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Quantitative Edge Analysis of Pancreatic Margins in Patients with Chronic Pancreatitis: A Correlation with Exocrine Function

Background: Many efforts have been made to improve accuracy and sensitivity in diagnosing chronic pancreatitis (CP), obtaining quantitative assessments related to functional data. Our purpose was to correlate a computer-assisted analysis of pancreatic morphology, focusing on glandular margins, with...

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Autores principales: Ambrosetti, Maria Chiara, Grecchi, Annamaria, Ambrosetti, Alberto, Amodio, Antonio, Mansueto, Giancarlo, Montemezzi, Stefania, Zamboni, Giulia A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341214/
https://www.ncbi.nlm.nih.gov/pubmed/37443666
http://dx.doi.org/10.3390/diagnostics13132272
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author Ambrosetti, Maria Chiara
Grecchi, Annamaria
Ambrosetti, Alberto
Amodio, Antonio
Mansueto, Giancarlo
Montemezzi, Stefania
Zamboni, Giulia A.
author_facet Ambrosetti, Maria Chiara
Grecchi, Annamaria
Ambrosetti, Alberto
Amodio, Antonio
Mansueto, Giancarlo
Montemezzi, Stefania
Zamboni, Giulia A.
author_sort Ambrosetti, Maria Chiara
collection PubMed
description Background: Many efforts have been made to improve accuracy and sensitivity in diagnosing chronic pancreatitis (CP), obtaining quantitative assessments related to functional data. Our purpose was to correlate a computer-assisted analysis of pancreatic morphology, focusing on glandular margins, with exocrine function—measured by fecal elastase values—in chronic pancreatitis patients. Methods: We retrospectively reviewed chronic pancreatitis patients who underwent fecal elastase assessment and abdominal MRI in our institute within 1 year. We identified 123 patients divided into three groups based on the fecal elastase value: group A with fecal elastase > 200 μg/g; group B with fecal elastase between 100 and 200 μg/g; and group C with fecal elastase < 100 μg/g. Computer-assisted quantitative edge analysis of pancreatic margins was made on non-contrast-enhanced water-only Dixon T1-weighted images, obtaining the pancreatic margin score (PMS). PMS values were compared across groups using a Kruskal–Wallis test and the correlation between PMS and fecal elastase values was tested with the Spearman’s test. Results: A significant difference in PMS was observed between the three groups (p < 0.0001), with a significant correlation between PMS and elastase values (r = 0.6080). Conclusions: Quantitative edge analysis may stratify chronic pancreatitis patients according to the degree of exocrine insufficiency, potentially contributing to the morphological and functional staging of this pathology.
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spelling pubmed-103412142023-07-14 Quantitative Edge Analysis of Pancreatic Margins in Patients with Chronic Pancreatitis: A Correlation with Exocrine Function Ambrosetti, Maria Chiara Grecchi, Annamaria Ambrosetti, Alberto Amodio, Antonio Mansueto, Giancarlo Montemezzi, Stefania Zamboni, Giulia A. Diagnostics (Basel) Article Background: Many efforts have been made to improve accuracy and sensitivity in diagnosing chronic pancreatitis (CP), obtaining quantitative assessments related to functional data. Our purpose was to correlate a computer-assisted analysis of pancreatic morphology, focusing on glandular margins, with exocrine function—measured by fecal elastase values—in chronic pancreatitis patients. Methods: We retrospectively reviewed chronic pancreatitis patients who underwent fecal elastase assessment and abdominal MRI in our institute within 1 year. We identified 123 patients divided into three groups based on the fecal elastase value: group A with fecal elastase > 200 μg/g; group B with fecal elastase between 100 and 200 μg/g; and group C with fecal elastase < 100 μg/g. Computer-assisted quantitative edge analysis of pancreatic margins was made on non-contrast-enhanced water-only Dixon T1-weighted images, obtaining the pancreatic margin score (PMS). PMS values were compared across groups using a Kruskal–Wallis test and the correlation between PMS and fecal elastase values was tested with the Spearman’s test. Results: A significant difference in PMS was observed between the three groups (p < 0.0001), with a significant correlation between PMS and elastase values (r = 0.6080). Conclusions: Quantitative edge analysis may stratify chronic pancreatitis patients according to the degree of exocrine insufficiency, potentially contributing to the morphological and functional staging of this pathology. MDPI 2023-07-05 /pmc/articles/PMC10341214/ /pubmed/37443666 http://dx.doi.org/10.3390/diagnostics13132272 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ambrosetti, Maria Chiara
Grecchi, Annamaria
Ambrosetti, Alberto
Amodio, Antonio
Mansueto, Giancarlo
Montemezzi, Stefania
Zamboni, Giulia A.
Quantitative Edge Analysis of Pancreatic Margins in Patients with Chronic Pancreatitis: A Correlation with Exocrine Function
title Quantitative Edge Analysis of Pancreatic Margins in Patients with Chronic Pancreatitis: A Correlation with Exocrine Function
title_full Quantitative Edge Analysis of Pancreatic Margins in Patients with Chronic Pancreatitis: A Correlation with Exocrine Function
title_fullStr Quantitative Edge Analysis of Pancreatic Margins in Patients with Chronic Pancreatitis: A Correlation with Exocrine Function
title_full_unstemmed Quantitative Edge Analysis of Pancreatic Margins in Patients with Chronic Pancreatitis: A Correlation with Exocrine Function
title_short Quantitative Edge Analysis of Pancreatic Margins in Patients with Chronic Pancreatitis: A Correlation with Exocrine Function
title_sort quantitative edge analysis of pancreatic margins in patients with chronic pancreatitis: a correlation with exocrine function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341214/
https://www.ncbi.nlm.nih.gov/pubmed/37443666
http://dx.doi.org/10.3390/diagnostics13132272
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