Fischer Larissa, Molloy Eóin N, Pichet Binette Alexa, Vockert Niklas, Marquardt Jonas, Pacha Pilar Andrea, Kreissl Michael C, Remz Jordana, Tremblay-Mercier Jennifer, Poirier Judes, Rajah Maria Natasha, Villeneuve Sylvia, Maass Anne
German Center for Neurodegenerative Diseases (DZNE), Magdeburg 39120, Germany
German Center for Neurodegenerative Diseases (DZNE), Magdeburg 39120, Germany.
J Neurosci. 2025 Feb 5;45(6):e1408242024. doi: 10.1523/JNEUROSCI.1408-24.2024.
The precuneus is a site of early amyloid-beta (Aβ) accumulation. Previous cross-sectional studies reported increased precuneus fMRI activity in older adults with mild cognitive deficits or elevated Aβ. However, longitudinal studies in early Alzheimer's disease (AD) are lacking and the relationship to the Apolipoprotein-E () genotype is unclear. Investigating the PREVENT-AD dataset, we assessed how baseline and longitudinal precuneus activity during successful memory retrieval relates to future Aβ and tau burden and change in memory performance. We further studied the moderation by 4 genotype. We included 165 older adults (age, 62.8 ± 4.4 years; 113 female; 66 4 carriers) who were cognitively normal at baseline with a family history of AD. All participants performed task-fMRI at baseline and underwent F-flortaucipir-PET and F-NAV4694-Aβ-PET on average 5 years later. We found that higher baseline activity and greater longitudinal increase in precuneus activity were associated with higher Aβ burden in 4 carriers but not noncarriers. We observed no effects of precuneus activity on tau burden. Finally, 4 noncarriers with low baseline precuneus activity exhibited better longitudinal performance in an independent memory test compared with (1) noncarriers with higher baseline activity and (2) 4 carriers. Our findings suggest that higher task-related precuneus activity during memory retrieval at baseline and over time are associated with greater Aβ burden in cognitively normal 4 carriers. Our results further indicate that the absence of "hyperactivation" and the absence of the 4 allele is related with better future cognitive outcomes in cognitively normal older adults at risk for AD.
楔前叶是早期β淀粉样蛋白(Aβ)积累的部位。以往的横断面研究报告称,患有轻度认知缺陷或Aβ水平升高的老年人楔前叶功能磁共振成像(fMRI)活动增强。然而,早期阿尔茨海默病(AD)的纵向研究尚缺乏,且与载脂蛋白E(APOE)基因型的关系尚不清楚。通过对PREVENT-AD数据集的研究,我们评估了成功记忆检索过程中基线和纵向的楔前叶活动与未来Aβ和tau蛋白负担以及记忆表现变化之间的关系。我们还进一步研究了APOE基因型的调节作用。我们纳入了165名基线时认知正常且有AD家族史的老年人(年龄62.8±4.4岁;113名女性;66名APOE ε4携带者)。所有参与者在基线时进行了任务功能磁共振成像检查,平均5年后接受了18F-氟替卡匹尔正电子发射断层扫描(PET)和18F-NAV4694-Aβ-PET检查。我们发现,较高的基线活动以及楔前叶活动的更大纵向增加与APOE ε4携带者而非非携带者的更高Aβ负担相关。我们未观察到楔前叶活动对tau蛋白负担有影响。最后,与(1)基线活动较高的非携带者和(2)APOE ε4携带者相比,基线楔前叶活动较低的APOE ε4非携带者在一项独立记忆测试中表现出更好的纵向记忆表现。我们的研究结果表明,在基线和随访期间,记忆检索过程中与任务相关的较高楔前叶活动与认知正常的APOE ε4携带者中更大的Aβ负担相关。我们的结果进一步表明,在有AD风险的认知正常老年人中,不存在“过度激活”以及不存在APOE ε4等位基因与更好的未来认知结果相关。