Interplay of atherosclerosis and medial degeneration in human ascending aorta.

Atherosclerosis ascending aorta collagen alteration elastic fibre medial degeneration smooth muscle cell

Journal

Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
ISSN: 1879-1336
Titre abrégé: Cardiovasc Pathol
Pays: United States
ID NLM: 9212060

Informations de publication

Date de publication:
08 Oct 2024
Historique:
received: 24 02 2024
revised: 18 09 2024
accepted: 08 10 2024
medline: 11 10 2024
pubmed: 11 10 2024
entrez: 10 10 2024
Statut: aheadofprint

Résumé

The previous understanding has been that atherosclerosis tends to increase distally from the ascending aorta, but recent studies and practical experience have indicated that atherosclerosis occurs in the ascending aorta more than previously thought. Medial degeneration is linked to aortic aneurysms, dissection and dilatation and has been related to increased mortality. There is a lack of data on the coexistence of atherosclerosis and medial degeneration in the ascending aorta and its outcome to clinical morbidity and mortality. Earlier studies have shown coexisting atherosclerosis and medial degeneration as significant risk indicators for coronary and cerebrovascular events. We aimed to analyze aortic specimens classified according to the consensus documents of the Society for Cardiovascular Pathology and the Association for European Cardiovascular Pathology particularly the comparison of variable morphological features with the atherosclerotic grade to gain more data about the coexistence of atherosclerosis and medial degeneration. We evaluated 217 specimens of human ascending aorta resected at Tampere University Heart Hospital because of aortic aneurysm, dissection or dilatation. None of the samples contained normal aortic morphology; atherosclerosis was found in a total of 75.8% of the samples and medial degeneration in all the samples. The present study is mostly in agreement with earlier research regarding the prevalence of different histological findings, even though a higher prevalence of atherosclerosis was found compared with most studies. There was no statistically significant association between atherosclerosis and medial degeneration, but a higher atherosclerotic grade was significantly associated with the presence of smooth muscle cell nuclei loss, smooth muscle cell disorganisation, elastic fibre thinning and medial fibrosis. Our study reinforces the perception that atherosclerotic lesions significantly occur in the ascending aorta and coexist with individual components of the medial degeneration.

Identifiants

pubmed: 39389219
pii: S1054-8807(24)00098-X
doi: 10.1016/j.carpath.2024.107702
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107702

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no conflict of interest. VTR Competitive Research Grant from Pirkanmaa Hospital District, Finland, the Aarne Koskelo Foundation and the Tampere Tuberculosis Foundation funded the research, but had no influence on design and performance of the study.

Auteurs

Aaron Huhta (A)

Department of Pathology, Fimlab Laboratories, Arvo Ylpön katu 4, 33520, Tampere, Finland; Faculty of Medicine and Health Technology, Tampere University, Arvo Ylpön katu 34, 33520, Tampere, Finland. Electronic address: aaron.huhta@tuni.fi.

Timo Paavonen (T)

Department of Pathology, Fimlab Laboratories, Arvo Ylpön katu 4, 33520, Tampere, Finland; Faculty of Medicine and Health Technology, Tampere University, Arvo Ylpön katu 34, 33520, Tampere, Finland. Electronic address: timo.paavonen@tuni.fi.

Ari Mennander (A)

Faculty of Medicine and Health Technology, Tampere University, Arvo Ylpön katu 34, 33520, Tampere, Finland; Division of Cardiothoracic Surgery, Tampere University Heart Hospital, Elämänaukio 1, 33520, Tampere, Finland. Electronic address: ari.mennander@sydansairaala.fi.

Ivana Kholová (I)

Department of Pathology, Fimlab Laboratories, Arvo Ylpön katu 4, 33520, Tampere, Finland; Faculty of Medicine and Health Technology, Tampere University, Arvo Ylpön katu 34, 33520, Tampere, Finland. Electronic address: ivana.kholova@tuni.fi.

Classifications MeSH