老年人偏头痛、认知能力下降和痴呆:一项基于人群的研究。

Yajun Liang, Ya-qin Gao, Rui Wang, G. Grande, R. Monastero, Yanhong Dong, Xin Jiang, Peiyuan Lv, C. Qiu
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引用次数: 3

摘要

背景:偏头痛对老年人认知老化的潜在影响仍然存在争议。目的探讨瑞典老年人群中偏头痛及其亚型与认知能力下降和痴呆的关系。方法本研究以人群为基础,纳入来自斯德哥尔摩Kungsholmen瑞典国家老龄化与护理研究的3069名参与者(年龄≥60岁)。基线检查于2001-2004年进行,每3年或6年随访一次,直到2013-2016年。通过面对面访谈、临床检查、实验室检查和与登记处联系收集数据。用简易精神状态检查(MMSE)测量整体认知功能。根据DSM-IV标准诊断痴呆。偏头痛及其亚型按照国际分类系统进行定义。数据分析采用logistic回归、Cox回归和线性混合效应模型。结果基线时,305名参与者被定义为非偏头痛,352名参与者被定义为偏头痛。横断面分析显示,偏头痛患者的多变量校正优势比(95%可信区间)为0.49(0.20-1.21),无先兆偏头痛患者的优势比为0.66(0.26-1.66)。纵向分析显示,偏头痛和亚型相关痴呆的多变量校正风险比为0.68 ~ 0.89 (p > 0.05)。此外,偏头痛及其亚型与基线MMSE评分或随访期间MMSE变化均无显著相关性(p > 0.05)。年龄、APOE / 4等位基因、脑血管疾病和抗偏头痛治疗没有显著相关性(相互作用p > 0.05)。结论本研究未发现偏头痛及其亚型与老年人认知能力下降和痴呆相关的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Migraine, Cognitive Decline, and Dementia in Older Adults: A Population-Based Study.
BACKGROUND The potential impact of migraine on cognitive aging among older adults remains controversial. OBJECTIVE To examine the relationship of migraine and subtypes with cognitive decline and dementia in an older Swedish population. METHODS This population-based study included 3069 participants (age≥60) from the Swedish National study on Aging and Care in Kungsholmen, Stockholm. Baseline examination was conducted in 2001-2004, and participants were followed every 3 or 6 years until 2013-2016. Data were collected through face-to-face interviews, clinical examinations, laboratory tests, and linkage with registers. Global cognitive function was measured with the Mini-Mental State Examination (MMSE). Dementia was diagnosed according to the DSM-IV criteria. Migraine and subtypes were defined following the international classification system. Data were analyzed using logistic regression, Cox regression, and linear mixed-effects models. RESULTS At baseline, 305 participants were defined with non-migraine headache and 352 with migraine. The cross-sectional analysis showed that the multivariable-adjusted odds ratio (95% confidence interval) of prevalent dementia was 0.49 (0.20-1.21) for migraine and 0.66 (0.26-1.66) for migraine without aura. The longitudinal analysis showed that the multivariable-adjusted hazard ratios of incident dementia associated with migraine and subtypes ranged 0.68-0.89 (p > 0.05). Furthermore, migraine and subtypes were not significantly associated with either baseline MMSE score or MMSE changes during follow-ups (p > 0.05). The nonsignificant associations did not vary substantially by age, APOEɛ4 allele, cerebrovascular disease, and antimigraine treatment (p for interactions > 0.05). CONCLUSION This study shows no evidence supporting the associations of migraine and its subtypes with cognitive decline and dementia among older adults.
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