Evidence map›Paper›PMID 40582536›Full record

ArticleActa biomaterialia2025

Dissection Propagation via Avalanches in Human Descending Thoracic Aorta: Effect of Aging.

Ruizhi Wang, Xunjie Yu, Samuel C Halvorsen, Béla Suki, Yanhang Zhang

Abstract read
In one paragraph

Article in Acta biomaterialia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Ruizhi WangDepartment of Mechanical Engineering, Boston University, Boston, MA 02215.
Xunjie YuDepartment of Mechanical Engineering, Boston University, Boston, MA 02215.
Samuel C HalvorsenDepartment of Mechanical Engineering, Boston University, Boston, MA 02215.
Béla SukiDepartment of Biomedical Engineering, Boston University, Boston, MA 02215; Divison of Materials Science & Engineering, Boston University, Boston, MA 02215.
Yanhang ZhangDepartment of Mechanical Engineering, Boston University, Boston, MA 02215; Department of Biomedical Engineering, Boston University, Boston, MA 02215; Divison of Materials Science & Engineering, Boston University, Boston, MA 02215. Electronic address: yanhang@bu.edu.

Funding

Multi-Scale Integration of Extracellular Matrix Mechanics in Vascular RemodelingR01HL098028 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI ZHANG, YANHANG KATHERINE · 2011 to 2025
$5.2M
Cerebrovascular Remodeling and Neurodegenerative Changes in Alzheimer's DiseaseR01AG075876 · NIA · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI Thor Stein, JOSEPH ZAIA · 2022 to 2026
$3.9M
NHLBI NIH HHS R01 HL098028NIA NIH HHS R01 AG075876
6 · The paper itself

Abstract

Understanding of the risk factors and underlying mechanisms of aortic dissection (AD) is critical for improved clinical management of the disease. How aging, a prominent risk factor for AD, impairs the dissection resistance capabilities of the aorta has not been elucidated. This study integrated mechanical testing, multiphoton imaging and finite element (FE) modeling to investigate the multiscale dissection behavior of human descending thoracic aortas (DTAs) from a wide range of ages. Mechanical testing demonstrated that aging diminishes bonding between the lamellar layers within the media of human DTA. Moreover, dissection propagation in aortic media is associated with dissection tension drops that follow a power-law distribution. Multiphoton imaging of dissected DTA media revealed less organized elastic lamellae and fewer visible collagen with aging. The discrete FE model of dissection propagation recapitulated the power-law behavior that originates from avalanches of interlamellar collagen fiber (ICF) failures. Simulation revealed prominent interlamellar structural rearrangement of ICFs in the aging DTA, including lower density and higher dispersion, of which the former strongly correlates with the weakened interlamellar bonding while the latter is vital in triggering the fast-propagating avalanches and power-law behavior of AD. Furthermore, small avalanches occur more often with aging, which makes dissection propagation faster and AD more dangerous for the elderly population. STATEMENT OF SIGNIFICANCE: Early diagnosis of aortic dissection (AD) is crucial for effective disease management, and it requires a comprehensive understanding of the risk factors. This study explores the microstructural mechanisms that underlie the age-augmented risk of AD through a multiscale investigation of the dissection mechanics of human descending thoracic aortas (DTAs). Our findings reveal the presence of avalanches and power-law behavior in dissection propagation, which is age-dependent and can be recapitulated using a novel computational model that accounts for the failure of discrete interlamellar fibers. Using this model, we demonstrated that aging weakens the dissection resistance of the DTA, characterized by a reduction in the number and increased dispersion of interlamellar collagen fibers. The avalanches and power-law behavior not only plays a fundamental role in the rapid progression of AD but also offers new perspectives on the interlamellar microstructure-function relationship in both aortic health and disease.

Indexed as

AgingAorta, ThoracicAortic DissectionModels, CardiovascularAdultAgedAged, 80 and overFemaleFinite Element AnalysisHumansMaleMiddle AgedAortic dissectiondiscrete finite element modelinterlamellar fibermicrostructural mechanismpeeling test

Identifiers

PMID40582536
PMCPMC12238761

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.