Department of Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Department of Biostatistics, University of Florida, Gainesville, FL, USA.
J Alzheimers Dis. 2021;79(3):1041-1054. doi: 10.3233/JAD-200176.
Understanding metabolic mechanisms associated with cognitive changes preceding an Alzheimer's disease (AD) diagnosis could advance our understanding of AD progression and inform preventive methods.
We investigated the metabolomics of the early changes in executive function and delayed recall, the earliest aspects of cognitive function to change in the course of AD development, in order to better understand mechanisms that could contribute to early stages and progression of this disease.
This investigation used longitudinal plasma samples from the Wisconsin Registry for Alzheimer's Prevention (WRAP), a cohort of participants who were dementia free at enrollment and enriched with a parental history of AD. Metabolomic profiles were quantified for 2,324 fasting plasma samples among 1,200 participants, each with up to three study visits, which occurred every two years. Metabolites were individually tested for association with executive function and delayed recall trajectories across age.
Of 1,097 metabolites tested, levels of seven were associated with executive function trajectories, including an amino acid cysteine S-sulfate and three fatty acids, including erucate (22 : 1n9), while none were associated with delayed recall trajectories. Replication was attempted for four of these metabolites that were present in the Vietnam Era Twin Study of Aging (VETSA). Although none reached statistical significance, three of these associations showed consistent effectdirections.
Our results suggest potential metabolomic mechanisms that could contribute to the earliest signs of cognitive decline. In particular, fatty acids may be associated with cognition in a manner that is more complex than previously suspected.
了解与阿尔茨海默病(AD)诊断前认知变化相关的代谢机制,可以增进我们对 AD 进展的理解,并为预防方法提供信息。
我们研究了执行功能和延迟回忆早期变化的代谢组学,这是 AD 发展过程中认知功能最早变化的方面,以便更好地了解可能导致该疾病早期和进展的机制。
这项研究使用了威斯康星州阿尔茨海默病预防注册中心(WRAP)的纵向血浆样本,该队列的参与者在入组时没有痴呆症,并且有 AD 的家族史。在 1200 名参与者中,对多达 3 次研究访问的 2324 个空腹血浆样本进行了代谢组学特征的定量分析,每次访问每两年进行一次。逐个测试代谢物与执行功能和延迟回忆轨迹随年龄的相关性。
在测试的 1097 种代谢物中,有 7 种代谢物的水平与执行功能轨迹相关,包括一种氨基酸半胱氨酸 S-硫酸盐和三种脂肪酸,包括芥酸(22 : 1n9),而没有代谢物与延迟回忆轨迹相关。对其中四种存在于越南时代双胞胎衰老研究(VETSA)中的代谢物进行了复制尝试。尽管没有达到统计学意义,但这些关联中的三个显示出一致的效应方向。
我们的研究结果表明,潜在的代谢组学机制可能有助于认知能力下降的最早迹象。特别是,脂肪酸可能以比以前怀疑的更复杂的方式与认知相关。