Intramuscular blood flow in Duchenne and Becker Muscular Dystrophy: Quantitative power Doppler sonography relates to disease severity

Abstract

ObjectiveAbsent or truncated dystrophin in Duchenne (DMD) and Becker (BMD) muscular dystrophies results in impaired vasodilatory pathways and exercise induced muscle ischemia. Here, we used power Doppler sonography to quantify changes in intramuscular blood flow immediately following exercise in boys with D/BMD. MethodWe quantified changes in intramuscular blood flow following exercise using power Doppler sonography in 14 boys with D/BMD and compared changes in muscle blood flow to disease severity and to historic controls. ResultPost exercise blood flow change in the anterior forearm muscles is lower in (1) DMD (median 0.25%; range −0.47 to 2.19%) than BMD (2.46%; 2.02–3.38%, p < 0.05) and historical controls (6.59%; 2.16–12.40%, p < 0.01); (2) in non-ambulatory (0.04%; −0.47 to 0.10%) than ambulatory DMD boys (0.71%; 0.07–2.19%, p < 0.05); and (3) in muscle with higher echointensity (rs = −0.7253, p = 0.005). The tibialis anterior showed similar findings. We estimate that a single sample clinical trial would require 19 subjects to detect a doubling of blood flow to the anterior forearm after the intervention. ConclusionPost-exercise blood flow is reduced in D/BMD and relates to disease severity. SignificanceOur protocol for quantifying post-exercise intramuscular blood flow is feasible for clinical trials in D/BMD.