Wang Hanyu, Yang Bowen, Zeng Xiaoyu, Zhang Shipeng, Jiang Yanjie, Wang Lu, Zhang Qinxiu
Clinical Medical College, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.
Dongguan Hospital, Guangzhou University of Chinese Medicine, Dongguan, Guangdong, China.
Arch Dermatol Res. 2024 Dec 10;317(1):94. doi: 10.1007/s00403-024-03619-4.
Observational studies have reported an association between obstructive sleep apnea (OSA) and psoriasis. Nonetheless, the presence of a causal relationship within this observed association remains to be confirmed. Consequently, we utilized the Mendelian Randomization (MR) method to assess the causal effects between OSA on psoriasis. Single-nucleotide polymorphisms associated with OSA were extracted from the FinnGen study. statistics for psoriasis were obtained from the publicly available IEU GWAS database. Inverse-variance weighted (IVW) method was chosen as the primary analysis, combined with several sensitivity analyses to evaluate the robustness of results. The study design included two-sample MR and two-step MR. Our primary MR analysis revealed that genetically predicted OSA was positively linked to psoriasis (OR = 1.26, 95% confidence interval [CI]: 1.12-1.42, p < 0.001), while no significant causal relationships were observed between psoriasis and OSA (p > 0.05). The two-step MR suggests that BMI might act as a mediating factor in the effect of OSA on psoriasis, with a mediated portion estimated at 23%. Our findings provide support for a causal relationship between genetically predicted OSA and psoriasis. Furthermore, our results suggest that BMI may play a role in mediating the influence of OSA on psoriasis.
观察性研究报告了阻塞性睡眠呼吸暂停(OSA)与银屑病之间存在关联。然而,在这种观察到的关联中是否存在因果关系仍有待证实。因此,我们采用孟德尔随机化(MR)方法来评估OSA对银屑病的因果效应。与OSA相关的单核苷酸多态性是从芬兰基因研究中提取的。银屑病的统计数据来自公开可用的IEU全基因组关联研究(GWAS)数据库。选择逆方差加权(IVW)方法作为主要分析方法,并结合几种敏感性分析来评估结果的稳健性。研究设计包括两样本MR和两步MR。我们的主要MR分析显示,基因预测的OSA与银屑病呈正相关(优势比[OR]=1.26,95%置信区间[CI]:1.12 - 1.42,p<0.001),而银屑病与OSA之间未观察到显著的因果关系(p>0.05)。两步MR表明,体重指数(BMI)可能在OSA对银屑病的影响中起中介作用,估计中介比例为23%。我们的研究结果支持基因预测的OSA与银屑病之间存在因果关系。此外,我们的结果表明BMI可能在介导OSA对银屑病的影响中发挥作用。