# Investigation of hemodynamic bulk flow patterns caused by aortic stenosis using a combined 4D Flow MRI-CFD framework

**Authors:** Tianai Wang, Christine Quast, Florian Bönner, Malte Kelm, Tobias Zeus, Teresa Lemainque, Ulrich Steinseifer, Michael Neidlin

PMC · DOI: 10.1371/journal.pcbi.1012467 · PLOS Computational Biology · 2025-03-27

## TL;DR

This study uses advanced imaging and simulations to show how aortic stenosis changes blood flow patterns, increasing red blood cell damage.

## Contribution

A validated 4D Flow MRI-based CFD model reveals altered turbulent and helical flow structures in aortic stenosis that may damage red blood cells.

## Key findings

- Pathological flow in aortic stenosis increases shear stress on red blood cells by 125% during late systole.
- A physiological bihelical flow structure is replaced by a left-handed helix in aortic stenosis, increasing turbulent kinetic energy.
- The 4D Flow MRI-based CFD model shows excellent agreement with in-vivo data (R² = 0.9).

## Abstract

Aortic stenosis (AS) leads to alterations of supra-valvular flow patterns which can cause increased damage of red blood cell (RBC) membranes. We investigated these patient specific patterns of a severe AS patient and their reversal in healthy flow through a 4D Flow MRI-based CFD methodology. Computational models of subject-specific aortic geometries were created using in-vivo medical imaging data. Temporally and spatially resolved boundary conditions derived from 4D Flow MRI were implemented for an AS patient and a healthy subject. After validation of the in-silico results with in-vivo data, a healthy inflow profile was set for the AS patient in the CFD model. Pathological versus healthy flow fields were compared regarding their blood flow characteristics, i.e., shear stresses on RBCs and helicity. The accuracy of the 4D Flow MRI-based CFD model was proven with excellent agreement between in-vivo and in-silico velocity fields and R² = 0.9. A pathological high shear stress region in the bulk flow was present during late systole with an increase of 125% compared to both healthy flow. The physiological bihelical structure with predominantly right-handed helices vanished for the pathological state. Instead, a left-handed helix appeared, accompanied by an overall increase in turbulent kinetic energy in areas of accumulated left-handed helicity. The validated 4D Flow MRI-based CFD model identified marked differences between AS and healthy flow. It suggests that altered turbulent and helical structures in the bulk flow are the cause for increased, potentially damaging forces acting upon RBCs in AS.

Aortic stenosis (AS) is a condition that alters the flow of blood through the aorta, potentially increasing damage to red blood cells (RBCs). It is therefore crucial to understand the precise nature of these changes, especially in the bulk region where the RBCs are mainly circulating. To investigate this, we developed a computational model based on patient-specific 4D Flow MRI data to simulate blood flow in a patient with severe AS and a healthy individual. Our high-fidelity models show high agreement with real-world data. We then imposed synthetically generated healthy flow conditions in the AS patient to eliminate age- and geometry-related uncertainties. Our results revealed significantly higher shear stresses and changes in helical flow patterns in the AS patient compared to healthy flow, suggesting that these alterations could increase the risk of RBC membrane damage. These findings underscore the importance of deepening our understanding about the interplay between bulk flow alterations and their impact on RBCs, as previous studies were mostly focused on near wall regions. This methodology could also be extended to other cardiovascular conditions, aiding in the development of patient-specific treatment strategies.

## Linked entities

- **Diseases:** aortic stenosis (MONDO:0042981)

## Full-text entities

- **Diseases:** AS (MESH:D001024), CFD (MESH:C563256)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC11996075/full.md

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Source: https://tomesphere.com/paper/PMC11996075