Center for Molecular & Behavioral Neuroscience, Rutgers University-Newark, 197 University Avenue, Suite 209, Newark, NJ, 07102, USA.
Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at the University of Gothenburg, Wallinsgatan 6, Mölndal, Gothenburg, 431 41, Sweden.
Alzheimers Res Ther. 2024 Nov 22;16(1):253. doi: 10.1186/s13195-024-01619-0.
Phosphorylated tau (p-tau) and amyloid beta (Aβ) in human plasma may provide an affordable and minimally invasive method to evaluate Alzheimer's disease (AD) pathophysiology. The medial temporal lobe (MTL) is susceptible to changes in structural integrity that are indicative of the disease progression. Among healthy adults, higher dynamic network flexibility within the MTL was shown to mediate better generalization of prior learning, a measure which has been demonstrated to predict cognitive decline and neural changes in preclinical AD longitudinally. Recent developments in cognitive, neural, and blood-based biomarkers of AD risk that may correspond with MTL changes. However, there is no comprehensive study on how these generalization biomarkers, long-term memory, MTL dynamic network flexibility, and plasma biomarkers are interrelated. This study investigated (1) the relationship between long-term memory, generalization performance, and MTL dynamic network flexibility and (2) how plasma p-tau231, p-tau181, and Aβ42/Aβ40 influence generalization, long-term memory, and MTL dynamics in cognitively unimpaired older African Americans.
148 participants (Mean: 70.88,SD: 6.05) were drawn from the ongoing longitudinal study, Pathways to Healthy Aging in African Americans conducted at Rutgers University-Newark. Cognition was evaluated with the Rutgers Acquired Equivalence Task (generalization task) and Rey Auditory Learning Test (RAVLT) delayed recall. MTL dynamic network connectivity was measured from functional Magnetic Resonance Imaging data. Plasma p-tau231, p-tau181, and Aβ42/Aβ40 were measured from blood samples.
There was a significant positive correlation between generalization performance and MTL Dynamic Network Flexibility (t = 3.372, β = 0.280, p < 0.001). There were significant negative correlations between generalization performance and plasma p-tau231 (t = -3.324, β = -0.265, p = 0.001) and p-tau181 (t = -2.408, β = -0.192, p = 0.017). A significant negative correlation was found between plasma p-tau231 and MTL Dynamic Network Flexibility (t = -2.825, β = -0.232, p = 0.005).
Increased levels of p-tau231 are associated with impaired generalization abilities and reduced dynamic network flexibility within the MTL. Plasma p-tau231 may serve as a potential biomarker for assessing cognitive decline and neural changes in cognitively unimpaired older African Americans.
人血浆中的磷酸化 tau(p-tau)和淀粉样蛋白 β(Aβ)可能提供一种负担得起且微创的方法来评估阿尔茨海默病(AD)的病理生理学。内侧颞叶(MTL)易发生结构完整性的变化,这些变化表明疾病的进展。在健康成年人中,MTL 内更高的动态网络灵活性被证明可以更好地概括先前的学习,这一指标已被证明可以预测认知能力下降和预临床 AD 的神经变化。最近在 AD 风险的认知、神经和基于血液的生物标志物方面取得了进展,这些标志物可能与 MTL 的变化相对应。然而,目前尚无综合研究来探讨这些概括生物标志物、长时记忆、MTL 动态网络灵活性以及血浆生物标志物之间的相互关系。本研究调查了(1)长时记忆、概括能力和 MTL 动态网络灵活性之间的关系,以及(2)在认知正常的老年非裔美国人中,血浆 p-tau231、p-tau181 和 Aβ42/Aβ40 如何影响概括、长时记忆和 MTL 动力学。
148 名参与者(平均年龄:70.88,标准差:6.05)来自罗格斯大学纽瓦克分校正在进行的纵向研究“非裔美国人健康老龄化途径”。认知通过罗格斯获得等价任务(概括任务)和 Rey 听觉学习测试(RAVLT)延迟回忆进行评估。MTL 动态网络连接性由功能磁共振成像数据测量。血浆 p-tau231、p-tau181 和 Aβ42/Aβ40 从血液样本中测量。
概括能力与 MTL 动态网络灵活性呈显著正相关(t=3.372,β=0.280,p<0.001)。概括能力与血浆 p-tau231(t=-3.324,β=-0.265,p=0.001)和 p-tau181(t=-2.408,β=-0.192,p=0.017)呈显著负相关。血浆 p-tau231 与 MTL 动态网络灵活性呈显著负相关(t=-2.825,β=-0.232,p=0.005)。
血浆 p-tau231 水平升高与 MTL 内概括能力受损和动态网络灵活性降低有关。血浆 p-tau231 可能成为评估认知能力下降和认知正常的老年非裔美国人神经变化的潜在生物标志物。