Aortic wall shear stress in bicuspid aortic valve disease—10-year follow-up
Highlight box
Key findings
• After a ten years’ follow-up of patients with isolated BAV disease, WSS decreased whilst indexed aortic diameters did not change in this patient cohort.
What is known and what is new?
• BAV disease may lead to aortic dilation, complex helical flow patterns and increased WSS, especially in the mid-ascending aorta.
• 4D flow CMR has been established as a valid imaging modality for flow visualization and WSS estimation.
• WSS reduction might be explained by slight alterations in hemodynamic flow patterns by the aging aorta as distensibility decreased and stiffness index increased both more than 20% after ten years.
What is the implication, and what should change now?
• Possibly a drop of WSS in BAV could serve as a marker for a benign long-term course and implementation of more conservative treatment strategies.
Introduction
Bicuspid aortic valve (BAV) disease is the most prevalent congenital heart defect, affecting 0.77% to 2% of the general population (1,2). It describes the fusion of two aortic cusps during valvulogenesis leading to an aortic valve consisting of two instead of three leaflets (3). The fusion of the right and left coronary cusp is the most common morphotype (RL-type) followed by RN-type (fusion of the right and noncoronary cusp) and LN-type (fusion of the left and noncoronary cusp) (4). Frequent complications of this malformation are valvular dysfunction, aortic stenosis (AS) as well as aortic regurgitation (AR) (5) and changes in hemodynamics, leading to complex helical flow patterns (6). Clinically relevant wall alterations may occur, especially in the mid-ascending aorta (AAo), such as dilation, aneurysm formation and dissection (7,8). However, the still unknown origin of these pathologies led to two conflicting theories: the genetic theory is based on a connective tissue disorder named “Erdheim’s cystic medial necrosis” (9) which leads to inborn wall weakness, also explaining the association of BAV with further congenital vascular defects, such as coarctation of the aorta (CoA) or patent ductus arteriosus (1). In contrast, the hemodynamic theory describes a BAV, which in itself is causing flow alterations, which affect the vessel wall, and leads to the development of an aortopathy (10).
Besides aortic diameter, several parameters like wall shear stress (WSS), aortic distensibility, aortic stiffness and flow displacement were established in recent years for quantification of disease severity and prediction of outcome (11,12). For assessment of these parameters, a combination of non-invasive techniques such as echocardiography (13) and cardiovascular magnetic resonance (CMR) is required. Based on CMR, 4D flow has been established as a valid imaging modality offering the possibility for direct, in vivo evaluation of vascular anatomy and cardiac function (14,15). It is applied for flow visualization and WSS estimation (16,17). Due to the gap in longitudinal studies in BAV disease, the aim of this study was to evaluate the diagnostic value of hemodynamic parameters such as flow patterns, distensibility and WSS in BAV but without further cardiovascular disease collecting ten-year follow-up data in the same patient cohort as in 2008/2009 using 4D flow CMR. We present the following article in accordance with the TREND reporting checklist (available at https://cdt.amegroups.com/article/view/10.21037/cdt-22-477/rc).
Methods
Study population
A specific patient cohort consisting of fifteen patients with congenital BAV previously evaluated in 2008/2009 were included for reevaluation, performed between October 2018 and September 2019 at a third level cardiac center. The patients were all contacted for this follow-up study. Among this patient group we could also reevaluate a child which was only aged 10 years at that time. In 2008/2009 originally 18 patients with BAV were included, 3 patients (17%) were lost during follow-up due to non-availability of contact data. Before CMR, all subjects underwent clinical examination including physical examination, 12-lead electrocardiography (ECG) and echocardiographic survey of valvular function. Exclusion criteria were equal as in 2008/2009: congenital heart disease other than BAV, aortic dissection, previous myocardial infarction or cardiovascular surgery, connective tissue disorders, hypertension, maximal flow velocity through the aortic valve (Vmax) of >2.9 m/s and contraindications for CMR imaging. All patients met the inclusion criteria. Patients with moderate or severe aortic valve stenosis or regurgitation were excluded from the initial study. The study was approved by the ethics committee of the Technical University of Munich (No. 29/18S) and all patients gave written informed consent. No participant received financial support. The trial was conducted in accordance with the Declaration of Helsinki (as revised in 2013).
CMR
All CMR scans in 2008/2009 and 2018/2019 were performed on the same 1.5 Tesla MRI system (MAGNETOM Avanto®, software version VD13, Siemens Healthineers, Erlangen, Germany) with a 12-channel body-coil. Re-assessment of aortic valve morphotype and measurement of aortic diameters and planimetric area for distensibility calculation were performed using an ECG-gated time-resolved (2D CINE) steady state free precession (SSFP) sequence over multiple cardiac timeframes during breath hold (slice thickness 6 mm, acquisition matrix 192×192, 25 phases/cardiac cycle). Measurements of aortic diameter and planimetric area were performed in double-oblique, cross-sectional orientation to the aortic root axis by choosing adequate slices representing the maximal aortic diameter at peak systole and end-diastole. Further, aortic blood flow patterns were evaluated using a time-resolved three-dimensional (3D) phase-contrast (PC) sequence with three-directional velocity encoding (4D flow CMR) with prospective gating. A sagittal oblique plane orientation for image acquisition provides 3D volumetric coverage of the entire aorta [from left ventricular outflow tract to the thoracic descending aorta (DAo)]. ECG-synchronization and respiratory navigator-gating were performed. Prospective gating was used due to sequence architecture, since same scanner and the same sequence parameters were set as in the initial study in 2008/2009. No contrast agent was used. Measurement parameters were: isotropic voxel size with a spatial resolution of 2.5×2.5×2.5 mm3, TE 2.44 ms, TR 39.2 ms, FOV 240×320 mm, FOV phase 75%, velocity encoding Vx, Vy, Vz 200–320 cm/s, flip angle 8°, band width 440 Hz/pixel. Image acquisition is displayed in Figure 1.
Aortic valve morphotype
Aortic valve morphotype was classified as previously described by Schaefer et al.: BAV type 1 describing the congenital fusion of the right and left coronary cusp, BAV type 2 as fusion of the right and noncoronary cusp and BAV type 3 as fusion of the left and noncoronary cusp (4).
Calculation of distensibility and stiffness index
By using Microsoft Excel software tool (Microsoft Corporation, 2018, Redmond, WA, USA) calculation of distensibility according to a previously described formula was performed:
where Amax = maximal systolic area (mm2), Amin = minimal diastolic area (mm2), Psys = systolic blood pressure (mmHg) and Pdia = diastolic blood pressure (mmHg) (18). Aortic stiffness index (SI) was calculated according to Nistri et al.:
with Dmax describing the maximal systolic aortic diameter and Dmin describing the minimal diastolic aortic diameter (19).
Data preprocessing
The generated 4D flow data sets were imported in DICOM format to the current software MEVISFlow (MEVISFlow; Fraunhofer Institute for Digital Medicine, software version 11.4, Bremen, Germany) for further editing. Data sets from 2008/2009, previously analyzed with EnSight® software package (EnSight®; CEI, Apex, NC, USA) and software tool based on Matlab (The MathWorks, Natick, MA, USA), were also reevaluated by software MEVISFlow using the same parameter settings. Vascular enhancement and suppression of background signal was performed applying noise filtering, eddy-current correction and anti-aliasing as presented by Walker et al. (20). After pre-processing, the squared sum of the 3D-PC images provided a time-averaged 3D phase-contrast MR angiography (PC-MRA) for watershed-based 3D segmentation of the complete thoracic aorta, also performed with MEVISFlow. By adjusting the threshold at eddy-current correction (optimum 0.023±0.003), manual correction of 3D segmentations could be reduced to a minimum. The workflow of data preprocessing is pictured in Figure 1.
Flow visualization and WSS estimation
By manually contouring the aortic vessel wall on reformatted cross-sectional magnitude image planes at a single temporal frame in systolic phase, we defined our regions of interest (ROI), displaying important anatomical landmarks (mid-ascending aorta at the level of bifurcation of the main pulmonary artery (MPA level) and at the level just before the branching of the brachiocephalic trunk (BCT level) (Figure 1). An automated algorithm further propagated the contour to all other temporal frames, but in a few cases manual correction was necessary to account for motion of the aorta and the most precise vessel lumen boundary definition as possible (21). 4D flow visualization in the mid-ascending aorta was performed using pathline tracing (22) (Figure 1). Flow was classified according to a grading scale previously described by Meierhofer et al., where Grade 0 was defined as linear flow and Grade 1–3 as helical flow (Grade 1: <180°, Grade 2: 180–360° and Grade 3: >360°) (6). WSS was calculated by separation of blood flow forces acting on the vessel wall into three vectors: axial WSS (WSSaxial) − parallel to flow direction; circumferential WSS (WSScirc) − in-plane, and magnitudinal WSS (WSSmag) as resulting net vector represents the entire aortic WSS (23) (Figure 1). WSS values were merged over a complete cardiac cycle for each vessel wall segment (Figure 1). CMR was operated by experienced investigators (MC, HM, BE and SN). Flow visualization and WSS estimation was performed by two investigators (HM and BE) both blinded to the findings in 2008/2009 and with more than 2 years of experience in post-processing.
Statistical analysis
Statistical analysis was performed using GraphPad Prism 9.02 statistical software. Data are presented as median and total range. Differences were analyzed using the Wilcoxon signed-rank test. Intra- and inter-observer variability concerning WSS were evaluated using Bland-Altman analysis of matched pairs analyzed by one investigator and two investigators, respectively. Correlation analyses were displayed by Spearman correlation coefficient r.
Results
Study population
The 10-year follow-up reevaluation (median follow-up 9.8 years, range 9.5 to 10.7 years) was successfully completed in fifteen asymptomatic patients (8 males; 53%), median age 34 years (range, 19.8 to 54.3 years), no one had to be excluded. Three patients of the original cohort of 18 patients (17%) were lost to follow-up due to non-availability of contact data. No adverse events or unintended effects occurred during the study. The echocardiographic survey revealed no pronounced valvular dysfunction. The velocity through the aortic valve was median 1.9 m/s (range 0.9 to 2.7 m/s). The regurgitation fraction was median 2.5% (range 0 to 13%). Eleven patients (73%) were identified as BAV type 1, the remaining 4 patients as BAV type 2, confirming the morphotypes of the aortic valve as evaluated in 2008/2009. The statistical analysis demonstrated good evidence of an important difference comparing 2008/2009 values with 2018/2019: weight (median difference 3 kg; range −3 to 25 kg; 95% CI: 1.9 to 9.7; P=0.005), body mass index (BMI) (median difference 1.63 kg/m2; range −1.91 to 5.73 kg/m2; 95% CI: 0.4 to 2.8; P=0.02), body surface area (BSA) (median difference 0.04 m2; range −0.04 to 0.49 m2; 95% CI: 0.02 to 0.2; P=0.004), diastolic blood pressure (median difference 2.5 mmHg; range −11 to 15 mmHg; 95% CI: 0.3 to 5.0; P=0.04), velocity through the aortic valve (median difference 0.3 m/s; range −1.4 to 0.8 m/s; 95% CI: −5.0 to 52.8; P=0.03) and absolute aortic diameter for AAo (median difference 0.3 cm; range −0.02 to 0.84 cm; 95 % CI: 0.25 to 0.54; P=0.009). The indexed aortic diameters in DAo and in the mid-ascending aorta did not change substantially, median difference 0.05 cm/m2 (range −0.1 to 0.5 cm/m2; 95% CI: 0.01 to 0.22; P=0.06) for AAo, median difference −0.08 cm/m2 (range −0.4 to 0.1 cm/m2; 95% CI: −0.12 to 0.01; P=0.07) for DAo. Values of the 10-year-old child are included in all analyses. Further baseline characteristics of the study population are displayed in Table 1. The three patients lost to follow-up are excluded in the column showing the data of 2008/2009.
Table 1
Characteristics | 2008/2009 (n=15) | 2018/2019 (n=15) | Median difference | 95% CI of median difference | P value | |||
---|---|---|---|---|---|---|---|---|
Median | Range | Median | Range | |||||
Age (years) | 24.5 | 10.1–43.6 | 34.0 | 19.8–54.3 | 9.5 | 9.8–10.3 | 0.004* | |
Height (cm) | 173 | 138–192 | 175 | 160–191 | 2.0 | −1.6 to 5.5 | 0.54 | |
Weight (kg) | 70.0 | 30.0–88.0 | 73.0 | 55.0–93.0 | 3.0 | 1.9–9.7 | 0.005* | |
BSA (m2) | 1.9 | 1.1–2.1 | 1.9 | 1.6–2.1 | 0 | 0.02–0.2 | 0.004* | |
BMI (kg/m2) | 22.8 | 15.8–28.1 | 24.4 | 20.8–30.4 | 1.6 | 0.4–2.8 | 0.02* | |
Psys (mmHg) | 110.5 | 92.0–128.0 | 112.0 | 111.0–130.0 | 1.5 | −1.4 to 4.0 | 0.33 | |
Pdia (mmHg) | 62.0 | 44.0–83.0 | 64.5 | 53.0–87.0 | 2.5 | 0.3–5.0 | 0.04* | |
MAP (mmHg) | 77.3 | 60.7–95.7 | 80.6 | 68.7–100.7 | 3.3 | −0.1 to 4.5 | 0.07 | |
Vmax (m/s) | 1.6 | 1.2–2.3 | 1.9 | 0.9–2.7 | 0.3 | −5.0 to 52.8 | 0.03* | |
Regurgitation fraction (%) | 1 | 0–6 | 2.5 | 0–13 | 1.5 | −0.6 to 3.3 | 0.16 | |
Absolute aortic diameter (cm) | ||||||||
AAo | 3.2 | 1.86–4.38 | 3.5 | 2.55–4.95 | 0.3 | 0.25–0.54 | 0.009* | |
DAo | 1.8 | 1.38–2.23 | 1.8 | 1.30–2.24 | 0 | −0.06 to 0.08 | 0.82 | |
Indexed aortic diameter (cm/m2) | ||||||||
AAo | 1.73 | 1.18–2.29 | 1.78 | 1.27–2.57 | 0.05 | 0.01–0.22 | 0.06 | |
DAo | 0.98 | 0.80–1.46 | 0.90 | 0.72–1.18 | −0.08 | −0.12 to 0.01 | 0.07 | |
Distensibility (10-3 mmHg−1) | ||||||||
AAo | 6.57 | 2.39–9.94 | 4.89 | 1.66–8.58 | −1.68 | −0.07 to 3.80 | 0.08 | |
DAo | 5.61 | 2.62–11.58 | 4.45 | 2.89–6.94 | −1.16 | −0.48 to 3.95 | 0.17 | |
Stiffness index | ||||||||
AAo | 4.12 | 2.50–5.86 | 5.09 | 2.95–13.39 | 0.97 | −4.83 to −0.13 | 0.02* | |
DAo | 3.99 | 2.91–6.69 | 4.89 | 3.66–8.15 | 0.90 | −3.02 to 0.33 | 0.17 | |
WSSaxial (N/m2) | ||||||||
MPA level | 0.45 | 0.29–0.74 | 0.28 | 0.22–0.51 | −0.17 | 0.1–0.21 | 0.001* | |
BCT level | 0.42 | 0.26–1.00 | 0.28 | 0.22–0.58 | −0.14 | 0.08–0.21 | 0.003* | |
WSScirc (N/m2) | ||||||||
MPA level | 0.50 | 0.23–0.71 | 0.24 | 0.19–0.43 | −0.16 | 0.15–0.29 | 0.001* | |
BCT level | 0.48 | 0.22–1.04 | 0.27 | 0.22–0.61 | −0.21 | 0.12–0.25 | 0.003* | |
WSSmag (N/m2) | ||||||||
MPA level | 0.75 | 0.40–1.15 | 0.43 | 0.34–0.75 | −0.32 | 0.2–0.4 | 0.001* | |
BCT level | 0.72 | 0.38–1.60 | 0.44 | 0.37–0.92 | −0.27 | 0.16–0.36 | 0.002* |
*, relevant changes after the follow-up period. BSA, body surface area; BMI, body mass index; Psys, systolic blood pressure; Pdia, diastolic blood pressure; MAP, mean arterial pressure; Vmax, maximal velocity through the aortic valve; AAo, (mid-) ascending aorta; DAo, descending aorta; BCT level, level before the branching of the brachiocephalic trunk; MPA level, level of bifurcation of the main pulmonary artery; WSS, wall shear stress; WSSaxial, axial WSS; WSScirc, circumferential WSS; WSSmag, magnitudinal WSS.
Aortic distensibility and stiffness index
On AAo level, distensibility decreased by 25.6% when simultaneously aortic stiffness index increased by 23.6%. Values on DAo level behave in the same manner: distensibility decreased by 20.7% whereas aortic stiffness index increased by 22.4%. Median values and ranges of distensibility and stiffness index are presented in Table 1.
Flow visualization and WSS estimation
All patients with BAV showed right-handed, helical flow patterns in the mid-ascending aorta. One patient (6.7%) was classified as Grade 0, 3 patients (20.0%) as Grade 2 and 11 patients (73.3%) as Grade 3 (Figure 2). All patients with BAV type 2 (4, 100%), but only 7 patients with BAV type 1 (63.6%) were categorized as Grade 3. Helical flow patterns increased by at least one grading level after the 10-year follow-up period in five patients (33.3%). Comparison of flow patterns are illustrated in Figure 3, exemplary in two patients.
WSS values are displayed in Table 1. WSSaxial, WSScirc and WSSmag are lower in 2018/2019 at the MPA level as well as at the BCT level compared to 2008/2009 (Figure 4) even in the above-mentioned patients with an increment in flow grading as well as comparing values of our youngest patient, which was a child back in 2008 (WSSmag decreased from 0.46 to 0.38 N/m2 at MPA level and from 0.63 to 0.41 N/m2 at BCT level). There were no relevant changes in all WSS directions on both aortic levels between BAV type 1 and BAV type 2. ROIs were placed at the identical levels as in the initial study, however we waived WSS measurement at the level of the aortic bulb due to weak resolution and therefore inadequate estimation of WSS since exact delineation of the aortic wall is crucial.
Intra- and inter-observer variability
Analysis showed good intra- and inter-observer variability: mean values of WSS were 0.35±0.10 and 0.34±0.11 N/m2 for the first and second measurement of one investigator (r=0.97) and 0.31±0.08 N/m2 (r=0.68) for the other investigator. Bland-Altman 95% limits of agreement were −0.03 to 0.05 N/m2 and −0.04 to 0.11 N/m2.
Discussion
In this prospectively designed study, we could show that indexed diameter of the ascending and descending aorta in patients with BAV did not increase substantially over a follow-up period of ten years. Based on strict and specific exclusion criteria, a well-described patient cohort was formed back in 2008/2009. Fortunately, we were able to reevaluate the same, particular patient collective, still lacking any further cardiovascular disease than BAV. WSS was essentially lower in all directions and at all measured levels in the aorta. In accordance with age, aortic distensibility decreased and stiffness index increased over the given period.
Studies have shown that aortic diameters in patients with BAV are larger than in controls, even with a normally functioning valve (8). Surgical interventions in BAV disease can prevent these patients from complications and provide an excellent outcome in terms of survival (24), but aortic dilation after valve replacement is still present (25). Accordingly, an individual approach for risk stratification is required. In the pre-selected patient cohort of this study, absolute aortic diameter in AAo slightly increased. Whilst comparing aortic diameters, confounders were limited by applying a relation to physical conditions of the patients. After indexing the aortic diameters on BSA, the values did not change in a 10-year follow-up period suggesting a potential benign long-term development and implementation of more conservative treatment strategies for the patients in our cohort study. Exact assessment of aortic size is under ongoing discussion in the literature, but though a height-based ratio seems to be sufficient, both correction for height as well as BSA improves prediction of complications (26,27). Semi-automatic assessment of aortic diameter may standardize measurements of aortic diameter (28).
Nevertheless, studies regarding outcome of BAV disease have revealed a higher prevalence for cardiac and vascular events compared to the general population (29). Besides aortic diameter, risk stratification includes severity of valvular dysfunction (30) or cardiovascular comorbidities such as CoA (31). The impact of flow alterations is also well demonstrated: helical flow patterns are present in BAV, especially in the mid-ascending aorta, including patients with concomitant aneurysm and aortic stenosis (AS) (32,33), creating “a higher friction of blood relative to the vessel wall with the consequence of increased WSS” (34). Several previous studies have shown, comparing BAV patients to subjects with normal, tricuspid valves (TAV), that WSS is clearly increased in patients with BAV compared to TAV (6,11,35). Especially circumferential WSS and progression of helicity seem to have an impact on aortic growth (36,37). Heterogeneous distribution of WSS leads to different affections of the vessel wall, including elastic fiber thinning (38) as well as intima-media thickening and plaque induction in initiation of atherosclerosis (39). A few studies reported different results, that may be explained by varying characteristics of patient collective, measured ROI and investigated primary disease (40-42).
However, in due consideration of valvular function, a differentiation within the spectrum of BAV disease is necessary: follow-up data of non- or mild stenotic and/or regurgitant, isolated BAVs and concomitant WSS already revealed an almost asymptomatic, progression-free disease development (43), with stable WSS values in childhood (44), starting to decrease at middle age (45). This latter study supports the hypothesis that compared to TAV with dilation, BAV patients demonstrated WSS reduction as a compensatory mechanism to reduce elevated WSS forces by aortic remodeling. These studies support our findings: WSS substantially decreased in all spatial vectors and measured levels in the ascending aorta in our patient cohort. Even regarding values of the child aged only 10 years back in 2008/2009, we found a reduction of WSS. It is most remarkable, that changes in aortic diameter are not responsible for this drop of WSS. Regarding valvular dysfunction, Farag et al. found significantly elevated values of WSS, correlating with the severity of aortic valve stenosis (46). Despite peak velocity through the aortic valve was higher in our study and in 5 patients (33.3%) helical flow patterns increased by at least one grading level after the 10-year follow-up period, absolute values do not indicate a moderate or severe level of stenosis, making any major impact on WSS reduction unlikely. Although comparison of cohorts may be contestable due to various variations in patient characteristics, the paradox of results needs to be addressed. Because rotational flow was assessed using a subjective method and therefore may be subject to minor deviations in reevaluation, a more objective assessment of circulation may be focus in future work when better software tools measuring helical flow are available.
WSS reduction might be explained by slight alterations in hemodynamic flow patterns by the aging aorta: in the ascending as well as descending part, distensibility decreased and stiffness index increased both more than 20% after ten years. In general, patients with BAV yet seem to exhibit altered elastic properties compared to normal controls, regardless of age (47). In addition, a positive correlation between age and stiffness suggests a continuous increase of stiffness over lifetime in BAV disease (48). Adjustment of distensibility to diameter may cause variation in changes of elastic properties and effects of valvular dysfunction have to be clarified (49,50), but our patients did not show any signs of disease progression. Numerical impairment of aortic elasticity may have led to changes in spatial and temporal distribution of helical flow. Slight alterations in flow direction, grade of rotation, angle to the vessel wall or intensity of helicity could have caused the decrease of WSS. It could serve as a marker for a benign long-term course, leading to prolonged intervals in serial reevaluation and a more conservative approach in therapy management.
Further studies are required for investigation of the impact of helical flow on WSS and the association between its severity and the development of aortopathy. Novel parameters may contribute to predict the outcome or even improve risk stratification: von Spiczak et al. described a quantitative analysis of vortical blood flow for visualization of pathological flow alterations (51), while Tiwari et al. successfully introduced so-called MRSD (maximal rate of systolic distension) and MRDR (maximal rate of diastolic recoil) for evaluation of biomechanical properties of the aorta (52). Future longitudinal studies should consider these parameters.
Limitations
Our study is a single-center study with a limited number of patients. Only adults, in 2008/2009 including one child, already pre-selected in 2008, especially concerning the absence of cardiac and vascular diseases further than BAV, were included [for information about initial recruitment refer to the previous study (6)]. Division into even smaller subgroups for comparison of different BAV morphologies is contestable, lacking statistical significance. Reevaluation of the exact same patient cohort as in 2008/2009 provides powerful long-term data, but results may not be interpreted as valid for the general population. Further longitudinal studies based on larger sample sizes are required.
Due to the study design, we were not aiming to gather histological specimens for the correlation of flow patterns and WSS with tissue alterations. Reevaluation of the reference group with TAV from the 2008/2009 study was also not included due to insufficient participation of former evaluated TAV volunteers. Future work could take these aspects into account.
Even though we were able to use the same CMR sequence as in 2008/2009, software version of the scanner changed over ten years. As software version VB15 was used for the initial study, reevaluation was performed with the current version VD13. By approximating software parameters as accurate as possible, confounders were set to a minimum.
To avoid a measurement bias in post-processing, all data of 2008/2009 were reevaluated with the software MEVISFlow. However, feasibility of flow visualization and measurement of WSS has been proven (21,53) and is not affected by ongoing upgrade processes of the used software.
Identifying the vessel lumen border and positioning of ROIs has to be re-adjusted manually in each case and therefore may be subject to minor deviations in WSS estimation in future possible reevaluations. Systematical underestimation of WSS due to limited spatial resolution or partial volume effect in PC-CMR is an already well-known side effect (23). Newly developed approaches such as an automated segmentation-free method for computing WSS might increase accuracy and reproducibility of assessment of hemodynamic parameters (54).
Conclusions
After a ten years’ follow-up period of patients with isolated BAV disease, indexed aortic diameters remained unchanged in the identical patient cohort. WSS was lower in all directions and at all measured aortic levels compared to values generated 10 years earlier. In accordance with a decreased aortic distensibility and an increased stiffness index, this might be explained by slight alterations in helical flow patterns by the aging aorta and due to remodeling. Possibly a drop in WSS in BAV could serve as a marker for a benign long-term course and implementation of more conservative treatment strategies in selected patients.
Acknowledgments
Funding: None.
Footnote
Provenance and Peer Review: This article was commissioned by the Guest Editors (Yskert von Kodolitsch, Harald Kaemmerer, Koichiro Niwa) for the series “Current Management Aspects in Adult Congenital Heart Disease (ACHD): Part V” published in Cardiovascular Diagnosis and Therapy. The article has undergone external peer review.
Reporting Checklist: The authors have completed the TREND reporting checklist. Available at https://cdt.amegroups.com/article/view/10.21037/cdt-22-477/rc
Data Sharing Statement: Available at https://cdt.amegroups.com/article/view/10.21037/cdt-22-477/dss
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://cdt.amegroups.com/article/view/10.21037/cdt-22-477/coif). The series “Current Management Aspects in Adult Congenital Heart Disease (ACHD): Part V” was commissioned by the editorial office without any funding or sponsorship. The authors have no other conflicts of interest to declare.
Ethical Statement:
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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