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Native T1 mapping detects both acute clinical rejection and graft dysfunction in pediatric heart transplant patients

BACKGROUND: Cardiovascular magnetic resonance (CMR) is emerging as an important tool for cardiac allograft assessment. Native T1 mapping may add value in identifying rejection and in assessing graft dysfunction and myocardial fibrosis burden. We hypothesized that CMR native T1 values and features of...

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Autores principales: Richmann, Devika P., Gurijala, Nyshidha, Mandell, Jason G., Doshi, Ashish, Hamman, Karin, Rossi, Christopher, Rosenberg, Avi Z., Cross, Russell, Kanter, Joshua, Berger, John T., Olivieri, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531384/
https://www.ncbi.nlm.nih.gov/pubmed/36192743
http://dx.doi.org/10.1186/s12968-022-00875-z
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author Richmann, Devika P.
Gurijala, Nyshidha
Mandell, Jason G.
Doshi, Ashish
Hamman, Karin
Rossi, Christopher
Rosenberg, Avi Z.
Cross, Russell
Kanter, Joshua
Berger, John T.
Olivieri, Laura
author_facet Richmann, Devika P.
Gurijala, Nyshidha
Mandell, Jason G.
Doshi, Ashish
Hamman, Karin
Rossi, Christopher
Rosenberg, Avi Z.
Cross, Russell
Kanter, Joshua
Berger, John T.
Olivieri, Laura
author_sort Richmann, Devika P.
collection PubMed
description BACKGROUND: Cardiovascular magnetic resonance (CMR) is emerging as an important tool for cardiac allograft assessment. Native T1 mapping may add value in identifying rejection and in assessing graft dysfunction and myocardial fibrosis burden. We hypothesized that CMR native T1 values and features of textural analysis of T1 maps would identify acute rejection, and in a secondary analysis, correlate with markers of graft dysfunction, and with fibrosis percentage from endomyocardial biopsy (EMB). METHODS: Fifty cases with simultaneous EMB, right heart catheterization, and 1.5 T CMR with breath-held T1 mapping via modified Look-Locker inversion recovery (MOLLI) in 8 short-axis slices and subsequent quantification of mean and peak native T1 values, were performed on 24 pediatric subjects. A single mid-ventricular slice was used for image texture analysis using nine gray-level co-occurrence matrix features. Digital quantification of Masson trichrome stained EMB samples established degree of fibrosis. Markers of graft dysfunction, including serum brain natriuretic peptide levels and hemodynamic measurements from echocardiography, catheterization, and CMR were collated. Subjects were divided into three groups based on degree of rejection: acute rejection requiring new therapy, mild rejection requiring increased ongoing therapy, and no rejection with no change in treatment. Statistical analysis included student’s t-test and linear regression. RESULTS: Peak and mean T1 values were significantly associated with acute rejection, with a monotonic trend observed with increased grade of rejection. Texture analysis demonstrated greater spatial heterogeneity in T1 values, as demonstrated by energy, entropy, and variance, in cases requiring treatment. Interestingly, 2 subjects who required increased therapy despite low grade EMB results had abnormal peak T1 values. Peak T1 values also correlated with increased BNP, right-sided filling pressures, and capillary wedge pressures. There was no difference in histopathological fibrosis percentage among the 3 groups; histopathological fibrosis did not correlate with T1 values or markers of graft dysfunction. CONCLUSION: In pediatric heart transplant patients, native T1 values identify acute rejection requiring treatment and may identify graft dysfunction. CMR shows promise as an important tool for evaluation of cardiac grafts in children, with T1 imaging outperforming biopsy findings in the assessment of rejection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12968-022-00875-z.
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spelling pubmed-95313842022-10-05 Native T1 mapping detects both acute clinical rejection and graft dysfunction in pediatric heart transplant patients Richmann, Devika P. Gurijala, Nyshidha Mandell, Jason G. Doshi, Ashish Hamman, Karin Rossi, Christopher Rosenberg, Avi Z. Cross, Russell Kanter, Joshua Berger, John T. Olivieri, Laura J Cardiovasc Magn Reson Research BACKGROUND: Cardiovascular magnetic resonance (CMR) is emerging as an important tool for cardiac allograft assessment. Native T1 mapping may add value in identifying rejection and in assessing graft dysfunction and myocardial fibrosis burden. We hypothesized that CMR native T1 values and features of textural analysis of T1 maps would identify acute rejection, and in a secondary analysis, correlate with markers of graft dysfunction, and with fibrosis percentage from endomyocardial biopsy (EMB). METHODS: Fifty cases with simultaneous EMB, right heart catheterization, and 1.5 T CMR with breath-held T1 mapping via modified Look-Locker inversion recovery (MOLLI) in 8 short-axis slices and subsequent quantification of mean and peak native T1 values, were performed on 24 pediatric subjects. A single mid-ventricular slice was used for image texture analysis using nine gray-level co-occurrence matrix features. Digital quantification of Masson trichrome stained EMB samples established degree of fibrosis. Markers of graft dysfunction, including serum brain natriuretic peptide levels and hemodynamic measurements from echocardiography, catheterization, and CMR were collated. Subjects were divided into three groups based on degree of rejection: acute rejection requiring new therapy, mild rejection requiring increased ongoing therapy, and no rejection with no change in treatment. Statistical analysis included student’s t-test and linear regression. RESULTS: Peak and mean T1 values were significantly associated with acute rejection, with a monotonic trend observed with increased grade of rejection. Texture analysis demonstrated greater spatial heterogeneity in T1 values, as demonstrated by energy, entropy, and variance, in cases requiring treatment. Interestingly, 2 subjects who required increased therapy despite low grade EMB results had abnormal peak T1 values. Peak T1 values also correlated with increased BNP, right-sided filling pressures, and capillary wedge pressures. There was no difference in histopathological fibrosis percentage among the 3 groups; histopathological fibrosis did not correlate with T1 values or markers of graft dysfunction. CONCLUSION: In pediatric heart transplant patients, native T1 values identify acute rejection requiring treatment and may identify graft dysfunction. CMR shows promise as an important tool for evaluation of cardiac grafts in children, with T1 imaging outperforming biopsy findings in the assessment of rejection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12968-022-00875-z. BioMed Central 2022-10-03 /pmc/articles/PMC9531384/ /pubmed/36192743 http://dx.doi.org/10.1186/s12968-022-00875-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Richmann, Devika P.
Gurijala, Nyshidha
Mandell, Jason G.
Doshi, Ashish
Hamman, Karin
Rossi, Christopher
Rosenberg, Avi Z.
Cross, Russell
Kanter, Joshua
Berger, John T.
Olivieri, Laura
Native T1 mapping detects both acute clinical rejection and graft dysfunction in pediatric heart transplant patients
title Native T1 mapping detects both acute clinical rejection and graft dysfunction in pediatric heart transplant patients
title_full Native T1 mapping detects both acute clinical rejection and graft dysfunction in pediatric heart transplant patients
title_fullStr Native T1 mapping detects both acute clinical rejection and graft dysfunction in pediatric heart transplant patients
title_full_unstemmed Native T1 mapping detects both acute clinical rejection and graft dysfunction in pediatric heart transplant patients
title_short Native T1 mapping detects both acute clinical rejection and graft dysfunction in pediatric heart transplant patients
title_sort native t1 mapping detects both acute clinical rejection and graft dysfunction in pediatric heart transplant patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531384/
https://www.ncbi.nlm.nih.gov/pubmed/36192743
http://dx.doi.org/10.1186/s12968-022-00875-z
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