Spinal Cord Stimulation Offers Hope for SMA Patients by Restoring Walking Ability

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Spinal Cord Stimulation Offers Hope for SMA Patients by Restoring Walking Ability
Spinal Muscle AtrophySMASpinal Cord Stimulation
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A new study shows that electrical spinal cord stimulation can improve muscle function and walking ability in people with spinal muscle atrophy (SMA), a debilitating genetic disease. The research, published in Nature Medicine, suggests that this treatment could offer a significant breakthrough for individuals with SMA by addressing the underlying cause of their paralysis.

People with spinal muscle atrophy ( SMA ), an inherited neuromuscular disease, often experience muscle weakness that significantly impacts their movement capabilities. Recent research suggests that electrical spinal cord stimulation holds promise for improving muscle function in these patients, potentially even enabling them to walk again.

Studies conducted at the University of Pittsburgh School of Medicine have demonstrated that sessions of spinal cord stimulation can restore motor neuron activity and enhance leg muscle strength in individuals with SMA. These findings were published in Nature Medicine on February 5th. The study involved three participants with SMA who underwent spinal cord stimulation five times a week for four hours for a month. At the conclusion of the trial, all participants exhibited notable improvements in motoneuron function, reduced fatigue, and increased strength and walking ability. Specifically, they experienced an average 40% improvement in step length, up to 180% improvement in muscle strength, and a 26-minute increase in walking time. Doug McCullough, one of the participants who was experiencing advanced symptoms and difficulty walking, remarked on the positive impact of the treatment. He described his pre-treatment gait as a waddle due to weak hip flexors, but noted that the stimulation therapy significantly improved his walking speed, gait, and stamina. Although SMA is a progressive disease that typically worsens over time, the participants in this study demonstrated noticeable improvements during the four-week treatment period. They reported advancements in their activities of daily living, with one patient even stating that they were able to walk from their home to the lab without experiencing fatigue. Study co-author Elvira Pirondini, assistant professor of physical medicine and rehabilitation at Pitt School of Medicine, highlighted these positive outcomes, emphasizing the improvements observed in several clinical measures. The researchers view this study as a 'proof of concept' that offers hope for individuals with this genetic disability. It demonstrates the potential of spinal cord stimulation and other neuromodulation techniques as safe and effective treatment options for paralysis, particularly in cases where medications or gene therapy provide limited relief. The research team plans to conduct further clinical trials with additional SMA patients to rigorously assess the treatment's safety and efficacy. They also aspire to explore the application of this therapy for other neurodegenerative diseases, including ALS and Huntington's disease

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