Evidence map›Paper›PMID 41514385›Full record

ArticleJournal of cannabis research2026

Sex-specific association between low oral doses of cannabidiol (CBD) and plasma concentration of anandamide (AEA), N-palmitoylethanolamine (PEA) and N-oleoylethanolamine (OEA) in healthy occasional cannabis users.

Anita Abboud, Lucy Ann Chester, Francois-Olivier Hébert, Didier Jutras-Aswad

Registry-linked trialAbstract read
In one paragraph

Article in Journal of cannabis research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05407285 (A Triple-blind, Placebo-controlled, Randomized, Crossover Study of Low Dose Oral Synthetic Cannabidiol Effects in Healthy Cannabis Occasional Users), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05407285 phase1 / phase2completednot on this map

A Triple-blind, Placebo-controlled, Randomized, Crossover Study of Low Dose Oral Synthetic Cannabidiol Effects in Healthy Cannabis Occasional Users

TypeinterventionalSponsorCentre hospitalier de l'Université de Montréal (CHUM)Ran2022 to 2023Enrolled70ConditionsCannabisArmscannabis 0 mg, placebo, Cannabis 20 mg,, Cannabis 50 mg, Cannabis 100 mg, Cannabis 200 mg
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Anita AbboudDepartment of Psychiatry and Addictology, Université de Montréal, Montréal, Québec, Canada.ORCID http://orcid.org/0000-0002-9356-9233
Lucy Ann ChesterDepartment of Psychiatry and Addictology, Université de Montréal, Montréal, Québec, Canada.ORCID http://orcid.org/0000-0002-7813-0281
Francois-Olivier HébertResearch Center, CHUM (CRCHUM), 900 St-Denis Street, Viger Tower, 5Th Floor, room R05.740, Montreal, QC, H2X 1P1, Canada.ORCID http://orcid.org/0000-0002-8111-0484
Didier Jutras-AswadDepartment of Psychiatry and Addictology, Université de Montréal, Montréal, Québec, Canada. didier.jutras-aswad@umontreal.ca.ORCID http://orcid.org/0000-0002-8474-508X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCannabidiol (CBD), a phytocannabinoid produced by Cannabis sativa, is widely consumed and interacts with components of the endocannabinoid system, including enzymes and receptors, through indirect and complex mechanisms. However, how CBD influences endogenous cannabinoids such as anandamide (AEA), and related N-acylethanolamines like N-palmitoylethanolamine (PEA) and N-oleoylethanolamine (OEA), remains poorly understood. This study investigates the acute impact of marketed CBD doses on the plasmatic levels of these signaling lipids in occasional cannabis users, addressing a critical gap in understanding the biological effects of low-dose CBD in non-therapeutic contexts.

methodsIn a triple-blind, placebo-controlled, randomized crossover trial, 70 healthy volunteers received ten sequences of four oral CBD doses (20, 50, 100, 200 mg) and placebo. Blood was sampled at baseline and five timepoints post-dose. Plasma AEA, PEA, and OEA were quantified by LC–MS, and dose–response assessed with linear mixed-effects models on plasma concentrations (model 1) and Area Under the Curve to increase (AUCi, model 2), including participant ID (nested in sequence) as random effect, and visit, sequence, sex, and baseline levels as fixed effects.

resultsModel 2 revealed a significant effect of CBD dose on AUCi of PEA and OEA, but not AEA. Pairwise comparisons showed that placebo was associated with significantly higher AUCi values than the 50 mg dose (p < 0.05; moderate effect sizes), and trended higher than the 200 mg dose (p < 0.10; small-to-moderate effect sizes). No differences were observed for other dose contrasts. Importantly, sex emerged as a significant factor: sub-group analyses indicated that these reductions in AUCi were driven by female participants, with lower PEA and OEA exposure confirmed at both 50 mg and 200 mg (only PEA) compared to placebo. No corresponding effects were observed in males. All plasma levels decreased overall throughout each visit, at every dose of CBD and placebo.

conclusionsThis study revealed that among healthy adults who consume cannabis occasionally, low-dose oral CBD formulations were able to significantly decrease the cumulative plasma levels of PEA and OEA in a female-specific fashion, confirming the importance of sex-differences in cannabinoid response, and emphasizing the relevance of a personalized approach to cannabis consumption and its effects, as well as public health messaging.

trial registration(ClinicalTrials.gov, registration: NCT05407285, Registration date: 2022–06-02).

Indexed as

Acute effectsAnandamideCannabidiolCrossover designOleoylethanolamidePalmitoylethanolamide

Identifiers

PMID41514385
PMCPMC12879445

What Socratic holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.