Mechanisms and Treatment of Exercise Intolerance and Persistent Fatigue in Spinal Muscular Atrophy
- Conditions
- Spinal Muscular Atrophy
- Interventions
- Other: Observational
- Registration Number
- NCT05518773
- Lead Sponsor
- Columbia University
- Brief Summary
This study will focus on the pathophysiological underpinnings of reduced exercise capacity and fatigue in ambulatory patients with spinal muscular atrophy (SMA). There has been laboratory evidence to suggest that the molecular mechanisms underlying mitochondrial biogenesis may be vulnerable to survival motor neuron (SMN) protein deficiency. This is an observational, single visit study including 34 ambulatory SMA patients treated with SMN repletion therapies (risdiplam or nusinersen) for at least 6 months at enrollment.
- Detailed Description
SMN depletion affects muscle mitochondria and thus muscle function as a result. The relationship between these and their effect(s) on fatigue in the context of SMN repletion treatment has not been evaluated. If muscle function is vulnerable to SMN insufficiency, treatment strategies targeting muscle in addition to the central nervous system (motor neurons) may ameliorate fatigue and improve exercise capacity, thereby improving quality of life and bringing SMA treatments closer to a cure. This project explores such an idea by comparing the effects of the two different SMN repletion modalities in patients. This is an observational cross-sectional study involving ambulatory SMA children and adults treated for at least 6 months with SMN repletion therapy, either (1) systemically with risdiplam, or (2) intrathecally (central nervous system-only), with nusinersen.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 34
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Genetic confirmation of SMA with laboratory documentation of homozygous deletion of survival motor neuron (SMN1) exon 7;
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At least 8 years of age at time of signing Informed Consent Form (or assent)
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Children or adults currently receiving treatment, for at least 6 months, with SMN repletion therapy, either with
(1) risdiplam, or (2) nusinersen
-
Able to walk independently at least 25 meters
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Able to tread a stationary cycle ergometer.
- Unable to walk 25 meters independently.
- Use of investigational medications intended for the treatment of SMA within 30 days prior to study entry.
- The presence of any contraindication to exercise according the American College of Sports Medicine (ACSM) criteria.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Nusinersen treated Observational Children and adults who are currently treated with nusinersen for at least 6 months prior to enrollment. Risdiplam treated Observational Children and adults who are currently treated with risdiplam for at least 6 months prior to enrollment.
- Primary Outcome Measures
Name Time Method Peak oxygen uptake Baseline Participants will undergo an exercise tolerance test performed by a clinical exercise physiologist using an electronically-braked recumbent cycle ergometer to determine peak oxygen uptake (VO2 max).
- Secondary Outcome Measures
Name Time Method Leg muscle composition Baseline To characterize leg muscle composition, quality and architecture using MRI and ultrasound in individuals with SMA treated with agents that restore SMN either systemically (risdiplam) or to central nervous system alone (nusinersen).
Distance walked during the Six Minute Walk Test (6MWT) Baseline 6MWT is an objective evaluation of functional exercise capacity, measures the maximum distance a person can walk in six minutes over a 25-meter linear course.
NIRS derived index of muscle oxygen extraction Baseline Near Infrared Spectroscopy (NIRS) is a simple, non-invasive method to measure oxygen in muscle and other tissues in vivo.
Trial Locations
- Locations (1)
Columbia University Irving Medical Center
🇺🇸New York, New York, United States