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Imaging of programmed cell death in arrhythmogenic right ventricle cardiomyopathy/dysplasia

BACKGROUND: Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a myocardial disease that predominantly affects the right ventricle (RV). Its hallmark feature is fibrofatty replacement of the RV myocardium. Apoptosis in ARVC/D has been proposed as an important process that mediates...

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Autores principales: Campian, Maria E., Tan, Hanno L., van Moerkerken, Astrid F., Tukkie, Raymond, van Eck-Smit, Berthe L. F., Verberne, Hein J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127016/
https://www.ncbi.nlm.nih.gov/pubmed/21553091
http://dx.doi.org/10.1007/s00259-011-1817-x
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author Campian, Maria E.
Tan, Hanno L.
van Moerkerken, Astrid F.
Tukkie, Raymond
van Eck-Smit, Berthe L. F.
Verberne, Hein J.
author_facet Campian, Maria E.
Tan, Hanno L.
van Moerkerken, Astrid F.
Tukkie, Raymond
van Eck-Smit, Berthe L. F.
Verberne, Hein J.
author_sort Campian, Maria E.
collection PubMed
description BACKGROUND: Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a myocardial disease that predominantly affects the right ventricle (RV). Its hallmark feature is fibrofatty replacement of the RV myocardium. Apoptosis in ARVC/D has been proposed as an important process that mediates the slow, ongoing loss of heart muscle cells which is followed by ventricular dysfunction. We aimed to establish whether cardiac apoptosis can be assessed noninvasively in patients with ARVC/D. METHODS: Six patients fulfilling the ARVC/D criteria were studied. Regional myocardial apoptosis was assessed with (99m)Tc-annexin V scintigraphy. RESULTS: Overall, the RV wall showed a higher (99m)Tc-annexin V signal than the left ventricular wall (p = 0.049) and the interventricular septum (p = 0.026). However, significantly increased uptake of (99m)Tc-annexin V in the RV was present in only three of the six ARVC/D patients (p = 0.001, compared to (99m)Tc-annexin V uptake in the RV wall of the other three patients). CONCLUSION: Our results are suggestive of a chamber-specific apoptotic process. Although the role of apoptosis in ARVC/D is unsolved, the ability to assess apoptosis noninvasively may aid in the diagnostic course. In addition, the ability to detect apoptosis in vivo with (99m)Tc-annexin V scintigraphy might allow individual monitoring of disease progression and response to diverse treatments aimed at counteracting ARVC/D progression.
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spelling pubmed-31270162011-08-09 Imaging of programmed cell death in arrhythmogenic right ventricle cardiomyopathy/dysplasia Campian, Maria E. Tan, Hanno L. van Moerkerken, Astrid F. Tukkie, Raymond van Eck-Smit, Berthe L. F. Verberne, Hein J. Eur J Nucl Med Mol Imaging Original Article BACKGROUND: Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a myocardial disease that predominantly affects the right ventricle (RV). Its hallmark feature is fibrofatty replacement of the RV myocardium. Apoptosis in ARVC/D has been proposed as an important process that mediates the slow, ongoing loss of heart muscle cells which is followed by ventricular dysfunction. We aimed to establish whether cardiac apoptosis can be assessed noninvasively in patients with ARVC/D. METHODS: Six patients fulfilling the ARVC/D criteria were studied. Regional myocardial apoptosis was assessed with (99m)Tc-annexin V scintigraphy. RESULTS: Overall, the RV wall showed a higher (99m)Tc-annexin V signal than the left ventricular wall (p = 0.049) and the interventricular septum (p = 0.026). However, significantly increased uptake of (99m)Tc-annexin V in the RV was present in only three of the six ARVC/D patients (p = 0.001, compared to (99m)Tc-annexin V uptake in the RV wall of the other three patients). CONCLUSION: Our results are suggestive of a chamber-specific apoptotic process. Although the role of apoptosis in ARVC/D is unsolved, the ability to assess apoptosis noninvasively may aid in the diagnostic course. In addition, the ability to detect apoptosis in vivo with (99m)Tc-annexin V scintigraphy might allow individual monitoring of disease progression and response to diverse treatments aimed at counteracting ARVC/D progression. Springer-Verlag 2011-05-07 2011 /pmc/articles/PMC3127016/ /pubmed/21553091 http://dx.doi.org/10.1007/s00259-011-1817-x Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
Campian, Maria E.
Tan, Hanno L.
van Moerkerken, Astrid F.
Tukkie, Raymond
van Eck-Smit, Berthe L. F.
Verberne, Hein J.
Imaging of programmed cell death in arrhythmogenic right ventricle cardiomyopathy/dysplasia
title Imaging of programmed cell death in arrhythmogenic right ventricle cardiomyopathy/dysplasia
title_full Imaging of programmed cell death in arrhythmogenic right ventricle cardiomyopathy/dysplasia
title_fullStr Imaging of programmed cell death in arrhythmogenic right ventricle cardiomyopathy/dysplasia
title_full_unstemmed Imaging of programmed cell death in arrhythmogenic right ventricle cardiomyopathy/dysplasia
title_short Imaging of programmed cell death in arrhythmogenic right ventricle cardiomyopathy/dysplasia
title_sort imaging of programmed cell death in arrhythmogenic right ventricle cardiomyopathy/dysplasia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127016/
https://www.ncbi.nlm.nih.gov/pubmed/21553091
http://dx.doi.org/10.1007/s00259-011-1817-x
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