Chronic cannabis use is associated with alterations in resting-state cerebellar-cortical connectivity.
Ilenia Salsano, Giorgia Picci, Nathan M Petro, Anna T Coutant, Lucy K Horne, Jason A John, Ryan Glesinger, Gaelle Doucet, Tony W Wilson
Psychopharmacology December 12, 2025 DOI: 10.1007/s00213-025-06981-x via PubMed
Summary
AI-generated from the abstractChronic cannabis use in middle-aged adults (average age 42) is linked to disrupted resting-state functional connectivity between the cerebellum and prefrontal-temporal brain regions. Using whole-brain analysis, adults with chronic cannabis use showed decreased connectivity between the right cerebellar Crus II and several frontal and temporal areas, and between the right cerebellar Crus I and the left pars triangularis, compared to demographically matched non-users. These findings suggest that sustained cannabis use may alter communication between brain regions rich in cannabinoid receptors, even in midlife, though the behavioral impact remains unknown.
Study at a glance
| Characteristics | Observational cohort Peer reviewed |
|---|---|
| Sample size | 45 |
| Population | Middle-aged adults (mean age 41.64 years) with chronic cannabis use and demographically matched controls who did not use cannabis or other illicit substances |
| Topics | Cannabis |
| Keywords | Cerebellum FMRI Functional connectivity |
| Key finding | Chronic cannabis use was associated with decreased resting-state functional connectivity between the right cerebellar Crus II and left pars triangularis, bilateral pars orbitalis, left superior frontal gyrus, left middle temporal gyrus, and left inferior temporal gyrus, and between the right cerebellar Crus I and left pars triangularis, compared to controls. |
Abstract
Cannabis is one of the most widely used psychoactive drugs in the United States, yet its long-term effects on brain function remain poorly understood. Prior resting-state functional connectivity (rsFC) studies have yielded inconsistent findings, likely due to variability in cannabis use thresholds, a predominant focus on younger populations, and region-of-interest (ROI)-based approaches limited to a small number of a priori brain regions. We aimed to address these limitations by examining rsFC across the entire brain using an atlas-based, whole-brain, ROI-to-ROI approach in a middle-aged sample (mean age = 41.64 years) of individuals with chronic cannabis use (CCU) and a demographically matched group of controls who did not use cannabis or other illicit substances. Based on the known neuroanatomical distribution of type 1 cannabinoid receptors (CB1Rs), we hypothesized that regions with high CB1R density would be the most affected. However, given our whole-brain approach, we were also sensitive to other regions that may exhibit altered connectivity. Using the Automated Anatomical Labeling (AAL) atlas, we computed rsFC matrices across 116 brain regions in 22 adults with CCU and 23 demographically matched controls. The CCU group showed decreased rsFC (pFDR< .05) between the right cerebellar Crus II and the left pars triangularis, bilateral pars orbitalis, left superior frontal gyrus, left middle temporal gyrus, and left inferior temporal gyrus compared with the control group. The CCU group also had lower rsFC (pFDR < .05) between the right cerebellar Crus I and the left pars triangularis compared with controls. Our findings revealed disrupted rsFC between cerebellar and prefrontal-temporal regions in the CCU group. This study advances the literature by using an atlas-based, whole-brain, ROI-to-ROI approach in a middle-aged sample with sustained cannabis use. Future studies should integrate neuropsychological assessments and task-based paradigms to understand how such alterations in rsFC affect behavioral outcomes.