Autism Spectrum Disorder
Study register · detail RCT · Autism Spectrum Disorder · 2019

The effect of cannabidiol (CBD) on low-frequency activity and functional connectivity in the brain of adults with and without autism spectrum disorder (ASD).

Unclear GRADE Moderate 104 citations
Samplen = 34 Pat.
DurationSingle dose
ControlMatched placebo
EndpointfALFF
Blindingdoppelblind
DesignRCT
Cannabinoidcbd
Max. dose600.0 mg
Routeoral
Key finding

CBD significantly increased fALFF in the cerebellar vermis and right fusiform gyrus, primarily in the ASD group, without clear clinical behavioral effects reported.

Summary

Pharmaco-fMRI study, n=34 adult men (50% with ASD); single oral CBD administration 600 mg vs. placebo. CBD significantly increased fALFF in the cerebellar vermis and right fusiform gyrus, primarily driven by the ASD group (no significant change in controls). Within the ASD group, CBD significantly altered vermal FC with subcortical and cortical target regions.

P
PopulationAdult men with and without autism spectrum disorder (ASD), n=34 (17 each with/without ASD)
I
InterventionOral CBD 600 mg, single dose, double-blind, cross-over
C
ControlMatched placebo (oral, single dose)
O
OutcomeCBD significantly increased fALFF in the cerebellar vermis and right fusiform gyrus; effect primarily driven by the ASD group; altered functional connectivity of the vermis with striatal and cortical target regions only in the ASD group
Confidence in the evidence
Moderate

The third of four GRADE levels, the effect estimate is probably reliable.

Downgraded for
Imprecision
Quality profile
Sample size
Blinding Double-blind
Effect size
Citations / year
Authors
Pretzsch CM, Voinescu B, Mendez MA, Wichers R, Ajram L, Ivin G, Heasman M, Williams S, Murphy DG, Daly E
Share
Abstract
Background: The potential benefits of cannabis and its major non-intoxicating component cannabidiol (CBD) are attracting attention, including as a potential treatment in neurodevelopmental disorders such as autism spectrum disorder (ASD). However, the neural action of CBD, and its relevance to ASD, remains unclear. We and others have previously shown that response to drug challenge can be measured using functional magnetic resonance imaging (fMRI), but that pharmacological responsivity is atypical in Asd. Aims: We hypothesized that there would be a (different) fMRI response to CBD in Asd. Methods: To test this, task-free fMRI was acquired in 34 healthy men (half with ASD) following oral administration of 600 mg CBD or matched placebo (random order; double-blind administration). The 'fractional amplitude of low-frequency fluctuations' (fALFF) was measured across the whole brain, and, where CBD significantly altered fALFF, we tested if functional connectivity (FC) of those regions was also affected by Cbd. Results: CBD significantly increased fALFF in the cerebellar vermis and the right fusiform gyrus. However, post-hoc within-group analyses revealed that this effect was primarily driven by the ASD group, with no significant change in controls. Within the ASD group only, CBD also significantly altered vermal FC with several of its subcortical (striatal) and cortical targets, but did not affect fusiform FC with other regions in either group. Conclusion: Our results suggest that, especially in ASD, CBD alters regional fALFF and FC in/between regions consistently implicated in ASD. Future studies should examine if this affects the complex behaviours these regions modulate.

The impediment to action advances action. — Marcus Aurelius