Published online before print January 19, 2009, doi: 10.1161/CIRCULATIONAHA.108.794529
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Circulation. 2009;119:524-529.)
© 2009 American Heart Association, Inc.
Heart Failure |
Long-Term Effects of Enzyme Replacement Therapy on Fabry Cardiomyopathy
Evidence for a Better Outcome With Early Treatment
From the Department of Medicine, Divisions of Cardiology and Nephrology (F.W., M.N., F.B., S.H., S.S., W.V., G.E., C.W., J.S.) and Department of Radiology (M.B.), University Hospital, Wuerzburg, Germany.
Correspondence to Frank Weidemann, Medizinische Klinik und Poliklinik I, Universitätsklinik Würzburg, Josef-Schneider Str 2, Bau 4, 97080 Würzburg, Germany. E-mail weidemann_f{at}medizin.uni-wuerzburg.de
Received May 27, 2008; accepted November 14, 2008.
 |
Abstract |
|---|
 Top Abstract IntroductionMethodsResultsDiscussionReferences |
|---|
Background— Enzyme replacement therapy with recombinant
-galactosidase A reduces left ventricular hypertrophy and improves regional myocardial function in patients with Fabry disease during short-term treatment. Whether enzyme replacement therapy is effective in all stages of Fabry cardiomyopathy during long-term follow-up is unknown. Methods and Results— We studied 32 Fabry patients over a period of 3 years regarding disease progression and clinical outcome under enzyme replacement therapy. Regional myocardial fibrosis was assessed by magnetic resonance imaging late-enhancement technique. Echocardiographic myocardial mass was calculated with the Devereux formula, and myocardial function was quantified by ultrasonic strain-rate imaging. In addition, exercise capacity was measured by bicycle stress test. All measurements were repeated at yearly intervals. At baseline, 9 patients demonstrated at least 2 fibrotic left ventricular segments (severe myocardial fibrosis), 11 had 1 left ventricular segment affected (mild fibrosis), and 12 were without fibrosis. In patients without fibrosis, enzyme replacement therapy resulted in a significant reduction in left ventricular mass (238±42 g at baseline, 202±46 g at 3 years; P for trend <0.001), an improvement in myocardial function (systolic radial strain rate, 2.3±0.4 and 2.9±0.6 seconds–1, respectively; P for trend=0.045), and a higher exercise capacity obtained by bicycle stress exercise (106±14 and 122±26 W, respectively; P for trend=0.014). In contrast, patients with mild or severe fibrosis showed a minor reduction in left ventricular hypertrophy and no improvement in myocardial function or exercise capacity.
Conclusions— These data suggest that treatment of Fabry cardiomyopathy with recombinant -galactosidase A should best be started before myocardial fibrosis has developed to achieve long-term improvement in myocardial morphology and function and exercise capacity.
Key Words: cardiomyopathy • echocardiography • Fabry disease • hypertrophy • treatment
|
Introduction |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Fabry disease is a relatively rare X-linked lysosomal storage disorder caused by
-galactosidase A deficiency. The enzymatic deficit results in progressive intracellular accumulation of globotriaosylceramide in different tissues. Cardiac involvement is frequent, presenting with left ventricular (LV) hypertrophy as the most common finding, and many patients die of heart failure.1
Clinical Perspective p 529
Enzyme replacement therapy (ERT) with recombinant -galactosidase A cleared microvascular deposits of globotriaosylceramide in biopsies of kidney, skin, and heart of most Fabry patients.2,3 We have shown a reduction in LV mass and an improvement in LV function after 1 year of ERT in 16 Fabry patients.4 However, the response to ERT was not consistent in this small cohort of Fabry patients. In addition, it remained unclear whether the effect of ERT could persist over longer periods of time. In a more recent study in a larger group of patients, we identified the coexistence of LV hypertrophy, myocardial fibrosis, and severely reduced regional LV function as a surrogate of advanced Fabry cardiomyopathy.5 It is conceivable that such severe morphological manifestation is irreversible and that the course of cardiomyopathy at this stage is unresponsive to therapy of the underlying disease.
The hypothesis of the present study was that patients at an early stage of the disease showing no or little myocardial fibrosis may consistently benefit from ERT over a period of 3 years. This hypothesis was tested in a cohort that was relatively large for this rare disease. Fibrosis was quantified by magnetic resonance imaging (MRI).
|
Methods |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Study Population
Thirty-two patients with genetically confirmed Fabry disease 42±7 years of age were observed over a period of 3 years. None of the Fabry patients had received ERT at study entry. A subgroup of these patients (n=16) who were under ERT for 1 year was already reported.4 The data from the Fabry group were compared with those from 20 age-matched healthy control subjects. The study conformed with the principles outlined in the Declaration of Helsinki. Informed consent was obtained from all patients.
Patients were treated with recombinant -galactosidase A (dosage of 1 mg/kg body weight) intravenously every 2 weeks (infusion time, 2 to 4 hours) for a period of 3 years.4 Patients underwent MRI, standard echocardiographic, color Doppler myocardial imaging studies, and bicycle stress tests at baseline and after 1, 2, and 3 years.
MRI Studies
Routine cine MRI with gadolinium was carried out in all patients with Fabry disease as part of the standard assessment. The late-enhancement (LE) technique (8-mm slice thickness, breath hold, short heart axis) was applied to detect changes in tissue integrity in the LV myocardium.6 Images were acquired with an inversion recovery sequence (field of view, 240x320 mm2; matrix, 165x256). Short-axis views at the basal, mid, and apical segments were used for the semiquantitative assessment of the appearance of LE in every LV segment (LE, yes or no) according to the standardized 16-segment model.7 With this LE technique, every LV segment was evaluated for the occurrence of intramyocardial fibrosis. All MRI data were analyzed by researchers blinded to the time point.
Standard Echocardiographic Measurements
LV end-diastolic and end-systolic dimensions and end-diastolic thickness of the posterior wall (PWT) and septum were measured with standard M-mode echocardiographic methods and parasternal LV long-axis images (3.5 MHz; GE Vingmed Vivid 7, Horten, Norway). Myocardial mass was calculated with the Devereux formula. Ejection fraction was calculated with the modified Simpson method. Blood pool pulsed Doppler of the mitral valve inflow was used to extract the ratio of early to late diastolic flow velocity (E/A ratio) and the deceleration time.
Color Doppler Myocardial Imaging
Real-time 2-dimensional color Doppler myocardial imaging data were recorded from the interventricular septum and the LV lateral wall with standard apical 4-chamber views to evaluate longitudinal function (3.5 MHz; GE Vingmed Vivid 7). To assess radial function of the posterior wall, parasternal long-axis views were used. Color Doppler myocardial imaging data were analyzed with dedicated software (Echopac, GE Ultrasound, Horten, Norway). Radial strain-rate curves of the midbasal posterior wall were extracted, as well as longitudinal strain-rate curves of the midapical septum and the basal midlateral wall. These longitudinal segments were chosen on the basis of experience gained in earlier studies on Fabry cardiomyopathy: The midapical septum is always without fibrosis, whereas the basal midlateral wall is the segment in which fibrosis usually starts.5,6,8 From the resulting strain-rate curves, peak systolic strain rate (SRSYS) was derived. All echocardiographic data were analyzed by researchers blinded to the time point and degree of fibrosis.
Bicycle Stress Test
Symptom-limited (fatigue or dyspnea) exercise was performed on a bicycle ergometer with a 25-W 3-minute step protocol starting at 50 W. The heart rate was continuously monitored, and a 12-lead ECG and blood pressure were recorded at every step. Criteria for termination were achievement of maximal heart rate, severe chest pain or dyspnea, horizontal or downsloping ST-segment depression 
2 mm, systolic blood pressure >220 mm Hg, diastolic blood pressure >120 mm Hg, reduction in systolic blood pressure 30 mm Hg, and supraventricular or ventricular tachyarrhythmia.
Patient Groups
Patients were assigned to 1 of 3 groups according to the amount of fibrosis in the MRI.5,6,8 Patients without detectable fibrosis were categorized as the no fibrosis group. Patients with fibrosis in no more than 1 LV segment were categorized as the mild fibrosis group, and patients with 2 fibrotic LV segments were categorized as the severe fibrosis group.
Data Analysis
Data are presented as mean±SD. Differences between control subjects and patients were tested with the unpaired Student t test or 
2 test as appropriate. Multiple comparisons between different groups were performed using ANOVA with Duncan’s posthoc test. Changes over time were analyzed with a general linear model for repeated measurements. The overall effect was assessed in a multivariable analysis after testing for sphericity to check the circular covariance assumption. If sphericity was not present, the Huyhn-Feldt 
correction factor was applied to correct the degrees of freedom, and the resulting probability value was then reported. Sidak’s t test was applied to account for multiple testing in analyses assessing between-subject effects. All tests were performed 2 sided. A value of P<0.05 was considered statistically significant. SPSS version 16.0.1 (SPSS Inc, Chicago, Ill) was used.
The authors had full access to and take full responsibility for the integrity of the data. All authors have read and agree to the manuscript as written.
|
Results |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
The baseline characteristics of the control subjects and Fabry patients are presented in Table 1. Fourteen patients had a history of hypertension. All were under hypertensive medication and therefore were almost normotensive at study entry. The types of antihypertensive medication and the number of patients receiving antihypertensive medication were very uniformly distributed in all 3 groups. The major clinical limitation at baseline was dyspnea. Two patients died during follow-up of heart failure as a consequence of the underlying disease.
|
MRI Studies
At baseline, 12 patients were LE negative, 11 patients had only 1 LE-positive segment, and 9 patients had LE in >1 segment (Figure 1). In general, LE was detected in basal or mid segments of the posterolateral walls. Only in the severe fibrosis group were fibrotic segments also found in the basal third of the other LV walls. None of the patients had an LE-positive segment in the apical septum. There was no change in the LE pattern after 3 years of ERT.
|
Standard Echocardiographic Measurements
Comparison Between the Complete Fabry Cohort and Control Subjects
Fabry patients had a longer deceleration time (248±65 ms) compared with control subjects (198±36 ms; P<0.01), but the E/A ratio did not differ (Fabry, 1.5±0.5; control subjects, 1.4±0.4). Patients showed a normal ejection fraction at baseline (62±1%), not different from control subjects (64±1%), and no change during ERT (Fabry, 64±1%). End-diastolic thicknesses of the LV posterior wall and septum were significantly higher in patients compared with control subjects (PWT: Fabry, 13.9±2.1 mm; control subjects, 8.6±1.4 mm; septum: Fabry, 14.3±2.1 mm; control subjects, 8.9±1.0 mm; both P<0.001). In Fabry patients, myocardial mass at study entry averaged 269±67 g, which was significantly higher compared with the control subjects (133±55 g; P<0.001). The standard echocardiographic measurements of the Fabry subgroups are shown in Table 2, and the changes in these parameters during ERT are given in Table 3. In all 3 subgroups, PWT and LV myocardial mass decreased significantly after 3 years of ERT.
|
|
Radial and Longitudinal Function
In the complete Fabry cohort, radial SRSYS averaged 2.0±0.5 seconds–1, which was significantly lower than in control subjects (SRSYS=2.7±0.5 seconds–1; P<0.001). The lowest radial SRSYS was seen in the severe fibrosis group. Figure 2 displays the change in radial SRSYS during the 3 years of treatment in the various subgroups. Radial SRSYS increased in the no fibrosis group (normal values after 3 years of ERT) and rather decreased in the severe fibrosis group (Figure 2). Septal longitudinal SRSYS in Fabry patients (–1.2±0.3 seconds–1) was similar to that of controls (–1.3±0.3 seconds–1) and among the 3 Fabry groups at baseline. Septal longitudinal SRSYS increased in the 3 Fabry groups (significantly for the no fibrosis group, P=0.045; Figure 3). Lateral longitudinal SRSYS was lower in Fabry patients (–0.9±0.3 seconds–1) compared with the control subjects (–1.3±0.2 seconds–1; P<0.001) and was lowest in the 2 groups with fibrosis. There was a nonsignificant decrease in lateral SRSYS in patients with severe fibrosis during 3 years of ERT (Figure 3).
|
|
The 2 patients who died during follow-up (1 after 1 year and another after 2 years) had low radial and longitudinal strain-rate values at baseline and were in the severe fibrosis group. Interestingly, both patients showed a decrease in lateral longitudinal systolic strain rate of >0.5 seconds–1 between the last 2 assessments (displaying a systolic strain rate of <–0.3 seconds–1 in the last assessment).
Bicycle Stress Test
The exercise capacity was lower in the Fabry severe fibrosis group compared with the other 2 groups. Figure 4 displays the change in exercise capacity in the 3 Fabry groups during follow-up. Only patients of the no fibrosis group showed an improvement after 3 years of ERT (baseline, 106±14 W; 3 years, 122±26 W; P for trend=0.014).
|
|
Discussion |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
The clearance of globotriaosylceramide from various tissues during ERT in Fabry disease has been well documented.2 This long-term observation evaluates the impact of ERT on the Fabry cardiomyopathy in relation to the baseline disease stages. The data presented here suggest that early treatment is desirable to achieve long-term improvement in myocardial morphology, function, and exercise capacity.
ERT in Fabry Disease
The safety of ERT was documented in 2 initial studies.2,3 Furthermore, Eng et al2 demonstrated in a placebo-controlled, double-blind study that ERT resulted in histological clearance of the deposits of globotriaosylceramide from cardiomyocytes. Subsequently, clinical short-term follow-up studies in relatively small Fabry cohorts or registries have documented that ERT leads to a regression of LV hypertrophy and an improvement in myocardial function.4,9,10 The present investigation shows that the long-term ERT effects on Fabry cardiomyopathy are related to the extent of myocardial fibrosis at baseline, when therapy is started. We and others have shown that Fabry patients at an early stage of the disease have virtually no myocardial fibrosis.5,8 These patients with no detectable fibrosis and mild hypertrophy at baseline showed a normalization of LV wall thickness and mass during ERT in the present study. Parallel to cardiac morphology, LV radial and longitudinal septal function improved to normal. Subsequently, the patients with no fibrosis also improved in exercise capacity, which might be at least partly related to the positive effects of ERT on the Fabry cardiomyopathy. Thus, in the largest group of our Fabry patients (those in the beginning of disease progression), cardiac and exercise improvement during long-term ERT was proven. The effect of ERT critically depended on the stage of the disease at baseline. In patients with localized myocardial fibrosis in only 1 LV segment, a reduction in LV hypertrophy could be achieved during ERT that was associated with a stabilization of LV function and exercise capacity. Patients in a more advanced stage with fibrosis in several LV segments still showed some reduction in hypertrophy but hardly any benefit in terms of LV function during long-term ERT.
Monitoring the Effects of ERT
The change in LV mass was used in several studies to monitor ERT effects.4,9,10 The present study proved LV mass to be in principle a useful parameter to monitor the cardiac effects of ERT. However, fibrosis spreading to the posterior wall may mimic a reduction in hypertrophy in more advanced stages of the cardiomyopathy. Thus, PWT, which is an echocardiographic standard parameter to monitor changes in LV hypertrophy, is probably not useful for monitoring ERT.11
Strain-rate imaging based on tissue Doppler is superior to global parameters like ejection fraction in monitoring and quantifying LV function in patients with Fabry disease.4,5,12,13 The increase in peak systolic strain rate appears to be more specific for regional contractility and rather independent of wall thickness.14 The present study shows that an increase in radial strain rate after 1 year of ERT may predict long-term improvement in regional myocardial function. A decrease in longitudinal lateral function is an ominous sign in advanced stages and predicts an adverse outcome. Interestingly, both patients who died during ERT showed a decrease in longitudinal lateral strain rate of >0.5 seconds–1 in the last year of life.
Most patients in our study sample who were treated with ERT reported an improvement in exercise capacity. The improvement could, however, be objectified only in the group of patients at an early stage of the disease. The reason might be that the mechanisms limiting exercise capacity are complex in Fabry patients and include cardiovascular factors, neuropathic pain, and hypohydrosis.
Clinical Impact and Limitations
The present study shows that an assessment of the baseline conditions before ERT is necessary. Knowledge of the presence or absence of myocardial fibrosis is crucial with respect to the treatment expectations. A recent phase IV ERT study focusing on renal function showed more benefit in patients starting with better renal function.15 We showed this finding here for Fabry cardiomyopathy, suggesting that the earlier the treatment is started, the better the long-term outcome is.
Conclusions
In patients with Fabry disease, early is probably superior to late treatment to achieve long-term improvements in cardiac morphology and function and exercise capacity.
|
Acknowledgments |
|---|
Disclosures
Dr Wanner is a member of the European Advisory Board of the Fabry Registry sponsored by Genzyme Corp and has received travel assistance, speaking fees, and research support. Drs Weidemann, Breunig, and Strotmann have received speaking fees from Genzyme Corp. The other authors report no conflicts.
|
References |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
1. Desnick RJ, Brady R, Barranger J, Collins AJ, Germain DP, Goldman M, Grabowski G, Packman S, Wilcox WR. Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy. Ann Intern Med. 2003; 138: 338–346.
2. Eng CM, Guffon N, Wilcox WR, Germain DP, Lee P, Waldek S, Caplan L, Linthorst GE, Desnick RJ. Safety and efficacy of recombinant human alpha-galactosidase A: replacement therapy in Fabry’s disease. N Engl J Med. 2001; 345: 9–16. 3. Schiffmann R, Kopp JB, Austin HA 3rd, Sabnis S, Moore DF, Weibel T, Balow JE, Brady RO. Enzyme replacement therapy in Fabry disease: a randomized controlled trial. JAMA. 2001; 285: 2743–2749. 4. Weidemann F, Breunig F, Beer M, Sandstede J, Turschner O, Voelker W, Ertl G, Knoll A, Wanner C, Strotmann JM. Improvement of cardiac function during enzyme replacement therapy in patients with Fabry disease: a prospective strain rate imaging study. Circulation. 2003; 108: 1299–1301. 5. Weidemann F, Breunig F, Beer M, Sandstede J, Stork S, Voelker W, Ertl G, Knoll A, Wanner C, Strotmann JM. The variation of morphological and functional cardiac manifestation in Fabry disease: potential implications for the time course of the disease. Eur Heart J. 2005; 26: 1221–1227. 6. Beer M, Weidemann F, Breunig F, Knoll A, Koeppe S, Machann W, Hahn D, Wanner C, Strotmann J, Sandstede J. Impact of enzyme replacement therapy on cardiac morphology and function and late enhancement in Fabry’s cardiomyopathy. Am J Cardiol. 2006; 97: 1515–1518. 7. Cerqueira MD, Weissman NJ, Dilsizian V, Jacobs AK, Kaul S, Laskey WK, Pennell DJ, Rumberger JA, Ryan T, Verani MS. Standardized myocardial segmentation and nomenclature for tomographic imaging of the heart: a statement for healthcare professionals from the Cardiac Imaging Committee of the Council on Clinical Cardiology of the American Heart Association. Circulation. 2002; 105: 539–542. 8. Moon JC, Sachdev B, Elkington AG, McKenna WJ, Mehta A, Pennell DJ, Leed PJ, Elliott PM. Gadolinium enhanced cardiovascular magnetic resonance in Anderson-Fabry disease: evidence for a disease specific abnormality of the myocardial interstitium. Eur Heart J. 2003; 24: 2151–2155. 9. Beck M, Ricci R, Widmer U, Dehout F, de Lorenzo AG, Kampmann C, Linhart A, Sunder-Plassmann G, Houge G, Ramaswami U, Gal A, Mehta A. Fabry disease: overall effects of agalsidase alfa treatment. Eur J Clin Invest. 2004; 34: 838–844. 10. Hughes DA, Elliott PM, Shah J, Zuckerman J, Coghlan G, Brookes J, Mehta AB. Effects of enzyme replacement therapy on the cardiomyopathy of Anderson-Fabry disease: a randomised, double-blind, placebo-controlled clinical trial of agalsidase alfa. Heart. 2008; 94: 153–158. 11. Eng CM, Germain DP, Banikazemi M, Warnock DG, Wanner C, Hopkin RJ, Bultas J, Lee P, Sims K, Brodie SE, Pastores GM, Strotmann JM, Wilcox WR. Fabry disease: guidelines for the evaluation and management of multi-organ system involvement. Genet Med. 2006; 8: 539–548. 12. Pieroni M, Chimenti C, Ricci R, Sale P, Russo MA, Frustaci A. Early detection of Fabry cardiomyopathy by tissue Doppler imaging. Circulation. 2003; 107: 1978–1984. 13. Weidemann F, Niemann M, Herrmann S, Kung M, Stork S, Waller C, Beer M, Breunig F, Wanner C, Voelker W, Ertl G, Bijnens B, Strotmann JM. A new echocardiographic approach for the detection of non-ischaemic fibrosis in hypertrophic myocardium. Eur Heart J. 2007; 28: 3020–3026. 14. Weidemann F, Jamal F, Sutherland GR, Claus P, Kowalski M, Hatle L, De Scheerder I, Bijnens B, Rademakers FE. Myocardial function defined by strain rate and strain during alterations in inotropic states and heart rate. Am J Physiol Heart Circ Physiol. 2002; 283: H792–H799. 15. Banikazemi M, Bultas J, Waldek S, Wilcox WR, Whitley CB, McDonald M, Finkel R, Packman S, Bichet DG, Warnock DG, Desnick RJ. Agalsidase-beta therapy for advanced Fabry disease: a randomized trial. Ann Intern Med. 2007; 146: 77–86.
Related Article:
This article has been cited by other articles:
Footnotes
*The first 2 authors contributed equally to this work. 
Circulation 2009 119: 487-488.
T. D. Karamitsos, J. M. Francis, S. Myerson, J. B. Selvanayagam, and S. Neubauer
The Role of Cardiovascular Magnetic Resonance Imaging in Heart Failure
J. Am. Coll. Cardiol.,
October 6, 2009;
54(15):
1407 - 1424.
[Abstract]
[Full Text]
[PDF]
H.-Y. Lin, K.-W. Chong, J.-H. Hsu, H.-C. Yu, C.-C. Shih, C.-H. Huang, S.-J. Lin, C.-H. Chen, C.-C. Chiang, H.-J. Ho, et al.
High Incidence of the Cardiac Variant of Fabry Disease Revealed by Newborn Screening in the Taiwan Chinese Population
Circ Cardiovasc Genet,
October 1, 2009;
2(5):
450 - 456.
[Abstract]
[Full Text]
[PDF]
This Article 
Abstract
Full Text (PDF)
All Versions of this Article:
119/4/524
most recent
CIRCULATIONAHA.108.794529v1
Alert me when this article is cited
Alert me if a correction is posted
Citation Map
Services
Email this article to a friend
Similar articles in this journal
Similar articles in PubMed
Alert me to new issues of the journal
Download to citation manager
Request Permissions Citing Articles
Citing Articles via HighWire
Citing Articles via Google Scholar
Google Scholar
Articles by Weidemann, F.
Articles by Strotmann, J.
Search for Related Content
PubMed
PubMed Citation
Articles by Weidemann, F.
Articles by Strotmann, J.
Related Collections
Other heart failure
Other Treatment
Related Article