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睡眠特征与自身免疫性关节炎之间的因果关联:来自双向孟德尔随机化研究的证据。

Causal association between sleep traits and autoimmune arthritis: Evidence from a bidirectional Mendelian randomization study.

作者信息

Li Yajia, Li Qiangxiang, Cao Ziqin, Wu Jianhuang

机构信息

Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China.

National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan, China; Ningxia Geriatric Disease Clinical Research Center, People's Hospital of Ningxia Hui Autonomous Region, Yinchuan, Ningxia Hui Autonomous Region, China; Hunan Provincial People's Hospital, Department of Hunan Institute of Geriatrics, Changsha, Hunan, China.

出版信息

Sleep Health. 2024 Feb;10(1):149-159. doi: 10.1016/j.sleh.2023.11.014. Epub 2024 Jan 19.

Abstract

OBJECTIVE

To explore whether there is a genetic causal relationship between sleep traits and the risk of autoimmune arthritis (AA).

METHODS

Univariable and multivariable Mendelian randomization was employed using genome-wide association studies data to assess sleep traits' associations with AAs, including rheumatoid arthritis (RA), ankylosing spondylitis, and psoriatic arthritis. The inverse-variance weighted method served as the primary analysis, supplemented by the CAUSE method to improve power and mitigate false positives. Mediation Mendelian randomization was used to quantify direct and indirect effects.

RESULTS

Significant associations were shown between insomnia symptoms and increased risk of overall RA (odds ratio = 2.75, 95% confidence interval 1.45-5.22) and seronegative RA (odds ratio = 6.95, 95% confidence interval 2.47-19.56). CAUSE results revealed an association of insomnia symptoms with overall RA and seronegative RA, as well as the sleep duration with overall RA. After the adjustment for body mass index, alcohol status, smoking status, and physical activity levels, multivariable analyses revealed that genetic predisposition to insomnia symptoms and prolonged sleep duration showed independent negative associations with the risk of overall RA and seropositive RA. In the reversed multivariable analyses, a borderline negative association was shown in the overall RA-sleep duration and a positive association of seropositive RA with the risk of insomnia symptoms.

CONCLUSION

This study demonstrated a potential bidirectional causal relationship that genetic predisposition to insomnia symptoms and shorter sleep duration was associated with the risk of AA, especially RA. Genetic predisposition to RA was also associated with decreased sleep duration, as well as increased insomnia symptom risk.

摘要

目的

探讨睡眠特征与自身免疫性关节炎(AA)风险之间是否存在遗传因果关系。

方法

利用全基因组关联研究数据进行单变量和多变量孟德尔随机化,以评估睡眠特征与包括类风湿关节炎(RA)、强直性脊柱炎和银屑病关节炎在内的自身免疫性关节炎的关联。采用逆方差加权法作为主要分析方法,并辅以CAUSE方法以提高检验效能并减少假阳性。采用中介孟德尔随机化来量化直接和间接效应。

结果

失眠症状与总体RA风险增加(比值比=2.75,95%置信区间1.45-5.22)以及血清阴性RA风险增加(比值比=6.95,95%置信区间2.47-19.56)之间存在显著关联。CAUSE结果显示失眠症状与总体RA和血清阴性RA有关,睡眠时长与总体RA有关。在对体重指数、饮酒状况、吸烟状况和身体活动水平进行调整后,多变量分析显示,失眠症状的遗传易感性和睡眠时长延长与总体RA和血清阳性RA风险呈独立负相关。在反向多变量分析中,总体RA-睡眠时长之间显示出临界负相关,血清阳性RA与失眠症状风险呈正相关。

结论

本研究证明了一种潜在的双向因果关系,即失眠症状的遗传易感性和较短的睡眠时长与自身免疫性关节炎风险相关,尤其是类风湿关节炎。类风湿关节炎的遗传易感性还与睡眠时长缩短以及失眠症状风险增加有关。

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