Cannabis use and atherosclerotic cardiovascular disease: a Mendelian randomization study

被引:2
|
作者
de La Harpe, Roxane [1 ]
Schoeler, Tabea [2 ,3 ]
Thorball, Christian W. [4 ]
Thomas, Aurelien [5 ]
Kutalik, Zoltan [2 ,3 ,6 ]
Vaucher, Julien [1 ,7 ]
机构
[1] Univ Hosp Lausanne, Dept Med, Div Internal Med, Rue Bugnon 46, CH-1011 Lausanne, Switzerland
[2] Swiss Inst Bioinformat, CH-1015 Lausanne, Switzerland
[3] Univ Lausanne, Dept Computat Biol, Lausanne, Switzerland
[4] Lausanne Univ Hosp Lausanne, Biomed Data Sci Ctr, Precis Med Unit, Chemin Roches 1a-1b, CH-1010 Lausanne, Switzerland
[5] Univ Lausanne, Fac Unit Toxicol, Fac Biol & Med, CURML, Lausanne, Switzerland
[6] Ctr Univ Med & Sante Publ, Lausanne, Switzerland
[7] HFR Freiburg Kantonspital, Lausanne, Switzerland
关键词
Cannabis; Atherosclerotic cardiovascular disease; Genetically predicted cannabis use; Causal inference; Mendelian randomization (MR); Modifiable risk factor; GENOME-WIDE ASSOCIATION; MARIJUANA USE; METAANALYSIS; RISK; PROTECTS; YOUNG; BIAS;
D O I
10.1186/s12872-023-03641-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundAssociation between cannabis use and development of atherosclerotic cardiovascular disease (ASCVD) is inconsistent and challenging to interpret, given existing study limitations.MethodsSixty five independent single-nucleotide polymorphisms (SNPs), obtained from a genome-wide association study on lifetime cannabis use, were employed as genetic instruments to estimate the effects of genetically indexed cannabis use on risk of coronary artery disease (CAD) and acute ischemic stroke (IS) using a two-sample Mendelian randomization (MR) approach. Summary statistics on CAD (CARDIoGRAMplusC4D; 60,801 cases and 123,504 controls) and IS (MEGASTROKE; 34,217 cases and 406,111 controls) were obtained separately. A comprehensive review of the observational literature on cannabis use and CAD or IS was also performed and contrasted with MR results.ResultsThere was no causal effect of cannabis use on the risk of CAD (odds ratio (OR) per ever-users vs. never-users 0.93; 95% confidence interval (CI), 0.83 to 1.03) or IS (OR 1.05; 95%CI, 0.93 to 1.19). Sensitivity analyses yielded similar results, and no heterogeneity and directional pleiotropy was observed. Our meta-analysis of observational studies showed no significant association between ever use of cannabis with risk of CAD (k = 6 studies; ORpooled = 1.23, 95%CI 0.78 to 1.69), nor with IS (k = 6 studies; ORpooled = 1.22, 95%CI 0.95 to 1.50).ConclusionUsing a genetic approach approximating a clinical trial does not provide evidence consistent with a causal effect of genetic predisposition to cannabis use on CAD or IS development. Further studies are needed to replicate our findinds, an to investigate more precisely the risk of ASCVD in relation to the quantity, type, route of administration, or the age at exposure to cannabis.
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页数:10
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