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Rapid quantification of myocardial fibrosis: a new macro-based automated analysis
BACKGROUND: Fibrosis is associated with various cardiac pathologies and dysfunction. Current quantification methods are time-consuming and laborious. We describe a semi-automated quantification technique for myocardial fibrosis and validated this using traditional methods. METHODS: Pulmonary Hyperte...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162624/ https://www.ncbi.nlm.nih.gov/pubmed/21538025 http://dx.doi.org/10.1007/s13402-011-0035-7 |
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author | Hadi, Awal M. Mouchaers, Koen T. B. Schalij, Ingrid Grunberg, Katrien Meijer, Gerrit A. Vonk-Noordegraaf, Anton van der Laarse, Willem J. Beliën, Jeroen A. M. |
author_facet | Hadi, Awal M. Mouchaers, Koen T. B. Schalij, Ingrid Grunberg, Katrien Meijer, Gerrit A. Vonk-Noordegraaf, Anton van der Laarse, Willem J. Beliën, Jeroen A. M. |
author_sort | Hadi, Awal M. |
collection | PubMed |
description | BACKGROUND: Fibrosis is associated with various cardiac pathologies and dysfunction. Current quantification methods are time-consuming and laborious. We describe a semi-automated quantification technique for myocardial fibrosis and validated this using traditional methods. METHODS: Pulmonary Hypertension (PH) was induced in adult Wistar rats by subcutaneous monocrotaline (MCT) injection(40 mg/kg). Cryosections of myocardial tissue (5 μm) of PH rats (n = 9) and controls (n = 9) were stained using Picrosirius red and scanned with a digital microscopic MIRAX slide scanner. From these sections 21 images were taken randomly of each heart. Using ImageJ software a macro for automated image analysis of the amount of fibrosis was developed. For comparison, fibrosis was quantified using traditional polarisation microscopy. Both methods were correlated and validated against stereology as the gold standard. Furthermore, the method was tested in paraffin-embedded human tissues. RESULTS: Automated analysis showed a significant increase of fibrosis in PH hearts vs. control. Automated analysis correlated with traditional polarisation and stereology analysis (r(2) = 0.92 and r(2) = 0.95 respectively). In human heart, lungs, kidney, and liver, a similar correlation with stereology (r(2) = 0.91) was observed. Time required for automated analysis was 22% and 33% of the time needed for stereology and polarisation analysis respectively. CONCLUSION: Automated quantification of fibrosis is feasible, objective, and time-efficient. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13402-011-0035-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3162624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-31626242011-09-26 Rapid quantification of myocardial fibrosis: a new macro-based automated analysis Hadi, Awal M. Mouchaers, Koen T. B. Schalij, Ingrid Grunberg, Katrien Meijer, Gerrit A. Vonk-Noordegraaf, Anton van der Laarse, Willem J. Beliën, Jeroen A. M. Cell Oncol (Dordr) Original Paper BACKGROUND: Fibrosis is associated with various cardiac pathologies and dysfunction. Current quantification methods are time-consuming and laborious. We describe a semi-automated quantification technique for myocardial fibrosis and validated this using traditional methods. METHODS: Pulmonary Hypertension (PH) was induced in adult Wistar rats by subcutaneous monocrotaline (MCT) injection(40 mg/kg). Cryosections of myocardial tissue (5 μm) of PH rats (n = 9) and controls (n = 9) were stained using Picrosirius red and scanned with a digital microscopic MIRAX slide scanner. From these sections 21 images were taken randomly of each heart. Using ImageJ software a macro for automated image analysis of the amount of fibrosis was developed. For comparison, fibrosis was quantified using traditional polarisation microscopy. Both methods were correlated and validated against stereology as the gold standard. Furthermore, the method was tested in paraffin-embedded human tissues. RESULTS: Automated analysis showed a significant increase of fibrosis in PH hearts vs. control. Automated analysis correlated with traditional polarisation and stereology analysis (r(2) = 0.92 and r(2) = 0.95 respectively). In human heart, lungs, kidney, and liver, a similar correlation with stereology (r(2) = 0.91) was observed. Time required for automated analysis was 22% and 33% of the time needed for stereology and polarisation analysis respectively. CONCLUSION: Automated quantification of fibrosis is feasible, objective, and time-efficient. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13402-011-0035-7) contains supplementary material, which is available to authorized users. Springer Netherlands 2011-05-03 2011-08 /pmc/articles/PMC3162624/ /pubmed/21538025 http://dx.doi.org/10.1007/s13402-011-0035-7 Text en © The Author(s) 2011 |
spellingShingle | Original Paper Hadi, Awal M. Mouchaers, Koen T. B. Schalij, Ingrid Grunberg, Katrien Meijer, Gerrit A. Vonk-Noordegraaf, Anton van der Laarse, Willem J. Beliën, Jeroen A. M. Rapid quantification of myocardial fibrosis: a new macro-based automated analysis |
title | Rapid quantification of myocardial fibrosis: a new macro-based
automated analysis |
title_full | Rapid quantification of myocardial fibrosis: a new macro-based
automated analysis |
title_fullStr | Rapid quantification of myocardial fibrosis: a new macro-based
automated analysis |
title_full_unstemmed | Rapid quantification of myocardial fibrosis: a new macro-based
automated analysis |
title_short | Rapid quantification of myocardial fibrosis: a new macro-based
automated analysis |
title_sort | rapid quantification of myocardial fibrosis: a new macro-based
automated analysis |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162624/ https://www.ncbi.nlm.nih.gov/pubmed/21538025 http://dx.doi.org/10.1007/s13402-011-0035-7 |
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