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|Year : 2008
: 1 | Issue : 2 | Page
|Role of beta-blockers in Marfan's syndrome and bicuspid aortic valve: A time for re-appraisal
Department of Pediatric Cardiology, Amrita Institute of Medical Sciences, Kochi, India
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Keywords: Marfan′s syndrome, aortic root dilatation, aneurysm
|How to cite this article:|
Vaidyanathan B. Role of beta-blockers in Marfan's syndrome and bicuspid aortic valve: A time for re-appraisal. Ann Pediatr Card 2008;1:149-52
|How to cite this URL:|
Vaidyanathan B. Role of beta-blockers in Marfan's syndrome and bicuspid aortic valve: A time for re-appraisal. Ann Pediatr Card [serial online] 2008 [cited 2019 Oct 21];1:149-52. Available from: http://www.annalspc.com/text.asp?2008/1/2/149/43885
| Introduction|| |
Marfan's syndrome is an autosomal dominant disorder with high penetrance having an incidence of 1 in 5000 live births.  It has heterogenous clinical presentation and the diagnosis is based on the Ghent's criteria. The recognized clinical features include tall stature, arachnodactyly, joint hypermobility, skeletal abnormalities, lens subluxation, and mitral valve prolapse. The genetic basis for Marfan's syndrome is a mutation in the fibrillin-1 gene, and till date about 600 different types of mutations in this gene have been reported. 
The major cause of morbidity and mortality in patients with Marfan's syndrome is related to aortic dilatation leading to aortic dissection or rupture and aortic valve regurgitation. This condition worsens with age and at the age of 30 years, men and women with Marfan's syndrome have an annual death risk of 2% and 1%, respectively - 20-40 times higher than normal population of the same age.  Seventy percent of the deaths in Marfan's syndrome can be directly attributed to acute cardiovascular complications, especially aortic dissection.  Hence, the most important target for improving survival in patients with Marfan's syndrome is to prevent or delay aortic dissection.
A review of clinical studies of medical treatment for Marfan's syndrome reveals that only three classes of drugs have been investigated - beta-blockers, angiotensin converting enzyme (ACE) inhibitors, and calcium channel blockers with primary focus being on beta-blockers.  The proposed mechanisms of benefit of beta-blockers in Marfan's syndrome include reduction in the rate of pressure increase in aorta (dP/dt) and reduction in heart rate, which reduces the number of systolic impulses in a given period.  To date, randomized control studies supporting this management approach has been limited, especially in children. The lacunae in our current knowledge about beta-blocker therapy in Marfan's syndrome include effects on reducing rate of aortic root dilatation, impact on clinical outcomes, and the timing to initiate therapy in patients who may have potential benefit with such therapy. The clinician will need to consider the potential side effects of such a long-term therapy in children, especially when the data supporting such treatment is not very robust.
Bicuspid aortic valve is perhaps the most common congenital heart disease occurring at a frequency of 1-2/1000 live births.  Several studies have shown the presence of an intrinsic aortic wall pathology in patients with bicuspid aortic valve characterized by abnormal distensibility and pulse wave velocity. , This impairs elasticity of the vessel wall leading to aortic dilatation. Studies have shown that Marfan's syndrome and bicuspid aortic valve have many histological and clinical similarities with respect to aortic dilatation and aortic complications like dissection.  Though, the effect of beta-blockers have been extensively studied in patients with Marfan's syndrome, there is no data regarding the use of beta-blockers in preventing aortic dilatation in patients with bicuspid aortic valve. Extending the data from Marfan's syndrome and considering the similarities in their pathology, it is intuitive to think that there could be potential benefit with such therapy.
This meta-analysis and e-mail survey of expert opinion attempts to clarify the issues involved in medical management of patients with Marfan's syndrome and bicuspid aortic valve with beta-blockers including effects on slowing aortic root dilatation and cardiovascular effects - death, aortic dissection, and surgery - and when to initiate therapy in patients who may potentially benefit from it.
| Review of Current Literature|| |
Role of beta-blockers in patients with Marfan's syndrome and bicuspid aortic valve
The first report describing a beneficial effect of beta-blockers in patients with Marfan's syndrome was published by Halpern et al., from Johns Hopkins university.  This small study in six adult patients showed that beta-blockers could slow the rate of aortic root dilatation in Marfan's syndrome through their negative inotropic and chronotropic effects. The landmark study showing the beneficial effect of beta-blockers on slowing the rate of aortic root dilatation was published by Shores et al., in 1994.  This open-label study conducted in 70 patients (adult and pediatric) reported lower incidence of clinical endpoints in patients treated with beta-blockers versus controls (16% vs. 24%). A recent study in children with Marfan's syndrome also reported decrease in the rate of aortic dilatation by a mean of 0.16 mm/year in patients treated with beta-blockers versus controls.  This study also reported a trend toward lower cardiac mortality, decreased need for preventive aortic surgery, and fewer dissections. However, a study by Tierney et al., in children reported that beta-blocker therapy does not significantly alter the rate of aortic root dilatation in children with Marfan's syndrome.  A recent meta-analysis also questioned the role of beta-blockers in the medical therapy of patients with Marfan's syndrome.  There is no data regarding the use of beta-blockers in patients with bicuspid aortic valve and aortic dilation.
Effect of beta-blockade on rate of aortic root dilatation and clinical endpoints
The randomized control study conducted by Shores et al., showed that the rate of enlargement of aorta in patients receiving treatment was less than one-third the rate of patients receiving no treatment (P < 0.001).  Also, clinical endpoints were fewer in treated patients (16% vs. 24%), and the study was underpowered to detect effect on mortality. In the study by Ladouceur et al.,  though the baseline aortic diameters were higher in patients treated with beta-blockers, there was significant slowing of the rate of aortic dilatation (0.16 mm/year) after commencement of beta-blocker therapy. More children required aortic surgery in the control group (6.4% vs. 2.6%), and of the four total deaths, three occurred in the control group. However, Tierney et al., reported no significant change in progression of aortic root dilatation between patients treated with beta-blockers versus controls, despite the fact that heart rate was significantly slower in those treated with beta-blockers.  A recent meta-analysis also concluded that there is no beneficial effect of beta-blocker therapy on aortic dilatation or clinical events in children with Marfan's syndrome.  The differential effects found in the various studies are probably related to variations in study design, the time of onset of therapy (diagnosis vs. onset of aortic dilatation), and different age groups studied.
When should beta-blocker therapy be initiated?
Most studies had left this decision to the discretion of the treating physician. Most of these decisions were made empirically. There is no clear consensus on whether treatment should be initiated as soon as the diagnosis of Marfan's syndrome is made or one can wait till significant aortic root dilatation has set in. No clear cut-off values of aortic root measurements have been suggested as an indication for starting the therapy. In one study, a greater proportion of treated patients had positive family history of Marfan's syndrome.  Some of these factors may have played a role in influencing the rather contradictory results of some of these trials.
Choice of beta-blocker and monitoring of therapy
Atenolol was the most commonly used agent in most studies. ,, In most of the adult studies, the dose of beta-blocker was adjusted based on heart rate response to exercise with a target heart rate of less than 100 beats/minute after exercise.  In most of the studies involving children , exercise testing was not performed and the dose of beta-blocker was empirically increased till the target dose was achieved or side-effects encountered. In children, the starting dose was 12.5-25 mg and the target dose was 25 mg, while in adolescents the target dose was 50 mg. 
What are the alternative therapeutic drugs for Marfan's syndrome?
Calcium channel blockers
These drugs are sometimes prescribed to patients in whom beta-blockers are contraindicated. In a small study, Rossi-Foulkes et al., reported a slower rate of enlargement of the aorta in patients receiving treatment compared with placebo. 
Angiotensin converting enzyme inhibitors
The potential benefit of these drugs in Marfan's syndrome maybe mediated through angiotensin-II type-2 receptor blockade, thereby, reducing apoptosis of vascular smooth muscle cells and cystic medial necrosis. A recent randomized controlled trial in children reported increased aortic distensibility and reduced stiffness index in patients treated with enalapril compared with beta-blockers. 
Angiotensin-II type-1 receptor blockers (AT1R blockers)
The postulated mechanism of benefit of these agents is mediated through their transforming growth factor (TGF)-beta receptor antagonism.  In a preliminary report, Habashi et al., demonstrated that losartan therapy in the mouse model of Marfan's syndrome resulted in complete correction of the phenotypic abnormalities in the aortic wall.  These results have prompted a multicenter randomized clinical trial, coordinated by the Pediatric Heart Network of the National Heart, Lung and Blood institute of the National Institutes of Health, comparing losartan with beta-blocker therapy in children and young adults with Marfan's syndrome.
Other drugs with theoretical rationale in patients with Marfan's syndrome include matrix metalloproteinase inhibitors (tetracycline, doxycycline), advanced glycation end-product (AGE) receptor blockers, aldosterone receptor antagonists, and drugs to reduce homocystenemia. 
E-mail survey and expert opinion
The e-mail survey was carried out using the following questionnaire. All the experts were requested to respond to the the following questions and a summary of the consensus is presented.
Do you think there is any role of beta-blockers in the medical therapy of patients with Marfan's syndrome and bicuspid aortic valve?
Survey opinion: Most of the respondents felt that beta-blockers are useful in patients with Marfan's syndrome. Regarding bicuspid aortic valve, most were of opinion that beta-blockers are not of much value, especially if there is no aortic root dilatation. Dr Wilson and Dr Saxena felt that beta-blockers may have a role in bicuspid aortic valve if there is aortic root dilatation. Dr Teirney and Dr Shrivatsava, however, were of opinion that beta-blockers are not effective in both Marfan's syndrome and bicuspid aortic valve.
What in your opinion is the effect of beta-blockers in patients with Marfan's syndrome and bicuspid aortic valve as regards:
- Reducing the rate of progression of aortic root dilatation.
- Delaying need for aortic root surgery.
- Reducing mortality and cardiovascular events.
Survey opinion: Most of the respondents were of opinion that beta-blockers were useful for all the three endpoints in patients with Marfan's syndrome.
If you think treatment with beta-blockers is beneficial, when would you recommend initiation of therapy?
- At time of diagnosis itself.
- Once aortic root dilatation has set in.
- Any cut-off value for aortic root dimension.
Survey opinion: Most of the experts preferred to start beta-blockers only after aortic root dilatation has set in. None offered any cut-off values for aortic root dilatation in children. Prof. Jondeau, however, was of opinion that beta-blockers should be started right from the time of diagnosis itself.
What is your beta-blocker of choice and how do you monitor adequacy of therapy?
Survey opinion: The overall opinion was that the choice of beta-blocker really does not matter, though most respondents preferred cardioselective beta-blockers like atenolol. Atenolol was recommended in standard tolerated doses (1-2 mg/kg/day). Most of the experts recommended monitoring of resting heart rate and tolerance before increasing the dose. Yearly monitoring of the aortic root dimension by echo was also recommended.
Do you use any other alternative drugs for medical management for patients with Marfan's syndrome or bicuspid aortic valve with aortic root dilatation?
Survey opinion: Most of the experts were not in favor of alternative drugs till more evidence is available. Dr. Wilson suggested use of ACE inhibitors in patients who cannot tolerate beta-blockers and use of calcium channel blockers in those who are intolerant to both beta-blockers and ACE inhibitors. Most of the experts felt that losartan is still in a trial phase for the medical treatment of patients with Marfan's syndrome.
| Conclusions|| |
It will be a reasonable practice to recommend beta-blockers in patients with Marfan's syndrome with aortic root dilatation, though there is some recent evidence suggesting that such therapy may not be beneficial. Based on available data, beta-blockers may be of value in delaying the progression of aortic root dilatation, while harder clinical endpoints like mortality and vascular complications may not be altered much. The role of newer drugs like losartan in Marfan's syndrome needs further evaluation. In patients with bicuspid aortic valve, there is no evidence base to support the use of any of these drugs at present.
| Acknowledgments|| |
The author would like to express his gratitude to the following experts for their opinion and expert comments:
- Professor Guillaume Jondeau, Service de Cardiologie et centre de reference de Marfan et apparentes; INSERM U 698 et Universite Paris VII - Denis Diderot; Hopital Bichat; Paris.
- Dr. Dirk G Wilson, Consultant Pediatric Cardiologist; University Hospital of Wales, UK.
- Dr. Savitri Shrivatsava, Consultant Pediatric Cardiologist, Escorts heart institute and research center, New Delhi, India
- Dr. Sieda Tierney, Children's hospital, Boston, Mass.
- Dr. Anita Saxena, Professor of Cardiology, AIIMS, New Delhi, India.
- Dr. SS Kothari, Professor of Cardiology, AIIMS, New Delhi, India.
- Dr. BRJ Kannan, Consultant Pediatric Cardiologist, Vadamalayan hospitals, Madurai, Tamil Nadu, India.
| References|| |
|1.||Dietz HC, Pyeiritz RE. Mutations in human gene for fibrillin-1 in the Marfans syndrome and related disorders. Hum Mol Genet 1995;4:1799-809. |
|2.||Silverman DI, Burton BS, Gray J, Bosner MS, Kouchoukos NT, Roman MJ, et al. Life expectancy in the Marfan syndrome. Am J Cardiol 1995;75:157-60. |
|3.||Williams A, Davies S, Stuart AG, Wilson DG, Fraser AG. Medical treatment of Marfan's syndrome: A time for change. Heart 2008;94:414-21. [PUBMED] [FULLTEXT]|
|4.||Prokop EK, Palmer RF, Wheat MW Jr. Hydrodyanamic forces in dissecting aneurysms: in vitro studies in a Tygon model and in dog aortas. Circ Res 1970;27:121-7. [PUBMED] |
|5.||Fedak PW, Verma S, David TE, Lesak RL, Weisel RD, Butany J. Clinical and pathophysiological implications of a bicuspid aortic valve. Circulation 2002;106:900-4. |
|6.||Grotenhuis HB, Ottenkamp J, Westenberg JJ, Bax JJ, Kroft LJ, de Roos A. Reduced aortic elasticity and dilatation are associated with aortic regurgitation and left ventricular hypertrophy in nonstenotic bicuspid aortic valve patients. J Am Coll Cardiol 2007;49:1660-5. [PUBMED] [FULLTEXT]|
|7.||Warren AE, Boyd ML, O'Connell C, Dodds L. Dilatation of the ascending aorta in pediatric patients with bicuspid aortic valve: Frequency, rate of progression and risk factors. Heart 2006;92:1496-500. [PUBMED] [FULLTEXT]|
|8.||Halpern BL, Char F, Murdoch JL, Horton WB, McKusick VA. A prospectus on the prevention of aortic rupture in the Marfan's syndrome with data on survivorship without treatment. Johns Hopkins Med J 1971;129:123-9. [PUBMED] |
|9.||Shores J, Berger KR, Murphy E, Pyeritz RE. Progression of aortic dilatation and the benefit of long-term beta-adrenergic blockade in Marfan's syndrome. N Engl J Med 1994;330:1335-41. |
|10.||Ladouceur M, Fermanian C, Lupoglazoff JM, Edouard T, Dulac Y, Acar P, et al. Effect of beta-blockade on ascending aortic dilatation in children with Marfan's syndrome. Am J Cardiol 2007;99:406-9. [PUBMED] [FULLTEXT]|
|11.||Selamet Tierney ES, Feingold B, Printiz BF, Park SC, Graham D, Kleinman CS, et al. Beta-blocker therapy does not alter the rate of aortic root dilation in pediatric patients with Marfan's syndrome. J Pediatr 2007;150:77-82. |
|12.||Gersony DR, McClaughlin MA, Jin Z, Gersony WM. The effect of beta-blocker therapy on clinical outcome in patients with Marfan's syndrome: A meta-analysis. Int J Cardiol 2007;114:303-8. [PUBMED] [FULLTEXT]|
|13.||Rossi-Foulkes R, Roman MJ, Rosen SE, Kramer-Fox R, Ehlers KH, O'Loughlin JE, et al. Phenotypic features and impact of beta-blocker or calcium antagonist therapy on aortic lumen size in the Marfan's syndrome. Am J Cardiol 1999;83:1364-8. [PUBMED] [FULLTEXT]|
|14.||Yetman AT, Bornermeier RA, McCrindle BW. Usefulness of enalapril versus propranolol or atenolol for the prevention of aortic dilatation in patients with the Marfan's syndrome. Am J Cardiol 2005;95:1125-7. |
|15.||Matt P, Habashi J, Carrel T, Cameron DE, Van Eyk JE, Dietz HC. Recent advances in understanding Marfan's syndrome: Should we now treat surgical patients with losartan? J Thorac Cardiovasc Surg 2008;135:389-94. [PUBMED] [FULLTEXT]|
|16.||Habashi JP, Judge DP, Holm TM, Cohn RD, Loeys BL, Cooper TK, et al. Losartan, an AT1 antagonist prevents aortic aneurysm in a mouse model of Marfan's syndrome. Science 2006;312:117-21. [PUBMED] [FULLTEXT]|
Department of Pediatric Cardiology, Amrita Institute of Medical Sciences, Elamakkara P. O. Kochi - 682 026, Kerala
Source of Support: None, Conflict of Interest: None
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