TB medication could fight fear and anxiety

An antibiotic that treats tuberculosis could help fight fear and anxiety disorders when combined with therapy, researchers report.
A young person bites their fingernails

A medication used as a second line of defense against tuberculosis could enhance therapy for fear and anxiety disorders, according to a new clinical study.

D-cycloserine (DCS) has landed itself on the World Health Organization’s list of essential medicines for its abilities to stop the growth of bacterial cell walls. In recent decades, however, mental health researchers have taken note of the antibiotic’s neurological influence, particularly within the amygdala, the brain’s emotional epicenter—where fear lives.

“The question is can we tailor this approach to be more effective for each patient?”

“Multiple studies have shown that DCS can help cement the safety learning that takes place during psychotherapy sessions that involve exposure therapy,” says Jasper Smits, professor of psychology at the University of Texas at Austin, who led the study in JAMA Network Open.

“The question is can we tailor this approach to be more effective for each patient?”

The amygdala is red in the illustration of the brain
Illustration highlights the amygdala portion of the brain. (Credit: UT Austin)

When paired with exposure therapy—which aims to correct anxiety responses by offering safe spaces for patients to engage with their fears—DCS acts as a “cognitive enhancer,” promoting strong neural connections that help augment the learning experience.

“This two-part approach aims to enhance the exposure and create a memory of safety that sticks,” says Smits, who also directs the Anxiety & Stress Clinic.

The researchers set out to refine the approach in a randomized clinical trial on social anxiety. They postulated that DCS would be more effective if it were only administered after sessions marked by “safety learning,” which they defined as evidencing low fear at the end of the exposure therapy session. But the strategy did not work.

Instead, the researchers found that the medication worked better as a blanket strategy, administrated before or after any therapy session. This confirmed the results of prior studies and emphasized new opportunities for exploration in the treatment of fear and anxiety disorders.

“The findings show again that this medication helps improve the outcomes of exposure-based therapy, adding to the evidence base for this,” Smits says.

“There undoubtedly are individual and session characteristics that influence the effectiveness of this augmentation strategy, which is an important area for future research.”

Source: UT Austin

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