TY - JOUR
T1 - From Biomechanical Properties to Morphological Variations
T2 - Exploring the Interplay between Aortic Valve Cuspidity and Ascending Aortic Aneurysm
AU - Brečs, Ivars
AU - Skuja, Sandra
AU - Kasyanov, Vladimir
AU - Groma, Valērija
AU - Kalējs, Mārtiņš
AU - Svirskis, Šimons
AU - Ozolanta, Iveta
AU - Stradiņš, Pēteris
N1 - Publisher Copyright:
© 2024 by the authors.
PY - 2024/7/19
Y1 - 2024/7/19
N2 -
Background: This research explores the biomechanical and structural characteristics of ascending thoracic aortic aneurysms (ATAAs), focusing on the differences between bicuspid aortic valve aneurysms (BAV-As) and tricuspid aortic valve aneurysms (TAV-As) with non-dilated aortas to identify specific traits of ATAAs.
Methods: Clinical characteristics, laboratory indices, and imaging data from 26 adult patients operated on for aneurysms (BAV-A:
n = 12; TAV-A:
n = 14) and 13 controls were analyzed. Biomechanical parameters (maximal aortic diameter, strain, and stress) and structural analyses (collagen fiber organization, density, fragmentation, adipocyte deposits, and immune cell infiltration) were assessed.
Results: Significant differences in biomechanical parameters were observed. Median maximal strain was 40.0% (control), 63.4% (BAV-A), and 45.3% (TAV-A); median maximal stress was 0.59 MPa (control), 0.78 MPa (BAV-A), and 0.48 MPa (TAV-A). BAV-A showed higher tangential modulus and smaller diameter, with substantial collagen fragmentation (
p < 0.001 vs. TAV and controls). TAV-A exhibited increased collagen density (
p = 0.025), thickening between media and adventitia layers, and disorganized fibers (
p = 0.036). BAV-A patients had elevated adipocyte deposits and immune cell infiltration.
Conclusions: This study highlights distinct pathological profiles associated with different valve anatomies. BAV-A is characterized by smaller diameters, higher biomechanical stress, and significant collagen deterioration, underscoring the necessity for tailored clinical strategies for effective management of thoracic aortic aneurysm.
AB -
Background: This research explores the biomechanical and structural characteristics of ascending thoracic aortic aneurysms (ATAAs), focusing on the differences between bicuspid aortic valve aneurysms (BAV-As) and tricuspid aortic valve aneurysms (TAV-As) with non-dilated aortas to identify specific traits of ATAAs.
Methods: Clinical characteristics, laboratory indices, and imaging data from 26 adult patients operated on for aneurysms (BAV-A:
n = 12; TAV-A:
n = 14) and 13 controls were analyzed. Biomechanical parameters (maximal aortic diameter, strain, and stress) and structural analyses (collagen fiber organization, density, fragmentation, adipocyte deposits, and immune cell infiltration) were assessed.
Results: Significant differences in biomechanical parameters were observed. Median maximal strain was 40.0% (control), 63.4% (BAV-A), and 45.3% (TAV-A); median maximal stress was 0.59 MPa (control), 0.78 MPa (BAV-A), and 0.48 MPa (TAV-A). BAV-A showed higher tangential modulus and smaller diameter, with substantial collagen fragmentation (
p < 0.001 vs. TAV and controls). TAV-A exhibited increased collagen density (
p = 0.025), thickening between media and adventitia layers, and disorganized fibers (
p = 0.036). BAV-A patients had elevated adipocyte deposits and immune cell infiltration.
Conclusions: This study highlights distinct pathological profiles associated with different valve anatomies. BAV-A is characterized by smaller diameters, higher biomechanical stress, and significant collagen deterioration, underscoring the necessity for tailored clinical strategies for effective management of thoracic aortic aneurysm.
KW - tricuspid aortic valve
KW - bicuspid aortic valve
KW - ascending thoracic aortic aneurysm
KW - biomechanical properties
KW - morphology
UR - https://www-webofscience-com.db.rsu.lv/wos/alldb/full-record/WOS:001278542000001
UR - http://www.scopus.com/inward/record.url?scp=85199861602&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/b00bda3f-d83c-32d0-a136-8e95e66d6eab/
U2 - 10.3390/jcm13144225
DO - 10.3390/jcm13144225
M3 - Article
C2 - 39064264
SN - 2077-0383
VL - 13
JO - Journal of clinical medicine
JF - Journal of clinical medicine
IS - 14
M1 - 4225
ER -