Bicuspid aortic valve
|Bicuspid aortic valve|
|Classification and external resources|
A bicuspid aortic valve (BAV) is most commonly a congenital condition of the aortic valve where two of the aortic valvular leaflets fuse during development resulting in a valve that is bicuspid instead of the normal tricuspid configuration. Normally the only cardiac valve that is bicuspid is the mitral valve (bicuspid valve) which is situated between the left atrium and left ventricle. Cardiac valves play a crucial role in ensuring the unidirectional flow of blood from the atrium to the ventricles, or the ventricle to the aorta or pulmonary trunk.
Bicuspid aortic valves are the most common cardiac valvular anomaly, occurring in 1–2% of the general population. It is twice as common in males as in females.
Bicuspid aortic valve is a heritable condition, with a demonstrated association with Notch 1. Its heritability () is as high as 89%. Both familial clustering and isolated valve defects have been documented. The incidence of bicuspid aortic valve can be as high as 10% in families affected with the valve problem. Recent studies suggest that BAV is an autosomal dominant condition with incomplete penetrance. Other congenital heart defects are associated with bicuspid aortic valve at various frequencies, including coarctation of the aorta.
Bicuspid aortic valves may assume three different types of configuration:
- "Real" bicuspid valves with two symmetric leaflets
- A tricuspid architecture with a fusion of two leaflets
- A tricuspid architecture with a fusion of three leaflets
In many cases, a bicuspid aortic valve will cause no problems. However BAV may become calcified later in life, which may lead to varying degrees of severity of aortic stenosis that will manifest as murmurs. If the leaflets do not close correctly, aortic regurgitation can occur. If these become severe enough, they may require heart surgery. People with BAV may become tired more easily than those with normal valvular function and have difficulty maintaining stamina for cardio-intensive activities-due to poor heart performance. The heart is put under more stress in order to either pump more blood through a stenotic valve or attempt to circulate regurgitation blood through a leaking valve.
Diagnosis, treatment, and prognosis
The condition can be associated with a heart murmur located at the right second intercostal space. Often there will be differences in blood pressures between upper and lower extremities. The diagnosis can be assisted with echocardiography (EchoCG) or magnetic resonance imaging (MRI). Four-dimensional magnetic resonance imaging (4D MRI) is a technique that defines blood flow characteristics and patterns throughout the vessels, across valves, and in compartments of the heart. Four-dimensional imaging enables accurate visualizations of blood flow patterns in a three-dimensional (3D) spatial volume, as well as in a fourth temporal dimension. Current 4D MRI systems produces high-resolution images of blood flow in just a single scan session.
Bicuspid Aortic Valve Morphology
Fusion of aortic valve leaflets occurs most commonly (≈80%) between the right coronary and left coronary leaflets (RL), which are the anterior leaflets of the aortic valve. Fusion also occurs between the right coronary and noncoronary leaflets (RN, ≈17%), and least commonly between the noncoronary and left coronary leaflets (≈2%). In comparison to other fusion patterns, RN leaflet fusion has a stronger association with future complications such as aortic valve regurgitation and stenosis. However, all fusion patterns associate with a specific area or areas of dilated enlargement in either the root of the ascending aorta, ascending aorta, or transverse aortic arch.
Identifying hemodynamic patterns in the aorta after left ventricle systole aids in predicting consequential complications of bicuspid aortic valve. The patient-specific risk of developing complications such as aortic aneurysms is dependent on the particular aortic leaflet fusion pattern, with each pattern varying in 4D MRI measurements of wall shear stress (WSS), blood flow velocity, asymmetrical flow displacement and flow angle of the aorta.
BAV outflow is helical and occurs at high velocities (>1 m/s) throughout the ascending aorta. This is potentially more damaging to the aorta in comparison to the streamline flow and short-lived burst of high velocity at the beginning of the aorta, as seen within a healthy tricuspid valve. This eccentric outflow from the BAV results in blood hitting and reflecting off the aortic wall in a non-streamline fashion. The specific zones where blood hits is dependent on the varying BAV leaflet fusion patterns and consequently correlates with increases in WSS. WSS measurements in RL fusion indicate an increase in pressure applied predominantly to the right-anterior side of the vessel wall, while RN fusion increases WSS on the right-posterior wall. The resulting rise in WSS is supported by the asymmetrical displacement of blood flow produced by an increased angle of outflow from the BAV. Displacement is measured as the distance in millimeters from the center of the aorta to the center of the high velocity outflow. Blood does not flow centrally through the aorta in BAV, but along the right-anterior and right-posterior vessel wall for RL and RN leaflet fusion respectively.
Identification of hemodynamics for RL, RN, and left coronary and noncoronary leaflet fusion patterns enables detection of specific aortic regions susceptible to dysfunction and the eventual development of disease. Specifically, RL and RN fusion patterns are more likely to develop into these aortic disease states. The blood flow information associated with RL fusion causes dilation of the mid-ascending aorta, while RN fusion is associated with dilation in the root, distal ascending aorta and transverse arch. BAV helical and high velocity outflow patterns are consistent with aortic dilation hemodynamics seen in those with tricuspid aortic valves. However, it is the increase and variance in WSS and flow displacement in BAV that demonstrate the importance of aortic leaflet morphology. Flow displacement measurements taken from 4D MRI may be best for detecting irregularities in hemodynamics. Displacement measurements were highly sensitive and distinguishable between different valve morphologies. Hemodynamic measurements from 4D MRI in patients with BAV are advantageous in determining the timing and location of repair surgery to the aorta in aortopathy states.
Most patients with bicuspid aortic valve whose valve becomes dysfunctional will need careful follow-up and potentially valve replacement at some point in life. Regular EchoCG and MRI may be performed. For diagnosed patients, genetic testing is done to allow for future offspring with the disease to be monitored and treated early in life.
Patients with bicuspid aortic valve should be followed by a cardiologist or cardiac surgeon with specific interest in this valve pathology.
If the valve is normally functioning or minimally dysfunctional, average lifespan is similar to that of those without the anomaly.
One of the most notable associations with BAV is the tendency for these patients to present with ascending aortic aneurysmal lesions. The extracellular matrix of the aorta in patients with BAV shows marked deviations from that of the normal tricuspid aortic valve. It is currently believed that an increase in the ratio of MMP2 (Matrix Metalloproteinases 2) to TIMP1 (Tissue Inhibitor Metalloproteinases 1) may be responsible for the abnormal degradation of the valve matrix and therefore lead to aortic dissection and aneurysm. However, other studies have also shown MMP9 involvement with no differences in TIMP expression. The size of the proximal aorta should be evaluated carefully during the work-up. The initial diameter of the aorta should be noted and annual evaluation with CT scan, or MRI to avoid ionizing radiation, should be recommended to the patient; the examination should be conducted more frequently if a change in aortic diameter is seen. From this monitoring, the type of surgery that should be offered to the patient can be determined based on the change in size of the aorta.
Co-arctation of the aorta (a congenital narrowing in the region of the ductus arteriosus) has also been associated with BAV.
- Tzemos N, Therrien J, Yip J et al. (September 2008). "Outcomes in adults with bicuspid aortic valves". JAMA 300 (11): 1317–25. doi:10.1001/jama.300.11.1317. PMID 18799444.
- Garg V; Muth AN; Ransom JF et al. (2005). "Mutations in NOTCH1 cause aortic valve disease". Nature 437 (7056): 270–274. Bibcode:2005Natur.437..270G. doi:10.1038/nature03940. PMID 16025100.
- Cripe L, Andelfinger G, Martin LJ, Shooner K, Benson DW (July 2004). "Bicuspid aortic valve is heritable". Journal of the American College of Cardiology 44 (1): 138–43. doi:10.1016/j.jacc.2004.03.050. PMID 15234422.
- Blackbourne, Lorne H.; Chhabra, Anikar, eds. (2002). "Congenital Heart Disease". Pathology Recall. Lippincott Williams & Wilkins. pp. 247–9. ISBN 978-0-7817-3406-6.
- Kumme, Anja (2007). Klassifikation bikuspider Aortenklappen. OCLC 254078723.[page needed]
- "Atrial Septal Defect". Commonly Asked Questions About Children and Heart Disease. October 29, 2012. Retrieved April 9, 2014.
- Mahadevia R, Barker AJ, Schnell S et al. (February 2014). "Bicuspid aortic cusp fusion morphology alters aortic three-dimensional outflow patterns, wall shear stress, and expression of aortopathy". Circulation 129 (6): 673–82. doi:10.1161/CIRCULATIONAHA.113.003026. PMID 24345403.
- Markl M, Chan FP, Alley MT et al. (April 2003). "Time-resolved three-dimensional phase-contrast MRI". Journal of Magnetic Resonance Imaging 17 (4): 499–506. doi:10.1002/jmri.10272. PMID 12655592.
- Bissell MM, Hess AT, Biasiolli L et al. (July 2013). "Aortic dilation in bicuspid aortic valve disease: flow pattern is a major contributor and differs with valve fusion type". Circulation. Cardiovascular Imaging 6 (4): 499–507. doi:10.1161/CIRCIMAGING.113.000528. PMC 3859916. PMID 23771987.
- Weigang E, Kari FA, Beyersdorf F et al. (July 2008). "Flow-sensitive four-dimensional magnetic resonance imaging: flow patterns in ascending aortic aneurysms". European Journal of Cardio-thoracic Surgery 34 (1): 11–6. doi:10.1016/j.ejcts.2008.03.047. PMID 18515137.
- Hope MD, Hope TA, Meadows AK et al. (April 2010). "Bicuspid aortic valve: four-dimensional MR evaluation of ascending aortic systolic flow patterns". Radiology 255 (1): 53–61. doi:10.1148/radiol.09091437. PMID 20308444.
- Fernandes SM, Sanders SP, Khairy P et al. (October 2004). "Morphology of bicuspid aortic valve in children and adolescents". Journal of the American College of Cardiology 44 (8): 1648–51. doi:10.1016/j.jacc.2004.05.063. PMID 15489098.
- Barker AJ, Lanning C, Shandas R (March 2010). "Quantification of hemodynamic wall shear stress in patients with bicuspid aortic valve using phase-contrast MRI". Annals of Biomedical Engineering 38 (3): 788–800. doi:10.1007/s10439-009-9854-3. PMC 2872988. PMID 19953319.
- Michelena HI, Desjardins VA, Avierinos JF et al. (May 2008). "Natural history of asymptomatic patients with normally functioning or minimally dysfunctional bicuspid aortic valve in the community". Circulation 117 (21): 2776–84. doi:10.1161/CIRCULATIONAHA.107.740878. PMC 2878133. PMID 18506017.
- Rison SC, Locke TP, Rosenthal E, Gandhi S (2012). "A man with hypertension and two murmurs". BMJ 344: e956. doi:10.1136/bmj.e956. PMID 22337753.
- Bicuspid Aortic Foundation Homepage
- Cedars Sinai Heart Center - Bicuspid Aortic Disease
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