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偏头痛与阿尔茨海默病风险的关联:来自英国生物银行队列研究和孟德尔随机化的证据。

Migraine Association with Alzheimer's Disease Risk: Evidence from the UK Biobank Cohort Study and Mendelian Randomization.

作者信息

Geng Chaofan, Chen Chen

机构信息

Department of Neurology & Innovation Center for Neurological Disorders, Xuanwu Hospital, Capital Medical University, National Center for Neurological Disorders, Beijing, China.

Department of Neurology, Zhengzhou University People's Hospital, Henan Provincial People's Hospital, Zhengzhou, China.

出版信息

Can J Neurol Sci. 2025 Jan;52(1):44-52. doi: 10.1017/cjn.2024.35. Epub 2024 Mar 13.

Abstract

BACKGROUND

Epidemiological studies on the association between migraine and Alzheimer's disease (AD) risk have yielded inconsistent conclusions. We aimed to characterize the phenotypic and genetic relationships between migraine and AD.

METHODS

To investigate the association between migraine and the risk of AD by analyzing data from a large sample of 404,318 individuals who were initially free from all-cause dementia or cognitive impairment, utilizing the UK Biobank dataset. We employed Cox regression modeling and propensity score matching techniques to examine the relationship between migraine and subsequent occurrences of AD. Additionally, the study utilized Mendelian randomization (MR) analysis to identify the genetic relationship between migraine and the risk of AD.

RESULTS

Migraine patients had a significantly increased risk of developing AD, compared to non-migraine patients (adjusted hazard ratio (HR) = 2.34, 95% confidence interval (CI) = 2.01-0.74, < 0.001). Moreover, the propensity scores matching analyses found that migraine patients had a significantly higher risk of developing AD compared to non-migraine patients (HR = 1.85, 95%CI = 1,68-2.05, < 0.001). Additionally, the MR suggested that significant causal effects of migraine on AD risks were observed [odds ratio (OR) = 2.315; 95% confidence interval (CI) = 1.029-5.234; = 0.002]. Moreover, no evidence supported the causal effects of AD on migraine (OR = 1.000; 95%CI = 0.999-1.006; = 0.971).

CONCLUSION

The present study concludes that migraine patients, compared to a matched control group, exhibit an increased risk of developing AD. Moreover, migraine patients exhibit an increased predisposition of genetic susceptibility to AD. These findings hold significant clinical value for early intervention and treatment of migraines to reduce the risk of AD.

摘要

背景

关于偏头痛与阿尔茨海默病(AD)风险之间关联的流行病学研究得出了不一致的结论。我们旨在描述偏头痛与AD之间的表型和遗传关系。

方法

通过分析来自英国生物银行数据集的404318名最初无全因性痴呆或认知障碍的个体的大样本数据,研究偏头痛与AD风险之间的关联。我们采用Cox回归模型和倾向评分匹配技术来检验偏头痛与AD后续发病之间的关系。此外,该研究利用孟德尔随机化(MR)分析来确定偏头痛与AD风险之间的遗传关系。

结果

与非偏头痛患者相比,偏头痛患者患AD的风险显著增加(调整后的风险比(HR)=2.34,95%置信区间(CI)=2.01 - 0.74,<0.001)。此外,倾向评分匹配分析发现,与非偏头痛患者相比,偏头痛患者患AD的风险显著更高(HR = 1.85,95%CI = 1,68 - 2.05,<0.001)。此外,MR分析表明观察到偏头痛对AD风险有显著的因果效应[优势比(OR)= 2.315;95%置信区间(CI)= 1.029 - 5.234;= 0.002]。此外,没有证据支持AD对偏头痛有因果效应(OR = 1.000;95%CI = 0.999 - 1.006;= 0.971)。

结论

本研究得出结论,与匹配的对照组相比,偏头痛患者患AD的风险增加。此外,偏头痛患者对AD的遗传易感性倾向增加。这些发现对于早期干预和治疗偏头痛以降低AD风险具有重要的临床价值。

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