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Deep brain stimulation offers relief to UTHealth patient with treatment-resistant depression

Deep brain stimulation offers relief to UTHealth patient with treatment-resistant depression

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For Shannon Paige McCann, the thought of having brain surgery – which would frighten most – paled in significance to the depression that had dragged her down most of her life.

McCann was one of the first people in North America to undergo an experimental treatment option for people struggling with treatment-resistant depression (TRD). The pilot study at the Center of Excellence on Mood Disorders at The University of Texas Health Science Center at Houston (UTHealth) is using deep brain stimulation (DBS) for patients with chronic TRD. The procedure targets an area of the brain called the medial forebrain bundle, which is thought to be important for reward processing.

DBS has actually been used for decades to help Parkinson’s patients whose tremors did not improve with medication, said Jair Soares, M.D., Ph.D., principal investigator, director of the center and professor and Pat R. Rutherford, Jr. Chair in Psychiatry at the McGovern Medical School at UTHealth. DBS targeting the medial forebrain bundle has also been successfully used, on an experimental basis, to treat TRD in Germany. The UTHealth trial is approved by the U.S. Food and Drug Administration (FDA).

McGann, a patient in her late 40s who enrolled in the pilot study, described the treatment as “a miracle.”

“I felt like someone turned on a lightbulb in my brain. Everything is brighter. It changed my life,” she said.

Since she was a child, McGann has suffered from depression off and on. She was diagnosed with depression as a college freshman and was stabilized with medications. She went on to become a teacher for seven years, but after getting a new teaching position, her depression returned severely.

After that, McGann switched careers and excelled in pharmaceutical sales. Then, in 2007, her mother died and her boyfriend broke up with her -; and she hit a new low. “It was a chore to get out of bed; I would lay in bed for days,” she said.

Thinking another change might be beneficial, she moved from Virginia to Houston in September 2016 to take a new job. However, she wasn’t able to handle it. At that point, no medications were working for her and she did not respond to electroconvulsive therapy.

Since these treatments weren’t effective, McGann says one of her doctors in Virginia told her about the UTHealth DBS trial and recommended it to her. The small trial, which is enrolling 10 patients, is studying whether DBS of the medial forebrain bundle is safe and effective.

In the procedure, a neurosurgeon permanently implants two electrodes that each have four small contacts, which deliver electrical stimulation to the target area.

McGann said she wasn’t scared to undergo the treatment. “I had exhausted all other options,” she said.

Candidates for the treatment undergo a screening evaluation to determine if they meet the criteria for the study. This includes a thorough examination of their medical history, neuropsychological testing, bloodwork, drug screening and a physical. Patients in the trial undergo the procedure at Memorial Hermann-Texas Medical Center.

The procedure involves the surgeon making an incision across the front of the head and drilling two holes down to the skull. Then, the surgeon places the electrodes and turns them on. The patient is kept awake during this time. But they don’t experience any pain because local anesthetic is used, and there are no pain receptors in the brain, said Albert Fenoy, M.D., associate professor at the Vivian L. Smith Department of Neurosurgery at McGovern Medical School at UTHealth and a member of the Mischer Neuroscience Institute at Memorial Hermann-TMC.

“Patients need to be awake because we ask them questions to assess their mood and feelings while we test the electrodes at different spots in order to find the one which improves mood to the highest extent, Fenoy said. “We will note changes in the patient’s energy or motivation, such as speaking more freely, smiling or laughing. That indicates that we are in the right spot. It is amazing to see, because it is provoked by the stimulation.”

Once that is complete, the patient is placed under anesthesia while a wire that connects the electrodes and a battery pack (called the neurostimulator) are implanted underneath the skin. The neurostimulator -; the system’s power source -; is placed inside a metal case below the clavicle. Similar to a small pacemaker, models range from 2 to 3 inches in diameter and are about 1/2 inch thick. The battery produces the electrical impulses needed to stimulate the electrodes.

McGann said she felt immediate relief when the surgery was over. She stayed in the hospital one night and went home the next day. “I remember wanting to do things, like going to the pool at my apartment complex, which I had no desire to do before,” she said.

Follow-up care includes visits with a neurosurgeon and a psychiatrist, who monitors improvement in depressive symptoms every week by having them rate their level of depression. Patients also have a neuropsychological evaluation once a year to ensure that DBS is not interfering with brain functions, such as memory. The study follows patients for at least two years after surgery.

Patients may not experience immediate symptom suppression from DBS. Frequent, non-invasive adjustment to the stimulation parameters may be required.

“The procedure is very experimental, so there’s no guarantee that someone will get better,” Soares said. “But the goal is to see patients get better. Because depression is a chronic condition, patients may have still bumps along the road. But hopefully their lows won’t be as low, and they won’t last as long. We hope to see an uptrend in the patient’s mood, and that they have normal energy and enthusiasm for life.”

Soares notes that in past decades DBS treatment was used to treat patients with depression who didn’t respond to commonly available treatments -; but different areas of the brain were targeted and it didn’t prove to be effective.

During a preliminary study published in 2013 and conducted in Germany at University Hospital Bonn, researchers targeted a new area of the brain -; the medial forebrain bundle -; with success. Six of the seven patients in the study experienced a positive response for at least 24 months after their surgery.

Inspired by the German study, Soares, chair of the Department of Psychiatry and Behavioral Health, paired up with faculty at the Vivian L. Smith Department of Neurosurgery at McGovern Medical School to design their own trial. To date, UTHealth has performed nine surgeries. “We are very impressed with the results so far,” he said. “Patients are functioning better. Some are now working full-time and are enjoying life with their families.”

If the trial continues to be successful, UTHealth researchers plan to ask the FDA to approve a study with a larger group of patients over a longer period of time. “For now, we are just trying to replicate and expand what our German colleagues reported,” Soares said.

Fenoy said the ultimate goal would be to have the FDA approve this treatment for TRD, so others can benefit. “It’s amazing to see patients who have been in a rut for years go back to a normal way of life,” he said.

“To find something that would help people who have run out of hope would be a major treatment advancement for TRD,” Soares said.

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