About this trial
Duchenne Muscular Dystrophy (DMD) is an X-linked disorder that causes muscle wasting, cardiopulmonary failure, and premature death. Heart failure is a leading cause of death in DMD, but substantial knowledge gaps exist regarding predisposing risk factors. In the general population, hyperglycemia, insulin resistance, and decreased heart rate variability (HRV; reflecting autonomic dysfunction) are associated with cardiomyopathy (CM). It is unclear whether these factors are associated with DMD-CM. Closing this knowledge gap may lead to novel screening and therapeutic strategies to delay progression of DMD related CM. Despite risk factors for hyperglycemia, including the use of glucocorticoids, low muscle mass, obesity, and reduced ambulation, little is known regarding glucose abnormalities in DMD. Some of these same risk factors, along with the distance needed to travel for specialty care, present significant barriers to research participation and clinical care for individuals with DMD. Remote wearable technology may improve research participation in this vulnerable population. Therefore, this study will leverage remote wearable technologies to overcome these barriers and define the relationship between dysglycemia and DMD-CM.
In this Aim of the study, the investigators will assess the utility of remote wearable technology to predict changes in traditional metrics of metabolism and cardiac function. In this pilot study, 10 individuals with DMD will undergo cardiac magnetic resonance imaging (CMR) and oral glucose tolerance tests (OGTTs) at baseline and two years. The investigators will remotely assess glycemia (using continuous glucose monitors), HRV (using extended Holter monitors), and activity (using accelerometers) every 6 months over the 2 years and evaluate if changes in wearable metrics predict changes in CMR and OGTT.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
Male- ≥10 years
Clinical phenotype of DMD confirmed with muscle biopsy or genotype.
Informed consent for individuals ≥18 years
Parent/guardian informed consent and child assent for individuals < 18 years
Trial population
10 adolescent and young adult males with DMD. DMD affects about 1/3500-6000 males and 1/50million females, therefore only male participants will be enrolled.
Trial design
Cohort
Cross-sectional
Treatments tested in this trial
wearable technology
DeviceThree wearable devices
Treatment groups
Trial outcomes
Primary outcomes
Rate of hyperglycemia
number of glucose measurements ≥140mg/dL over total number of glucoses
Standard deviation of the mean R-to-R segment (SDANN)
correlation of rate of hyperglycemia and SDANN, which reflects heart rate variability
Secondary outcomes
Coefficient of variation on CGM
variability of glucose levels on CGM measured by coefficient of variation (COV)
Rate of significant hyperglycemia
number of glucose measurements ≥200mg/dL over total number of glucoses
Activity level
Time spent in sedentary, low intensity, and moderate to vigorous physical activity
Standard deviation of normal R to R intervals (SDNN)
correlation of rate of hyperglycemia and SDNN
Sponsors and contacts
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