A Systematic Histopathologic Evaluation of Type-A Aortic Dissections Implies a Uniform Multiple-Hit Causation
(1) Background: The pathophysiologic basis of an acute type A aortic dissection (TAAD) is largely unknown. In an effort to evaluate vessel wall defects, we systematically studied aortic specimens in TAAD patients. (2) Methods: Ascending aortic wall specimens (<i>n</i> = 58, mean age 63 y...
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doaj-8f7adedca2714adfa2a0c356d7833e572021-01-28T00:04:17ZengMDPI AGJournal of Cardiovascular Development and Disease2308-34252021-01-018121210.3390/jcdd8020012A Systematic Histopathologic Evaluation of Type-A Aortic Dissections Implies a Uniform Multiple-Hit CausationNimrat Grewal0Bart J. J. Velders1Adriana C. Gittenberger-de Groot2Robert Poelmann3Robert J. M. Klautz4Thomas J. Van Brakel5Jan H. N. Lindeman6Department of Cardiothoracic Surgery, Leiden University Medical Center, 2333ZA Leiden, The NetherlandsDepartment of Cardiothoracic Surgery, Leiden University Medical Center, 2333ZA Leiden, The NetherlandsDepartment of Anatomy and Embryology, Leiden University Medical Center, 2333ZA Leiden, The NetherlandsInstitute of Biology, Animal Sciences and Health, Leiden University, 2333 BE Leiden, The NetherlandsDepartment of Cardiothoracic Surgery, Leiden University Medical Center, 2333ZA Leiden, The NetherlandsDepartment of Cardiothoracic Surgery, Leiden University Medical Center, 2333ZA Leiden, The NetherlandsDepartment of Vascular Surgery, Leiden University Medical Center, 2333ZA Leiden, The Netherlands(1) Background: The pathophysiologic basis of an acute type A aortic dissection (TAAD) is largely unknown. In an effort to evaluate vessel wall defects, we systematically studied aortic specimens in TAAD patients. (2) Methods: Ascending aortic wall specimens (<i>n</i> = 58, mean age 63 years) with TAAD were collected. Autopsy tissues (<i>n</i> = 17, mean age 63 years) served as controls. All sections were studied histopathologically. (3) Results: Pathomorphology in TAAD showed predominantly moderate elastic fiber fragmentation/loss, elastic fiber thinning, elastic fiber degeneration, mucoid extracellular matrix accumulation, smooth muscle cell nuclei loss, and overall medial degeneration. The control group showed significantly fewer signs of those histopathological features (none-mild, <i>p</i> = 0.00). It was concluded that the dissection plane consistently coincides with the vasa vasorum network, and that TAAD associates with a significantly thinner intimal layer <i>p</i> = 0.005). (4) Conclusions: On the basis of the systematic evaluation and the consistent presence of diffuse, pre-existing medial defects, we hypothesize that TAAD relates to a developmental defect of the ascending aorta and is caused by a triple-hit mechanism that involves (I) an intimal tear; and (II) a diseased media, which allows (III) propagation of the tear towards the plane of the vasa vasorum where the dissection further progresses.https://www.mdpi.com/2308-3425/8/2/12acute aortic syndromecardiovascular diseaseaorta |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nimrat Grewal Bart J. J. Velders Adriana C. Gittenberger-de Groot Robert Poelmann Robert J. M. Klautz Thomas J. Van Brakel Jan H. N. Lindeman |
spellingShingle |
Nimrat Grewal Bart J. J. Velders Adriana C. Gittenberger-de Groot Robert Poelmann Robert J. M. Klautz Thomas J. Van Brakel Jan H. N. Lindeman A Systematic Histopathologic Evaluation of Type-A Aortic Dissections Implies a Uniform Multiple-Hit Causation Journal of Cardiovascular Development and Disease acute aortic syndrome cardiovascular disease aorta |
author_facet |
Nimrat Grewal Bart J. J. Velders Adriana C. Gittenberger-de Groot Robert Poelmann Robert J. M. Klautz Thomas J. Van Brakel Jan H. N. Lindeman |
author_sort |
Nimrat Grewal |
title |
A Systematic Histopathologic Evaluation of Type-A Aortic Dissections Implies a Uniform Multiple-Hit Causation |
title_short |
A Systematic Histopathologic Evaluation of Type-A Aortic Dissections Implies a Uniform Multiple-Hit Causation |
title_full |
A Systematic Histopathologic Evaluation of Type-A Aortic Dissections Implies a Uniform Multiple-Hit Causation |
title_fullStr |
A Systematic Histopathologic Evaluation of Type-A Aortic Dissections Implies a Uniform Multiple-Hit Causation |
title_full_unstemmed |
A Systematic Histopathologic Evaluation of Type-A Aortic Dissections Implies a Uniform Multiple-Hit Causation |
title_sort |
systematic histopathologic evaluation of type-a aortic dissections implies a uniform multiple-hit causation |
publisher |
MDPI AG |
series |
Journal of Cardiovascular Development and Disease |
issn |
2308-3425 |
publishDate |
2021-01-01 |
description |
(1) Background: The pathophysiologic basis of an acute type A aortic dissection (TAAD) is largely unknown. In an effort to evaluate vessel wall defects, we systematically studied aortic specimens in TAAD patients. (2) Methods: Ascending aortic wall specimens (<i>n</i> = 58, mean age 63 years) with TAAD were collected. Autopsy tissues (<i>n</i> = 17, mean age 63 years) served as controls. All sections were studied histopathologically. (3) Results: Pathomorphology in TAAD showed predominantly moderate elastic fiber fragmentation/loss, elastic fiber thinning, elastic fiber degeneration, mucoid extracellular matrix accumulation, smooth muscle cell nuclei loss, and overall medial degeneration. The control group showed significantly fewer signs of those histopathological features (none-mild, <i>p</i> = 0.00). It was concluded that the dissection plane consistently coincides with the vasa vasorum network, and that TAAD associates with a significantly thinner intimal layer <i>p</i> = 0.005). (4) Conclusions: On the basis of the systematic evaluation and the consistent presence of diffuse, pre-existing medial defects, we hypothesize that TAAD relates to a developmental defect of the ascending aorta and is caused by a triple-hit mechanism that involves (I) an intimal tear; and (II) a diseased media, which allows (III) propagation of the tear towards the plane of the vasa vasorum where the dissection further progresses. |
topic |
acute aortic syndrome cardiovascular disease aorta |
url |
https://www.mdpi.com/2308-3425/8/2/12 |
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