|Exercise Stress Echocardiography with Tissue Doppler Imaging (TDI) Detects Early Systolic Dysfunction in Beta-Thalassemia Major Patients without Cardiac Iron Overload.|
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|OBJECTIVES: To evaluate left and right myocardial performance at rest and after maximal exercise by conventional and Tissue Doppler Imaging (TDI) echocardiography. BACKGROUND: Iron Overload Cardiomyopathy (IOC) is the main cause of death in thalassemia major (TM) patients but conventional Echocardiography fails to predict early cardiac dysfunction. As TDI is able to demonstrate regional myocardial dysfunction and stress test may reveal abnormalities which are not evident at rest, we wondered if echocardiographic parameters may reveal abnormalities when applied first at rest and then after a physical effort. METHODS: We enrolled 46 consecutive beta-TM patients and 39 control subjects without evidence of cardiac disease; two echocardiograms, at baseline and at the end of maximal exercise on supine bicycle ergometer, were done. All TM patients had a liver iron assessment by SQUID (Superconducting Quantum Interference Device) and a cardiac iron one by MRI (T2*) evaluation. RESULTS: 38 TM patients had no evidence of cardiac iron overload. Whereas TM patients did not shown diastolic dysfunction and all of them presented a good global response to exercise, TDI detected a reduced increase of the S' waves of left ventricle basal segment during exercise. This finding seems to have some weak but interesting relations with iron overload markers. Pulmonary artery systolic pressure (PAPs) values were greater than in control subjects both at rest and after exercise CONCLUSIONS: in our study, exercise stress TDI-echocardiography was able to demonstrate subtle systolic abnormalities that were missed by Conventional Echocardiography. Further studies are required to determine the meaning and the clinical impact of these results.|
|Umberto Barbero; Paola Destefanis; Roberto Pozzi; Filomena Longo; Antonio Piga|
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|Type: JOURNAL ARTICLE Date: 2012-6-14|
|Title: Mediterranean journal of hematology and infectious diseases Volume: 4 ISSN: 2035-3006 ISO Abbreviation: - Publication Date: 2012|
|Created Date: 2012-7-19 Completed Date: - Revised Date: -|
Medline Journal Info:
|Nlm Unique ID: 101530512 Medline TA: Mediterr J Hematol Infect Dis Country: -|
|Languages: ENG Pagination: e2012037 Citation Subset: -|
|Cardiology Division, San Luigi Gonzaga Hospital, Orbassano, Italy.|
|APA/MLA Format Download EndNote Download BibTex|
Journal ID (nlm-ta): Mediterr J Hematol Infect Dis
Journal ID (iso-abbrev): Mediterr J Hematol Infect Dis
Journal ID (publisher-id): Mediterranean Journal of Hematology and Infectious Diseases
Publisher: Università Cattolica del Sacro Cuore
Received Day: 31 Month: 3 Year: 2012
Accepted Day: 18 Month: 5 Year: 2012
collection publication date: Year: 2012
Electronic publication date: Day: 14 Month: 6 Year: 2012
Volume: 4 Issue: 1
E-location ID: e2012037
PubMed Id: 22811786
Publisher Id: mjhid-4-1-e2012037
|Exercise Stress Echocardiography with Tissue Doppler Imaging (TDI) Detects Early Systolic Dysfunction in Beta-Thalassemia Major Patients without Cardiac Iron Overload|
1Cardiology Division, San Luigi Gonzaga Hospital, Orbassano, Italy
2Thalassemia Center, University of Turin, Orbassano, Italy
|Correspondence: Correspondence to: Umberto Barbero, Cardiology Division, San Luigi Gonzaga Hospital, Regione Gonzole 10, 10043 Orbassano (TO), Italy. E-mail: firstname.lastname@example.org
Some previous studies reported interesting results about the utility of Tissue Doppler Imaging for the echocardiographic evaluation of patients with beta-talassemia major.1 Because all these studies considered echocardiographic evaluation at rest, we wondered if TDI evaluation during exercise stress echocardiography could be more sensitive to early abnormalities. Since a few years, cardiac iron overload evaluation by Magnetic Resonance with T2* technique is available to identify patients at high risk of heart failure and arrhythmia from myocardial siderosis; nevertheless, it is not a fast and bedside technique as echocardiography.
TM patients are prone to iron overload due to chronic blood transfusion and increased intestinal absorption.2 Within iron-related complications, iron overload cardiomyopathy (IOC) represents the leading cause of death in these patients.3 IOC is characterized by a restrictive pattern with early diastolic dysfunction which progresses to an end-stage dilated cardiomyopathy and heart failure. It is now clear that chelation therapy can prevent, delay or even reverse the signs of cardiac dysfunction, but once overt heart failure is present, only 50% of patients survive.1 Early diagnosis of iron toxicity may be crucial to modify iron chelation therapy before heart failure appears, even if symptoms, as well as abnormalities at standard echocardiography, appear late.4 The demonstration of a change in contractility of longitudinal myocardial fibers by recent TDI technique could be useful for early detection of regional myocardial dysfunction before the occurrence of abnormal indices of global ventricular function.5,6
With our study we evaluated the effectiveness of TDI in TM patients without clinical or instrumental signs of heart failure in early detection of regional myocardial dysfunction at rest and after maximal exercise.
From January to October 2011 we examined 46 consecutive patients with beta-thalassemia major (TM) on regular blood transfusion and iron chelation. Inclusion criteria were a recent Biosusceptometry SQUID (Superconducting Quantum Interference Device) to quantify liver iron concentration (LIC) and a cardiac iron assessment by MRI T2* technique in the previous year. Exclusion criteria were: clinical signs of heart failure, pulmonary hypertension, arrhythmias, left ventricular ejection fraction (LVEF) <55%, ongoing pregnancy, age <18 years, reduced exercise capacity or dyspnea at six minutes walking test (6MWT).
We also examined 39 healthy age-, and sex-matched volunteers. The study protocol was approved by local ethics committee/boards, and all patients and control subjects were enrolled after informed consent.
Transthoracic echocardiography was performed 4–9 days after blood transfusion to ensure hemodynamic stability, using a Aloka Prosound Alfa 10 ultrasound system (2.5–3.5 MHz), by a single expert investigator that was blinded to clinical information about patients until the end of the study. Cardiac cycles were stored in a digital format. Chamber dimension were determined by standard procedures7 and valve flow Doppler and TDI were recorded in the apical 4-chamber view according to guidelines.8 Mitral and tricuspid in-flow measurements included peak early (E) and late (A) flow velocities, E/A ratio, deceleration time of mitral E (DT) and right isovolumic relaxation time (IVRT). Systolic (S’), early (E’) and late (A’) diastolic peak velocities of TDI were assessed on three beats at septal and lateral mitral origin and at lateral tricuspid origin, and expressed as a mean. Mean values of the E/E’ and E’/A’ were determined.
For all measurements, intervals from 3 consecutive cardiac cycles were measured and averaged.8
During the same session all patients underwent a complete echocardiographic examination (standard and TDI) after maximal exercise performed on a supine ergometer ER-900, Bitz-Germany, increasing workload by 25 Watts every 2 minutes, until they experienced fatigue or symptoms or until 85% of the age-predicted maximum heart rate was achieved.11 The ergometer was very close to the ultrasound system allowing execution of echocardiogram at peak of exercise.
Data are expressed as mean ± standard deviation for continuous variables or count (%) for categoric variables. Variables between the 2 groups were compared using the unpaired Student t test or Fisher’s exact test. The degree of association between clinical and laboratory variables were determined using the Pearson’s correlation coefficient. Differences were considered significant at a probability value of p<0.05.
The characteristics of patients and control subjects are summarized in Table 1. Although patients and control subjects were matched for age and gender, body surface area was significantly smaller in TM patients than in control subjects. Eight TM patients (17.4%) had cardiac iron overload at MRI while 38 had not.
Echo at rest (table 3 and 4): in patients with TM the morphological data were within normal ranges, with a mild atrial dilation compared to control group (left atria 19.8±3.2 cm2 vs 16.8±1.4; p<0.0001). Left atria’s area had a significantly negative relation with mean haemoglobin levels of the previous year (r=0.328; p=0.03).
As regards systolic function, in TM patients EF was normal, left S’-waves by TDI were comparable to controls and the average value of Tricuspid Anular Plane Systolic Excursion (TAPSE) was normal (23.9±3 mm).
Diastolic parameters were in ranges of normality in both groups, even if right isovolumic relaxation time (IVRT) was higher in TM patients (59.6±19.6 ms) then in the control group (19.7±3.5; p<0.0001).
Also PAPs value was within normal limit even if higher in TM patients than in control subjects (24.38±3 mmHg vs 20.8±4.8 mmHg), due to different tricuspid regurgitation jet velocity (TRV) between the two groups (2.18±0.16 m/s vs 1.97±0.3 m/s; p<0.0001). There were no remarkably echocardiographic differences at rest between patients with and without cardiac iron overload detected by MRI (table 6).
After maximal exercise (table 5): patients showed a good fit, with increase in EF and no signs of ventricular filling pressures’ elevation.
S’ waves of the left ventricle increased with stress as expected, but at a significantly lower degree in TM patients than in controls (S’ lateral mitral ring: 0.16±0.05 vs 0.22±0.04 m/sec; p<0.0001 – S’ septal: 0.15±0.04 vs 0.19±0.03; p<0.0001) as showed in figure 1.
Right S’ wave increased more in TM cases than in controls (p<0.0001); also TAPSE, used to evaluate the systolic function of the right ventricle, followed this way, although without statistic significance (p=0.14). TAPSE values significantly differed between patients with and without cardiac iron overload (26.88±3.98 vs 31.26±4.12 mm; p=0.008).
PAPs value increased in both groups, due to TRV rising after exercise (2.63±0.18 m/s in TM patients vs 2.27±0.28 m/s in control group) and remained higher in TM patients (p<0.0001).
Heart disease is till today the major cause of mortality in thalassemic patients.3 Iron deposition in myocardial cells induces the production of oxygen free radicals with free fatty acid oxidation, ATP decreased production and Ca2+ metabolism abnormalities.12 Over that, others factors have been suggested to act in these patients: chronic anemia, resulting in the hyperdynamic circulation; tissue hypoxia; altered coronary regulation and myocarditis;13 chronic hemolysis with arginase release and consumption of nitric oxide leading to elevated pulmonary arteriolar resistance and right ventricle dilatation and dysfunction.14
Cardiomyopathy from iron toxicity has a silent course, with late onset of symptoms of congestive heart failure,15 therefore an instrumental early recognition of cardiac dysfunction may be useful in modifying therapy before cardiac damage occurs.16 Cardiac T2* magnetic resonance was demonstrated to have a significant prognostic value in predicting such complications17 but, althought giving a strong information about the risks associated with the level of iron load, it does not give an actual knowledge about myocardial damage.
In clinical practice echocardiography provides a fast bedside and relatively cheap technique to study heart function; however, conventional echocardiographic parameters remain normal until late, mainly due to the anemia-related hyperdynamic state. Pulsed Doppler tissue imaging is a relatively new technique which allows the assessment of ventricular regional function, myocardial velocity, time intervals of the cardiac cycle and, most importantly, is preload independent.
There is evidence that long axis function measured by TDI is a more sensitive index of myocardial contractility than conventional echocardiographic parameters. Impairment of longitudinal fiber motion is therefore a sensitive and early marker of myocardial dysfunction, with prognostic value.18 This new modality has been applied during the last years in some studies for quantitative assessment of regional myocardial function of TM Patients, leading to interesting expected results.1,6,19 In fact these papers considered mostly patients with cardiac iron overload that were evaluated by echocardiograms performed at rest.
Conversely, in our work only 17.4% of patients had some evidence of cardiac iron and 38 of 46 (82.6%) had no evidence of cardiac iron overload. They underwent physical exercise to highlight by stress a contractile dysfunction that is not evident at rest, because this may potentially be an early sign of cardiomyopathy. The exercise capacity of this group of patients was comparable to that of healthy controls. The absence of ventricular hypertrophy and dilation may be due to the good clinical care, while dilation of the atria (50% of patients) is probably a consequence of residual anemia with transfusional regimens that keep the haemoglobin between 9.5 and 13.5 g%.
As expected in patients whose iron overload cardiomyopathy is presumably in very early stages, the global and segmental LV systolic functions were normal at rest.
The most interesting data on the systolic function came from TDI. The average values of S’ waves measured on the basal septum and on the lateral mitral ring were normal at rest in TM. As expected, the S’ waves increased with exercise, in both groups, but in TM patients it achieved significantly lower values than in the control group (Figure 1).
Our data show a weak correlation between LV S’ waves values after exercise and LIC and also with mean ferritin values (Figure 2). A significant, negative, correlation of post-exercise S’ of interventricular septum with transfusional Iron Input was also shown (Figure 3). Finally we found a weak but interesting positive relation between LV S’ waves and heart T2* that decrease together (Figure 4).
Subgrouping patients according to the presence of cardiac iron at MRI, we did not found any significant difference in the echocardiographic values, except for TAPSE. Even for the TDI parameters of systolic velocity we did not showed a significant difference, although a trend to lower values was present in patients with T2 * <20 (Table 6).
The possible explanation for this finding could be that the group of patients with cardiac iron accumulation is too small to have sufficient statistical power and moreover the range of cardiac iron load is moderate-mild (7–19 ms with a mean of 13,4±3,7 ms). We should also keep in mind that some patients presenting without accumulation on MRI have had heart iron accumulation in the past then regressed after regular chelation therapy over the years. Finally, it is possible that the reduced systolic regional performance detected by TDI and likely to be attributed to iron damage, could be due to other factors, such as chronic anemia, that all patients with TM have in common.
Nevertheless, systolic S’ velocity at TDI evaluation done after a physical exercise were lower also in TM patients without evidence of cardiac iron overload when compared to a healty group: this is a new result, not yet described in TM patients, and further studies are needed to understand if the reduced shortening of longitudinal fibers could represent a very early sign of initial myocardial dysfunction.
The preservation of global systolic function could be explained by the patchy iron deposition in the heart,20 primarily involving the longitudinal subendocardial fibers. This may justify our observation of abnormal regional contraction that becomes evident in TM patients only during physical exercise, without any signs of global dysfunction. A recent study21 found that in TM patients, LV lateral systolic velocity was more reduced at rest in comparison to a control group, but no relation with iron overload parameters was investigated. Nevertheless, our observation that TDI waves are not reduced at rest confirms previous observational studies which found an inverse relation between TDI waves and iron overload.1 This emphasizes the utility of a diagnostic technique to demonstrate a possible iron-related dysfunction in patient considered at low risk because of a normal T2* value.
Conversely, in RV, systolic function - measured with TAPSE, FAC and S’ wave - is preserved, with a pattern similar to control group. The only difference we found is about the S’ wave measured at the tricuspid ring: under exercise, it increases more in TM patients than in control group. This difference recalls what described by Hamdy et al.5 using rest echocardiography. We hypothesize that this different response could be related to differences in the myosin isoforms between myocytes of the two ventricles,22 probably in response to increased pulmonary pressure that characterizes TM patients23 as in our study group. These facts could explain also the higher values of TAPSE we measured in TM patients with MRI evidence of iron load.
Doppler analysis of flows through the AV valves shows normal average values of both mitral and tricuspid E/A ratio. The response to stress is normal, with filling velocities increase and non-significant decrease in E/A ratio bilaterally. According to Kremastinos et al.,24 also in our group of young asymptomatic patients, left ventricular compliance is normal, as is expected in well-treated patients in early stage of iron overload cardiomyopathy. On the other hand the lower tricuspidal E/A ratio, the longer isovolumetric relaxation time of the right ventricle and the higher PAPs in TM than in healthy controls suggest that the pulmonary circulation and the right heart are also affected by the disease since early stages, without any clinical symptoms. This aspect underlines the need of more focus on pulmonary hypertension and right heart function in thalassemia major. 16,23
We have not yet provided an adequate follow-up to validate the clinical impact of our findings. Because of the need to acquire data quickly after stopping the exercise, we could not conduct a full assessment of all myocardial segments to the TDI, but only the basal ones. However, these are generally considered the most reliable.8
Our study shows that patients with beta thalassemia major, without clinical signs of heart failure and with normal EF under exercise stress may have a reduced response to exercise of left ventricle longitudinal fibers that could be detected with TDI echocardiography, even without MRI evidence of iron overload. To our knowledge this is a novel finding and we hypothesize that it may be a very early sign of initial myocardial damage by iron. Further investigations are warranted to confirm this hypothesis, in order to clarify if it could influence the clinical and therapeutic choices. A follow-up with the same technique could also confirm the stabilization, the exacerbation or regression of the dysfunction, and therefore the response to therapies.
From our data we conclude that stress echocardiography with TDI may be a non-invasive and repeatable imaging technique to assess the efficacy of chelation therapy and to identify early signs of myocardial involvement, even when MRI is not indicated or is negative for cardiac iron overload.
fn1-mjhid-4-1-e2012037Competing interests: The authors have declared that no competing interests exist.
|1.||Vogel M,et al. Tissue Doppler echocardiography in patients with thalassaemia detects early myocardial dysfunction related to myocardial iron overloadEur Heart JYear: 20032411139 http://dx.doi.org/10.1016/S0195-668X(02)00381-0. 12559943|
|2.||Olivieri NF. The beta-thalassemiasN Engl J MedYear: 1999341299109 http://dx.doi.org/10.1056/NEJM199907083410207. 10395635|
|3.||Borgna-Pignatti C,et al. Survival and complications in thalassemiaAnn N Y Acad SciYear: 20051054407 http://dx.doi.org/10.1196/annals.1345.006. 16339650|
|4.||Trikas A,et al. Exercise capacity in patients with beta-thalassemia major: relation to left ventricular and atrial size and functionAm Heart JYear: 1998136698890 http://dx.doi.org/10.1016/S0002-8703(98)70154-1. 9842011|
|5.||Hamdy AM. Use of strain and tissue velocity imaging for early detection of regional myocardial dysfunction in patients with beta thalassemiaEur J EchocardiogrYear: 2007821029 http://dx.doi.org/10.1016/j.euje.2006.02.004. 16564231|
|6.||Silvilairat S,et al. Tissue Doppler echocardiography reliably reflects severity of iron overload in pediatric patients with beta thalassemiaEur J EchocardiogrYear: 2008933687217689292|
|7.||Lang RM,et al. Recommendations for chamber quantification: a report from the American Society of Echocardiography’s Guidelines and Standards Committee and the Chamber Quantification Writing Group, developed in conjunction with the European Association of Echocardiography, a branch of the European Society of CardiologyJ Am Soc EchocardiogrYear: 20051812144063 http://dx.doi.org/10.1016/j.echo.2005.10.005. 16376782|
|8.||Nagueh SF,et al. Recommendations for the evaluation of left ventricular diastolic function by echocardiographyEur J EchocardiogrYear: 200910216593 http://dx.doi.org/10.1093/ejechocard/jep007. 19270053|
|9.||Currie PJ,et al. Continuous wave Doppler determination of right ventricular pressure: a simultaneous Doppler-catheterization study in 127 patientsJ Am Coll CardiolYear: 1985647506 http://dx.doi.org/10.1016/S0735-1097(85)80477-0. 4031289|
|10.||Kircher BJ,Himelman RB,Schiller NB. Noninvasive estimation of right atrial pressure from the inspiratory collapse of the inferior vena cavaAm J CardiolYear: 19906644936 http://dx.doi.org/10.1016/0002-9149(90)90711-9. 2386120|
|11.||Sicari R,et al. Stress Echocardiography Expert Consensus Statement--Executive Summary: European Association of Echocardiography (EAE) (a registered branch of the ESC)Eur Heart JYear: 200930327889 http://dx.doi.org/10.1093/eurheartj/ehn492. 19001473|
|12.||Murphy CJ,Oudit GY. Iron-overload cardiomyopathy: pathophysiology, diagnosis, and treatmentJ Card FailYear: 20101611888900 http://dx.doi.org/10.1016/j.cardfail.2010.05.009. 21055653|
|13.||Kremastinos DT,et al. Myocarditis in beta-thalassemia major. A cause of heart failureCirculationYear: 199591166717805220|
|14.||Atichartakarn V,et al. Pulmonary arterial hypertension in previously splenectomized patients with beta-thalassemic disordersInt J HematolYear: 200378213945 http://dx.doi.org/10.1007/BF02983382. 12953808|
|15.||Aessopos A,et al. Cardiac status in well-treated patients with thalassemia majorEur J HaematolYear: 200473535966 http://dx.doi.org/10.1111/j.1600-0609.2004.00304.x. 15458515|
|16.||Hahalis G,et al. Right ventricular diastolic function in beta-thalassemia major: echocardiographic and clinical correlatesAm Heart JYear: 2001141342834 http://dx.doi.org/10.1067/mhj.2001.113077. 11231441|
|17.||Kirk P,et al. Cardiac T2* magnetic resonance for prediction of cardiac complications in thalassemia majorCirculationYear: 20091202019618 http://dx.doi.org/10.1161/CIRCULATIONAHA.109.874487. 278419819801505|
|18.||Mogelvang R,et al. Cardiac dysfunction assessed by echocardiographic tissue Doppler imaging is an independent predictor of mortality in the general populationCirculationYear: 200911920267985 http://dx.doi.org/10.1161/CIRCULATIONAHA.108.793471. 19433761|
|19.||Marci M,et al. Detection of early cardiac dysfunction in patients with Beta thalassemia by tissue Doppler echocardiographyEchocardiographyYear: 201128217580 http://dx.doi.org/10.1111/j.1540-8175.2010.01270.x. 20738369|
|20.||Fitchett DH,et al. Cardiac involvement in secondary haemochromatosis: a catheter biopsy study and analysis of myocardiumCardiovasc ResYear: 1980141271924 http://dx.doi.org/10.1093/cvr/14.12.719. 7260965|
|21.||Bilge AK,et al. Early detection of left ventricular dysfunction with strain imaging in thalassemia patientsClin CardiolYear: 2010337E2934 http://dx.doi.org/10.1002/clc.20584. 20641107|
|22.||Brooks WW,et al. Comparison of contractile state and myosin isozymes of rat right and left ventricular myocardiumJ Mol Cell CardiolYear: 198719543340 http://dx.doi.org/10.1016/S0022-2828(87)80395-4. 3625780|
|23.||Hahalis G,et al. Right ventricular cardiomyopathy in beta-thalassaemia majorEur Heart JYear: 200223214756 http://dx.doi.org/10.1053/euhj.2001.2709. 11785997|
|24.||Kremastinos DT,et al. Left ventricular diastolic Doppler characteristics in beta-thalassemia majorCirculationYear: 19938831127358353874|
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