Major ALS Breakthrough – Common Cause of All Forms of ALS Discovered
By Dell Hill
A major breakthrough has been reported that could soon allow very specific drug testing to control, or perhaps even eliminate, all forms of ALS - commonly known as Lou Gehrig's Disease.
This outstanding medical news was reported by NeuroScienceNews.com.
“The underlying disease process of amyotrophic lateral sclerosis (ALS and Lou Gehrig’s disease), a fatal neurodegenerative disease that paralyzes its victims, has long eluded scientists and prevented development of effective therapies. Scientists weren’t even sure all its forms actually converged into a common disease process.
But a new Northwestern Medicine study for the first time has identified a common cause of all forms of ALS.
The basis of the disorder is a broken down protein recycling system in the neurons of the spinal cord and the brain. Optimal functioning of the neurons relies on efficient recycling of the protein building blocks in the cells. In ALS, that recycling system is broken. The cell can’t repair or maintain itself and becomes severely damaged.
The discovery by Northwestern University Feinberg School of Medicine researchers, published in the journal Nature, provides a common target for drug therapy and shows that all types of ALS are, indeed, tributaries, pouring into a common river of cellular incompetence.
“This opens up a whole new field for finding an effective treatment for ALS,” said senior author Teepu Siddique, M.D., the Les Turner ALS Foundation/Herbert C. Wenske Professor of the Davee Department of Neurology and Clinical Neurosciences at Northwestern’s Feinberg School and a neurologist at Northwestern Memorial Hospital. ”We can now test for drugs that would regulate this protein pathway or optimize it, so it functions as it should in a normal state.”
The discovery of the breakdown in protein recycling may also have a wider role in other neurodegenerative diseases, specifically the dementias. These include Alzheimer’s disease and frontotemporal dementia as well as Parkinson’s disease, all of which are characterized by aggregations of proteins, Siddique said. The removal of damaged or misfolded proteins is critical for optimal cell functioning, he noted.
This breakdown occurs in all three forms of ALS: hereditary, which is called familial; ALS that is not hereditary, called sporadic; and ALS that targets the brain, ALS/dementia.
In related research, Feinberg School researchers also discovered a new gene mutation present in familial ALS and ALS/dementia, linking these two forms of the disease.”
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Absolutely wonderful news from the science of medical research. It’s discoveries such as this that will one day lead to the prevention or cure for cancer and other deadly diseases.
Just a word of cautious optimism; specific drug testing and the subsequent approval by the FDA for treatment usually takes years. But, the process could never start without this discovery, so the ball is rolling...hopefully, on a steep, downhill grade.
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