Abstract

Psilocybin has shown promise for the treatment of mood disorders, which are often accompanied by cognitive dysfunction including cognitive rigidity. Recent studies have proposed neuropsychoplastogenic effects as mechanisms underlying the enduring therapeutic effects of psilocybin. In an open-label study of 24 patients with major depressive disorder, we tested the enduring effects of psilocybin therapy on cognitive flexibility (perseverative errors on a set-shifting task), neural flexibility (dynamics of functional connectivity or dFC via functional magnetic resonance imaging), and neurometabolite concentrations (via magnetic resonance spectroscopy) in brain regions supporting cognitive flexibility and implicated in acute psilocybin effects (e.g., the anterior cingulate cortex, or ACC). Psilocybin therapy increased cognitive flexibility for at least 4 weeks post-treatment, though these improvements were not correlated with the previously reported antidepressant effects. One week after psilocybin therapy, glutamate and N-acetylaspartate concentrations were decreased in the ACC, and dFC was increased between the ACC and the posterior cingulate cortex (PCC). Surprisingly, greater increases in dFC between the ACC and PCC were associated with less improvement in cognitive flexibility after psilocybin therapy. Connectome-based predictive modeling demonstrated that baseline dFC emanating from the ACC predicted improvements in cognitive flexibility. In these models, greater baseline dFC was associated with better baseline cognitive flexibility but less improvement in cognitive flexibility. These findings suggest a nuanced relationship between cognitive and neural flexibility. Whereas some enduring increases in neural dynamics may allow for shifting out of a maladaptively rigid state, larger persisting increases in neural dynamics may be of less benefit to psilocybin therapy.

Highlights

  • Classic psychedelics have shown potential efficacy for treating a variety of psychiatric disorders [1,2,3,4,5,6], including major depressive disorder (MDD)

  • We focused our analyses on the anterior cingulate cortex (ACC) and posterior cingulate cortex (PCC) based on their roles in cognitive flexibility and psychedelic drug action

  • The effect of psilocybin therapy on Penn Conditional Exclusion Test (PCET) perseverative errors was unlikely to be explained by practice effects, as there was moderate evidence supporting the null hypothesis that perseverative errors did not change in the delayed group prior to receiving psilocybin (95% CI = [−9.77, 10.57], t(9) = 0.09, p > 0.250, BF = 0.31)

Read more

Summary

INTRODUCTION

Classic psychedelics (serotonin 2A or 5-HT2A agonists such as psilocybin, lysergic acid diethylamide or LSD, and N,N-dimethyltryptamine or DMT) have shown potential efficacy for treating a variety of psychiatric disorders [1,2,3,4,5,6], including major depressive disorder (MDD). The durability of these effects is unclear in patients with MDD, one small study of 12 healthy adults did not find enduring modulation of neural flexibility or ACC function 1 week and 4 weeks after a completed baseline clinical, cognitive, and neuroimaging measurements followed by ~8 h of preparatory therapy sessions conducted over 2 weeks to build rapport with research personnel Following these preparatory sessions, participants attended two psilocybin sessions separated by ~1.6 weeks. In order to test whether baseline measures of sFC and dFC predicted post-treatment changes in depression and cognitive flexibility, we constructed and tested the performance of several connectome-based predictive models [90,91,92] Because of the relatively small N and number of edges from which to select, we report the robustness of different models across a range of thresholds for feature selection (p < 0.010–0.050)

RESULTS
DISCUSSION
CODE AVAILABILITY
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call