Bauer Christopher E, Zachariou Valentinos, Sudduth Tiffany L, Van Eldik Linda J, Jicha Gregory A, Nelson Peter T, Wilcock Donna M, Gold Brian T
Department of Neuroscience University of Kentucky Lexington Kentucky USA.
Sanders-Brown Center on Aging University of Kentucky Lexington Kentucky USA.
Alzheimers Dement (Amst). 2023 May 31;15(2):e12437. doi: 10.1002/dad2.12437. eCollection 2023 Apr-Jun.
We evaluated the relationship between plasma levels of transactive response DNA binding protein of 43 kDa (TDP-43) and neuroimaging (magnetic resonance imaging [MRI]) measures of brain structure in aging.
Plasma samples were collected from 72 non-demented older adults (age range 60-94 years) in the University of Kentucky Alzheimer's Disease Research Center cohort. Multivariate linear regression models were run with plasma TDP-43 level as the predictor variable and brain structure (volumetric or cortical thickness) measurements as the dependent variable. Covariates included age, sex, intracranial volume, and plasma markers of Alzheimer's disease neuropathological change (ADNC).
Negative associations were observed between plasma TDP-43 level and both the volume of the entorhinal cortex, and cortical thickness in the cingulate/parahippocampal gyrus, after controlling for ADNC plasma markers.
Plasma TDP-43 levels may be directly associated with structural MRI measures. Plasma TDP-43 assays may prove useful in clinical trial stratification.
Plasma transactive response DNA binding protein of 43 kDa (TDP-43) levels were associated with entorhinal cortex volume.Biomarkers of TDP-43 and Alzheimer's disease neuropathologic change (ADNC) may help distinguish limbic-predominant age-related TDP-43 encephalopathy neuropathologic change (LATE-NC) from ADNC.A comprehensive biomarker kit could aid enrollment in LATE-NC clinical trials.
我们评估了43 kDa的反式激活反应DNA结合蛋白(TDP-43)的血浆水平与衰老过程中脑结构的神经影像学(磁共振成像[MRI])测量值之间的关系。
从肯塔基大学阿尔茨海默病研究中心队列中的72名非痴呆老年人(年龄范围60 - 94岁)采集血浆样本。以血浆TDP-43水平作为预测变量,脑结构(体积或皮质厚度)测量值作为因变量,运行多元线性回归模型。协变量包括年龄、性别、颅内体积以及阿尔茨海默病神经病理改变(ADNC)的血浆标志物。
在控制了ADNC血浆标志物后,观察到血浆TDP-43水平与内嗅皮质体积以及扣带回/海马旁回的皮质厚度之间均呈负相关。
血浆TDP-43水平可能与MRI结构测量值直接相关。血浆TDP-43检测可能在临床试验分层中有用。
43 kDa的反式激活反应DNA结合蛋白(TDP-43)的血浆水平与内嗅皮质体积相关。TDP-43和阿尔茨海默病神经病理改变(ADNC)的生物标志物可能有助于区分以边缘系统为主的年龄相关性TDP-43脑病神经病理改变(LATE-NC)与ADNC。一套综合的生物标志物试剂盒可能有助于LATE-NC临床试验的入组。