Lo Lindsay A, Christiansen April, Eadie Lauren, Strickland Justin C, Kim David D, Boivin Michael, Barr Alasdair M, MacCallum Caroline A
Department of Public Health Sciences, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Centre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada.
J Intern Med. 2023 Jun;293(6):724-752. doi: 10.1111/joim.13627. Epub 2023 Mar 13.
Findings 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).
In 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.
Cannabidiol 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.
Cannabidiol-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.
近期大麻二酚研究中发现的肝酶升高现象引发了对肝脏安全性的担忧。本研究旨在确定使用大麻二酚、肝酶升高与药物性肝损伤(DILI)之间的关联。
在这项系统评价和荟萃分析中,检索了截至2022年2月的EMBASE、CENTRAL、CINAHL、Clinicaltrials.gov、Medline、medRxiv和Web of Science数据库。纳入了启动每日大麻二酚治疗并进行系列肝酶检测的临床试验。从已发表的报告中独立提取肝酶升高和DILI的比例。进行了合并比例和概率荟萃分析。
与安慰剂对照相比,使用大麻二酚与肝酶升高(N = 12项试验,n = 1229;OR = 5.85,95% CI = 3.84 - 8.92,p < 0.001)和DILI(N = 12项试验,n = 1229;OR = 4.82,95% CI = 2.46 - 9.45,p < 0.001)的概率增加相关。在服用大麻二酚的参与者中(N = 28项试验,n = 1533),肝酶升高的合并比例为0.074(95% CI 0.0448 - 0.1212),DILI为0.0296(95% CI 0.0136 - 0.0631)。高剂量CBD(≥1000毫克/天或≥20毫克/千克/天)和同时使用抗癫痫药物被确定为危险因素。使用大麻二酚剂量<300毫克/天的成年人中未报告病例。未报告严重DILI病例。
大麻二酚相关的肝酶升高和DILI符合常见药物不良事件的标准。鼓励临床医生对使用大麻二酚的情况进行筛查,并对风险增加的患者监测肝功能。