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|Year : 2021
: 14 | Issue : 2 | Page
|Carvedilol improves left ventricular diastolic dysfunction in patients with transfusion-dependent thalassemia
Suchaya Silvilairat1, Pimlak Charoenkwan1, Suwit Saekho2, Adisak Tantiworawit3, Nipon Chattipakorn4
1 Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand
2 Department of Radiologic Technology, Faculty of Associated Medical Sciences; Biomedical Engineering Center, Faculty of Engineering, Chiang Mai University, Chiang Mai, Thailand
3 Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand
4 Cardiac Electrophysiology Research and Training Center; Department of Physiology, Cardiac Electrophysiology Unit, Faculty of Medicine, Chiang Mai University; Center of Excellence in Cardiac Electrophysiology Research, Chiang Mai University, Chiang Mai, Thailand
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|Date of Submission||07-Apr-2020|
|Date of Decision||12-Oct-2020|
|Date of Acceptance||27-Jan-2021|
|Date of Web Publication||03-May-2021|
| Abstract|| |
Background: Iron overload cardiomyopathy is the most common cause of death in patients with transfusion-dependent thalassemia.
Aim: The aim of this study was to determine the efficacy of carvedilol treatment in patients with transfusion-dependent thalassemia who had left ventricular diastolic dysfunction.
Methods: Eighteen patients with transfusion-dependent thalassemia who had left ventricular diastolic dysfunction were enrolled. All patients had normal left ventricular systolic function and were given carvedilol with the target dose of 0.8 mg/kg/day. Ventricular function and the level of cardiac iron were assessed by echocardiography and magnetic resonance imaging at 0, 3, and 6 months.
Results: The median age of the patients was 19 years (range 13–25 years). Four patients had severe left ventricular Grade III diastolic dysfunction and fourteen patients had Grade II diastolic dysfunction. The grade of left ventricular diastolic dysfunction was improved at 3 months after the carvedilol treatment. The Doppler parameters, including pulmonary vein atrial reversal velocity, pulmonary vein atrial reversal duration, and the difference of pulmonary vein atrial reversal and the mitral valve atrial contraction wave duration at 3 months after the carvedilol treatment, were significantly lower than these parameters before the treatment.
Conclusions: Among patients with transfusion-dependent thalassemia who had left ventricular diastolic dysfunction without systolic dysfunction, treatment with carvedilol for 3 months was associated with improvement in Doppler parameters of left ventricular diastolic function. However, this finding and its clinical significance need to be confirmed in further double-blind controlled studies.
Keywords: CARDIAC T2*, carvedilol, tissue Doppler echocardiography, transfusion-dependent thalassemia
|How to cite this article:|
Silvilairat S, Charoenkwan P, Saekho S, Tantiworawit A, Chattipakorn N. Carvedilol improves left ventricular diastolic dysfunction in patients with transfusion-dependent thalassemia. Ann Pediatr Card 2021;14:152-8
|How to cite this URL:|
Silvilairat S, Charoenkwan P, Saekho S, Tantiworawit A, Chattipakorn N. Carvedilol improves left ventricular diastolic dysfunction in patients with transfusion-dependent thalassemia. Ann Pediatr Card [serial online] 2021 [cited 2021 Oct 16];14:152-8. Available from: https://www.annalspc.com/text.asp?2021/14/2/152/315285
| Introduction|| |
Patients with severe forms of homozygous beta-thalassemia and beta-thalassemia/hemoglobin E disease often display symptoms related to hemolysis and ineffective erythropoiesis, including anemia, jaundice, hepatosplenomegaly, skeleton change, and delayed growth. The mainstay of treatment in these patients is regular blood transfusion with an aim to inhibit the synthesis of abnormal red blood cells and iron chelation to reduce iron deposition in the vital organs. Consequences of transfusional iron overload are ventricular dysfunction, arrhythmia, hepatitis, diabetes mellitus, failure of sexual maturation, and growth retardation., Iron overload cardiomyopathy is the most common cause of death in patients with transfusion-dependent thalassemia.,,,, To reduce the risk of both mortality and morbidity, these patients need to receive iron chelation therapy to reduce iron in the body.,,,, Although iron chelation is widely used in patients with transfusion-dependent thalassemia, iron overload cardiomyopathy remains one of the major causes of death., The factors affecting mortality are the presence of a left ventricular restrictive filling pattern and a low left ventricular ejection fraction., The pathophysiology of iron overload cardiomyopathy is the formation of highly reactive oxygen free radicals that cause oxidative damage-associated ischemia–reperfusion injury., An angiotensin-converting enzyme inhibitor used in adult patients with thalassemia has been shown to be capable of improving both systolic and diastolic left ventricular impairments. Amlodipine used in conjunction with standard chelation therapy shows a potential for reducing cardiac iron overload as voltage-gated calcium channel blockade might prevent iron uptake into the cardiomyocytes., However, there has been no study of whether the effect of the amlodipine therapy improves ventricular function.
Carvedilol is a nonselective adrenergic blocker combining an antioxidant effect. Several studies show that carvedilol can improve both systolic and diastolic ventricular function, reduce free radical release and apoptosis, and reduce mortality in children and adults with congestive heart failure.,,, The hypothesis for this study was that carvedilol can attenuate left ventricular diastolic dysfunction due to iron overload in patients with transfusion-dependent thalassemia who had ventricular dysfunction.
| Methods|| |
Sixty-one patients with transfusion-dependent thalassemia were evaluated in this study between January 2014 and December 2016. All consecutive patients with transfusion-dependent thalassemia who had left ventricular diastolic dysfunction were enrolled in this study. All patients or their parents provided written informed consent for research participation. All patients were initially given carvedilol in doses of 0.1 mg/kg/day, with the medication being divided into two separate doses. The dosage was doubled every 2 weeks until the target dose of 0.8 mg/kg/day was reached and was continued for 6 months. The maximum dose was 50 mg/day. All patients had normal left ventricular systolic function and no symptom of congestive heart failure. The patients who received other medications for congestive heart failure were excluded. All patients had their cardiac function assessed by echocardiography as the primary outcome at 0, 3, and 6 months, and the level of iron in the heart was also evaluated at 0, 3, and 6 months using cardiac magnetic resonance imaging (MRI). Side effects of the drug were monitored through the study.
Echocardiographic data were obtained using the Philips iE33 system (Philips Healthcare, Bothell, WA, USA). Echocardiography was performed in nonfasting state after the blood transfusion. Complete two-dimensional, M-mode, Doppler (pulsed wave, continuous wave, and color) echocardiography was performed according to the American Society of Echocardiography recommendations., The quality of Doppler echocardiographic imaging was satisfactory enough for measurement. Echocardiographic parameters included left ventricular end-diastolic dimension, left ventricular end-systolic dimension, and left ventricular fractional shortening. Echocardiographic data included pulse wave Doppler assessment of mitral and pulmonary venous flows (ventricular diastolic filling analysis) and tissue Doppler imaging. Pulse wave Doppler of mitral valve flow included peak early ventricular filling velocity, peak atrial contraction velocity, and atrial contraction wave duration and deceleration time. Pulse wave Doppler of pulmonary venous flow included systolic forward flow velocity, diastolic forward flow velocity, atrial reversal flow velocity, and atrial reversal flow duration. Tissue Doppler imaging signals were obtained from an apical four-chamber view at the septal mitral annulus. Tissue Doppler imaging variables included systolic myocardial velocity, early diastolic myocardial velocity, and late diastolic myocardial velocity. Doppler characteristics of left ventricular diastolic dysfunction with increased ventricular end-diastolic and left atrial pressure included increased atrial reversal flow velocity and atrial reversal flow duration, pulmonary vein atrial reversal duration exceeding the A wave duration, decreased early diastolic myocardial velocity, and increased mitral early ventricular filling velocity-to-early diastolic myocardial velocity ratio. Myocardial performance index derived from tissue Doppler imaging was calculated by adding the isovolumic contraction and isovolumic relaxation times together and then dividing this value by the ejection time. Mitral annular plane systolic excursion was assessed with the M-mode in an apical four-chamber view, placing the cursor on the lateral mitral annulus. Diastolic left ventricular dysfunction was graded according to pulse wave Doppler of mitral and pulmonary venous flows and tissue Doppler imaging.,
Cardiac T2* magnetic resonance
All patients had a cardiac T2* MRI, with the imaging carried out using a 1.5 Tesla MRI scanner (Philips Achieva, the Netherlands) with a sense cardiac phase array of a five-element coil, or SENSE XL Torso 16-element coil, as was used in previous studies. Cardiac T2* was measured from a single short-axis view at the mid-left ventricle with 10 echo times (1.70–26.10 ms with an increment of 2.70 ms). The cardiac T2* protocol included a double inversion recovery black blood gradient echo. A multiecho sequence was applied with a flip angle of 25°, matrix 164 × 154, field of view 36 cm, TR 28 ms, slice thickness 10 mm, and number of signal averages = 1. Data analysis was performed on the workstation with the validated in-house software developed on the MATLAB R2014b (Mathworks, Natick, MA, USA).
All statistical calculations were assessed using commercially available software (SPSS version 23, SPSS Inc., Chicago, IL, USA). Continuous data were expressed as median and range or mean and standard deviation. Categorical data were summarized as number and percentage. The differences in the Doppler parameters of ventricular function were assessed using a nonparametric test. P < 0.05 was considered statistically significant.
| Results|| |
Eighteen patients with transfusion-dependent thalassemia and left ventricular diastolic dysfunction with the median age of 19 years (range 13–25 years) were enrolled in this study. Ten (56%) patients were male. Four patients had severe left ventricular Grade III diastolic dysfunction, and fourteen patients had grade II diastolic dysfunction. All patients tolerated carvedilol with the target dose of 0.8 mg/kg/day with good compliance. No side effects were reported. The clinical characteristics and the results of the cardiac T2* MRI data are summarized in [Table 1]. Systolic blood pressure 6 months after treatment was lower than that before the carvedilol treatment. At the end of the study, heart rate and diastolic blood pressure were not significantly different from before the treatment. In addition, levels of serum ferritin and cardiac T2* before and after the treatment were not different.
|Table 1: Clinical and laboratory characteristics at baseline and after 3 and 6 months of treatment with carvedilol|
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Conventional Doppler parameters, including mitral valve inflow, pulmonary vein inflow, fractional shortening, and mitral annular plane systolic excursion, were compared before treatment and then at 3 and 6 months after treatment [Table 2]. Pulmonary vein atrial reversal flow velocity, pulmonary vein atrial reversal flow duration, and the difference of pulmonary vein atrial reversal duration and the mitral valve atrial contraction wave duration in patients 3 and 6 months after the carvedilol treatment were significantly lower than those before the treatment [Figure 1]. Mitral annular plane systolic excursion, left ventricular fractional shortening, and cardiac index were not different after the treatment.
|Figure 1: Graph comparing the pulse wave Doppler of mitral valve and pulmonary venous flow after 3 and 6 months of carvedilol treatment. (a) Pulmonary venous atrial reversal flow velocity; (b): The difference in the pulmonary vein atrial reversal duration and the mitral valve A wave (Pulmonary venous atrial reversal-mitral valve atrial filling velocity) duration|
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|Table 2: Comparison of the pulse wave Doppler parameters at baseline and after 3 and 6 months of treatment|
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Tissue Doppler echocardiography
Tissue Doppler imaging and the grade of left ventricular diastolic dysfunction are summarized in [Table 3]. The grade of left ventricular diastolic dysfunction significantly improved after 3 and 6 months of carvedilol treatment [Figure 2]. Systolic myocardial velocity readings 3 and 6 months after the carvedilol treatment was started were higher than those before the treatment. Early diastolic myocardial velocity, early ventricular filling velocity-to-early diastolic myocardial velocity ratio, and tissue Doppler imaging-derived myocardial performance index were not different after the treatment.
|Figure 2: Graph comparing the grade of left ventricular diastolic dysfunction after 3 and 6 months of carvedilol treatment|
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|Table 3: Comparison of the tissue Doppler data before and after 3 and 6 months of treatment|
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| Discussion|| |
The results of this study supported the hypothesis in that the carvedilol treatment led to improved left ventricular diastolic function in patients with iron overload cardiomyopathy. Diastolic echocardiographic parameters, including atrial reversal flow velocity, atrial reversal flow duration, and the difference of pulmonary vein atrial reversal duration and the mitral valve atrial contraction wave duration, were significantly improved at 3 months after the treatment. In addition, the grade of left ventricular diastolic dysfunction was significantly improved at 3 months after the carvedilol treatment.
Tissue Doppler echocardiography has been the noninvasive method used in the assessment of early ventricular dysfunction. Left ventricular diastolic dysfunction demonstrated in patients with thalassemia preceded the onset of systolic impairment. Complete assessment of left ventricular diastolic function should be interpreted by both mitral valve and pulmonary venous Doppler inflow. Tissue Doppler imaging has been the additional assessment for grading left ventricular diastolic function. The grading system using a semiquantitative method can classify the severity of left ventricular diastolic ventricular function. In the present study, pulse wave Doppler of mitral valve and pulmonary venous Doppler inflow, including tissue Doppler imaging, were assessed for grading the left ventricular diastolic function. Doppler parameters indicating left ventricular diastolic function, including atrial reversal flow velocity, atrial reversal flow duration, and pulmonary vein atrial reversal duration exceeding the mitral valve atrial contraction wave duration improved during carvedilol treatment. The E/e' ratio was somewhat lower at 3 months after the treatment. We believe that the pulse Doppler of pulmonary venous and mitral valve inflow parameters had more sensitivity for the detection of LV diastolic dysfunction. Conversely, cardiac T2* MRI which is used as a gold standard for early detection of iron overload cardiomyopathy did not change during the treatment. Therefore, the Doppler parameter of left ventricular diastolic function improved as a result of the carvedilol treatment.
Several studies in pediatric patients have shown that carvedilol improved ventricular function, both in cases of dilated cardiomyopathy and in those of congenital heart disease with heart failure.,, Bajcetic et al. reported that a 1-year treatment of carvedilol in pediatric patients with dilated cardiomyopathy improved left ventricular function and increased antioxidant enzyme activity. Only one study, involving a randomized controlled trial with 14 adolescent patients with beta-thalassemia major who had left ventricular ejection fraction <55%, revealed that a pulsed Doppler E/A ratio of mitral valve flow in a group undergoing carvedilol treatment and a control group changed from 1.1 ± 0.37 m/s to 1.8 ± 0.40 m/s and from 1.34 ± 0.30 m/s to 2.6 ± 0.23 m/s, respectively. However, this study did not demonstrate that carvedilol therapy led to improvements in both left ventricular systolic and diastolic functions in these patients. In our study, 18 pediatric and adolescent patients with transfusion-dependent thalassemia who had left ventricular diastolic dysfunction showed improvement in left ventricular diastolic function after 3 months of carvedilol treatment. These improvements were demonstrated by pulse wave Doppler of the pulmonary vein and mitral valve flow parameters. Carvedilol can improve left ventricular diastolic function by acting as a nonselective adrenergic blocker and through its antioxidant effects that include reducing free radical release and apoptosis.,,,,
Use of an angiotensin-converting enzyme inhibitor in a study including 14 adult patients with beta-thalassemia major who had asymptomatic or minimally symptomatic left ventricular dysfunction showed increased left ventricular fractional shortening and deceleration time and decreased E/A ratio of mitral valve Doppler flow in the patients. Recently, amlodipine used in combination with standard chelation therapy in patients with thalassemia major who had myocardial T2* <35 ms led to a more effective reduction in cardiac iron overload than chelation therapy alone., However, there has been no study into the effect of the amlodipine therapy on the improvement of left ventricular function.
The limitation of this study was that a double-blinded randomized controlled trial could not be conducted because of the small number of patients with transfusion-dependent thalassemia who had left ventricular diastolic dysfunction. However, the improvement in left ventricular diastolic function in the medium-term follow-up was effectively measured and documented using complete conventional pulse wave Doppler of both the pulmonary vein and mitral valve inflow and tissue Doppler imaging. The encouraging results from the study show that a double-blinded randomized controlled trial of a large number of patients with transfusion-dependent thalassemia is warranted.
| Conclusions|| |
For patients with transfusion-dependent thalassemia who had left ventricular diastolic dysfunction without systolic dysfunction, treatment with carvedilol for 3 months was associated with improvement in Doppler parameters of diastolic function. Doppler parameters, indicating left ventricular diastolic dysfunction including pulmonary vein atrial reversal flow velocity, pulmonary vein atrial reversal flow duration, and the difference of pulmonary vein atrial reversal duration and mitral valve atrial contraction wave duration, were significantly decreased after 3 months of carvedilol treatment. However, this finding and its clinical significance need to be confirmed in further double-blind controlled studies.
Financial support and sponsorship
This work was supported by a grant from the Thailand Research Fund RSA5680014 (SS) and NSTDA Research chair grant from the National Science and Technology Development Agency Thailand (NC).
Conflicts of interest
There are no conflicts of interest.
| References|| |
Origa R. β-Thalassemia. Genet Med 2017;19:609-19.
Galanello R, Origa R. Beta-thalassemia. Orphanet J Rare Dis 2010;5:11.
Modell B, Khan M, Darlison M. Survival in beta-thalassaemia major in the UK: Data from the UK Thalassaemia Register. Lancet 2000;355:2051-2.
Li CK, Luk CW, Ling SC, Chik KW, Yuen HL, Li CK, et al.
Morbidity and mortality patterns of thalassaemia major patients in Hong Kong: Retrospective study. Hong Kong Med J 2002;8:255-60.
Kremastinos DT, Farmakis D, Aessopos A, Hahalis G, Hamodraka E, Tsiapras D, et al
. Beta-thalassemia cardiomyopathy: History, present considerations, and future perspectives. Circ Heart Fail 2010;3:451-8.
Rund D, Rachmilewitz E. Beta-thalassemia. N Engl J Med 2005;353:1135-46.
Ehlers KH, Giardina PJ, Lesser ML, Engle MA, Hilgartner MW. Prolonged survival in patients with beta-thalassemia major treated with deferoxamine. J Pediatr 1991;118:540-5.
Aessopos A, Farmakis D, Hatziliami A, Fragodimitri C, Karabatsos F, Joussef J, et al
. Cardiac status in well-treated patients with thalassemia major. Eur J Haematol 2004;73:359-66.
Neufeld EJ. Update on iron chelators in thalassemia. Hematology Am Soc Hematol Educ Program 2010;2010:451-5.
Fernandes JL. Iron chelation therapy in the management of transfusion-related cardiac iron overload. Transfusion 2012;52:2256-68.
Ware HM, Kwiatkowski JL. Evaluation and treatment of transfusional iron overload in children. Pediatr Clin North Am 2013;60:1393-406.
Marsella M, Borgna-Pignatti C. Transfusional iron overload and iron chelation therapy in thalassemia major and sickle cell disease. Hematol Oncol Clin North Am 2014;28:703-27, vi.
Efthimiadis GK, Hassapopoulou HP, Tsikaderis DD, Karvounis HI, Giannakoulas GA, Parharidis GE, et al
. Survival in thalassemia major patients: Prognostic value of Doppler-demonstrated left ventricular restrictive filling pattern. Circ J 2006;70:1037-42.
Chrysohoou C, Panagiotakos DB, Barbetseas Y, Brilli S, Lambrou S, Karagiorga M, et al.
Echocardiographic and electrocardiographic prognostic factors of heart failure in young patients with β-thalassemia: A 10-year (1995-2000) follow up. Int J Hematol 2004;80:336-40.
Murphy CJ, Oudit GY. Iron-overload cardiomyopathy: Pathophysiology, diagnosis, and treatment. J Card Fail 2010;16:888-900.
Gujja P, Rosing DR, Tripodi DJ, Shizukuda Y. Iron overload cardiomyopathy: Better understanding of an increasing disorder. J Am Coll Cardiol 2010;56:1001-12.
Karvounis HI, Zaglavara TA, Parharidis GE, Nouskas IG, Hassapopoulou EP, Gemitzis KD, et al
. An angiotensin-converting enzyme inhibitor improves left ventricular systolic and diastolic function in transfusion-dependent patients with beta-thalassemia major. Am Heart J 2001;141:281.
Fernandes JL, Sampaio EF, Fertrin K, Coelho OR, Loggetto S, Piga A, et al.
Amlodipine reduces cardiac iron overload in patients with thalassemia major: A pilot trial. Am J Med 2013;126:834-7.
Fernandes JL, Loggetto SR, Veríssimo MP, Fertrin KY, Baldanzi GR, Fioravante LA, et al
. A randomized trial of amlodipine in addition to standard chelation therapy in patients with thalassemia major. Blood 2016;128:1555-61.
Yue TL, Cheng HY, Lysko PG, McKenna PJ, Feuerstein R, Gu JL, et al.
Carvedilol, a new vasodilator and beta adrenoceptor antagonist, is an antioxidant and free radical scavenger. J Pharmacol Exp Ther 1992;263:92-8.
Nishiyama M, Park IS, Yoshikawa T, Hatai Y, Ando M, Takahashi Y, et al
. Efficacy and safety of carvedilol for heart failure in children and patients with congenital heart disease. Heart Vessels 2009;24:187-92.
Läer S, Mir TS, Behn F, Eiselt M, Scholz H, Venzke A, et al
. Carvedilol therapy in pediatric patients with congestive heart failure: A study investigating clinical and pharmacokinetic parameters. Am Heart J 2002;143:916-22.
Rusconi P, Gómez-Marín O, Rossique-González M, Redha E, Marín JR, Lon-Young M, et al
. Carvedilol in children with cardiomyopathy: 3-year experience at a single institution. J Heart Lung Transplant 2004;23:832-8.
Bajcetic M, Kokic Nikolic A, Djukic M, Kosutic J, Mitrovic J, Mijalkovic D, et al
. Effects of carvedilol on left ventricular function and oxidative stress in infants and children with idiopathic dilated cardiomyopathy: A 12-month, two-center, open-label study. Clin Ther 2008;30:702-14.
Lai WW, Geva T, Shirali GS, Frommelt PC, Humes RA, Brook MM, et al
. Guidelines and standards for performance of a pediatric echocardiogram: A report from the Task Force of the Pediatric Council of the American Society of Echocardiography. J Am Soc Echocardiogr 2006;19:1413-30.
Lopez L, Colan SD, Frommelt PC, Ensing GJ, Kendall K, Younoszai AK, et al
. Recommendations for quantification methods during the performance of a pediatric echocardiogram: A report from the Pediatric Measurements Writing Group of the American Society of Echocardiography Pediatric and Congenital Heart Disease Council. J Am Soc Echocardiogr 2010;23:465-95.
Frommelt PC. Diastolic ventricular function assessment. In: Echocardiography in Pediatric and Congenital Heart Disease: From Fetus to Adult. 2nd
ed. Wiley-Blackwell: John Wiley & Sons Ltd.; 2016. p. 132-53.
Nagueh SF, Smiseth OA, Appleton CP, Byrd BF 3rd
, Dokainish H, Edvardsen T, et al
. Recommendations for the Evaluation of Left Ventricular Diastolic Function by Echocardiography: An Update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr 2016;29:277-314.
Silvilairat S, Charoenkwan P, Saekho S, Tantiworawit A, Phrommintikul A, Srichairatanakool S, et al
. Heart rate variability for early detection of cardiac iron deposition in patients with transfusion-dependent thalassemia. PLoS One 2016;11:e0164300.
Ajami GH, Amoozgar H, Borzouee M, Karimi M, Piravian F, Ashrafi A, et al
. Efficacy of carvedilol in patients with dilated cardiomyopathy due to beta-thalassemia major; a double-blind randomized controlled trial. Iran J Pediatr 2010;20:277-83.
Dr. Suchaya Silvilairat
Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200
Source of Support: None, Conflict of Interest: None
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3]