Mild Amyloid Burden in the Brains of Cognitively Unimpaired Individuals is Associated with Long-Term Cognitive Impairment.

IF 7.5 1区 医学 Q1 CLINICAL NEUROLOGY
Chengjie Xiong, Jingqin Luo, Sarah Hartz, Suzanne E Schindler, Walter Kukull, Jason Hassenstab, David A Wolk, Carey E Gleason, Sterling C Johnson, Reisa Sperling, Keith Johnson, Erik D Roberson, Krista L Moulder, Emily Gremminger, Folasade Agboola, Elizabeth A Grant, Russ Hornbeck, Parinaz Massoumzadeh, Sarah Keefe, Donna Dierker, David Holtzman, John C Morris
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Abstract

Objective: We aimed to identify the minimal amount of amyloid burden measured by positron emission tomography (PET) in amyloid-negative cognitively unimpaired individuals that predicts the development of cognitive impairment.

Methods: A total of 1,896 cognitively unimpaired participants underwent longitudinal clinical/cognitive assessments for up to 20.3 years after amyloid PET imaging. Cox proportional hazards models were used to assess how the risk of cognitive impairment was associated with subthresholds of amyloid PET Centiloid. Linear mixed effects models were used to associate the longitudinal cognitive decline and amyloid accumulation with baseline amyloid burden.

Results: Amyloid-positive participants (Centiloid >20; n = 421) were 154% (hazard ratio 2.54, p < 0.0001) more likely to develop cognitive impairment than amyloid-negative participants. Approximately 48.7% of the amyloid-negative participants had mild amyloid burden (defined by Centiloid from 0.93 to 20) and were 43% more likely to develop cognitive impairment (hazard ratio 1.43, p = 0.008) than the lowest amyloid group (Centiloid <0.93) approximately 10 years post baseline. Longitudinal changes in amyloid PET Centiloid and cognition followed a similar pattern: amyloid-positive participants were the fastest, followed by the mild amyloid burden group and finally the lowest amyloid group, and the cognitive trajectories for the latter 2 started to separate only approximately 10 years post baseline (p = 0.003).

Interpretation: Almost half of amyloid-negative cognitively unimpaired individuals were at an elevated long-term risk of cognitive impairment, when compared with those with the lowest amyloid levels. These findings suggest that the current threshold for amyloid positivity may be overly restrictive, potentially excluding a large portion of high-risk participants from prevention trials. ANN NEUROL 2026.

认知功能未受损个体大脑中的轻度淀粉样蛋白负担与长期认知障碍有关。
目的:我们旨在确定通过正电子发射断层扫描(PET)在淀粉样蛋白阴性认知未受损个体中测量的淀粉样蛋白负荷的最小量,以预测认知障碍的发展。方法:在淀粉样蛋白PET成像后,共有1896名认知功能未受损的参与者接受了长达20.3年的纵向临床/认知评估。使用Cox比例风险模型来评估认知障碍风险与淀粉样蛋白PET Centiloid亚阈值之间的关系。使用线性混合效应模型将纵向认知能力下降和淀粉样蛋白积累与基线淀粉样蛋白负担联系起来。结果:淀粉样蛋白阳性的参与者(Centiloid bbb20; n = 421)为154%(危险比2.54,p)解释:与淀粉样蛋白水平最低的人相比,几乎一半的淀粉样蛋白阴性的认知功能正常的个体长期认知功能障碍的风险升高。这些发现表明,目前淀粉样蛋白阳性的阈值可能过于严格,可能会将很大一部分高风险参与者排除在预防试验之外。Ann neurol 2026。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of Neurology
Annals of Neurology 医学-临床神经学
CiteScore
18.00
自引率
1.80%
发文量
270
审稿时长
3-8 weeks
期刊介绍: Annals of Neurology publishes original articles with potential for high impact in understanding the pathogenesis, clinical and laboratory features, diagnosis, treatment, outcomes and science underlying diseases of the human nervous system. Articles should ideally be of broad interest to the academic neurological community rather than solely to subspecialists in a particular field. Studies involving experimental model system, including those in cell and organ cultures and animals, of direct translational relevance to the understanding of neurological disease are also encouraged.
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