IMR Press / RCM / Volume 26 / Issue 3 / DOI: 10.31083/RCM26735
Open Access Review
The Role of 4D Flow MRI-derived Wall Shear Stress in Aortic Disease: A Comprehensive Review
Ying Liu1,2,†Xiaolin Mu1,*,†Yixin Wang1Zhe Xu1Yang Song1,*
Show Less
Affiliation
1 Department of Radiology, Central Hospital of Dalian University of Technology, 116033 Dalian, Liaoning, China
2 Department of Graduate School, Dalian Medical University, 116044 Dalian, Liaoning, China
*Correspondence: dugumuxin@163.com (Xiaolin Mu); sy_zxyy@163.com (Yang Song)
These authors contributed equally.
Rev. Cardiovasc. Med. 2025, 26(3), 26735; https://doi.org/10.31083/RCM26735
Submitted: 25 September 2024 | Revised: 16 December 2024 | Accepted: 20 December 2024 | Published: 5 March 2025
Copyright: © 2025 The Author(s). Published by IMR Press.
This is an open access article under the CC BY 4.0 license.
Abstract

Aortic diseases, such as aortic dissection and aortic rupture, often lead to catastrophic complications, significantly increasing morbidity and mortality. Population-based screening for early detection in asymptomatic individuals is not feasible due to high costs and practical challenges. However, recent advancements in four dimensions (4D) Flow magnetic resonance imaging (MRI) offer a comprehensive tool for evaluating hemodynamic changes within the aortic lumen. This technology allows for the quantification and visualization of flow patterns and the calculation of advanced hemodynamic parameters, such as wall shear stress (WSS). WSS is crucial in the development, risk stratification, and surgical outcomes of aortic diseases and their complications, enabling noninvasive and quantitative screening of high-risk populations. This review explores the current status and limitations of 4D flow MRI-derived WSS imaging for aortic disease.

Keywords
4D flow
magnetic resonance imaging
wall shear stress
aortic
1. Introduction

Complications from aortic disease, such as aortic dissection and aortic rupture, are often catastrophic, resulting in increased morbidity and mortality [1]. The development of aortic disease is closely related to the luminal hemodynamic environment, with wall shear stress (WSS) playing an important role. Under physiological conditions, vascular endothelial cells possess mechanosensors that detect the magnitude and direction of WSS, including ion channels, cell-cell junctions, G protein-coupled receptors, integrins, and glycocalyx [2, 3, 4]. These mechanosensors regulate the expression of relevant genes and their proteins by activating signal transduction pathways [5]. Normal WSS maintains vascular homeostasis and exerts anti-proliferative, anti-apoptotic, anti-inflammatory and anti-thrombotic effects. Conversely, abnormal WSS can lead to vascular dysfunction, inflammation and thrombosis [6, 7]. This underscores the importance of WSS in the physiological stages and progression of vascular diseases.

The aorta is mainly evaluated by Color Doppler ultrasound, computed tomography angiography (CTA), digital subtraction angiography (DSA) and other techniques. But these techniques have some defects, for example, ultrasound is susceptible to gas and the quality and accuracy of its images are related to the level of the imaging physician; CTA and DSA require the introduction of contrast agents, which can only obtain information on the morphology of the aorta. They need to be combined with hydrodynamic post-processing software in order to provide hemodynamics. Computational fluid dynamics (CFD) is a common hemodynamic measurement that provides high spatial and temporal resolution [8], but it simulates the real blood flow information by computer modeling, and the data obtained are to some extent virtual. Four dimensions (4D) flow magnetic resonance imaging (MRI) is a new non-invasive, contrast-free imaging technique that can truly reflect the status of intravascular blood flow and retrospectively analyze the aortic hemodynamic information to dynamically evaluate the abnormal blood flow status in the aorta for early intervention. This article summarizes the current status and limitations of 4D flow MRI-derived WSS in aortic disease, aiming to provide new insights into the clinical management of aortic disease and its complications.

2. 4D Flow MRI-derived WSS Imaging Technology and Post-processing Software

Currently, Siemens, Philips and GE MRI vendors are able to perform 4D Flow MRI acquisitions, and the WSS obtained from two consecutive 4D Flow scans on the same magnetic resonance (MR) scanner has good consistency and reproducibility [9, 10, 11, 12]. However, the quantitative values of WSS obtained by different MR vendors have not been standardized [13]. In addition, there was variability in WSS values between 1.5 T and 3.0 T from the same MR supplier [14, 15].

Efficient post-processing software is essential for the quantification and visualization of hemodynamic parameters in both scientific research and clinical applications. The example of 4D flow MRI–based visualization of aortic hemodynamics is shown in Fig. 1. Current post-processing software includes CAAS 5.1 (Pie Medical Imaging, Maastricht, Limburg, the Netherlands), CVI42 6.0.2 (Circle Cardiovascular Imaging, Calgary, Alberta, Canada), GT Flow 3.1.14 (GyroTools, Zurich, Switzerland), iT Flow 1.9 (Cardio Flow Design Inc., Chiyoda-ku, Tokyo, Japan) and MEVISFlow 10.3 (Fraunhofer MEVIS, Bremen, Germany). In addition, some researchers have developed advanced flow analysis parameters using MATLAB R2022b (MathWorks Inc., Natick, MA, USA) or other programming languages to visualize the advanced flow data using post-processing tools in the field of fluid dynamics, such as Ensight and Paraview. It is important to note that there are significant differences in WSS quantitative reference values derived from different post-processing software [16]. These discrepancies may be related to variations in background phase offset corrections, contour splitting, and software algorithms.

Fig. 1.

4D flow magnetic resonance imaging (MRI)–based visualization of aortic hemodynamics in a healthy volunteer. (A) 4D-flow-Image streamlines for the aorta. (B) 4D-flow-Image wall shear stress for the aorta. The color gradient change reflects the magnitude of velocity and wall shear stress (WSS). Red and blue are the maximum and minimum values, respectively. 4D, four dimensions.

Limitations: The lack of uniformity in WSS measurement limits its clinical application. However, it has been suggested that aortic remodeling can be predicted by differentiating between areas of high and low WSS [17]. In the future, standardization of scanning protocols and uniformity of post-processing methods are needed before 4D Flow can be introduced into routine clinical applications.

3. 4D Flow MRI-derived WSS Clinical Applications

In recent years, 4D Flow MRI-derived WSS is a hemodynamic parameter highly relevant to aortic disease. It plays a significant role in the occurrence, development, risk stratification, and surgical evaluation of aortic diseases such as aortic aneurysm, aortic dissection, aortic atherosclerosis, bicuspid aortic valve, and Marfan syndrome (Table 1, Ref. [12, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59]).

Table 1. Research status of the application of 4D Flow MRI-derived WSS in aortic diseases.
Type of disease Author Date published Research Research Finding
Aneurysm Natsume et al. [26] 2017 16 aortic arch aneurysms, 8 young healthy volunteers and age-matched control subjects Aneurysm geometry affects WSS distribution
Jamaleddin Mousavi et al. [21] 2021 2 ATAA, 2 healthy subjects Computational modeling coupling hemodynamics with mechanobiology as a promising approach for exploring aneurysm progression
Ramaekers et al. [20] 2021 25 TAA, 22 controls Asymmetrically distributed peak WSS values in TAA
Salmasi et al. [24] 2021 10 ATAA Elevated WSS values associated with aortic wall degradation in ATAA disease
Trenti et al. [18] 2022 18 AAA, 22 age-matched controls, 23 young subjects RRT as a marker for abnormal AAA hemodynamics
Aalbregt et al. [12] 2024 22 asymptomatic AAA A 4D flow MRI is robust for assessing the hemodynamics within AAAs
Bouaou et al. [19] 2024 17 ATAA, 17 healthy controls, 13 younger healthy subjects Flow and pressure indices associated with WSS
Zeng et al. [25] 2024 11 TAAA, 19 AAA, 21 controls Lower WSS in TAAA
Dissection Veger et al. [28] 2021 A porcine aorta dissection model Strict heart rate control is of major importance in reducing the mean and peak WSS in uncomplicated acute TBAD
Ruiz-Muñoz et al. [27] 2022 54 Patients with chronic AD WSS positively correlated with aortic growth rate
Stokes et al. [29] 2023 A 56-year-old male patient with chronic TBAD Oscillatory shear is highly sensitive to inlet velocity distribution and flow volume
Atherosclerosis Harloff et al. [30] 2010 62 aortic atherosclerosis, 31 healthy volunteers 4D flow MRI was successfully used to analyze multiplanar WSS distribution
Markl et al. [33] 2013 70 patients with complex plaques, 12 healthy volunteers Decreased WSS and increased OSI in patients with atherosclerosis
Winter et al. [31] 2021 5 wildtype and 5 ApoE mice A new post processing method with 4D flow MRI
Andelovic et al. [32] 2021 6 healthy wildtype and 6 atherosclerotic ApoE mice WSScirc as potential marker of plaque size and composition in advanced atherosclerosis
Bicuspid aortic valve Barker et al. [43] 2012 15 BAV, 45 controls Increased and asymmetric WSS according to BAV fusion pattern
Meierhofer et al. [36] 2013 18 BAV, 18 healthy individuals Increased WSS in healthy BAV individuals
van Ooij et al. [35] 2015 13 BAV, 10 controls Elevated WSS correlated with peak systolic velocity
Guzzardi et al. [22] 2015 20 BAV Regions of increased WSS show greater medial elastin degradation
Shan et al. [41] 2017 50 BAV, 15 TAV Severe aortic insufficiency or stenosis resulted in further elevated WSS
van Ooij et al. [45] 2017 270 BAV, 245 TAV with aortic dilatation, 56 healthy subjects Increased WSS in BAV and TAV with AS
Rodríguez-Palomares et al. [44] 2018 101 BAV, 20 healthy subjects Different BAV-phenotypes present different flow patterns
Farag et al. [40] 2018 48 BAV, 25 healthy individuals Increased WSS in BAV patients with AS
Bollache et al. [37] 2018 27 BAV Increased aortic valve-mediated WSS associated with elastic fiber thinning
Soulat et al. [38] 2022 72 BAV, 136 controls WSS correlated with AAO dilation
Guala et al. [23] 2022 47 BAV Circumferential WSS predict progressive dilation of the ascending aorta in patients with BAV
Minderhoud et al. [39] 2022 32 BAV, 28 healthy controls WSS angle associated with aortic growth
Trenti et al. [42] 2024 42 BAV, 22 normal controls Elevated OSI in BAV with aortic regurgitation
Maroun et al. [34] 2024 20 BAV, 125 controls The long-term stability of 4D flow MRI-derived WSS and WSS-derived heatmaps
Aortic valve replacement von Knobelsdorff-Brenkenhoff et al. [49] 2014 38 AVR, 9 healthy controls AVR types affect WSS
Trauzeddel et al. [53] 2016 17 TAVI, 12 AVR, 9 healthy controls Increased WSS after TAVI and AVR compared to healthy controls
van Kesteren et al. [50] 2018 14 stented and 14 stentless bioprosthesis Lower WSS for stentless prosthesis
Bissell et al. [51] 2018 30 AVR, 30 patients with a native aortic valve, 30 healthy subjects. Decreased WSS after mechanical AVR or Ross procedures
Bollache et al. [47] 2018 33 patients received operation, 20 control patients did not Proximal aortic WSS decreased after AVR
Farag et al. [52] 2019 14 post-TAVR patients and 10 healthy controls Increased WSS in the ascending aorta after TAVR
Komoriyama et al. [48] 2021 32 Pre-TAVR and post-TAVR patients TAVR improves blood flow dynamics
Wiesemann et al. [46] 2023 7 patients received an AVR, 13 control patients did not Decreased WSS compared to patients who were not operated on
Marfan syndrome Geiger et al. [54] 2013 24 MFS, 12 older healthy volunteers Higher WSS at the inner curvature in the proximal AAO and at the anterior part in the more distal AAO
Wang et al. [57] 2016 20 MFS and 12 age-matched normal subjects Lower WSSaxial in the aortic root and the WSScirc in the arch
van der Palen et al. [58] 2017 25 MFS, 21 healthy controls Lower WSS in pediatric MFS patients
Geiger et al. [55] 2017 19 adolescent MFS, 10 healthy volunteers Lower WSS in the inner proximal DAO in a 3-year follow-up
Guala et al. [59] 2019 75 Marfan, 48 healthy subjects Abnormal circumferential WSS in Marfan patients
van Andel et al. [56] 2022 55 MFS, 25 healthy subjects Deviant directed WSS in the DAO was more frequently seen in male patients and in patients with a HI mutation type

ATAA, ascending thoracic aortic aneurysm; TAA, thoracic aortic aneurysm; AAA, abdominal aortic aneurysm; RRT, relative residence time; TAAA, thoracoabdominal aortic aneurysm; TBAD, type B aortic dissection; AD, aortic dissection; OSI, oscillatory shear stress; ApoE, apolipoprotein E-deficient; WSScirc, circumferential WSS; BAV, bicuspid aortic valve; TAV, tricuspid aortic valve; AS, aortic valve stenosis; AAO, ascending aorta; AVR, aortic valve replacement; TAVR, transcatheter aortic valve replacement; MFS, Marfan syndrome; WSSaxial, axial WSS; DAO, descending aorta; HI, haploinsufficient.

Additionally, some scholars have derived the oscillatory shear index (OSI) based on WSS [60, 61], which indicates the degree of directional change of WSS during a cardiac cycle [62, 63]. A high OSI implies significant directional changes in WSS, reflecting large shear stress fluctuation. Another study introduced relative residence time (RRT), a parameter based on the values of WSS and OSI [18]. RRT can identify areas with low WSS and high OSI, which are prone to aortic diseases such as plaque formation. Therefore, high RRT can be used to locate high-risk areas [18, 64].

3.1 Aortic Aneurysm

Risk stratification of aortic aneurysms is a prominent and challenging research topic, with increasing attention being paid to the influence of hemodynamics on aneurysms [19, 20, 21]. WSS is closely related to aneurysm formation, growth, and rupture, and it changes continuously during aneurysm progression.

A series of histopathological studies have revealed that high WSS leads to dysregulation of the extracellular matrix and degeneration of elastic fibers, resulting in thinning of the arterial wall, promoting aneurysm formation [22, 65, 66]. A study utilizing 4D Flow MRI has reached similar conclusions, showing that elevated WSS is strongly associated with an increased rate of aortic diameter growth. In particular, high circumferential WSS may be an independent predictor of aneurysm formation [23].

During aneurysm evolution, there are morphological and hemodynamic differences between aneurysms with different WSS, and both high and low WSS potentially contributing to aneurysm growth and rupture [67, 68]. Salmasi et al. [24] assessed the relationship between preoperative 4D Flow MRI images and postoperative tissue specimen characteristics in patients with ascending aortic aneurysms, finding that areas of high WSS were associated with aortic wall thinning, elastin abundance, and decreased smooth muscle cell counts. This suggests that degradation and thinning of the aneurysm wall are associated with hemodynamic impairment and high WSS (Fig. 2). Conversely, low WSS leads to inflammatory cell-mediated endothelial injury and apoptosis, with low and oscillating WSS areas being prone to plaque formation. This results in large, thick-walled aneurysms due to the combination of the inflammatory response and plaque buildup [69].

Fig. 2.

A patient with descending aortic aneurysm. (A) 4D-flow-Image with streamlines demonstrates low velocity inside the thoracic aortic aneurysm (blue arrow) and high velocity around the aneurysm (red arrow). (B) 4D-flow-Image demonstrates high WSS inside the thoracic aortic aneurysm (blue arrow).

Aortic aneurysms often exhibit vortex or helical flow, with lesion areas showing low WSS and high OSI [25, 26, 60, 61]. These abnormal hemodynamics tend to promote aortic atherosclerosis, which in turn leads to progressive aortic dilatation and increases the risk of aneurysm rupture. Additionally, it has been found that RRT seems to be a more powerful predictor of hemodynamic changes in aortic aneurysms than the commonly used OSI [18], as it accounts for both the magnitude and direction of WSS.

3.2 Aortic Dissection

Aortic dissection is one of the common types of acute aortic syndrome (AAS) with rapid onset and high mortality. Early screening for the potential risk of aortic dissection in high-risk groups would facilitate clinical preventive measures and reduce patient mortality. Fig. 3 shows aortic dissection evaluated by imaging modalities. Research has found that the area of highest WSS is highly coincident with the location of the tear in stanford type A aortic dissection [70]. This suggests that increased WSS may be an important factor in endovascular injury. Patients with stanford type B aortic dissection can be treated medically or surgically based on clinical assessment, and real-time monitoring of the dynamic evolution of the aortic dissection is mandatory. Increased aortic diameter and partial thrombosis of the false lumen are associated with late adverse events in type B aortic dissection [71, 72]. WSS may be a good indicator for monitoring these changes. On the one hand, WSS is positively correlated with the aortic growth rate [27], which could be used as a predictor of the distant expansion of aortic dissection. On the other hand, low WSS, high RRT, flow patterns are correlated with thrombosis [73]. There is increasing evidence to indicate that 4D flow MRI-based hemodynamics plays an important role in aortic dissection management and prognosis [27, 28, 29, 74].

Fig. 3.

A patient with stanford type B aortic dissection. (A) 2D sagittal view, showing true and false lumen as well as entry tear (blue arrow). (B) 3D VR displays true lumen, false lumen. (C) 4D-flow-Image with streamlines demonstrates high velocity at the entry tear (red arrow). (D) 4D-flow-Image demonstrates high WSS at the entry tear (red arrow). 2D, two dimensions; 3D, three dimensions; VR, volume rendering.

3.3 Aortic Atherosclerosis

WSS is one of the most important hemodynamic parameters in the formation and progression of atherosclerosis. Previous studies have demonstrated that persistent abnormal WSS can cause pathophysiological changes such as vascular remodeling, cell death, extracellular matrix degradation, and pro-inflammatory responses, which can promote plaque formation [75, 76, 77]. 4D Flow MRI provides a powerful tool for monitoring the distribution of aortic WSS in patients with atherosclerosis, allowing measurement of vessel wall parameters in the region of interest from any direction and angle [30, 31]. Circumferential WSS may be an important parameter in the noninvasive assessment of atherosclerotic plaque characteristics, correlating with plaque size, macrophage content, calcification, and necrotic core area [32], suggesting that abnormal circumferential WSS is critical for plaque growth and progression towards vulnerability. A study [33] analyzing 140 complex plaque locations using 4D Flow MRI found that aortic branches, bifurcations, or bends near the aorta are susceptible to disturbed and flocculated flow, generating areas of low and oscillating WSS, which are common areas of plaque formation. 4D Flow MRI-based study confirms that low WSS and high OSI promote the occurrence and development of atherosclerotic plaque [78, 79].

The rupture of atherosclerotic plaques can lead to vascular obstruction and trigger serious adverse consequences. High WSS increases metalloproteinase activity, accelerates angiogenesis and transformation, thereby enhancing plaque vulnerability and inducing plaque rupture [80, 81]. There are few studies applying 4D Flow to predict aortic plaque rupture. In a study of carotid plaques, high-risk plaques were found to have higher WSS, which proved that high WSS might be related to plaque rupture and more likely to cause cerebrovascular events [82].

3.4 Bicuspid Aortic Valve

The bicuspid aortic valve (BAV) is a common malformation of the aortic valve, occurring most often in males. 4D Flow MRI-derived WSS has demonstrated great potential for hemodynamic measurements in patients with BAV [34, 35]. Even in patients with normal BAV, the ascending aorta shows elevated WSS [36]. Areas with increased WSS are prone to aortic extracellular matrix dysregulation and elastic fiber thinning, which are associated with subsequent aortic disease [22, 37]. A prospective longitudinal study [23] found that elevated circumferential WSS predicted the growth rate of ascending aortic diameter in patients with BAV and may be a marker for the risk of ascending aortic dilatation. Other studies have confirmed the relationship between high WSS and aortic growth [38, 39]. BAV can be associated with valvular dysfunction, with elevated WSS observed in cases of aortic stenosis [40, 41] and elevated OSI observed in cases of aortic regurgitation [42].

Hemodynamic changes are also associated with the BAV valve fusion phenotype [43]. Right-left bicuspid aortic valve (RL-BAV) patients present a higher axial WSS at the aortic root while right-non coronary bicuspid aortic valve (RN-BAV) present a higher circumferential WSS in the mid and distal ascending aorta (AAO) [44]. However, moderate-to-severe aortic stenosis blurs the difference in WSS between these valve types, as the presence of aortic stenosis dominates ascending aortic hemodynamics irrespective of the valve fusion phenotype [41, 45].

3.5 Aortic Valve Replacement

Aortic valve replacement (AVR) significantly improves symptoms, quality of life, and prolongs survival in patients with aortic stenosis. A 4D Flow MRI-based study found improved aortic hemodynamics and reduced WSS after AVR compared with preoperative patients with aortic disease [46, 47, 48]. Different types of AVR present different hemodynamic changes post-surgery [49, 50]. Bissell et al. [51] compared the mechanical parameters of blood flow in 30 patients with BAV who underwent AVR using different surgical modalities and found that the aorta returned to a normal flow pattern in patients after mechanical valve replacement or the Ross procedure. However, higher WSS and abnormal spiral flow persisted in patients after bioprosthetic AVR. Transcatheter aortic valve replacement (TAVR) is an effective alternative to surgical aortic valve replacement (SAVR) for elderly and high-risk patients with aortic stenosis [83]. Ascending aortic WSS was increased and asymmetrically distributed after TAVR compared to healthy controls [52, 53].

3.6 Marfan Syndrome

Marfan syndrome (MFS) is a hereditary connective tissue disorder in which aortic complications are the main cause of death, including aortic dissection and aortic aneurysm rupture. Early prediction of the development of aortic complications in patients with Marfan syndrome by hemodynamic parameters is of great significance. Local helix flow patterns in the ascending aorta and proximal descending aorta were confirmed in a study of adolescent MFS patients using 4D Flow MRI [84]. This resulted in a heterogeneous regional WSS distribution, with elevated WSS in the proximal inner curvature of the ascending aorta [54] and decreased segmental WSS in the inner proximal descending aorta [55]. At follow-up after 3 years, WSS was reduced in the inner proximal descending aorta, which may be related to the risk of aortic dissection [55, 56]. Some scholars have disagreed, suggesting that proximal WSS in the ascending aorta is reduced, hypothesizing that the inconsistent results are due to the fact that young MFS patients exhibit higher WSS [57, 58]. In addition, both circumferential and axial WSS of the proximal descending aorta are independently correlated with local lumen diameter, and decreased circumferential WSS may be one of the early markers of descending aortic dilatation in patients with Marfan syndrome [59]. Patients with MFS need to be monitored for a long period of time, and in the future, 4D Flow MRI could be added as part of regular observations, which may help clinicians to predict the occurrence of MFS complications at an early stage.

4. Shortcomings and Prospects

Currently, 4D flow MRI technology still has many shortcomings and is mainly used for small-sample studies. First of all, 4D flow MRI scanning time is long, but the clinical environment still needs shorter imaging time, and image resolution is relatively low, which makes it difficult to accurately recognize aortic complex anatomies and cases, and at the same time affects the accuracy of WSS parameter values. In the future, we need to improve the K-space sampling, compression perception technology and deep learning to shorten the scanning time and enhance the spatial and temporal resolution. Second, the variability in parameters obtained from different post-processing vendors makes it difficult to establish a unified normal reference value for WSS. Therefore, developing and establishing a standardized workflow is crucial. Third, research based on 4D Flow MRI-derived WSS in aortic disease is limited. There is a need for more and larger prospective cohorts to explore how this technology could be integrated into existing clinical workflows and its expected impact on patient management and treatment outcomes.

5. Conclusions

In conclusion, 4D flow MRI-derived WSS is a promising tool for assessing the occurrence and development, risk stratification, and surgical efficacy of aortic disease and its complications.

Author Contributions

YL and XLM contributed to the design and implementation of the article, data collection and article writing. YXW and ZX contributed to the literature search and figure production. YS led the research team, provided critical guidance on the study design and methodology, and ensured the scientific rigor of the work. YS was responsible for finalizing the manuscript, managing all aspects of the publication process. All authors contributed to editorial changes in the manuscript. All authors read and approved the final manuscript. All authors have participated sufficiently in the work and agreed to be accountable for all aspects of the work.

Ethics Approval and Consent to Participate

Not applicable.

Acknowledgment

Not applicable.

Funding

This research received no external funding.

Conflict of Interest

The authors declare no conflict of interest.

References
[1]
Isselbacher EM, Preventza O, Hamilton Black J, 3rd, Augoustides JG, Beck AW, Bolen MA, et al. 2022 ACC/AHA Guideline for the Diagnosis and Management of Aortic Disease: A Report of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines. Circulation. 2022; 146: e334–e482. https://doi.org/10.1161/CIR.0000000000001106.
[2]
Dominguez A, Iruela-Arispe ML. Integration of Chemo-mechanical signaling in response to fluid shear stress by the endothelium. Current Opinion in Cell Biology. 2023; 85: 102232. https://doi.org/10.1016/j.ceb.2023.102232.
[3]
Heo KS, Fujiwara K, Abe JI. Shear stress and atherosclerosis. Molecules and Cells. 2014; 37: 435–440. https://doi.org/10.14348/molcells.2014.0078.
[4]
Davies PF. Hemodynamic shear stress and the endothelium in cardiovascular pathophysiology. Nature Clinical Practice. Cardiovascular Medicine. 2009; 6: 16–26. https://doi.org/10.1038/ncpcardio1397.
[5]
Zhou HL, Jiang XZ, Ventikos Y. Role of blood flow in endothelial functionality: a review. Frontiers in Cell and Developmental Biology. 2023; 11: 1259280. https://doi.org/10.3389/fcell.2023.1259280.
[6]
Kwak BR, Bäck M, Bochaton-Piallat ML, Caligiuri G, Daemen MJAP, Davies PF, et al. Biomechanical factors in atherosclerosis: mechanisms and clinical implications. European Heart Journal. 2014; 35: 3013–3013–20, 3020a–3020d. https://doi.org/10.1093/eurheartj/ehu353.
[7]
Pan S. Molecular mechanisms responsible for the atheroprotective effects of laminar shear stress. Antioxidants & Redox Signaling. 2009; 11: 1669–1682. https://doi.org/10.1089/ars.2009.2487.
[8]
Urschel K, Tauchi M, Achenbach S, Dietel B. Investigation of Wall Shear Stress in Cardiovascular Research and in Clinical Practice-From Bench to Bedside. International Journal of Molecular Sciences. 2021; 22: 5635. https://doi.org/10.3390/ijms22115635.
[9]
van der Palen RLF, Roest AAW, van den Boogaard PJ, de Roos A, Blom NA, Westenberg JJM. Scan-rescan reproducibility of segmental aortic wall shear stress as assessed by phase-specific segmentation with 4D flow MRI in healthy volunteers. Magma (New York, N.Y.). 2018; 31: 653–663. https://doi.org/10.1007/s10334-018-0688-6.
[10]
Markl M, Wallis W, Harloff A. Reproducibility of flow and wall shear stress analysis using flow-sensitive four-dimensional MRI. Journal of Magnetic Resonance Imaging: JMRI. 2011; 33: 988–994. https://doi.org/10.1002/jmri.22519.
[11]
van Ooij P, Powell AL, Potters WV, Carr JC, Markl M, Barker AJ. Reproducibility and interobserver variability of systolic blood flow velocity and 3D wall shear stress derived from 4D flow MRI in the healthy aorta. Journal of Magnetic Resonance Imaging: JMRI. 2016; 43: 236–248. https://doi.org/10.1002/jmri.24959.
[12]
Aalbregt E, Indrakusuma R, Jalalzadeh H, Planken RN, van Schuppen J, Meijboom L, et al. Four-Dimensional Flow MRI-Derived Hemodynamics in Abdominal Aortic Aneurysms: Reproducibility and Associations With Diameter, Intraluminal Thrombus Volume, and Vorticity. Journal of Magnetic Resonance Imaging: JMRI. 2024; 60: 878–888. https://doi.org/10.1002/jmri.29138.
[13]
Demir A, Wiesemann S, Erley J, Schmitter S, Trauzeddel RF, Pieske B, et al. Traveling Volunteers: A Multi-Vendor, Multi-Center Study on Reproducibility and Comparability of 4D Flow Derived Aortic Hemodynamics in Cardiovascular Magnetic Resonance. Journal of Magnetic Resonance Imaging: JMRI. 2022; 55: 211–222. https://doi.org/10.1002/jmri.27804.
[14]
Punzo B, Ranieri B, Tramontano L, Affinito O, Franzese M, Bossone E, et al. 4D-Flow Cardiovascular Magnetic Resonance Sequence for Aortic Assessment: Multi-Vendor and Multi-Magnetic Field Reproducibility in Healthy Volunteers. Journal of Clinical Medicine. 2023; 12: 2960. https://doi.org/10.3390/jcm12082960.
[15]
Strecker C, Harloff A, Wallis W, Markl M. Flow-sensitive 4D MRI of the thoracic aorta: comparison of image quality, quantitative flow, and wall parameters at 1.5 T and 3 T. Journal of Magnetic Resonance Imaging: JMRI. 2012; 36: 1097–1103. https://doi.org/10.1002/jmri.23735.
[16]
Oechtering TH, Nowak A, Sieren MM, Stroth AM, Kirschke N, Wegner F, et al. Repeatability and reproducibility of various 4D Flow MRI postprocessing software programs in a multi-software and multi-vendor cross-over comparison study. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2023; 25: 22. https://doi.org/10.1186/s12968-023-00921-4.
[17]
Ramaekers MJFG, Westenberg JJM, Adriaans BP, Nijssen EC, Wildberger JE, Lamb HJ, et al. A clinician’s guide to understanding aortic 4D flow MRI. Insights into Imaging. 2023; 14: 114. https://doi.org/10.1186/s13244-023-01458-x.
[18]
Trenti C, Ziegler M, Bjarnegård N, Ebbers T, Lindenberger M, Dyverfeldt P. Wall shear stress and relative residence time as potential risk factors for abdominal aortic aneurysms in males: a 4D flow cardiovascular magnetic resonance case-control study. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2022; 24: 18. https://doi.org/10.1186/s12968-022-00848-2.
[19]
Bouaou K, Dietenbeck T, Soulat G, Bargiotas I, Houriez-Gombaud-Saintonge S, De Cesare A, et al. Four-dimensional flow cardiovascular magnetic resonance aortic cross-sectional pressure changes and their associations with flow patterns in health and ascending thoracic aortic aneurysm. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2024; 26: 101030. https://doi.org/10.1016/j.jocmr.2024.101030.
[20]
Ramaekers MJFG, Adriaans BP, Juffermans JF, van Assen HC, Bekkers SCAM, Scholte AJHA, et al. Characterization of Ascending Aortic Flow in Patients With Degenerative Aneurysms: A 4D Flow Magnetic Resonance Study. Investigative Radiology. 2021; 56: 494–500. https://doi.org/10.1097/RLI.0000000000000768.
[21]
Jamaleddin Mousavi S, Jayendiran R, Farzaneh S, Campisi S, Viallon M, Croisille P, et al. Coupling hemodynamics with mechanobiology in patient-specific computational models of ascending thoracic aortic aneurysms. Computer Methods and Programs in Biomedicine. 2021; 205: 106107. https://doi.org/10.1016/j.cmpb.2021.106107.
[22]
Guzzardi DG, Barker AJ, van Ooij P, Malaisrie SC, Puthumana JJ, Belke DD, et al. Valve-Related Hemodynamics Mediate Human Bicuspid Aortopathy: Insights From Wall Shear Stress Mapping. Journal of the American College of Cardiology. 2015; 66: 892–900. https://doi.org/10.1016/j.jacc.2015.06.1310.
[23]
Guala A, Dux-Santoy L, Teixido-Tura G, Ruiz-Muñoz A, Galian-Gay L, Servato ML, et al. Wall Shear Stress Predicts Aortic Dilation in Patients With Bicuspid Aortic Valve. JACC. Cardiovascular Imaging. 2022; 15: 46–56. https://doi.org/10.1016/j.jcmg.2021.09.023.
[24]
Salmasi MY, Pirola S, Sasidharan S, Fisichella SM, Redaelli A, Jarral OA, et al. High Wall Shear Stress can Predict Wall Degradation in Ascending Aortic Aneurysms: An Integrated Biomechanics Study. Frontiers in Bioengineering and Biotechnology. 2021; 9: 750656. https://doi.org/10.3389/fbioe.2021.750656.
[25]
Zeng W, Wang J, Weng C, Peng W, Wang T, Yuan D, et al. Assessment of aortic hemodynamics in patients with thoracoabdominal aortic aneurysm using four-dimensional magnetic resonance imaging: a cross-sectional study. Quantitative Imaging in Medicine and Surgery. 2024; 14: 2800–2815. https://doi.org/10.21037/qims-23-1321.
[26]
Natsume K, Shiiya N, Takehara Y, Sugiyama M, Satoh H, Yamashita K, et al. Characterizing saccular aortic arch aneurysms from the geometry-flow dynamics relationship. The Journal of Thoracic and Cardiovascular Surgery. 2017; 153: 1413–1420.e1. https://doi.org/10.1016/j.jtcvs.2016.11.032.
[27]
Ruiz-Muñoz A, Guala A, Dux-Santoy L, Teixidó-Turà G, Servato ML, Valente F, et al. False lumen rotational flow and aortic stiffness are associated with aortic growth rate in patients with chronic aortic dissection of the descending aorta: a 4D flow cardiovascular magnetic resonance study. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2022; 24: 20. https://doi.org/10.1186/s12968-022-00852-6.
[28]
Veger HTC, Pasveer EH, Westenberg JJM, Wever JJ, van Eps RGS. Wall Shear Stress Assessment of the False Lumen in Acute Type B Aortic Dissection Visualized by 4-Dimensional Flow Magnetic Resonance Imaging: An Ex-Vivo Study. Vascular and Endovascular Surgery. 2021; 55: 696–701. https://doi.org/10.1177/15385744211017117.
[29]
Stokes C, Ahmed D, Lind N, Haupt F, Becker D, Hamilton J, et al. Aneurysmal growth in type-B aortic dissection: assessing the impact of patient-specific inlet conditions on key haemodynamic indices. Journal of the Royal Society, Interface. 2023; 20: 20230281. https://doi.org/10.1098/rsif.2023.0281.
[30]
Harloff A, Nussbaumer A, Bauer S, Stalder AF, Frydrychowicz A, Weiller C, et al. In vivo assessment of wall shear stress in the atherosclerotic aorta using flow-sensitive 4D MRI. Magnetic Resonance in Medicine. 2010; 63: 1529–1536. https://doi.org/10.1002/mrm.22383.
[31]
Winter P, Andelovic K, Kampf T, Hansmann J, Jakob PM, Bauer WR, et al. Simultaneous measurements of 3D wall shear stress and pulse wave velocity in the murine aortic arch. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2021; 23: 34. https://doi.org/10.1186/s12968-021-00725-4.
[32]
Andelovic K, Winter P, Kampf T, Xu A, Jakob PM, Herold V, et al. 2D Projection Maps of WSS and OSI Reveal Distinct Spatiotemporal Changes in Hemodynamics in the Murine Aorta during Ageing and Atherosclerosis. Biomedicines. 2021; 9: 1856. https://doi.org/10.3390/biomedicines9121856.
[33]
Markl M, Brendecke SM, Simon J, Barker AJ, Weiller C, Harloff A. Co-registration of the distribution of wall shear stress and 140 complex plaques of the aorta. Magnetic Resonance Imaging. 2013; 31: 1156–1162. https://doi.org/10.1016/j.mri.2013.05.001.
[34]
Maroun A, Scott MB, Catania R, Berhane H, Jarvis K, Allen BD, et al. Multiyear Interval Changes in Aortic Wall Shear Stress in Patients with Bicuspid Aortic Valve Assessed by 4D Flow MRI. Journal of Magnetic Resonance Imaging: JMRI. 2024; 60: 2580–2589. https://doi.org/10.1002/jmri.29305.
[35]
van Ooij P, Potters WV, Collins J, Carr M, Carr J, Malaisrie SC, et al. Characterization of abnormal wall shear stress using 4D flow MRI in human bicuspid aortopathy. Annals of Biomedical Engineering. 2015; 43: 1385–1397. https://doi.org/10.1007/s10439-014-1092-7.
[36]
Meierhofer C, Schneider EP, Lyko C, Hutter A, Martinoff S, Markl M, et al. Wall shear stress and flow patterns in the ascending aorta in patients with bicuspid aortic valves differ significantly from tricuspid aortic valves: a prospective study. European Heart Journal. Cardiovascular Imaging. 2013; 14: 797–804. https://doi.org/10.1093/ehjci/jes273.
[37]
Bollache E, Guzzardi DG, Sattari S, Olsen KE, Di Martino ES, Malaisrie SC, et al. Aortic valve-mediated wall shear stress is heterogeneous and predicts regional aortic elastic fiber thinning in bicuspid aortic valve-associated aortopathy. The Journal of Thoracic and Cardiovascular Surgery. 2018; 156: 2112–2120.e2. https://doi.org/10.1016/j.jtcvs.2018.05.095.
[38]
Soulat G, Scott MB, Allen BD, Avery R, Bonow RO, Malaisrie SC, et al. Association of Regional Wall Shear Stress and Progressive Ascending Aorta Dilation in Bicuspid Aortic Valve. JACC. Cardiovascular Imaging. 2022; 15: 33–42. https://doi.org/10.1016/j.jcmg.2021.06.020.
[39]
Minderhoud SCS, Roos-Hesselink JW, Chelu RG, Bons LR, van den Hoven AT, Korteland SA, et al. Wall shear stress angle is associated with aortic growth in bicuspid aortic valve patients. European Heart Journal. Cardiovascular Imaging. 2022; 23: 1680–1689. https://doi.org/10.1093/ehjci/jeab290.
[40]
Farag ES, van Ooij P, Planken RN, Dukker KCP, de Heer F, Bouma BJ, et al. Aortic valve stenosis and aortic diameters determine the extent of increased wall shear stress in bicuspid aortic valve disease. Journal of Magnetic Resonance Imaging: JMRI. 2018; 48: 522–530. https://doi.org/10.1002/jmri.25956.
[41]
Shan Y, Li J, Wang Y, Wu B, Barker AJ, Markl M, et al. Aortic shear stress in patients with bicuspid aortic valve with stenosis and insufficiency. The Journal of Thoracic and Cardiovascular Surgery. 2017; 153: 1263–1272.e1. https://doi.org/10.1016/j.jtcvs.2016.12.059.
[42]
Trenti C, Fedak PWM, White JA, Garcia J, Dyverfeldt P. Oscillatory shear stress is elevated in patients with bicuspid aortic valve and aortic regurgitation: a 4D flow cardiovascular magnetic resonance cross-sectional study. European Heart Journal. Cardiovascular Imaging. 2024; 25: 404–412. https://doi.org/10.1093/ehjci/jead283.
[43]
Barker AJ, Markl M, Bürk J, Lorenz R, Bock J, Bauer S, et al. Bicuspid aortic valve is associated with altered wall shear stress in the ascending aorta. Circulation. Cardiovascular Imaging. 2012; 5: 457–466. https://doi.org/10.1161/CIRCIMAGING.112.973370.
[44]
Rodríguez-Palomares JF, Dux-Santoy L, Guala A, Kale R, Maldonado G, Teixidó-Turà G, et al. Aortic flow patterns and wall shear stress maps by 4D-flow cardiovascular magnetic resonance in the assessment of aortic dilatation in bicuspid aortic valve disease. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2018; 20: 28. https://doi.org/10.1186/s12968-018-0451-1.
[45]
van Ooij P, Markl M, Collins JD, Carr JC, Rigsby C, Bonow RO, et al. Aortic Valve Stenosis Alters Expression of Regional Aortic Wall Shear Stress: New Insights From a 4-Dimensional Flow Magnetic Resonance Imaging Study of 571 Subjects. Journal of the American Heart Association. 2017; 6: e005959. https://doi.org/10.1161/JAHA.117.005959.
[46]
Wiesemann S, Trauzeddel RF, Musa A, Hickstein R, Mayr T, von Knobelsdorff-Brenkenhoff F, et al. Changes of aortic hemodynamics after aortic valve replacement-A four dimensional flow cardiovascular magnetic resonance follow up study. Frontiers in Cardiovascular Medicine. 2023; 10: 1071643. https://doi.org/10.3389/fcvm.2023.1071643.
[47]
Bollache E, Fedak PWM, van Ooij P, Rahman O, Malaisrie SC, McCarthy PM, et al. Perioperative evaluation of regional aortic wall shear stress patterns in patients undergoing aortic valve and/or proximal thoracic aortic replacement. The Journal of Thoracic and Cardiovascular Surgery. 2018; 155: 2277–2286.e2. https://doi.org/10.1016/j.jtcvs.2017.11.007.
[48]
Komoriyama H, Kamiya K, Nagai T, Oyama-Manabe N, Tsuneta S, Kobayashi Y, et al. Blood flow dynamics with four-dimensional flow cardiovascular magnetic resonance in patients with aortic stenosis before and after transcatheter aortic valve replacement. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2021; 23: 81. https://doi.org/10.1186/s12968-021-00771-y.
[49]
von Knobelsdorff-Brenkenhoff F, Trauzeddel RF, Barker AJ, Gruettner H, Markl M, Schulz-Menger J. Blood flow characteristics in the ascending aorta after aortic valve replacement–a pilot study using 4D-flow MRI. International Journal of Cardiology. 2014; 170: 426–433. https://doi.org/10.1016/j.ijcard.2013.11.034.
[50]
van Kesteren F, Wollersheim LW, Baan J, Jr, Nederveen AJ, Kaya A, Boekholdt SM, et al. Four-dimensional flow MRI of stented versus stentless aortic valve bioprostheses. European Radiology. 2018; 28: 257–264. https://doi.org/10.1007/s00330-017-4953-2.
[51]
Bissell MM, Loudon M, Hess AT, Stoll V, Orchard E, Neubauer S, et al. Differential flow improvements after valve replacements in bicuspid aortic valve disease: a cardiovascular magnetic resonance assessment. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2018; 20: 10. https://doi.org/10.1186/s12968-018-0431-5.
[52]
Farag ES, Vendrik J, van Ooij P, Poortvliet QL, van Kesteren F, Wollersheim LW, et al. Transcatheter aortic valve replacement alters ascending aortic blood flow and wall shear stress patterns: A 4D flow MRI comparison with age-matched, elderly controls. European Radiology. 2019; 29: 1444–1451. https://doi.org/10.1007/s00330-018-5672-z.
[53]
Trauzeddel RF, Löbe U, Barker AJ, Gelsinger C, Butter C, Markl M, et al. Blood flow characteristics in the ascending aorta after TAVI compared to surgical aortic valve replacement. The International Journal of Cardiovascular Imaging. 2016; 32: 461–467. https://doi.org/10.1007/s10554-015-0792-x.
[54]
Geiger J, Arnold R, Herzer L, Hirtler D, Stankovic Z, Russe M, et al. Aortic wall shear stress in Marfan syndrome. Magnetic Resonance in Medicine. 2013; 70: 1137–1144. https://doi.org/10.1002/mrm.24562.
[55]
Geiger J, Hirtler D, Gottfried K, Rahman O, Bollache E, Barker AJ, et al. Longitudinal Evaluation of Aortic Hemodynamics in Marfan Syndrome: New Insights from a 4D Flow Cardiovascular Magnetic Resonance Multi-Year Follow-Up Study. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2017; 19: 33. https://doi.org/10.1186/s12968-017-0347-5.
[56]
van Andel MM, van Ooij P, de Waard V, Gottwald LM, van Kimmenade RRJ, Scholte AJ, et al. Abnormal aortic hemodynamics are associated with risk factors for aortic complications in patients with marfan syndrome. International Journal of Cardiology. Heart & Vasculature. 2022; 43: 101128. https://doi.org/10.1016/j.ijcha.2022.101128.
[57]
Wang HH, Chiu HH, Tseng WYI, Peng HH. Does altered aortic flow in marfan syndrome relate to aortic root dilatation? Journal of Magnetic Resonance Imaging: JMRI. 2016; 44: 500–508. https://doi.org/10.1002/jmri.25174.
[58]
van der Palen RLF, Barker AJ, Bollache E, Garcia J, Rose MJ, van Ooij P, et al. Altered aortic 3D hemodynamics and geometry in pediatric Marfan syndrome patients. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2017; 19: 30. https://doi.org/10.1186/s12968-017-0345-7.
[59]
Guala A, Teixido-Tura G, Dux-Santoy L, Granato C, Ruiz-Muñoz A, Valente F, et al. Decreased rotational flow and circumferential wall shear stress as early markers of descending aorta dilation in Marfan syndrome: a 4D flow CMR study. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2019; 21: 63. https://doi.org/10.1186/s12968-019-0572-1.
[60]
Takehara Y, Isoda H, Takahashi M, Unno N, Shiiya N, Ushio T, et al. Abnormal Flow Dynamics Result in Low Wall Shear Stress and High Oscillatory Shear Index in Abdominal Aortic Dilatation: Initial in vivo Assessment with 4D-flow MRI. Magnetic Resonance in Medical Sciences: MRMS: an Official Journal of Japan Society of Magnetic Resonance in Medicine. 2020; 19: 235–246. https://doi.org/10.2463/mrms.mp.2019-0188.
[61]
Bürk J, Blanke P, Stankovic Z, Barker A, Russe M, Geiger J, et al. Evaluation of 3D blood flow patterns and wall shear stress in the normal and dilated thoracic aorta using flow-sensitive 4D CMR. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2012; 14: 84. https://doi.org/10.1186/1532-429X-14-84.
[62]
He X, Ku DN. Pulsatile flow in the human left coronary artery bifurcation: average conditions. Journal of Biomechanical Engineering. 1996; 118: 74–82. https://doi.org/10.1115/1.2795948.
[63]
Zhang JM, Chua LP, Ghista DN, Yu SCM, Tan YS. Numerical investigation and identification of susceptible sites of atherosclerotic lesion formation in a complete coronary artery bypass model. Medical & Biological Engineering & Computing. 2008; 46: 689–699. https://doi.org/10.1007/s11517-008-0320-4.
[64]
Himburg HA, Grzybowski DM, Hazel AL, LaMack JA, Li XM, Friedman MH. Spatial comparison between wall shear stress measures and porcine arterial endothelial permeability. American Journal of Physiology. Heart and Circulatory Physiology. 2004; 286: H1916–H1922. https://doi.org/10.1152/ajpheart.00897.2003.
[65]
Koseki H, Miyata H, Shimo S, Ohno N, Mifune K, Shimano K, et al. Two Diverse Hemodynamic Forces, a Mechanical Stretch and a High Wall Shear Stress, Determine Intracranial Aneurysm Formation. Translational Stroke Research. 2020; 11: 80–92. https://doi.org/10.1007/s12975-019-0690-y.
[66]
Meng H, Wang Z, Hoi Y, Gao L, Metaxa E, Swartz DD, et al. Complex hemodynamics at the apex of an arterial bifurcation induces vascular remodeling resembling cerebral aneurysm initiation. Stroke. 2007; 38: 1924–1931. https://doi.org/10.1161/STROKEAHA.106.481234.
[67]
Staarmann B, Smith M, Prestigiacomo CJ. Shear stress and aneurysms: a review. Neurosurgical Focus. 2019; 47: E2. https://doi.org/10.3171/2019.4.FOCUS19225.
[68]
Meng H, Tutino VM, Xiang J, Siddiqui A. High WSS or low WSS? Complex interactions of hemodynamics with intracranial aneurysm initiation, growth, and rupture: toward a unifying hypothesis. AJNR. American Journal of Neuroradiology. 2014; 35: 1254–1262. https://doi.org/10.3174/ajnr.A3558.
[69]
Takehara Y. Clinical Application of 4D Flow MR Imaging for the Abdominal Aorta. Magnetic Resonance in Medical Sciences: MRMS: an Official Journal of Japan Society of Magnetic Resonance in Medicine. 2022; 21: 354–364. https://doi.org/10.2463/mrms.rev.2021-0156.
[70]
Chi Q, He Y, Luan Y, Qin K, Mu L. Numerical analysis of wall shear stress in ascending aorta before tearing in type A aortic dissection. Computers in Biology and Medicine. 2017; 89: 236–247. https://doi.org/10.1016/j.compbiomed.2017.07.029.
[71]
Higashigaito K, Sailer AM, van Kuijk SMJ, Willemink MJ, Hahn LD, Hastie TJ, et al. Aortic growth and development of partial false lumen thrombosis are associated with late adverse events in type B aortic dissection. The Journal of Thoracic and Cardiovascular Surgery. 2021; 161: 1184–1190.e2. https://doi.org/10.1016/j.jtcvs.2019.10.074.
[72]
Tsai TT, Evangelista A, Nienaber CA, Myrmel T, Meinhardt G, Cooper JV, et al. Partial thrombosis of the false lumen in patients with acute type B aortic dissection. The New England Journal of Medicine. 2007; 357: 349–359. https://doi.org/10.1056/NEJMoa063232.
[73]
Cheng Z, Riga C, Chan J, Hamady M, Wood NB, Cheshire NJW, et al. Initial findings and potential applicability of computational simulation of the aorta in acute type B dissection. Journal of Vascular Surgery. 2013; 57: 35S–43S. https://doi.org/10.1016/j.jvs.2012.07.061.
[74]
Sherrah AG, Callaghan FM, Puranik R, Jeremy RW, Bannon PG, Vallely MP, et al. Multi-Velocity Encoding Four-Dimensional Flow Magnetic Resonance Imaging in the Assessment of Chronic Aortic Dissection. Aorta (Stamford, Conn.). 2017; 5: 80–90. https://doi.org/10.12945/j.aorta.2017.16.046.
[75]
Malek AM, Alper SL, Izumo S. Hemodynamic shear stress and its role in atherosclerosis. JAMA. 1999; 282: 2035–2042. https://doi.org/10.1001/jama.282.21.2035.
[76]
Chiu JJ, Chien S. Effects of disturbed flow on vascular endothelium: pathophysiological basis and clinical perspectives. Physiological Reviews. 2011; 91: 327–387. https://doi.org/10.1152/physrev.00047.2009.
[77]
Weinberg PD. Haemodynamic Wall Shear Stress, Endothelial Permeability and Atherosclerosis-A Triad of Controversy. Frontiers in Bioengineering and Biotechnology. 2022; 10: 836680. https://doi.org/10.3389/fbioe.2022.836680.
[78]
Strecker C, Krafft AJ, Kaufhold L, Hüllebrandt M, Weber S, Ludwig U, et al. Carotid geometry is an independent predictor of wall thickness - a 3D cardiovascular magnetic resonance study in patients with high cardiovascular risk. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance. 2020; 22: 67. https://doi.org/10.1186/s12968-020-00657-5.
[79]
Strecker C, Krafft AJ, Kaufhold L, Hüllebrandt M, Treppner M, Ludwig U, et al. Carotid Geometry and Wall Shear Stress Independently Predict Increased Wall Thickness-A Longitudinal 3D MRI Study in High-Risk Patients. Frontiers in Cardiovascular Medicine. 2021; 8: 723860. https://doi.org/10.3389/fcvm.2021.723860.
[80]
Eshtehardi P, Brown AJ, Bhargava A, Costopoulos C, Hung OY, Corban MT, et al. High wall shear stress and high-risk plaque: an emerging concept. The International Journal of Cardiovascular Imaging. 2017; 33: 1089–1099. https://doi.org/10.1007/s10554-016-1055-1.
[81]
Kojima K, Hiro T, Koyama Y, Ohgaku A, Fujito H, Ebuchi Y, et al. High Wall Shear Stress Is Related to Atherosclerotic Plaque Rupture in the Aortic Arch of Patients with Cardiovascular Disease: A Study with Computational Fluid Dynamics Model and Non-Obstructive General Angioscopy. Journal of Atherosclerosis and Thrombosis. 2021; 28: 742–753. https://doi.org/10.5551/jat.56598.
[82]
Zhang G, Zhang S, Qin Y, Fang J, Tang X, Li L, et al. Differences in Wall Shear Stress Between High-Risk and Low-Risk Plaques in Patients With Moderate Carotid Artery Stenosis: A 4D Flow MRI Study. Frontiers in Neuroscience. 2021; 15: 678358. https://doi.org/10.3389/fnins.2021.678358.
[83]
Vahanian A, Beyersdorf F, Praz F, Milojevic M, Baldus S, Bauersachs J, et al. 2021 ESC/EACTS Guidelines for the management of valvular heart disease. European Heart Journal. 2022; 43: 561–632. https://doi.org/10.1093/eurheartj/ehab395.
[84]
Geiger J, Markl M, Herzer L, Hirtler D, Loeffelbein F, Stiller B, et al. Aortic flow patterns in patients with Marfan syndrome assessed by flow-sensitive four-dimensional MRI. Journal of Magnetic Resonance Imaging: JMRI. 2012; 35: 594–600. https://doi.org/10.1002/jmri.23500.

Publisher’s Note: IMR Press stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share
Back to top