Association of Cardiovascular Risk Trajectory With Cognitive Decline and Incident Dementia

被引:43
|
作者
Farnsworth von Cederwald, Bryn [1 ,2 ]
Josefsson, Maria [1 ,3 ,4 ]
Wahlin, Anders [1 ,6 ]
Nyberg, Lars [1 ,2 ,5 ]
Karalija, Nina [1 ,5 ]
机构
[1] Umea Sch Business Econ & Stat, Umea Ctr Funct Brain Imaging, Umea, Sweden
[2] Umea Sch Business Econ & Stat, Dept Integrat Med Biol, Umea, Sweden
[3] Umea Sch Business Econ & Stat, Ctr Demog & Aging Res, Umea, Sweden
[4] Umea Sch Business Econ & Stat, Dept Stat, Umea, Sweden
[5] Umea Univ, Dept Radiat Sci, Diagnost Radiol, Umea, Sweden
[6] Umea Univ, Radiat Phys, Umea, Sweden
关键词
ALZHEIMERS-DISEASE; BLOOD-PRESSURE; PROGRESSION; MEMORY; IMPAIRMENT; ATROPHY; PROFILE; MIDLIFE; STROKE; HEALTH;
D O I
10.1212/WNL.0000000000200255
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Objectives Cardiovascular risk factors have a recently established association with cognitive decline and dementia, yet most studies examine this association through cross-sectional data, precluding an understanding of the longitudinal dynamics of such risk. The current study aims to explore how the ongoing trajectory of cardiovascular risk affects subsequent dementia and memory decline risk. We hypothesize that an accelerated, long-term accumulation of cardiovascular risk, as determined by the Framingham Risk Score (FRS), will be more detrimental to cognitive and dementia state outcomes than a stable cardiovascular risk. Methods We assessed an initially healthy, community-dwelling sample recruited from the prospective cohort Betula study. Cardiovascular disease risk, as assessed by the FRS, episodic memory performance, and dementia status were measured at each 5-year time point (T) across 20 to 25 years. Analysis was performed with bayesian additive regression tree, a semiparametric machine-learning method, applied herein as a multistate survival analysis method. Results Of the 1,244 participants, cardiovascular risk increased moderately over time in 60% of sample, with observations of an accelerated increase in 18% of individuals and minimal change in 22% of individuals. An accelerated, as opposed to a stable, cardiovascular risk trajectory predicted an increased risk of developing Alzheimer disease dementia (average risk ratio [RR] 3.3-5.7, 95% CI 2.6-17.5 at T2, 1.9-6.7 at T5) or vascular dementia (average RR 3.3-4.1, 95% CI 1.1-16.6 at T2, 1.5-7.6 at T5) and was associated with an increased risk of memory decline (average RR 1.4-1.2, 95% CI 1-1.9 at T2, 1-1.5 at T5). A stable cardiovascular risk trajectory appeared to partially mitigate Alzheimer disease dementia risk for APOE epsilon 4 carriers. Discussion The findings of the current study show that the longitudinal, cumulative trajectory of cardiovascular risk is predictive of dementia risk and associated with the emergence of memory decline. As a result, clinical practice may benefit from directing interventions at individuals with accelerating cardiovascular risk.
引用
收藏
页码:E2013 / E2022
页数:10
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