Tarawneh Hadeel Y, Jayakody Dona M P, Verma Shipra, Doré Vincent, Xia Ying, Mulders Wilhelmina H A M, Martins Ralph N, Sohrabi Hamid R
School of Human Sciences, The University of Western Australia, Perth, Australia.
Ear Science Institute Australia, Perth, Australia.
J Alzheimers Dis. 2023;92(3):1093-1109. doi: 10.3233/JAD-221119.
Auditory event-related potentials (AERPs) have been suggested as possible biomarkers for the early diagnosis of Alzheimer's disease (AD). However, no study has investigated AERP measures in individuals with subjective memory complaints (SMCs), who have been suggested to be at a pre-clinical stage of AD.
This study investigated whether AERPs in older adults with SMC can be used to objectively identify those at high risk of developing AD.
AERPs were measured in older adults. Presence of SMC was determined using the Memory Assessment Clinics Questionnaire (MAC-Q). Hearing thresholds using pure-tone audiometry, neuropsychological data, levels of amyloid-β burden and Apolipoprotein E (APOE)ɛ genotype were also obtained A classic two-tone discrimination (oddball) paradigm was used to elicit AERPs (i.e., P50, N100, P200, N200, and P300).
Sixty-two individuals (14 male, mean age 71.9±5.2 years) participated in this study, of which, 43 (11 male, mean age 72.4±5.5 years) were SMC and 19 (3 male, mean age 70.8±4.3 years) were non-SMC (controls). P50 latency was weakly but significantly correlated with MAC-Q scores. In addition, P50 latencies were significantly longer in Aβ+ individuals compared to Aβ- individuals.
Results suggest that P50 latencies may be a useful tool to identify individuals at higher risk (i.e., participants with high Aβ burden) of developing measurable cognitive decline. Further longitudinal and cross-sectional studies in a larger cohort on SMC individuals are warranted to determine if AERP measures could be of significance for the detection of pre-clinical AD.
听觉事件相关电位(AERP)已被认为可能是阿尔茨海默病(AD)早期诊断的生物标志物。然而,尚无研究对有主观记忆主诉(SMC)的个体进行AERP测量,这些个体被认为处于AD的临床前期。
本研究调查了有SMC的老年人的AERP是否可用于客观识别有患AD高风险的个体。
对老年人进行AERP测量。使用记忆评估诊所问卷(MAC-Q)确定是否存在SMC。还获得了纯音听力计测量的听力阈值、神经心理学数据、淀粉样β蛋白负荷水平和载脂蛋白E(APOE)ɛ基因型。采用经典的双音辨别(oddball)范式诱发AERP(即P50、N100、P200、N200和P300)。
62名个体(14名男性,平均年龄71.9±岁)参与了本研究,其中43名(11名男性,平均年龄72.4±5.5岁)有SMC,19名(3名男性,平均年龄70.8±4.3岁)无SMC(对照组)。P50潜伏期与MAC-Q评分呈弱但显著的相关性。此外,与Aβ-个体相比,Aβ+个体的P50潜伏期显著更长。
结果表明,P50潜伏期可能是识别有发生可测量认知衰退高风险个体(即Aβ负荷高的参与者)的有用工具。有必要在更大的SMC个体队列中进行进一步纵向和横断面研究,以确定AERP测量对于临床前期AD的检测是否具有重要意义。