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Quantitative collagen assessment in right ventricular myectomies from patients with tetralogy of Fallot

AIMS: Patients with tetralogy of Fallot (TOF) are often affected by right ventricular fibrosis, which has been associated with arrhythmias. This study aimed to assess fibrosis distribution in right ventricular outflow tract (RVOT) myocardium of TOF patients to evaluate the utility of single histolog...

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Autores principales: Wülfers, Eike M, Greiner, Joachim, Giese, Max, Madl, Josef, Kroll, Johannes, Stiller, Brigitte, Kohl, Peter, Rog-Zielinska, Eva A, Fürniss, Hannah E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943371/
https://www.ncbi.nlm.nih.gov/pubmed/33404047
http://dx.doi.org/10.1093/europace/euaa389
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author Wülfers, Eike M
Greiner, Joachim
Giese, Max
Madl, Josef
Kroll, Johannes
Stiller, Brigitte
Kohl, Peter
Rog-Zielinska, Eva A
Fürniss, Hannah E
author_facet Wülfers, Eike M
Greiner, Joachim
Giese, Max
Madl, Josef
Kroll, Johannes
Stiller, Brigitte
Kohl, Peter
Rog-Zielinska, Eva A
Fürniss, Hannah E
author_sort Wülfers, Eike M
collection PubMed
description AIMS: Patients with tetralogy of Fallot (TOF) are often affected by right ventricular fibrosis, which has been associated with arrhythmias. This study aimed to assess fibrosis distribution in right ventricular outflow tract (RVOT) myocardium of TOF patients to evaluate the utility of single histology-section analyses, and to explore the possibility of fibrosis quantification in unlabelled tissue by second harmonic generation imaging (SHGI) as an alternative to conventional histology-based assays. METHODS AND RESULTS: We quantified fibrosis in 11 TOF RVOT samples, using a tailor-made automated image analysis method on Picrosirius red-stained sections. In a subset of samples, histology- and SHGI-based fibrosis quantification approaches were compared. Fibrosis distribution was highly heterogeneous, with significant and comparable variability between and within samples. We found that, on average, 67.8 mm(2) of 10 µm thick, histologically processed tissue per patient had to be analysed for accurate fibrosis quantification. SHGI provided data faster and on live tissue, additionally enabling quantification of collagen anisotropy. CONCLUSION: Given the high intra-individual heterogeneity, fibrosis quantification should not be conducted on single sections of TOF RVOT myectomies. We provide an analysis algorithm for fibrosis quantification in histological images, which enables the required extended volume analyses in these patients.
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spelling pubmed-79433712021-03-15 Quantitative collagen assessment in right ventricular myectomies from patients with tetralogy of Fallot Wülfers, Eike M Greiner, Joachim Giese, Max Madl, Josef Kroll, Johannes Stiller, Brigitte Kohl, Peter Rog-Zielinska, Eva A Fürniss, Hannah E Europace Supplement Papers AIMS: Patients with tetralogy of Fallot (TOF) are often affected by right ventricular fibrosis, which has been associated with arrhythmias. This study aimed to assess fibrosis distribution in right ventricular outflow tract (RVOT) myocardium of TOF patients to evaluate the utility of single histology-section analyses, and to explore the possibility of fibrosis quantification in unlabelled tissue by second harmonic generation imaging (SHGI) as an alternative to conventional histology-based assays. METHODS AND RESULTS: We quantified fibrosis in 11 TOF RVOT samples, using a tailor-made automated image analysis method on Picrosirius red-stained sections. In a subset of samples, histology- and SHGI-based fibrosis quantification approaches were compared. Fibrosis distribution was highly heterogeneous, with significant and comparable variability between and within samples. We found that, on average, 67.8 mm(2) of 10 µm thick, histologically processed tissue per patient had to be analysed for accurate fibrosis quantification. SHGI provided data faster and on live tissue, additionally enabling quantification of collagen anisotropy. CONCLUSION: Given the high intra-individual heterogeneity, fibrosis quantification should not be conducted on single sections of TOF RVOT myectomies. We provide an analysis algorithm for fibrosis quantification in histological images, which enables the required extended volume analyses in these patients. Oxford University Press 2021-01-06 /pmc/articles/PMC7943371/ /pubmed/33404047 http://dx.doi.org/10.1093/europace/euaa389 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Supplement Papers
Wülfers, Eike M
Greiner, Joachim
Giese, Max
Madl, Josef
Kroll, Johannes
Stiller, Brigitte
Kohl, Peter
Rog-Zielinska, Eva A
Fürniss, Hannah E
Quantitative collagen assessment in right ventricular myectomies from patients with tetralogy of Fallot
title Quantitative collagen assessment in right ventricular myectomies from patients with tetralogy of Fallot
title_full Quantitative collagen assessment in right ventricular myectomies from patients with tetralogy of Fallot
title_fullStr Quantitative collagen assessment in right ventricular myectomies from patients with tetralogy of Fallot
title_full_unstemmed Quantitative collagen assessment in right ventricular myectomies from patients with tetralogy of Fallot
title_short Quantitative collagen assessment in right ventricular myectomies from patients with tetralogy of Fallot
title_sort quantitative collagen assessment in right ventricular myectomies from patients with tetralogy of fallot
topic Supplement Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943371/
https://www.ncbi.nlm.nih.gov/pubmed/33404047
http://dx.doi.org/10.1093/europace/euaa389
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