Effect of Agalsidase Alfa on Cardiac Inflammation in Patients With Fabry Disease: A [18F]-FDG PET-CMR Study (ESCAPE-FABRY Trial)

Visit 1. Screening At screening, for potential eligible patients, after obtaining their informed consent, inclusion/exclusion criteria will be reviewed and enrollment will be determined. Demography (date of birth, gender), prior and concomitant medication and relevant medical history will be recorded. Height, body weight, vital signs, and laboratory assessments will be needed. Women of childbearing potential will be tested for pregnancy.

Visit 2. Baseline Study At visit 2, subjects have following baseline evaluations performed

• Laboratory test: CBC+PLT, WBC Differential Count, Routine Chemistry (Calcium, Inorganic P, BUN, Creatinine, Fasting Glucose, Cholesterol, Total Protein, Albumin, Total. Bilirubin, Alkaline Phosphatase, AST, ALT), Electrolyte(Na, K, Cl), Lipid profile(Triglyceride, HDL-Cholesterol, LDL-Cholesterol), Plasma Lyso-GB3, NT-proBNP, Troponin T, high-sensitive C-reactive protein, ESR, Interleukin 6, Soluble urokinase plasminogen activator receptor (suPAR), monocyte chemoattractant protein-1(MCP-1), matrix metalloprotease-9(MMP-9), Tumor necrosis factor receptor 2(TNFR2), Urinalysis with Microscopy, Urine test(Microalbumin, Creatinine, Microprotein,Total), Anti-body testing for agalsidase alfa
• Concomitant medication
• Vital signs, weight
• 12-lead ECG
• QOL questionnaire
• PET-CMR
• MIBG cardiac scintigraphy (not mandatory)
• Conventional Echocardiography including strain imaging

Two-dimensional echocardiography Standard 2-dimensional measurements (LV diastolic and systolic dimensions, ventricular septum and posterior wall thickness, left atrial volume, and LV outflow tract diameter) will be obtained with the patients in the left lateral position. LV ejection fraction (EF) will be calculated by the Simpson's method. From the apical window, a 1- to 2-mm pulsed Doppler sample volume will be placed at the mitral valve tip and mitral flow velocities from 5-10 cardiac cycles will be recorded. Mitral inflow velocities are traced and the following variables will be obtained: peak velocity of early (E) and late (A) filling, and deceleration time of E-wave velocity. Stroke volume (SV) will be measured from LV outflow tract diameter and pulse-wave Doppler signal as previously described. Mitral annular velocity will be measured by Doppler tissue imaging using pulse-wave Doppler mode. The filter will be set to exclude high frequency signal, and the Nyquist limit will be adjusted to a range of 15-20 cm/s. Gain and sample volume will be minimized to allow for a clear tissue signal with minimal background noise. Early diastolic (E') and systolic (S') velocities of the mitral annulus will be measured from the apical 4-chamber view with a 2- to 5-mm sample volume placed at the septal corner of the mitral annulus. All data will be stored digitally and measurements will be taken at the completion of each study. Two-dimensional echocardiographic images from apical views at rest will be acquired, digitized, recorded, and analyzed for the wall motion analysis. Using a dedicated software package (EchoPAC PC), LV-GLS, LV global circumferential strain (LV-GCS), and LV global radial strain (LV-GRS) will be calculated automatically. 2D strain is a non-Doppler-based method for the evaluation of systolic strain using standard 2D acquisitions. LV-GLS strain will be assessed in three apical views, and LV-GCS and LV-GRS will be assessed in three levels of parasternal short-axis views. Left atrial (LA) strain also will be assessed by the same software.

Positron Emission Tomography - Cardiac Magnetic Resonance Imaging (PET-CMR) The PET-CMR procedure will be conducted prior to and within 12 months after initiating Enzyme Replacement Therapy (ERT). All patients are instructed to take a high-fat low-carbohydrate diet the day prior with overnight fast. Administer intravenous unfractionated heparin at a dose of 50 units/kg approximately 15 minutes before the intravenous injection of 10-12 mCi of 18F-FDG. This method is suitable for patients without any bleeding tendencies. After a 90-minute uptake period, cardiac and partial whole body PET images (cerebellum to mid-thigh) are acquired.The F-18 FDG study commences following an oral glucose load of 50 grams, administered one hour prior to injecting 370 MBq of F-18 FDG. A simultaneous cardiac PET/MR study is conducted on an integrated PET/MR scanner (Biograph mMR, Siemens Healthcare, Erlangen, Germany) beginning one hour after the tracer injection. Initially, a standard Dixon sequence is acquired for attenuation correction. Subsequently, comprehensive cardiac MR (CMR) sequences are performed. These include steady-state free precession cine imaging in two-chamber, three-chamber, and four-chamber views, as well as in short-axis images, to ensure detailed cardiac assessment. MR perfusion imaging is performed following gadolinium contrast infusion, and post-contrast late gadolinium enhancement (LGE) studies are executed for detailed tissue characterization. Static F-18 FDG myocardial PET imaging is acquired concurrently during the MRI scans, utilizing list mode for a duration of 30 minutes. The maximal myocardial thickness is noted as 30 mm at end-diastole on cine MRI. The first-pass MR perfusion imaging indicates reduced myocardial blood flow, while patchy F-18 FDG defect areas correspond to regions of LGE, indicative of myocardial fibrosis. Correlate findings from PET and CMR to gain for evaluation of Fabry cardiomyopathy, including assessment of myocardial viability, detection of ischemia, and characterization of tissue.