Media Contacts:
Renee Tessman, [email protected], (612) 928-6137
Carissa Jackson, [email protected], (612) 928-6169 

Newswise — MINNEAPOLIS – A drug shown to be effective in the treatment of babies with the rare muscle-wasting disease spinal muscular atrophy may be effective for muscle control even when treatment is started in children seven months and older, according to a study published in the August 29, 2018, online issue of Neurology®, the medical journal of the American Academy of Neurology. Previous studies focused on children younger than seven months old.

“This study is exciting because we found participants had motor function improvement six months after receiving treatment, even an 8-year-old participant,” said study author Laurent Servais, MD, PhD, of Pitié-Salpêtrière Hospital in Paris, France and Citadelle Hospital in Liège, Belgium. “The overall response was to the same extent as that in the previously studied younger population.”

Spinal muscular atrophy (SMA) is a leading genetic cause of death in infant children worldwide. It is a neurodegenerative disease that attacks nerve cells in the spinal cord, leading to muscle weakness. This can affect breathing, swallowing, walking and head control.

There are several different types of SMA; some of them fatal. SMA type 1 is the most common and most severe form of the disease. It starts before the age of six months, with infants never gaining the ability to sit up. The median survival rate is eight to 14 months old.

For the study, 33 children between the ages of eight months and 9 years old with SMA type 1 were given an injection of the drug nusinersen into the spinal canal. The drug, which was approved by the Food and Drug Administration in December 2016, is the first and only approved treatment for all types of SMA. It works by increasing the production of a certain protein that is essential for motor neurons in the spinal cord to survive.

Participants were evaluated before the injection, as well as at two and six months after the treatment. Researchers collected data about survival, breathing, need for help with feeding and participants’ ability to move.

Six months after the injection, all 33 participants were alive and continuing treatment. There were no safety concerns. The response to the drug was highly variable from person to person, but on average the participants had significant muscle control improvements – even the 8-year-old participant.

In one test that measured muscle control, with scores that ranged between zero and 26, the median improvement among study participants was 1.5 points after six months of treatment. Five of the study’s participants, ranging from 18 months to 4 years old when they received their first injection, were able to sit up without support for the first time.

None of the participants had changes in whether they needed a feeding tube, but some did have worsening respiratory problems. Researchers say this may suggest that nusinersen is slower to act on respiratory symptoms and related infections that might destabilize weak patients.

The results of the study were comparable to previous studies that looked only at infants younger than seven months old.

“Spinal muscular atrophy type 1 is a devastating disease, and it is encouraging to see that nusinersen may also help people who are at a later stage in the disease process,” said Servais. “More studies need to be done as it is likely that there are still unidentified genetic factors that contribute to the differences in participants’ responses to the treatment.”

A limitation of the study is that the majority of the participants were under 4-1/2 years old, so the results cannot be applied to older patients.

Learn more about spinal muscular atrophy at www.BrainandLife.org, the American Academy of Neurology’s free patient and caregiver magazine and website focused on the intersection of neurologic disease and brain health. Follow Brain & LifeTM on Facebook, Twitter and Instagram.

The American Academy of Neurology is the world’s largest association of neurologists and neuroscience professionals, with over 34,000 members. The AAN is dedicated to promoting the highest quality patient-centered neurologic care. A neurologist is a doctor with specialized training in diagnosing, treating and managing disorders of the brain and nervous system such as Alzheimer’s disease, stroke, migraine, multiple sclerosis, concussion, Parkinson’s disease and epilepsy.

For more information about the American Academy of Neurology, visit http://www.aan.com or find us on Facebook, Twitter, Instagram, LinkedIn and YouTube.