Bob Shepard
UAB Media Relations

CBD Oil graphic 2

Investigators with the University of Alabama at Birmingham Cannabidiol Program will present the first results drawn from the CBD oil studies underway at UAB and Children’s of Alabama. Three abstracts will be presented at the annual meeting of the American Academy of Neurology in Vancouver, Canada.The abstracts describe results from the first 51 subjects enrolled in the studies. Among other findings, the researchers report that approximately 50 percent of the subjects responded to the CBD oil therapy with overall sustained improvement inseizure control over a six-month period. Seizures declined between 32 and 45 percent in the responders, depending on the CBD dose. Two patients were seizure-free, and nine dropped out due to side effects or lack of efficacy.

UAB launched the studies of CBD oil as a treatment for severe, intractable seizures in April of 2015. The studies, an adult study at UAB and a pediatric study at Children’s of Alabama, were authorized by the Alabama Legislature in 2014 by legislation known as Carly’s Law.

The studies are designed to test the safety and tolerability of CBD oil in patients with intractable seizures. CBD oil, a derivative of the cannabis plant, is delivered orally as an oily liquid.

“The studies are ongoing, and we have a lot more to learn; but these preliminary findings are encouraging,” said Jerzy Szaflarski, M.D., Ph.D., professor in the Department of Neurology, principal investigator of the adult study. “Among our goals was to determine the safety of CBD oil therapy, and it appears that, in many cases, patients tolerate the oil quite well. The evidence of seizure reduction gives us hope that, the more we learn about CBD oil, the better we will be able to tailor this therapy to provide relief for those with severe epilepsy.”

The oil used in the studies is produced under stringent requirements of the United States Food and Drug Administration by a licensed pharmaceutical company. It contains only traces of THC, the psychoactive component of marijuana. The process developed by GW Pharmaceuticals guarantees the consistency of the product that is provided to study participants.

“Some patients respond well, but others either have no improvement or experience significant side effects. CBD is not a panacea, and it’s not for everyone. But many patients do have a reduction in seizure activity, and we hope our efforts will further define how to best utilize CBD oil for maximum benefit to the appropriate patient population.”
“The studies thus far show that the administration of CBD oil is a complex undertaking,” said Martina Bebin, M.D., professor of neurology and principal investigator for the pediatric study. “Some patients respond well, but others either have no improvement or experience significant side effects. CBD is not a panacea, and it’s not for everyone. But many patients do have a reduction in seizure activity, and we hope our efforts will further define how to best utilize CBD oil for maximum benefit to the appropriate patient population.”

Tyler Gaston, M.D., a clinical neurophysiology fellow, led a study of potential interactions between CBD and clobazam, a commonly prescribed anti-epileptic medication. The investigators suspected that CBD treatment might cause an increase in the blood levels of clobazam and its metabolite, N-desmethylclobazam, leading to adverse events including sedation. Seventeen patients in the studies were taking clobazam, and investigators found clear evidence for an interaction, with rising clobazam levels during CBD therapy. This finding highlights the importance of monitoring clobazam and N-desmethylclobazam levels when treating patients with CBD, and the results underscore the importance of the new knowledge gained through the UAB CBD program.

A study headed by Leslie Perry, M.D., also a clinical neurophysiology fellow, looked at the effect of CBD oil therapy on electroencephalography, or EEG. EEG is the standard test to measure electrical activity in the brain. The same cohort of 51 patients received EEG tests prior to beginning CBD therapy and then again after CBD therapy had begun. The investigators report that CBD does not appear to have a negative effect on standard EEG parameters. However, the authors acknowledge that the conclusion is limited by the relatively short duration of both the EEG and the length of time from the tests done prior to beginning CBD therapy and then during therapy.  

Another abstract, led by Jane Allendorfer, Ph.D., assistant professor of neurology, will be presented at the annual meeting of the Organization for Human Brain Mapping in Geneva, Switzerland. In her work, she evaluated the effects of CBDtreatment on attention circuits in the brain using functional MRI. Eight patients underwent fMRI before treatment with CBD and while taking CBD. Their scanning showed improved activation of brain regions important for attention. The authors conclude that these preliminary results are promising and illustrate the potential of CBD treatment to improve not only seizure control but also cognition in patients with poorly controlled epilepsy.  

The ongoing UAB CBD studies currently have 40 children and 39 adults enrolled.


                             MiRNA JRHA small regulatory RNA called microRNA-155 appears to play a key role in the brain inflammation that helps foster Parkinson’s disease. This finding, using a mouse model, implicates microRNA-155 as both a potential therapeutic target and biomarker for this progressive neurodegenerative disorder, according to a University of Alabama at Birmingham study published Feb. 23 in The Journal of Neuroscience.

Parkinson’s disease, the most common neurodegenerative movement disorder, affects as many as 1 million Americans, more than multiple sclerosis, muscular dystrophy and Lou Gehrig’s disease combined. About 60,000 new U.S. cases are diagnosed each year, and thousands more go undetected.

standaart 2016Parkinson’s disease can progress undetected for years before symptoms appear. The UAB researchers, led by David Standaert, M.D., Ph.D., professor and chair of the UAB Department of Neurology, write that their results “suggest that microRNA-155 is involved early in Parkinson’s disease pathogenesis and is important for initiating the inflammatory response to alpha-synuclein.”

Widespread intracellular aggregates of alpha-synuclein protein, or α-syn, are a hallmark of Parkinson’s disease, along with progressive loss of neurons in a region of the brain called the substantia nigra pars compacta, or SNpc.

The mouse model used by the UAB team uses a virus to deliver a human α-syn gene to the brain, where it is overexpressed, leading to inflammation and neurodegeneration. The researchers examined whether this overexpression α-syn also changed expression of any microRNAs. MicroRNAs — which interact with messenger RNAs after their export from the cell nucleus — act to regulate gene expression in cells, and there are more than 1,300 distinct microRNAs at work in the brain.

The UAB researchers probed with an array of 84 inflammation- and autoimmune-associated microRNAs and found that microRNA-155 was significantly overexpressed in the SNpc, two weeks after viral delivery of the α-syn gene.

To see whether microRNA-155 was involved in inflammation and neurodegeneration, they tested mice with a deletion of the microRNA-155 gene. In the mouse α-syn model, this deletion prevented the increased expression two immune-cell markers — MHCII and CD68 — in the SNpc. Similarly, knock-out of the microRNA-155 gene prevented the α-syn-associated neurodegeneration that is seen six months later in wild-type mice challenged with α-syn.

The toll of Parkinson’s

  • As many as 1 million Americans have Parkinson’s disease, a chronic and progressive movement disorder. This is more than multiple sclerosis, muscular dystrophy and Lou Gehrig’s disease combined.
  • About 60,000 new U.S. cases are diagnosed each year, but thousands of others go undetected.
  • Worldwide, about 7 million to 10 million have Parkinson’s disease.
Source: Parkinson’s Disease Foundation
Finally, the researchers tested isolated microglia, the resident macrophages that are the first line of immune defense in the brain. They found that the addition of α-syn fibrils to isolated microglia activated an immune response, as shown by increased expression of MHCII, a part of the inflammatory cascade, and inducible nitric oxide synthase, a pro-inflammatory enzyme. Microglia with the microRNA-155 gene deletion showed no increase in MHCII or inducible nitric oxide synthase, but a low-concentration transfection with a microRNA-155 mimic oligonucleotide restored the inflammatory response against α-syn fibrils in microglia with the microRNA-155 gene deletion.

“Our studies suggest,” the authors wrote, “that microRNA-155 is a key inflammation-initiating molecule that could be a viable target for Parkinson’s disease therapeutics.”

Authors of the paper, “MicroRNA-155 Regulates Alpha-Synuclein-Induced Inflammatory Responses in Models of Parkinson Disease,” are Aaron D. Thome, Ashley S. Harms, Laura A. Volpicelli-Daley and David G. Standaert, all of the Center for Neurodegeneration and Experimental Therapeutics, UAB Department of Neurology.

The work was supported by the American Parkinson Disease Association, and NIH grants F31 NS084722 and P20 NS092530.



before i forget B. Smith — restaurateur, magazine publisher, celebrity chef and nationally known lifestyle maven — and her husband, Dan Gasby, will visit the Barnes & Noble store at The Summit in Birmingham for a special event to discuss and sign copies of their book, “Before I Forget,” written with Vanity Fair contributing editor Michael Shnayerson. Smith has been diagnosed with Alzheimer’s disease, and “Before I Forget” describes her and Gasby’s journey with the disease and offers practical advice about dealing with Alzheimer’s day-to-day challenges, the family realities and tensions, ways of coping, and lessons learned along the way. 

Erik Roberson, M.D., Ph.D., Virginia B. Spencer Professor of Neuroscience and director of the Alzheimer’s Disease Center at the University of Alabama at Birmingham School of Medicine, will participate in the discussion to share research on the disease and answer questions from the audience.

The event is at 7 p.m., Tuesday, Feb. 23, at the Barnes & Noble at The Summit, 201 Summit Blvd., Suite 100.

By Bob Shepard
UAB Media Relations
peter king Peter King, M.D., professor in the Department of Neurology in the School of Medicine at the University of Alabama at Birmingham, will receive the 2016 Spirit of Lou Gehrig Award from the ALS Association’s Alabama Chapter. King has spent 20 years treating patients with the disease and is a leading researcher working to find a cure for ALS. Amyotrophic lateral sclerosis is a progressive neurodegenerative disease affecting nerve cells in the brain and spinal cord. The disease robs victims of the ability to walk, talk and eventually even blink an eye.

King will receive the award at the second annual “Changing the Game” awards dinner, 6 p.m. Wednesday, Feb. 24, at The Club on Robert Smith Drive in Birmingham. Guest speakers at the event will be former Auburn great Bo Jackson and former University of Alabama star Tony Nathan.

The award is named for baseball player Lou Gehrig, nicknamed “the Iron Horse.” Gehrig showed extraordinary courage and commitment to the game of baseball in the face of a devastating ALS diagnosis.

For more information about The ALS Association Alabama Chapter and the “Changing the Game” event, visit or