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中年止血措施、20 年认知能力下降与痴呆症发病。

Midlife Hemostasis Measures, 20-Year Cognitive Decline, and Incident Dementia.

机构信息

From the Johns Hopkins University (A.W., A.R.S., A.L.G., J.C.), Bloomberg School of Public Health, Baltimore, MD; University of Minnesota (A.R.F.), School of Public Health, Minneapolis; Department of Epidemiology (A.A.), Rollins School of Public Health, Emory University, Atlanta, GA; Laboratory of Behavioral Neuroscience (K.A.W.), Intramural Research Program, National Institute on Aging, Baltimore; National Institute of Neurological Disorders and Stroke Intramural Program (R.F.G.), NIH, Bethesda, MD; Sanofi (A.M.R.), Cambridge, MA; and Division of Neurocritical Care (A.L.C.S.), Department of Neurology, University of Pennsylvania Perelman School of Medicine, Philadelphia.

出版信息

Neurology. 2023 Oct 24;101(17):e1697-e1707. doi: 10.1212/WNL.0000000000207771. Epub 2023 Aug 31.

Abstract

BACKGROUND AND OBJECTIVES

Blood concentrations of hemostatic factors affect thrombosis and bleeding diathesis and may contribute to cognitive impairment through modifiable vascular pathologies. Whether hemostasis, assessed in middle age, is associated with late-life cognitive impairment remains largely unknown in a community-dwelling population.

METHODS

Using data from 14,128 participants with cognitive function measurements in 1990-1992 from the Atherosclerosis Risk in Communities study, we assessed the associations of hemostasis measures with 20-year changes in cognitive performance and incident dementia. Activated partial thromboplastin time (aPTT) and level of fibrinogen, von Willebrand factor (VWF), factor VIII, factor VII, factor XI, d-dimer, and soluble thrombomodulin were measured in 1987-1989 or 1993-1995. Hemostasis measures were categorized into quintiles, with the lowest quintile indicating low coagulability. Cognitive performance was characterized using a combined z-score from 3 tests (that is, delayed word recall test [DWRT], digit symbol substitution [DSST], and word fluency test [WFT]), assessed in 1990-1992, 1996-1998, and 2011-2013. Dementia was determined either from in-person evaluations or using dementia surveillance through 2017. Mixed-effects models and Cox proportional hazards models were used to assess cognitive trajectories and risk of dementia, respectively.

RESULTS

Among 12,765 participants with hemostasis measures in 1987-1989, who were aged 47-70 years at the first cognitive assessment, we observed significant trends of shorter aPTT ( for trend <0.001; difference in 20-year cognitive decline for fifth vs first quintile [Q5 vs Q1]: -0.104 [95% CI -0.160 to -0.048]) and higher levels of factor VII ( < 0.002; Q5 vs Q1: -0.085 [-0.142, -0.028]) and factor VIII ( = 0.033; Q4 vs Q1: -0.055 [-0.111, -0.000]) with greater 20-year cognitive declines. The associations with the decline in DSST were stronger than those with the decline in WFT or DWRT. Consistently, shorter aPTT and higher factor VIII levels were associated with higher dementia risk with HRs for Q5 vs Q1 of 1.23 (95% CI 1.07 to 1.42) and 1.17 (1.01-1.36), respectively, and p for trend of 0.008 and 0.024, respectively.

DISCUSSION

Overall, our study found consistent trend associations of aPTT and factor VIII measured in midlife with cognitive decline and incident dementia over 20 years, likely driven by vascular pathologies.

摘要

背景与目的

止血因子的血液浓度会影响血栓形成和出血倾向,并且可能通过可改变的血管病理导致认知障碍。在社区居住人群中,中年期评估的止血状态与晚年认知障碍之间的关联在很大程度上仍未知。

方法

利用来自动脉粥样硬化风险社区研究(Atherosclerosis Risk in Communities study)中 1990-1992 年具有认知功能测量的 14128 名参与者的数据,我们评估了止血测量值与 20 年认知表现和新发痴呆的变化之间的关联。在 1987-1989 年或 1993-1995 年测量了活化部分凝血活酶时间(activated partial thromboplastin time,aPTT)和纤维蛋白原、血管性血友病因子(von Willebrand factor,VWF)、因子 VIII、因子 VII、因子 XI、D-二聚体和可溶性血栓调节蛋白的水平。将止血测量值分为五组,最低五分位数表示凝血能力较低。认知表现使用 3 项测试的综合 z 评分进行描述(即延迟单词回忆测试(delayed word recall test,DWRT)、数字符号替换测试(digit symbol substitution,DSST)和单词流畅性测试(word fluency test,WFT)),在 1990-1992 年、1996-1998 年和 2011-2013 年进行评估。痴呆症要么通过面对面评估,要么通过 2017 年的痴呆症监测确定。混合效应模型和 Cox 比例风险模型分别用于评估认知轨迹和痴呆风险。

结果

在具有 1987-1989 年止血测量值的 12765 名参与者中,他们在首次认知评估时年龄在 47-70 岁,我们观察到 aPTT 缩短的显著趋势(趋势<0.001;第五五分位数与第一五分位数(Q5 与 Q1)的 20 年认知下降差异[Q5 与 Q1]:-0.104[95%CI -0.160 至-0.048])和因子 VII 水平升高(<0.002;Q5 与 Q1:-0.085[-0.142,-0.028])与更大的 20 年认知下降有关。与 WFT 或 DWRT 下降的关联比与 DSST 下降的关联更强。同样,较短的 aPTT 和较高的因子 VIII 水平与更高的痴呆风险相关,Q5 与 Q1 的 HR 分别为 1.23(95%CI 1.07 至 1.42)和 1.17(1.01-1.36),p 趋势分别为 0.008 和 0.024。

讨论

总体而言,我们的研究发现,中年期测量的 aPTT 和因子 VIII 与 20 年认知下降和新发痴呆之间存在一致的趋势关联,这可能是由血管病理引起的。

相似文献

1
Midlife Hemostasis Measures, 20-Year Cognitive Decline, and Incident Dementia.中年止血措施、20 年认知能力下降与痴呆症发病。
Neurology. 2023 Oct 24;101(17):e1697-e1707. doi: 10.1212/WNL.0000000000207771. Epub 2023 Aug 31.

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2
Hemostatic Abnormalities in Dementia: A Systematic Review and Meta-Analysis.痴呆患者的止血异常:系统评价和荟萃分析。
Semin Thromb Hemost. 2019 Jul;45(5):514-522. doi: 10.1055/s-0039-1688444. Epub 2019 May 16.

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