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Continuous Grading of Early Fibrosis in NAFLD Using Label-Free Imaging: A Proof-of-Concept Study

BACKGROUND AND AIMS: Early detection of fibrosis is important in identifying individuals at risk for advanced liver disease in non-alcoholic fatty liver disease (NAFLD). We tested whether second-harmonic generation (SHG) and coherent anti-Stokes Raman scattering (CARS) microscopy, detecting fibrilla...

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Autores principales: Pirhonen, Juho, Arola, Johanna, Sädevirta, Sanja, Luukkonen, Panu, Karppinen, Sanna-Maria, Pihlajaniemi, Taina, Isomäki, Antti, Hukkanen, Mika, Yki-Järvinen, Hannele, Ikonen, Elina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726624/
https://www.ncbi.nlm.nih.gov/pubmed/26808140
http://dx.doi.org/10.1371/journal.pone.0147804
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author Pirhonen, Juho
Arola, Johanna
Sädevirta, Sanja
Luukkonen, Panu
Karppinen, Sanna-Maria
Pihlajaniemi, Taina
Isomäki, Antti
Hukkanen, Mika
Yki-Järvinen, Hannele
Ikonen, Elina
author_facet Pirhonen, Juho
Arola, Johanna
Sädevirta, Sanja
Luukkonen, Panu
Karppinen, Sanna-Maria
Pihlajaniemi, Taina
Isomäki, Antti
Hukkanen, Mika
Yki-Järvinen, Hannele
Ikonen, Elina
author_sort Pirhonen, Juho
collection PubMed
description BACKGROUND AND AIMS: Early detection of fibrosis is important in identifying individuals at risk for advanced liver disease in non-alcoholic fatty liver disease (NAFLD). We tested whether second-harmonic generation (SHG) and coherent anti-Stokes Raman scattering (CARS) microscopy, detecting fibrillar collagen and fat in a label-free manner, might allow automated and sensitive quantification of early fibrosis in NAFLD. METHODS: We analyzed 32 surgical biopsies from patients covering histological fibrosis stages 0–4, using multimodal label-free microscopy. Native samples were visualized by SHG and CARS imaging for detecting fibrillar collagen and fat. Furthermore, we developed a method for quantitative assessment of early fibrosis using automated analysis of SHG signals. RESULTS: We found that the SHG mean signal intensity correlated well with fibrosis stage and the mean CARS signal intensity with liver fat. Little overlap in SHG signal intensities between fibrosis stages 0 and 1 was observed. A specific fibrillar SHG signal was detected in the liver parenchyma outside portal areas in all samples histologically classified as having no fibrosis. This signal correlated with immunohistochemical location of fibrillar collagens I and III. CONCLUSIONS: This study demonstrates that label-free SHG imaging detects fibrillar collagen deposition in NAFLD more sensitively than routine histological staging and enables observer-independent quantification of early fibrosis in NAFLD with continuous grading.
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spelling pubmed-47266242016-02-03 Continuous Grading of Early Fibrosis in NAFLD Using Label-Free Imaging: A Proof-of-Concept Study Pirhonen, Juho Arola, Johanna Sädevirta, Sanja Luukkonen, Panu Karppinen, Sanna-Maria Pihlajaniemi, Taina Isomäki, Antti Hukkanen, Mika Yki-Järvinen, Hannele Ikonen, Elina PLoS One Research Article BACKGROUND AND AIMS: Early detection of fibrosis is important in identifying individuals at risk for advanced liver disease in non-alcoholic fatty liver disease (NAFLD). We tested whether second-harmonic generation (SHG) and coherent anti-Stokes Raman scattering (CARS) microscopy, detecting fibrillar collagen and fat in a label-free manner, might allow automated and sensitive quantification of early fibrosis in NAFLD. METHODS: We analyzed 32 surgical biopsies from patients covering histological fibrosis stages 0–4, using multimodal label-free microscopy. Native samples were visualized by SHG and CARS imaging for detecting fibrillar collagen and fat. Furthermore, we developed a method for quantitative assessment of early fibrosis using automated analysis of SHG signals. RESULTS: We found that the SHG mean signal intensity correlated well with fibrosis stage and the mean CARS signal intensity with liver fat. Little overlap in SHG signal intensities between fibrosis stages 0 and 1 was observed. A specific fibrillar SHG signal was detected in the liver parenchyma outside portal areas in all samples histologically classified as having no fibrosis. This signal correlated with immunohistochemical location of fibrillar collagens I and III. CONCLUSIONS: This study demonstrates that label-free SHG imaging detects fibrillar collagen deposition in NAFLD more sensitively than routine histological staging and enables observer-independent quantification of early fibrosis in NAFLD with continuous grading. Public Library of Science 2016-01-25 /pmc/articles/PMC4726624/ /pubmed/26808140 http://dx.doi.org/10.1371/journal.pone.0147804 Text en © 2016 Pirhonen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Pirhonen, Juho
Arola, Johanna
Sädevirta, Sanja
Luukkonen, Panu
Karppinen, Sanna-Maria
Pihlajaniemi, Taina
Isomäki, Antti
Hukkanen, Mika
Yki-Järvinen, Hannele
Ikonen, Elina
Continuous Grading of Early Fibrosis in NAFLD Using Label-Free Imaging: A Proof-of-Concept Study
title Continuous Grading of Early Fibrosis in NAFLD Using Label-Free Imaging: A Proof-of-Concept Study
title_full Continuous Grading of Early Fibrosis in NAFLD Using Label-Free Imaging: A Proof-of-Concept Study
title_fullStr Continuous Grading of Early Fibrosis in NAFLD Using Label-Free Imaging: A Proof-of-Concept Study
title_full_unstemmed Continuous Grading of Early Fibrosis in NAFLD Using Label-Free Imaging: A Proof-of-Concept Study
title_short Continuous Grading of Early Fibrosis in NAFLD Using Label-Free Imaging: A Proof-of-Concept Study
title_sort continuous grading of early fibrosis in nafld using label-free imaging: a proof-of-concept study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726624/
https://www.ncbi.nlm.nih.gov/pubmed/26808140
http://dx.doi.org/10.1371/journal.pone.0147804
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