Jordan Alexander, Näslund-Koch Charlotte, Vedel-Krogh Signe, Egil Bojesen Stig, Skov Lone
Department of Dermatology and Allergy, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark.
Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
JAAD Int. 2024 Mar 20;15:197-205. doi: 10.1016/j.jdin.2024.03.003. eCollection 2024 Jun.
Psoriasis is associated with high alcohol consumption, but the causality of this relationship is unclear.
We aimed to use a Mendelian randomization approach to investigate the causal effects of alcohol on incident psoriasis.
We included 102,655 adults from the prospective Copenhagen studies. All participants filled out a questionnaire on alcohol consumption, were physically examined, and had blood drawn for biochemical and genetic analyses. We created a genetic instrument based on the number of fast-metabolizing alleles in alcohol dehydrogenase 1B and alcohol dehydrogenase 1C, known to be associated with alcohol consumption, to test whether alcohol consumption was causally associated with psoriasis.
Observationally, we found an increased risk of incident psoriasis among individuals with high alcohol consumption compared to those with low alcohol consumption with a hazard ratio of 1.30 (95% confidence interval 1.05-1.60) in the fully adjusted model. Using genetic data to predict alcohol consumption to avoid confounding and reverse causation, we found no association between number of fast-metabolizing alleles and risk of psoriasis.
Alcohol consumption was self-reported and psoriasis was defined using the International Classification of Diseases 10th revision and 8th revision codes.
Alcohol consumption is observationally but not causally associated with incident psoriasis.
银屑病与高酒精摄入量有关,但这种关系的因果性尚不清楚。
我们旨在采用孟德尔随机化方法研究酒精对银屑病发病的因果效应。
我们纳入了来自哥本哈根前瞻性研究的102,655名成年人。所有参与者都填写了一份关于酒精消费的问卷,接受了身体检查,并抽取血液进行生化和基因分析。我们基于已知与酒精消费相关的乙醇脱氢酶1B和乙醇脱氢酶1C中快速代谢等位基因的数量创建了一个遗传工具,以测试酒精消费是否与银屑病存在因果关联。
在观察性研究中,我们发现与低酒精摄入量者相比,高酒精摄入量者患银屑病的风险增加,在完全调整模型中风险比为1.30(95%置信区间1.05 - 1.60)。利用遗传数据预测酒精消费以避免混杂和反向因果关系,我们发现快速代谢等位基因的数量与银屑病风险之间没有关联。
酒精消费是自我报告的,银屑病是使用国际疾病分类第10版和第8版编码定义的。
从观察结果来看,酒精消费与银屑病发病有关,但并非因果关系。