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Murine cardiac fibrosis localization using adaptive Bayesian cardiac strain imaging in vivo

An adaptive Bayesian regularized cardiac strain imaging (ABR-CSI) algorithm for in vivo murine myocardial function assessment is presented. We report on 31 BALB/CJ mice (n = 17 females, n = 14 males), randomly stratified into three surgical groups: myocardial infarction (MI, n = 10), ischemia–reperf...

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Autores principales: Al Mukaddim, Rashid, Weichmann, Ashley M., Taylor, Rachel, Hacker, Timothy A., Pier, Thomas, Hardin, Joseph, Graham, Melissa, Mitchell, Carol C., Varghese, Tomy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122999/
https://www.ncbi.nlm.nih.gov/pubmed/35595876
http://dx.doi.org/10.1038/s41598-022-12579-6
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author Al Mukaddim, Rashid
Weichmann, Ashley M.
Taylor, Rachel
Hacker, Timothy A.
Pier, Thomas
Hardin, Joseph
Graham, Melissa
Mitchell, Carol C.
Varghese, Tomy
author_facet Al Mukaddim, Rashid
Weichmann, Ashley M.
Taylor, Rachel
Hacker, Timothy A.
Pier, Thomas
Hardin, Joseph
Graham, Melissa
Mitchell, Carol C.
Varghese, Tomy
author_sort Al Mukaddim, Rashid
collection PubMed
description An adaptive Bayesian regularized cardiac strain imaging (ABR-CSI) algorithm for in vivo murine myocardial function assessment is presented. We report on 31 BALB/CJ mice (n = 17 females, n = 14 males), randomly stratified into three surgical groups: myocardial infarction (MI, n = 10), ischemia–reperfusion (IR, n = 13) and control (sham, n = 8) imaged pre-surgery (baseline- BL), and 1, 2, 7 and 14 days post-surgery using a high frequency ultrasound imaging system (Vevo 2100). End-systole (ES) radial and longitudinal strain images were used to generate cardiac fibrosis maps using binary thresholding. Percentage fibrotic myocardium (PFM) computed from regional fibrosis maps demonstrated statistically significant differences post-surgery in scar regions. For example, the MI group had significantly higher PFM(Radial) (%) values in the anterior mid region (p = 0.006) at Day 14 (n = 8, 42.30 ± 14.57) compared to BL (n = 12, 1.32 ± 0.85). A random forest classifier automatically detected fibrotic regions from ground truth Masson’s trichrome stained histopathology whole slide images. Both PFM(Radial) (r = 0.70) and PFM(Longitudinal) (r = 0.60) results demonstrated strong, positive correlation with PFM(Histopathology) (p < 0.001).
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spelling pubmed-91229992022-05-22 Murine cardiac fibrosis localization using adaptive Bayesian cardiac strain imaging in vivo Al Mukaddim, Rashid Weichmann, Ashley M. Taylor, Rachel Hacker, Timothy A. Pier, Thomas Hardin, Joseph Graham, Melissa Mitchell, Carol C. Varghese, Tomy Sci Rep Article An adaptive Bayesian regularized cardiac strain imaging (ABR-CSI) algorithm for in vivo murine myocardial function assessment is presented. We report on 31 BALB/CJ mice (n = 17 females, n = 14 males), randomly stratified into three surgical groups: myocardial infarction (MI, n = 10), ischemia–reperfusion (IR, n = 13) and control (sham, n = 8) imaged pre-surgery (baseline- BL), and 1, 2, 7 and 14 days post-surgery using a high frequency ultrasound imaging system (Vevo 2100). End-systole (ES) radial and longitudinal strain images were used to generate cardiac fibrosis maps using binary thresholding. Percentage fibrotic myocardium (PFM) computed from regional fibrosis maps demonstrated statistically significant differences post-surgery in scar regions. For example, the MI group had significantly higher PFM(Radial) (%) values in the anterior mid region (p = 0.006) at Day 14 (n = 8, 42.30 ± 14.57) compared to BL (n = 12, 1.32 ± 0.85). A random forest classifier automatically detected fibrotic regions from ground truth Masson’s trichrome stained histopathology whole slide images. Both PFM(Radial) (r = 0.70) and PFM(Longitudinal) (r = 0.60) results demonstrated strong, positive correlation with PFM(Histopathology) (p < 0.001). Nature Publishing Group UK 2022-05-20 /pmc/articles/PMC9122999/ /pubmed/35595876 http://dx.doi.org/10.1038/s41598-022-12579-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Al Mukaddim, Rashid
Weichmann, Ashley M.
Taylor, Rachel
Hacker, Timothy A.
Pier, Thomas
Hardin, Joseph
Graham, Melissa
Mitchell, Carol C.
Varghese, Tomy
Murine cardiac fibrosis localization using adaptive Bayesian cardiac strain imaging in vivo
title Murine cardiac fibrosis localization using adaptive Bayesian cardiac strain imaging in vivo
title_full Murine cardiac fibrosis localization using adaptive Bayesian cardiac strain imaging in vivo
title_fullStr Murine cardiac fibrosis localization using adaptive Bayesian cardiac strain imaging in vivo
title_full_unstemmed Murine cardiac fibrosis localization using adaptive Bayesian cardiac strain imaging in vivo
title_short Murine cardiac fibrosis localization using adaptive Bayesian cardiac strain imaging in vivo
title_sort murine cardiac fibrosis localization using adaptive bayesian cardiac strain imaging in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122999/
https://www.ncbi.nlm.nih.gov/pubmed/35595876
http://dx.doi.org/10.1038/s41598-022-12579-6
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