Cannabinoid receptor type 1 availability in individuals with a history of childhood trauma: a positron emission tomography study
Ardavan Mohammad Aghaei, Brian Pittman, Nachshon Korem, Marc Nicholas Potenza, Deepak Cyril D’souza, Ansel T. Hillmer, Mohini Ranganathan, Ilan Harpaz-Rotem, Anahita Bassir Nia
Molecular Psychiatry October 31, 2026 DOI: 10.1038/s41380-026-03931-7 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Case-control study using PET imaging Peer reviewed |
|---|---|
| Sample size | 44 |
| Population | Adults with childhood trauma (N = 22) and age- and sex-matched healthy controls without childhood trauma (n = 22) |
| Measures | CB1R availability measured by positron emission tomography (PET) with the CB1R-specific radiotracer [11C]OMAR |
| Citations | 1 |
| Key findings | Compared with healthy controls, adults with childhood trauma had lower CB1R availability globally (-11.36%), in the amygdala (-13.70%), and in the hippocampus (-14.50%), but not in the frontal cortex (-8.08%). The authors interpret this preliminary result as suggesting endocannabinoid dysregulation associated with childhood trauma. |
Abstract
Abstract Early life adversity has a lasting impact on the endocannabinoid (eCB) system based on animal models. However, the impact of early life adversity such as childhood trauma (CT) on the eCB system has not been thoroughly studied. We assessed the availability of cannabinoid receptor type 1 (CB1R) in individuals with CT compared to healthy controls without CT (HCs). Cannabinoid receptor type 1 (CB1R) availability was compared in adults with CT (N = 22) and age- and sex-matched HCs (n = 22), using positron emission tomography (PET) imaging with the CB1R-specific radiotracer [ 11 C]OMAR. Using linear models, the effect of the group was assessed on global and trauma-relevant brain regions (amygdala, hippocampus, and frontal cortex). Compared to HCs, lower CB1R availability was observed in CT globally (difference= -11.36%, F (1,42) = 4.35, p = 0.04), in amygdala (-13.70%, F (1,84) = 6.66, p = 0.01), and in hippocampus (-14.50%, F (1,84) = 6.59, p = 0.01), but not in frontal cortex (-8.08%, F (1,84) = 2.17, p = 0.14). There were no effects of a diagnosis of posttraumatic stress disorder, major depressive disorder, nicotine dependence, or the use of antidepressant medication. This preliminary result of lower CB1R availability in adults with CT compared with HCs suggests eCB dysregulation associated with CT. Future studies should replicate and extend this finding and examine the potential effects of various trauma features on the eCB system.