文献速递心律失常血脂与心血管预防

心律失常、痴呆风险与神经退行性变:一项队列研究

Arrhythmias, dementia risk, and neurodegeneration: a cohort study.
PubMed 文献 · Eur Heart J · 2026-05-27

BACKGROUND AND AIMS: Evidence linking arrhythmias to dementia predominantly focuses on atrial fibrillation/flutter (AF), leaving non-AF subtypes under-researched.…

要点

  • 新发房颤、缓慢性心律失常/传导阻滞和室性心律失常均与痴呆风险升高独立相关。
  • 累积心律失常暴露与痴呆风险呈剂量反应关系,主要由房颤+缓慢性心律失常/传导阻滞驱动。
  • 心律失常相关脑MRI改变包括脑萎缩、脉络丛增大和白质损伤。

核心结论

  • 新发心律失常(包括房颤和非房颤)与痴呆风险存在独立且累积的关联,并伴随一致的神经退行性变。

主要发现

  • 随访期间50 243名(12.85%)发生新发心律失常(房颤33 182例,缓慢性心律失常/传导阻滞21 244例,室性心律失常6296例),10 564名(2.70%)发生全因痴呆(血管性2034例,阿尔茨海默4329例)。
  • 新发心律失常、房颤、缓慢性心律失常/传导阻滞和室性心律失常均与所有痴呆结局风险升高独立相关(完全调整模型3)。
  • 累积心律失常暴露与痴呆风险呈正剂量反应关系,主要由房颤+缓慢性心律失常/传导阻滞驱动。
  • 并发房颤和房室传导阻滞/窦房结功能障碍(或束支传导阻滞)的痴呆风险高于任一单独暴露,而起搏器植入与较低风险相关(相较于无起搏的房室传导阻滞/窦房结功能障碍)。
  • 脑MRI分析显示心律失常相关神经退行性改变,包括脑萎缩、脉络丛增大和白质损伤。

临床怎么用

  • 心律失常(包括非房颤亚型)应纳入痴呆风险评估框架,超越仅关注房颤的传统模式。
  • 非房颤心律失常在常规危险因素之外提供增量预测价值,类似房颤。

以上解读依据论文摘要(全文未开放获取或许可不允许翻译转载)。

原文

BACKGROUND AND AIMS: Evidence linking arrhythmias to dementia predominantly focuses on atrial fibrillation/flutter (AF), leaving non-AF subtypes under-researched. This study investigated associations of multiple incident and accumulated arrhythmia exposures with dementia and brain magnetic resonance imaging (MRI) to address these gaps. METHODS: UK Biobank participants without baseline arrhythmias, dementia, or organic central nervous system diseases were included. Cox models estimated associations of incident arrhythmia (AR), AF, bradyarrhythmia/conduction block (Brady/Block), ventricular arrhythmia (VA), and accumulated arrhythmia exposure (types) with all-cause, vascular and Alzheimer's dementia. Specific subtypes-including atrioventricular block (AVB), sinus node dysfunction (SND), and bundle branch block (BBB)-were also evaluated. Arrhythmia-related brain MRI alterations were analysed. RESULTS: Among 391 078 participants (median follow-up 13.35 years), 50 243 (12.85%) developed incident AR (AF, n = 33 182; Brady/Block, n = 21 244; VA, n = 6296), and 10 564 (2.70%) developed all-cause dementia (vascular, n = 2034; Alzheimer, n = 4329). Incident AR, AF, Brady/Block, and VA were independently associated with increased risk of all dementia outcomes (fully adjusted Model 3). Accumulated arrhythmia exposure exhibited a positive dose-response relationship with dementia risk, driven largely by AF+Brady/Block. Concurrent AF and AVB/SND (or BBB) showed higher dementia risk than either exposure alone, whereas pacemaker implantation related to lower risk than AVB/SND without pacing. These associations remained robust to incident stroke or cardiac arrest, genetic dementia risk, baseline cognition, and sensitivity analyses. Non-AF arrhythmias provided incremental predictive value beyond conventional risk factors, similar to AF. Brain MRI analysis revealed arrhythmia-related neurodegenerative changes, including brain atrophy, choroid-plexus enlargement, and white-matter injury. CONCLUSIONS: Incident arrhythmias (both AF and non-AF) exhibit independent and accumulated associations with dementia risk and consistent neurodegeneration. These findings extend the arrhythmia-dementia association beyond AF and suggest multi-arrhythmic framework for dementia risk assessment.

来源:Eur Heart J,查看原文。版权归原作者所有。

引用

  1. Lu W, Weng S, Wang Y, et al. Arrhythmias, dementia risk, and neurodegeneration: a cohort study. Eur Heart J. 2026. PMID: 42200489. doi:10.1093/eurheartj/ehag401

供执业医师工作参考,不替代临床判断;数值与分级以指南原文为准。