected bowel cross-sections. Matching with histological sampling sites was facilitated via scanning of the resected specimen. A histopathologist scored acute and chronic inflammation, and fibrosis (using histological scoring systems) following analysis of whole mount block sections. The association between sonographic observations and histopathological scores was examined via univariable and multivariable analysis. RESULTS: In univariate analyses, bowel wall thickness (regression co-efficient and 95% CI 0.8 (0.3, 1.3) p = 0.001), mesenteric fat echogenicity (8.7(3.0, 14.5) p = 0.005), submucosal layer thickness (7.4(1.2, 13.5) p = 0.02), submucosal layer clarity (4.4(0.6, 8.2) p = 0.02) and mucosal layer thickness (4.6(1.8, 7.4) p = 0.001) were all significantly associated with acute inflammation. Mesenteric fat echogenicity (674(8.67, 52404) p = 0.009), submucosal layer thickness (79.9(2.16, 2951) p = 0.02) and mucosal layer thickness (13.6(1.54, 121) p = 0.02) were significantly associated with chronic inflammation. Submucosal layer echogenicity (p = 0.03), clarity (25.0(1.76, 356) p = 0.02) and mucosal layer thickness (53.8(3.19, 908) p = 0.006) were significantly associated with fibrosis. In multivariate analyses, wall and mucosal thickness remained significantly associated with acute inflammation (p = 0.02), mesenteric fat echogenicity with chronic inflammation (p = 0.009) and mucosal thickness (p = 0.006) with fibrosis. CONCLUSION: Multiple sonographic parameters are associated with histological phenotypes in Crohn’s disease although there is overlap between ultrasonic stigmata of acute inflammation, chronic inflammation and fibrosis. GRAPHIC ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00261-020-02603-6) contains supplementary material, which is available to authorized users. Springer US 2020-06-20 2021 /pmc/articles/PMC7864849/ /pubmed/32564208 http://dx.doi.org/10.1007/s00261-020-02603-6 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Hollow Organ GI
Bhatnagar, Gauraang
Rodriguez-Justo, Manuel
Higginson, Antony
Bassett, Paul
Windsor, Alastair
Cohen, Richard
Halligan, Steve
Taylor, Stuart A.
Inflammation and fibrosis in Crohn’s disease: location-matched histological correlation of small bowel ultrasound features
title Inflammation and fibrosis in Crohn’s disease: location-matched histological correlation of small bowel ultrasound features
title_full Inflammation and fibrosis in Crohn’s disease: location-matched histological correlation of small bowel ultrasound features
title_fullStr Inflammation and fibrosis in Crohn’s disease: location-matched histological correlation of small bowel ultrasound features
title_full_unstemmed Inflammation and fibrosis in Crohn’s disease: location-matched histological correlation of small bowel ultrasound features
title_short Inflammation and fibrosis in Crohn’s disease: location-matched histological correlation of small bowel ultrasound features
title_sort inflammation and fibrosis in crohn’s disease: location-matched histological correlation of small bowel ultrasound features
topic Hollow Organ GI
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864849/
https://www.ncbi.nlm.nih.gov/pubmed/32564208
http://dx.doi.org/10.1007/s00261-020-02603-6
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