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Development of liver surface nodularity quantification program and its clinical application in nonalcoholic fatty liver disease

The liver morphological changes in relation to fibrosis stage in nonalcoholic fatty liver disease (NAFLD) have not yet been clearly understood. This study was to develop a liver surface nodularity (LSN) quantification program and to compare the fibrosis grades in simple steatosis (SS) and nonalcohol...

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Autores principales: Kim, Tae-Hoon, Kim, Ji Eon, Ryu, Jong-Hyun, Jeong, Chang-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620281/
https://www.ncbi.nlm.nih.gov/pubmed/31292497
http://dx.doi.org/10.1038/s41598-019-46442-y
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author Kim, Tae-Hoon
Kim, Ji Eon
Ryu, Jong-Hyun
Jeong, Chang-Won
author_facet Kim, Tae-Hoon
Kim, Ji Eon
Ryu, Jong-Hyun
Jeong, Chang-Won
author_sort Kim, Tae-Hoon
collection PubMed
description The liver morphological changes in relation to fibrosis stage in nonalcoholic fatty liver disease (NAFLD) have not yet been clearly understood. This study was to develop a liver surface nodularity (LSN) quantification program and to compare the fibrosis grades in simple steatosis (SS) and nonalcoholic steatohepatitis (NASH). Thirty subjects (7 normal controls [NC], 12 SS and 11 NASH) were studied. LSN quantification procedure was bias correction, boundary detection, segmentation and LSN measurement. LSN scores among three groups and fibrosis grades compared using Kruskal–Wallis H test. Diagnostic accuracy was determined by calculating the area under the receiver operating characteristics (ROC) curve. Mean LSN scores were NC 1.30 ± 0.09, SS 1.54 ± 0.21 and NASH 1.59 ± 0.23 (p = 0.008). Mean LSN scores according to fibrosis grade (F) were F0 1.30 ± 0.09, F1 1.45 ± 0.17 and F2&F3 1.67 ± 0.20 (p = 0.001). The mean LSN score in F2&F3 is significantly higher than that in F1 (p = 0.019). The AUROC curve to distinguish F1 and F2&F3 was 0.788 (95% CI 0.595–0.981, p = 0.019) at a cut-off LSN score greater than 1.48, and its diagnostic accuracy had 0.833 sensitivity and 0.727 specificity. This study developed LSN program and its clinical application demonstrated that the quantitative LSN scores can help to differentially diagnose fibrosis stage in NAFLD.
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spelling pubmed-66202812019-07-18 Development of liver surface nodularity quantification program and its clinical application in nonalcoholic fatty liver disease Kim, Tae-Hoon Kim, Ji Eon Ryu, Jong-Hyun Jeong, Chang-Won Sci Rep Article The liver morphological changes in relation to fibrosis stage in nonalcoholic fatty liver disease (NAFLD) have not yet been clearly understood. This study was to develop a liver surface nodularity (LSN) quantification program and to compare the fibrosis grades in simple steatosis (SS) and nonalcoholic steatohepatitis (NASH). Thirty subjects (7 normal controls [NC], 12 SS and 11 NASH) were studied. LSN quantification procedure was bias correction, boundary detection, segmentation and LSN measurement. LSN scores among three groups and fibrosis grades compared using Kruskal–Wallis H test. Diagnostic accuracy was determined by calculating the area under the receiver operating characteristics (ROC) curve. Mean LSN scores were NC 1.30 ± 0.09, SS 1.54 ± 0.21 and NASH 1.59 ± 0.23 (p = 0.008). Mean LSN scores according to fibrosis grade (F) were F0 1.30 ± 0.09, F1 1.45 ± 0.17 and F2&F3 1.67 ± 0.20 (p = 0.001). The mean LSN score in F2&F3 is significantly higher than that in F1 (p = 0.019). The AUROC curve to distinguish F1 and F2&F3 was 0.788 (95% CI 0.595–0.981, p = 0.019) at a cut-off LSN score greater than 1.48, and its diagnostic accuracy had 0.833 sensitivity and 0.727 specificity. This study developed LSN program and its clinical application demonstrated that the quantitative LSN scores can help to differentially diagnose fibrosis stage in NAFLD. Nature Publishing Group UK 2019-07-10 /pmc/articles/PMC6620281/ /pubmed/31292497 http://dx.doi.org/10.1038/s41598-019-46442-y Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Tae-Hoon
Kim, Ji Eon
Ryu, Jong-Hyun
Jeong, Chang-Won
Development of liver surface nodularity quantification program and its clinical application in nonalcoholic fatty liver disease
title Development of liver surface nodularity quantification program and its clinical application in nonalcoholic fatty liver disease
title_full Development of liver surface nodularity quantification program and its clinical application in nonalcoholic fatty liver disease
title_fullStr Development of liver surface nodularity quantification program and its clinical application in nonalcoholic fatty liver disease
title_full_unstemmed Development of liver surface nodularity quantification program and its clinical application in nonalcoholic fatty liver disease
title_short Development of liver surface nodularity quantification program and its clinical application in nonalcoholic fatty liver disease
title_sort development of liver surface nodularity quantification program and its clinical application in nonalcoholic fatty liver disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620281/
https://www.ncbi.nlm.nih.gov/pubmed/31292497
http://dx.doi.org/10.1038/s41598-019-46442-y
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