by Marylee MacDonald, author of MONTPELIER TOMORROW, a novel about caregiving, a mid-life mom, and ALS
Look in your average yearbook. Can you tell who is going to get ALS and who is not? On January 26, 2014 Anthony Carbajal was diagnosed with ALS. His grandmother had ALS, his mother had it, and now he has it.
ALS begins with small signs that something is wrong. Tiredness. Weakness in a finger. A moment when your tongue gets tangled and it sounds like you’re half-way sloshed.
After graduating from college, Anthony started a wedding photography business. The work allowed him to have a flexible schedule and help with his mother’s care. Now, he can no longer pick up his camera, let alone his mom. Anthony has “familial ALS.”
Anthony Carbajal on CNN
What Is Familial ALS?
According to ARC (“The ALS Research Collaboration) at the University of Miami, “ALS that runs in the family is known as “familial ALS” (or “fALS” for short). The type of ALS that doesn’t run in families is often called “sporadic ALS”. Familial ALS is very rare. Only about 10% of all ALS cases are familial. If more than one member of your family has had ALS, then it is very likely that you belong to a fALS family. If only one person in your family has ever had ALS, then it is most likely that ALS does not run in your family.” Here’s more from ARC
Finding the disease mechanisms for fALS has proven to be a needle-in-a-haystack proposition. Finally, an article in the November issue of Nature reports that Teepu Siddique, MD–a leading researcher in familial ALS–has made a breakthrough. Dr. Siddique is one of a handful of scientists who have consistently sought answers to the many enigmas of ALS. These enigmas all happen at the cellular level. Dr. Siddique and a team of colleagues reported the discovery of an enzyme responsible for repairing or getting rid of damaged proteins. The faulty enzyme is called Ubuiquilin-2. The gene UBQLN2 is responsible for encoding it.
A small number of fALS patients (but not all) have a mutation in the UBQLN2 gene. The faulty UBQLN2 gene creates a malfunctioning Ubiquilin-2 enzyme. This enzyme is responsible for breaking down certain kinds of proteins (ubiquinated proteins). If the enzyme isn’t functioning, these proteins accumulate in the lower motor neurons and upper cortical motor neurons.
The build-up of ubiquinated proteins can happen even when a person does not have the UBQLN2 genetic mutation. Mutations in the TDP-43 and C9ORF72 genes also cause the enzyme to malfunction.
“This is the first time we could connect ALS to a clear-cut biomedical mechanism,” Dr. Siddique said. “It has really made the direction we have to take very clear and sharp. 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.”
When the Ubiquilin 2 enzyme is unable to remove or repair damaged proteins, they begin to pile up in the cells, eventually blocking normal transmission of brain signals in the spinal cord and brain, leading to paralysis.
Ninety percent of people with ALS do not have a family history of the disease. What about them? Is something else going on? Actually, there is a breakthrough on that front, too. It looks like genetic mutations determine who gets ALS and at what age they get it.
According to an article in Annals of Neurology, scientists at the Washington University School of Medicine in St. Louis and Cedars Sinai Hospital in Los Angeles were able to link genetic mutations to ALS patients who had no family history of the disease. “The scientists used a sequencing technique devised at Washington University to look at 17 known ALS genes in the DNA of 391 patients with ALS. Like the overall ALS patient population, 90 percent of the patients had no family history of disease, according to an article on Washington University’s website. The researchers found that if a patient had one genetic mutation, the onset of disease occurred later. Patients who came down with ALS at a younger age had more than one mutation.