Zeng Yi-Fan, Wei Xin-Yu, Wang Qiu-Guo, Qi Zhen, Li Jingyu, Cheng Quan, Zeng Wenjing, Dong Alan
Department of Cardiovascular Surgery, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Department of Pharmacy, Xiangya Hospital Central South University, Changsha, Hunan, China.
BMJ Open. 2025 Jul 13;15(7):e095098. doi: 10.1136/bmjopen-2024-095098.
The causal relationship between sleep characteristics and aortic aneurysm and dissection (AAD) is little known.
In this two-sample Mendelian randomisation (MR) study, we selected seven sleep-related traits (sleep duration, getting up in the morning, chronotype, nap during day, insomnia, snoring, and narcolepsy) from published genome-wide association study (GWAS)-related genetic variants as instrumental variables. Causality was assessed by two-sample MR analysis using inverse-variance weighting (IVW), MR-Egger regression, weighted median, weighted mode and simple model. Horizontal pleiotropy was tested using MR-Egger regression and MR-polytropic residuals and outliers, and heterogeneity was calculated by Cochran's Q test.
There was no evidence of causality among sleep duration (IVW: OR=0.759, 95% CI: 0.489 to 1.177, p=0.218), getting up in the morning (IVW: OR=1.148, 95% CI: 0.768 to 1.716, p=0.502), chronotype (IVW: OR=0.960, 95% CI: 0.796 to 1.158, p=0.670), nap during day (IVW: OR=1.248, 95% CI: 0.771 to 2.020, p=0.367), sleeplessness/insomnia (IVW: OR=1.280, 95% CI: 0.678 to 2.414, p=0.447), snoring (IVW: OR=0.963, 95% CI: 0.770 to 1.203, p=0.738), narcolepsy (IVW: OR=1.025, 95% CI: 0.367 to 2.863, p=0.962) and aortic aneurysm. Moreover, there was no evidence to suggest a causal relationship among sleep traits and abdominal aneurysm, thoracic aneurysm and aortic dissection. Sensitivity analyses, including leave-one-out, horizontal pleiotropy and heterogeneity tests, indicated that our results were robust and reliable.
Overall, our study found no genetic evidence of a causal relationship between sleep characteristics and AAD. Large-scale randomised controlled trial experiments are also needed to further verify the causal relationship between sleep and AAD.
睡眠特征与主动脉瘤及主动脉夹层(AAD)之间的因果关系鲜为人知。
在这项两样本孟德尔随机化(MR)研究中,我们从已发表的全基因组关联研究(GWAS)相关基因变异中选择了七个与睡眠相关的特征(睡眠时间、早晨起床时间、生物钟类型、白天小睡、失眠、打鼾和发作性睡病)作为工具变量。使用逆方差加权(IVW)、MR-Egger回归、加权中位数、加权模式和简单模型通过两样本MR分析评估因果关系。使用MR-Egger回归以及MR-多效性残差和异常值检验水平多效性,并通过Cochran's Q检验计算异质性。
睡眠时间(IVW:OR=0.759,95%CI:0.489至1.177,p=0.218)、早晨起床时间(IVW:OR=1.148,95%CI:0.768至1.716,p=0.502)、生物钟类型(IVW:OR=0.960,95%CI:0.796至1.158,p=0.670)、白天小睡(IVW:OR=1.248,95%CI:0.771至2.020,p=0.367)、失眠(IVW:OR=1.280,95%CI:0.678至2.414,p=0.447)、打鼾(IVW:OR=0.963,95%CI:0.770至1.203,p=0.738)、发作性睡病(IVW:OR=1.025,95%CI:0.367至2.863,p=0.962)与主动脉瘤之间均无因果关系证据。此外,也没有证据表明睡眠特征与腹主动脉瘤、胸主动脉瘤和主动脉夹层之间存在因果关系。敏感性分析,包括留一法、水平多效性和异质性检验,表明我们的结果是稳健且可靠的。
总体而言,我们的研究未发现睡眠特征与AAD之间存在因果关系的遗传证据。还需要大规模随机对照试验来进一步验证睡眠与AAD之间的因果关系。