Evidence mapPaperPMID 42479047Full record

ArticleBiomechanics and modeling in mechanobiology2026

Haemodynamic and biomechanical biomarker analysis of carotid fibromuscular dysplasia via fluid-structure interaction.

Kaveh Moghadasi, Mergen H Ghayesh, Eric Hu, Shahid Hussain, Marco Amabili, Robert Fitridge, Jiawen Li

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Article in Biomechanics and modeling in mechanobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Kaveh MoghadasiSchool of Electrical and Mechanical Engineering, Adelaide University, Adelaide, SA, 5005, Australia. kaveh.moghadasikoohi@adelaide.edu.au.
Mergen H GhayeshSchool of Electrical and Mechanical Engineering, Adelaide University, Adelaide, SA, 5005, Australia.
Eric HuSchool of Electrical and Mechanical Engineering, Adelaide University, Adelaide, SA, 5005, Australia.
Shahid HussainSchool of Information Technology and Systems, University of Canberra, Canberra, ACT, Australia.
Marco AmabiliSchool of Engineering, Westlake University, Hangzhou, China.
Robert FitridgeVascular and Endovascular Service, Royal Adelaide Hospital, Adelaide, Australia.
Jiawen LiSchool of Electrical and Mechanical Engineering, Adelaide University, Adelaide, SA, 5005, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aims to investigate the biomechanical behaviour of the carotid artery in patients with fibromuscular dysplasia (FMD) disease. Carotid FMD is an arterial disease lacking either inflammatory or atherosclerotic pathology, which is characterised by segmental disruptions in arterial wall architecture. It is of considerable interest to examine carotid FMD haemodynamics for the identification of clinically meaningful biomechanical biomarkers. Thus, a two-way coupled three-dimensional (3D) fluid-structure interaction (FSI) model was developed that integrates patient-specific vascular geometries, non-Newtonian turbulent blood flow, an orthotropic hyperelastic representation of the arterial wall, and a Windkessel boundary formulation, with emphasis on characterising haemodynamic biomarkers and biomechanical wall responses. The results showed distinct severity-dependent trends among healthy, focal, non-focal, and severe non-focal carotid geometry types. FMD cases exhibited increased velocities and wall shear stresses, while their pressure gradients at the distal end decreased. Additionally, elevation of OSI (oscillatory shear index) and RRT (relative residence time) values was observed in each FMD model indicating higher levels of flow disruption, oscillatory shear, and localised flow stagnation. Non-focal phenotypes showed the largest radial deformation, whereas the focal configuration displayed the highest von-Mises stresses. These findings indicate that as FMD progresses through increasing complexity in its morphological structure, it will be subjected to increasingly adverse haemodynamics and mechanical forces, which are likely to promote endothelial dysfunction and further progression of the disease.Kindly check and confirm the corresponding author of the article and the first/last name of the authors are correctly identified.All others' names and affiliations have been checked.

Indexed as

BiomarkersCarotid ArteriesFibromuscular DysplasiaHemodynamicsBiomechanical PhenomenaBlood Flow VelocityHumansModels, CardiovascularStress, MechanicalBiomarkersAnisotropic artery tissueCarotid arteryFibromuscular dysplasia diseaseFluid–structure interactionWall shear biomarkers

Identifiers

PMID42479047
PMCPMC13388523

What Socratic holds

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Registered trials

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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 Socratic graph.