Those who can muster their brain’s own chemical forces against depression, it appears, have a head start in overcoming its symptoms with help from a medication. But those whose brain chemistry doesn’t react as much to a fake medicine, or placebo, struggle even after getting an active drug.
The findings, published in JAMA Psychiatry and made at the University of Michigan Medical School, help explain the variation in treatment response and resiliency that bedevils depression patients and their care teams.
The discovery also opens up the door to new research on how to amplify the brain’s natural response in new ways — to improve depression treatment for the estimated 350 million people worldwide who have depression at any given time.
The findings could also help those developing and testing new drugs, helping them correct for the placebo effect that gets in the way of measuring a drug’s true effect.
Natural painkillers
The study comes from a team that has studied the placebo effect for more than a decade, using sophisticated brain scanning techniques in healthy people.
They were pioneers in showing that the brain’s natural “painkiller” system — called the mu-opioid system — responded to pain when patients got a placebo. They’ve also studied the genetic variation that makes certain people more likely to respond to sham painkillers.
For the new study, they studied the brain chemistry of 35 people with untreated major depression, who agreed to try what they thought was a new depression drug, before receiving actual drugs already approved to treat depression.
The team found that participants who reported improvement of depression symptoms after getting the placebo also had the strongest mu-opioid response in brain regions involved in emotion and depression. And these individuals were also more likely to experience even fewer symptoms once they got a real drug.
In fact, response to placebo predicted nearly half of the variation between individuals in total response to the entire study, including actual drug treatment.
“This is the first objective evidence that the brain’s own opioid system involved in response to both antidepressants and placebos, and that variation in this response is associated with variation in symptom relief,” says the paper’s first author Marta Pecina, M.D., Ph.D., a research assistant professor in the U-M Department of Psychiatry and member of the U-M Depression Center.
“This finding gives us a biomarker for treatment response in depression — an objective way to measure neurochemical compounds involved in response,” she continues. “We can envision that by enhancing placebo effects, we might be able to develop faster-acting or better antidepressants.”
The research team was led by Jon-Kar Zubieta, M.D., Ph.D., a former U-M faculty member who now chairs the Department of Psychiatry at the University of Utah. He notes that the placebo effect in the study came not only from participants’ belief that they were receiving a real drug, but also from the sheer impact of being in a treatment environment.
Even as scientists work to understand this effect further, clinicians who treat people with depression may want to take heed of the findings, he notes.
“These results suggest that some people are more responsive to the intention to treat their depression, and may do better if psychotherapies or cognitive therapies that enhance the clinician-patient relationship are incorporated into their care as well as antidepressant medications,” he says. “We need to find out how to enhance the natural resiliency that some people appear to have.”
Studies testing antidepressants against placebos suggest that 40 percent of response is due to the placebo effect. To drug developers, this is a nuisance. But to placebo researchers, it’s like catnip.
“If 40 percent of people recover from a chronic illness without a medication, I want to know why,” says Zubieta. “And if you respond to a medication and half your response is due to a placebo effect, we need to know what makes you different from those who don’t respond as well.” This could include genetic effects that are still to be discovered.
Probing placebo power
The new findings were made using position emission tomography, or PET, scanning, and a substance that attaches to the receptors on brain cells that mu-opioid molecules bind to. In the single-blind randomized crossover design, the participants went in knowing that they wouldn’t be told full details about the purpose of the study until the end.
They then received two weeks of placebo pill treatment — but during one of those weeks, each was told they were taking a substance that is believed to activate internal mechanisms and may have antidepressant properties. At the end of this week, they also came for a brain scan and received an injection of harmless salt water that they were told might have fast-acting antidepressant properties. After these two weeks and scan, they were prescribed a real antidepressant. They reported their depression symptoms using standard measurement scales throughout the study period.
The researchers are also studying other molecules in the brain that are involved in depression and treatment response, and are recruiting people for further brain-scanning studies; see http://umhealth.me/placebodep for more information.
In addition to aiding the search for better depression drugs to help placebo non-responders, the new study could help identify which patients might benefit from non-drug strategies known to help people who don’t get relief from antidepressant drugs. These include electroconvulsive therapy or ECT, deep-brain stimulation or DBS, and transcranial magnetic stimulation or TMS.
The study done by University of Michigan Health System.