Why the study?
Duchenne muscular dystrophy shares overlapping clinical features with other disorders, leading to the hypothesis that some patients have secondary neuromuscular disorders that could skew clinical trial data and lead to incomplete treatment plans.
Does genetic panel testing reveal coexisting neuromuscular disorders in patients with Duchenne muscular dystrophy?
Does genetic panel testing reveal coexisting neuromuscular disorders in patients with Duchenne muscular dystrophy?
Nearly 10% of patients with Duchenne muscular dystrophy may have a coexisting secondary neuromuscular disorder, highlighting the importance of expanded genetic testing to prevent confounding in clinical trials and treatment plans.
Comorbid neuromuscular disorders may skew DMD trial data; leaves open prevalence and screening needs in larger cohorts.
Duchenne muscular dystrophy is a genetically based neuromuscular disorder characterized by progressive physical impairment and cardiomyopathy in children, leading to fatal cardiac or respiratory failure. Duchenne muscular dystrophy shares some overlapping clinical features with other disorders, complicating clinical differentiation. We hypothesized that some Duchenne muscular dystrophy patients may have a secondary neuromuscular disorders that could negatively skew data during pharmaceutical clinical trials and lead to incomplete treatment plans. Consecutive genetic panels on 353 patients were reviewed. Thirty-two (32; 9.1%) patients with Duchenne muscular dystrophy were identified. Three (3; 9.4%) were found to have at least 1 genetically confirmed secondary neuromuscular disorder. Overlooking these coexisting disorders could lead to unexpected treatment failures, potentially affecting medication efficacy in trials or commercial use. Secondary neuromuscular disorders should be considered in Duchenne muscular dystrophy patients before clinical trial enrollment or treatment planning, with expanded genetic testing, such as whole exome sequencing or whole genome sequencing, likely to reveal even more secondary disorders.
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Butson et al. (2024) studied this question.
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