From the Stroke Research Group, Department of Clinical Neurosciences, University of Cambridge, United Kingdom.
Neurology. 2024 Mar 12;102(5):e209141. doi: 10.1212/WNL.0000000000209141. Epub 2024 Feb 13.
Sleep disturbances are implicated as risk factors of both stroke and dementia. However, whether these associations are causal and whether treatment of sleep disorders could reduce stroke and dementia risk remain uncertain. We aimed to evaluate associations and ascertain causal relationships between sleep characteristics and stroke/dementia risk and MRI markers of small vessel disease (SVD).
We used data sets from a multicenter population-based study and summary statistics from genome-wide association studies (GWASs) of sleep characteristics and outcomes. We analyzed 502,383 UK Biobank participants with self-reported sleep measurements, including sleep duration, insomnia, chronotype, napping, daytime dozing, and snoring. In observational analyses, the primary outcomes were incident stroke, dementia, and their subtypes, alongside SVD markers. Hazard ratios (HRs) and odds ratios (ORs) were adjusted for age, sex, and ethnicity, and additional vascular risk factors. In Mendelian randomization (MR) analyses, ORs or risk ratios are reported for the association of each genetic score with clinical or MRI end points.
Among 502,383 participants (mean [SD] age, 56.5 [8.1] years; 54.4% female), there were 7,668 cases of all-cause dementia and 10,334 strokes. In longitudinal analyses, after controlling for cardiovascular risk factors, participants with insomnia, daytime napping, and dozing were associated with increased risk of any stroke (HR 1.05, 95% CI 1.01-1.11, = 8.53 × 10; HR 1.09, 95% CI 1.05-1.14, = 3.20 × 10; HR 1.19, 95% CI 1.08-1.32, = 4.89 × 10, respectively). Almost all sleep measures were associated with dementia risk (all < 0.001, except insomnia). Cross-sectional analyses identified associations between napping, snoring, and MRI markers of SVD (all < 0.001). MR analyses supported a causal link between genetically predicted insomnia and increased stroke risk (OR 1.31, 95% CI 1.13-1.51, = 0.00072), but not with dementia or SVD markers.
We found that multiple sleep measures predicted future risk of stroke and dementia, but these associations were attenuated after controlling for cardiovascular risk factors and were absent in MR analyses for Alzheimer disease. This suggests possible confounding or reverse causation, implying caution before proposing sleep disorder modifications for dementia treatment.
睡眠障碍被认为是中风和痴呆的危险因素。然而,这些关联是否具有因果关系,以及治疗睡眠障碍是否可以降低中风和痴呆的风险仍然不确定。我们旨在评估睡眠特征与中风/痴呆风险以及小血管疾病(SVD)的 MRI 标志物之间的关联,并确定因果关系。
我们使用了来自多中心人群基础研究的数据和睡眠特征与结局的全基因组关联研究(GWAS)的汇总统计数据。我们分析了 502383 名英国生物库参与者的自我报告睡眠测量结果,包括睡眠时间、失眠、昼夜节律、午睡、白天打盹和打鼾。在观察性分析中,主要结局是新发中风、痴呆及其亚型,以及 SVD 标志物。风险比(HRs)和优势比(ORs)经过年龄、性别和种族以及其他血管危险因素的调整。在孟德尔随机化(MR)分析中,报告了每个遗传评分与临床或 MRI 终点的关联的 OR 或风险比。
在 502383 名参与者(平均[标准差]年龄 56.5[8.1]岁,54.4%为女性)中,有 7668 例全因痴呆和 10334 例中风。在纵向分析中,在控制心血管危险因素后,有失眠、白天午睡和打盹的参与者发生任何中风的风险增加(HR 1.05,95%CI 1.01-1.11, = 8.53×10;HR 1.09,95%CI 1.05-1.14, = 3.20×10;HR 1.19,95%CI 1.08-1.32, = 4.89×10,分别)。几乎所有的睡眠指标都与痴呆风险相关(除失眠外,均 < 0.001)。横断面分析确定了午睡、打鼾与 SVD 的 MRI 标志物之间的关联(均 < 0.001)。MR 分析支持遗传预测的失眠与中风风险增加之间存在因果关系(OR 1.31,95%CI 1.13-1.51, = 0.00072),但与痴呆或 SVD 标志物无关。
我们发现,多种睡眠指标可预测未来中风和痴呆的风险,但这些关联在控制心血管危险因素后减弱,并且在针对阿尔茨海默病的 MR 分析中不存在。这表明可能存在混杂或反向因果关系,因此在提出治疗痴呆的睡眠障碍治疗方法之前应谨慎行事。