Abstract

BackgroundCardiac involvement in patients with Becker muscular dystrophy (BMD) is an important predictor of mortality. The cardiac phenotype of BMD patients is characterized by slowly progressive myocardial fibrosis that starts in the left ventricular (LV) free wall segments and extends into the septal wall during the disease course.PurposeSince the reason for this characteristic cardiac phenotype is unknown and comprehensive approaches using e.g. hybrid imaging combining cardiovascular magnetic resonance (CMR) with 18F-fluorodeoxyglucose (FDG) positron emission tomography (PET) are limited, the present study addressed this issue by a comprehensive non-invasive imaging approach.MethodsHybrid CMR- and FDG-PET-imaging was performed in N = 14 patients with BMD on a whole-body Biograph mMR system (Siemens, Erlangen, Germany). The CMR protocol comprised cine- and late-gadolinium-enhancement (LGE)-imaging. Metabolism was assessed with FDG-PET after oral glucose loading to effect myocardial carbohydrate uptake. PET was acquired for 65 min starting with tracer injection. Uptake values from 60 to 65 min p.i. were divided by the area under the blood activity curve and reported as percentages relative to the segment with maximal myocardial FDG uptake.ResultsA characteristic pattern of LGE in the LV lateral wall was observed in 13/14 patients whereas an additional septal LGE pattern was documented in 6/14 patients only. There was one patient without any LGE. Segmental FDG uptake was 88 ± 6% in the LV lateral wall vs. 77 ± 10% in the septal wall (p < 0.001). There was an inverse relationship between segmental FDG activity compared to segmental LGE extent (r = −0.33, p = 0.089). There were N = 6 LGE-positive patients with a segmental difference in FDG uptake of >15% in the LV lateral wall compared to the septal wall = ΔFDG-high group (lateral FDG = 91±3% vs. septal FDG = 69±8%; p < 0.001) while the remaining N = 7 LGE-positive patients showed a segmental difference in FDG uptake of ≤ 15% = ΔFDG-low group (lateral FDG = 85±7% vs. septal FDG = 83 ± 5%; p = 0.37). Patients in the ΔFDG-high group showed only a minor difference in the LGE extent between the LV lateral wall vs. septal wall (p = 0.09) whereas large differences were observed in the ΔFDG-low group (p < 0.004).ConclusionsSegmental FDG uptake—reflecting myocardial metabolic activity—is higher in the LV free wall of BMD patients—possibly due to a higher segmental work load. However, segmental metabolic activity seems to be dependent on and limited by the respective segmental extent of myocardial fibrosis as depicted by LGE-imaging.

Highlights

  • Duchenne and Becker muscular dystrophies (DMD and Becker muscular dystrophy (BMD)) are the most frequent X-chromosomal recessive neuromuscular disorders and are caused by mutations in the dystrophin gene

  • Our group described a characteristic pattern of cardiomyopathy in patients with BMD [5], the potential for predicting adverse cardiac events [7] and the detection of diffuse interstitial fibrosis [9] based on multi-parametric Cardiovascular magnetic resonance (CMR) data

  • We present the first preliminary data of our ongoing positron emission tomography (PET)-CMR-MD research project

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Summary

Introduction

Duchenne and Becker muscular dystrophies (DMD and BMD) are the most frequent X-chromosomal recessive neuromuscular disorders and are caused by mutations in the dystrophin gene. Cardiac involvement in BMD patients is characterized by a non-ischemic pattern of left ventricular (LV) myocardial fibrosis starting in the LV free wall and leading to non-ischemic dilated cardiomyopathy [2, 4,5,6]. Cardiovascular magnetic resonance (CMR) imaging has developed into the most relevant clinical imaging technique regarding detection of cardiac involvement and monitoring of cardiac disease progression— for BMD patients. It cannot only measure shape and function of the heart, and reveals even subtle structural changes in the myocardium such as fibrosis. Purpose: Since the reason for this characteristic cardiac phenotype is unknown and comprehensive approaches using e.g. hybrid imaging combining cardiovascular magnetic resonance (CMR) with 18F-fluorodeoxyglucose (FDG) positron emission tomography (PET) are limited, the present study addressed this issue by a comprehensive non-invasive imaging approach

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