Key result
Segmental FDG uptake was significantly higher in the left ventricular lateral wall compared to the septal wall (88% vs. 77%, p<0.001) in patients with Becker muscular dystrophy, though metabolic activity appeared limited by the extent of myocardial fibrosis.
Why the study?
The reason for the characteristic cardiac phenotype in Becker muscular dystrophy and data from comprehensive hybrid CMR and FDG-PET imaging were limited.
Does hybrid CMR- and FDG-PET-imaging reveal a relationship between myocardial metabolic activity and fibrosis in patients with Becker muscular dystrophy?
Cross-Sectional (n=14)
No
Does hybrid CMR- and FDG-PET-imaging reveal a relationship between myocardial metabolic activity and fibrosis in patients with Becker muscular dystrophy?
Absolute Event Rate: 88% vs 77%
p-value: p=<0.001
Simultaneous PET-CMR imaging in Becker muscular dystrophy patients reveals that myocardial metabolic activity is higher in the LV free wall but is limited by the extent of myocardial fibrosis, providing insights into early disease stages.
May reflect regional metabolic heterogeneity in Becker cardiomyopathy; hypothesis-generating for hybrid PET-CMR in fibrosis monitoring.
Background Cardiac 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. 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. Methods Hybrid 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. Results A 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). Conclusions Segmental 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.
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Vehof et al. (2022) conducted a cross-sectional in Becker Muscular Dystrophy (n=14). Left ventricular lateral wall vs. Septal wall was evaluated on Segmental FDG uptake (p=<0.001). Segmental FDG uptake was significantly higher in the left ventricular lateral wall compared to the septal wall (88% vs. 77%, p<0.001) in patients with Becker muscular dystrophy, though metabolic activity appeared limited by the extent of myocardial fibrosis.
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