Cannabidiol‐associated hepatotoxicity: A systematic review and meta‐analysis

Author:

Lo Lindsay A.1,Christiansen April2,Eadie Lauren3,Strickland Justin C.4,Kim David D.5,Boivin Michael6,Barr Alasdair M.57,MacCallum Caroline A.3ORCID

Affiliation:

1. Department of Public Health Sciences, Dalla Lana School of Public Health University of Toronto Toronto Ontario Canada

2. Centre for Neuroscience Studies Queen's University Kingston Ontario Canada

3. Department of Medicine, Faculty of Medicine University of British Columbia Vancouver British Columbia Canada

4. Department of Psychiatry and Behavioral Sciences Johns Hopkins University School of Medicine Baltimore Maryland USA

5. Department of Anesthesiology, Pharmacology & Therapeutics, Faculty of Medicine University of British Columbia Vancouver British Columbia Canada

6. CommPharm Consulting Barrie Ontario Canada

7. British Columbia Mental Health & Substance Use Services Research Institute Vancouver British Columbia Canada

Abstract

AbstractBackgroundFindings of liver enzyme elevations in recent cannabidiol studies have raised concerns over liver safety. This study aimed to determine the association between cannabidiol use, liver enzyme elevation, and drug‐induced liver injury (DILI).MethodsIn this systematic review and meta‐analysis, a search of EMBASE, CENTRAL, CINAHL, Clinicaltrials.gov, Medline, medRxiv, and Web of Science of records up to February 2022 was conducted. Clinical trials initiating daily cannabidiol treatment with serial liver enzyme measures were included. The proportion of liver enzyme elevations and DILI were independently extracted from published reports. Pooled proportions and probability meta‐analyses were conducted.ResultsCannabidiol use was associated with an increased probability of liver enzyme elevation (N = 12 trials, n = 1229; OR = 5.85 95% CI = 3.84–8.92, p < 0.001) and DILI (N = 12 trials, n = 1229; OR = 4.82 95% CI = 2.46–9.45, p < 0.001) compared to placebo controls. In participants taking cannabidiol (N = 28 trials, n = 1533), the pooled proportion of liver enzyme elevations was 0.074 (95% CI 0.0448–0.1212), and DILI was 0.0296 (95% CI 0.0136–0.0631). High‐dose CBD (≥1000 mg/day or ≥20 mg/kg/day) and concomitant antiepileptic drug use were identified as risk factors. No cases were reported in adults using cannabidiol doses <300 mg/day. No cases of severe DILI were reported.ConclusionsCannabidiol‐associated liver enzyme elevations and DILI meet the criteria of common adverse drug events. Clinicians are encouraged to screen for cannabidiol use and monitor liver function in patients at increased risk.

Publisher

Wiley

Subject

Internal Medicine

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