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  4. Predicting and understanding arterial elasticity from key microstructural features by bidirectional deep learning
 
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Predicting and understanding arterial elasticity from key microstructural features by bidirectional deep learning

Citation Link: https://doi.org/10.15480/882.4916
Publikationstyp
Journal Article
Date Issued
2022-05-25
Sprache
English
Author(s)
Linka, Kevin  
Cavinato, Cristina  
Humphrey, Jay Dowell  
Cyron, Christian J.  
Institut
Kontinuums- und Werkstoffmechanik M-15  
TORE-DOI
10.15480/882.4916
TORE-URI
http://hdl.handle.net/11420/12920
Journal
Acta biomaterialia  
Volume
147
Start Page
63
End Page
72
Citation
Acta Biomaterialia 147: 63-72 (2022)
Publisher DOI
10.1016/j.actbio.2022.05.039
Scopus ID
2-s2.0-85131577662
PubMed ID
35643194
Publisher
Elsevier
Microstructural features and mechanical properties are closely related in all soft biological tissues. Both yet exhibit considerable inter-individual differences and are affected by factors such as aging and disease and its progression. Histological analysis, modern in situ imaging, and biomechanical testing have deepened our understanding of these complex interrelations, yet two key questions remain: (1) Given the specific microstructure, can one predict the macroscopic mechanical properties without mechanical testing? (2) Can one quantify individual contributions of the different microstructural features to the macroscopic mechanical properties in an automated, systematic and largely unbiased way? Here we propose a bidirectional deep learning architecture to address these two questions. Our architecture uses data from standard histological analyses, two-photon microscopy and biaxial biomechanical testing. Its capabilities are demonstrated by predicting with high accuracy (R2=0.92) the evolving mechanical properties of the murine aorta during maturation and aging. Moreover, our architecture reveals that the extracellular matrix composition and organization are the most prominent factors governing the macroscopic mechanical properties of the tissues studied herein. Statement of significance:
Subjects
arterial tissues
explainable AI
hybrid modeling
tissue maturation
MLE@TUHH
DDC Class
620: Ingenieurwissenschaften
More Funding Information
This work was supported, in part, by grants from the US NIH (R01 HL105297, U01 HL142518).
Publication version
publishedVersion
Lizenz
https://creativecommons.org/licenses/by-nc-nd/4.0/
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