Liver biopsy in the quantitative assessment of liver fibrosis in nonalcoholic fatty liver disease

Nonalcoholic fatty liver disease/nonalcoholic steatohepatitis (NAFLD/NASH) is a major cause of liver fibrosis/cirrhosis and liver-related mortality. Despite emergence of noninvasive tests, liver biopsy remains the mainstay for the diagnosis and assessment of disease severity and chronicity. Accurate...

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Autores principales: Gwyneth Shook Ting Soon, Aileen Wee
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Publicado: Wolters Kluwer Medknow Publications 2021
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spelling oai:doaj.org-article:86e35ff04b0b4afda29654ecb13f3e752021-12-02T17:28:22ZLiver biopsy in the quantitative assessment of liver fibrosis in nonalcoholic fatty liver disease0377-492910.4103/IJPM.IJPM_947_20https://doaj.org/article/86e35ff04b0b4afda29654ecb13f3e752021-01-01T00:00:00Zhttp://www.ijpmonline.org/article.asp?issn=0377-4929;year=2021;volume=64;issue=5;spage=104;epage=111;aulast=Tinghttps://doaj.org/toc/0377-4929Nonalcoholic fatty liver disease/nonalcoholic steatohepatitis (NAFLD/NASH) is a major cause of liver fibrosis/cirrhosis and liver-related mortality. Despite emergence of noninvasive tests, liver biopsy remains the mainstay for the diagnosis and assessment of disease severity and chronicity. Accurate detection and quantification of liver fibrosis with architectural localization are essential for assessing the severity of NAFLD and its response to antifibrotic therapy in clinical trials. Conventional histological scoring systems for liver fibrosis are semiquantitative. Collagen proportionate area is morphometric by measuring the percentage of fibrosis on a continuous scale but is limited by the absence of architectural input. Ultra-fast laser microscopy, e.g., second harmonic generation (SHG) imaging, has enabled in-depth analysis of fibrillary collagen based on intrinsic optical signals. Quantification and calculation of different detailed variables of collagen fibers can be used to establish algorithm-based quantitative fibrosis scores (e.g. qFibrosis, q-FPs) in NAFLD. Artificial intelligence is being explored to further develop quantitative fibrosis scoring methods. SHG microscopy should be considered the new gold standard for the quantitative assessment of liver fibrosis, reaffirming the pivotal role of the liver biopsy in NAFLD, at least for the near-future. The ability of SHG-derived algorithms to intuitively detect subtle nuances in liver fibrosis changes over a continuous scale should be employed to redress the efficacy endpoint for fibrosis in NASH clinical trials. The current decrease by 1-point or more in fibrosis stage may not be realistic for the evaluation of therapeutic response to antifibrotic drugs in relatively short-term trials.Gwyneth Shook Ting SoonAileen WeeWolters Kluwer Medknow Publicationsarticleliver biopsyliver fibrosisnonalcoholic fatty liver diseasequantificationPathologyRB1-214MicrobiologyQR1-502ENIndian Journal of Pathology and Microbiology, Vol 64, Iss 5, Pp 104-111 (2021)
institution DOAJ
collection DOAJ
language EN
topic liver biopsy
liver fibrosis
nonalcoholic fatty liver disease
quantification
Pathology
RB1-214
Microbiology
QR1-502
spellingShingle liver biopsy
liver fibrosis
nonalcoholic fatty liver disease
quantification
Pathology
RB1-214
Microbiology
QR1-502
Gwyneth Shook Ting Soon
Aileen Wee
Liver biopsy in the quantitative assessment of liver fibrosis in nonalcoholic fatty liver disease
description Nonalcoholic fatty liver disease/nonalcoholic steatohepatitis (NAFLD/NASH) is a major cause of liver fibrosis/cirrhosis and liver-related mortality. Despite emergence of noninvasive tests, liver biopsy remains the mainstay for the diagnosis and assessment of disease severity and chronicity. Accurate detection and quantification of liver fibrosis with architectural localization are essential for assessing the severity of NAFLD and its response to antifibrotic therapy in clinical trials. Conventional histological scoring systems for liver fibrosis are semiquantitative. Collagen proportionate area is morphometric by measuring the percentage of fibrosis on a continuous scale but is limited by the absence of architectural input. Ultra-fast laser microscopy, e.g., second harmonic generation (SHG) imaging, has enabled in-depth analysis of fibrillary collagen based on intrinsic optical signals. Quantification and calculation of different detailed variables of collagen fibers can be used to establish algorithm-based quantitative fibrosis scores (e.g. qFibrosis, q-FPs) in NAFLD. Artificial intelligence is being explored to further develop quantitative fibrosis scoring methods. SHG microscopy should be considered the new gold standard for the quantitative assessment of liver fibrosis, reaffirming the pivotal role of the liver biopsy in NAFLD, at least for the near-future. The ability of SHG-derived algorithms to intuitively detect subtle nuances in liver fibrosis changes over a continuous scale should be employed to redress the efficacy endpoint for fibrosis in NASH clinical trials. The current decrease by 1-point or more in fibrosis stage may not be realistic for the evaluation of therapeutic response to antifibrotic drugs in relatively short-term trials.
format article
author Gwyneth Shook Ting Soon
Aileen Wee
author_facet Gwyneth Shook Ting Soon
Aileen Wee
author_sort Gwyneth Shook Ting Soon
title Liver biopsy in the quantitative assessment of liver fibrosis in nonalcoholic fatty liver disease
title_short Liver biopsy in the quantitative assessment of liver fibrosis in nonalcoholic fatty liver disease
title_full Liver biopsy in the quantitative assessment of liver fibrosis in nonalcoholic fatty liver disease
title_fullStr Liver biopsy in the quantitative assessment of liver fibrosis in nonalcoholic fatty liver disease
title_full_unstemmed Liver biopsy in the quantitative assessment of liver fibrosis in nonalcoholic fatty liver disease
title_sort liver biopsy in the quantitative assessment of liver fibrosis in nonalcoholic fatty liver disease
publisher Wolters Kluwer Medknow Publications
publishDate 2021
url https://doaj.org/article/86e35ff04b0b4afda29654ecb13f3e75
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