Population-based cohort study of modifiable risk factors for dementia and Alzheimer disease mortality in Spain.

Communications health Pub Date : 2026-01-01 Epub Date: 2026-09-02 DOI:10.1038/s44528-026-00022-5
Julián Benito-León, José Ignacio Serrano, María Dolores Del Castillo, Álex Escolà-Gascón, Carla María Benito-Rodríguez, Cristina Ramo-Tello, Ritwik Ghosh, Félix Bermejo-Pareja
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Abstract

Background: Although many modifiable factors are linked to dementia risk, their association with dementia and Alzheimer disease (AD) mortality remains unclear. We aimed to identify late-life modifiable factors associated with these outcomes and assess sex differences.

Methods: In the population-based Neurological Disorders in Central Spain (NEDICES) cohort, we followed 3085 older adults enrolled in 1994-1995 through 2017. We examined 13 modifiable factors measured at study entry. Dementia and AD deaths were defined by the underlying cause recorded on death certificates. Fine-Gray competing risk models accounted for death from other causes and generated subdistribution hazard ratio (SHR) estimates and adjusted population attributable fractions (PAFs).

Results: During follow-up, there were 182 dementia-coded deaths (including 105 AD-coded deaths) and 2423 deaths from other causes. Here we show that depressive symptoms are associated with higher dementia-coded mortality in women (SHR 1.52, 95% confidence interval [CI] 1.00-2.30; PAF 13.6%, 95% CI 0.0-28.4) and higher AD-coded mortality overall (SHR 1.76, 95% CI 1.11-2.79; PAF 15.4%, 95% CI 2.6-29.9), with a stronger association in women (SHR 2.23, 95% CI 1.28-3.88; PAF 27.2%, 95% CI 7.8-46.7). Several exposures show inverse associations (e.g., smoking, obesity, and arterial hypertension in men), consistent with competing mortality and late-life reverse causation. Combined positive PAFs are 10.8% for dementia-coded mortality and 18.2% for AD-coded mortality overall, reaching 41.1% in women for AD-coded mortality.

Conclusions: Late-life depressive symptoms, particularly among women, emerged as the most prominent modifiable correlate of dementia- and AD-coded mortality, supporting improved recognition and management of depressive symptoms in older adults.

西班牙痴呆和阿尔茨海默病死亡率可改变危险因素的人群队列研究
背景:尽管许多可改变的因素与痴呆风险有关,但它们与痴呆和阿尔茨海默病(AD)死亡率的关系尚不清楚。我们的目的是确定与这些结果相关的晚年可改变因素,并评估性别差异。方法:在以人群为基础的西班牙中部神经系统疾病(ne迪斯)队列中,我们随访了1994-1995年至2017年招募的3085名老年人。我们检查了研究开始时测量的13个可修改因素。痴呆症和阿尔茨海默病的死亡是根据死亡证明上记录的潜在原因来定义的。细灰色竞争风险模型考虑了其他原因导致的死亡,并产生了亚分布风险比(SHR)估计值和调整的人口归因分数(paf)。结果:随访期间,痴呆编码死亡182例(其中ad编码死亡105例),其他原因死亡2423例。在这里,我们发现抑郁症状与女性较高的痴呆编码死亡率(SHR 1.52, 95%可信区间[CI] 1.00-2.30; PAF 13.6%, 95% CI 0-28.4)和较高的ad编码总体死亡率(SHR 1.76, 95% CI 1.11-2.79; PAF 15.4%, 95% CI 2.6-29.9)相关,与女性的相关性更强(SHR 2.23, 95% CI 1.28-3.88; PAF 27.2%, 95% CI 7.8-46.7)。一些暴露显示出负相关(例如,男性吸烟、肥胖和动脉高血压),与竞争死亡率和晚年反向因果关系一致。综合阳性paf在痴呆编码死亡率中占10.8%,在ad编码总体死亡率中占18.2%,在女性ad编码死亡率中达到41.1%。结论:老年抑郁症状,特别是在女性中,成为痴呆症和ad编码死亡率最显著的可改变相关性,支持改善老年人抑郁症状的识别和管理。
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