van Amerongen Suzan, Das Shreyasee, Kamps Suzie, Goossens Julie, Bongers Bram, Pijnenburg Yolande A L, Vanmechelen Eugeen, Vijverberg Everard G B, Teunissen Charlotte E, Verberk Inge M W
Amsterdam Neuroscience, Neurodegeneration, De Boelelaan 1085, Amsterdam 1081 HV, the Netherlands; Alzheimer Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc, De Boelelaan 1118, Amsterdam 1081 HV, the Netherlands.
Neurochemistry Laboratory, Department of Laboratory Medicine, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc, Boelelaan 1117, Amsterdam 1081 HV, the Netherlands; ADx NeuroSciences, Technologiepark-Zwijnaarde 6, Gent 9052, Belgium.
Neurobiol Aging. 2024 Sep;141:121-128. doi: 10.1016/j.neurobiolaging.2024.06.001. Epub 2024 Jun 14.
Traumatic brain injury (TBI) and Alzheimer's disease (AD) have overlapping mechanisms but it remains unknown if pathophysiological characteristics and cognitive trajectories in AD patients are influenced by TBI history. Here, we studied AD patients (stage MCI or dementia) with TBI history (AD n=110), or without (AD, n=110) and compared baseline CSF concentrations of amyloid beta 1-42 (Aβ42), phosphorylated tau181 (pTau181), total tau, neurofilament light chain (NfL), synaptosomal associated protein-25kDa (SNAP25), neurogranin (Ng), neuronal pentraxin-2 (NPTX2) and glutamate receptor-4 (GluR4), as well as differences in cognitive trajectories using linear mixed models. Explorative, analyses were repeated within stratified TBI groups by TBI characteristics (timing, severity, number). We found no differences in baseline CSF biomarker concentrations nor in cognitive trajectories between AD and AD patients. TBI >5 years ago was associated with higher NPTX2 and a tendency for higher SNAP25 concentrations compared to TBI ≤ 5 years ago, suggesting that TBI may be associated with long-term synaptic dysfunction only when occurring before onset or in a pre-clinical disease stage of AD.
创伤性脑损伤(TBI)和阿尔茨海默病(AD)具有重叠的机制,但AD患者的病理生理特征和认知轨迹是否受TBI病史影响仍不清楚。在此,我们研究了有TBI病史的AD患者(轻度认知障碍或痴呆阶段,n = 110)和无TBI病史的AD患者(n = 110),比较了脑脊液中β淀粉样蛋白1-42(Aβ42)、磷酸化tau181(pTau181)、总tau、神经丝轻链(NfL)、突触体相关蛋白25kDa(SNAP25)、神经颗粒蛋白(Ng)、神经元五聚体蛋白-2(NPTX2)和谷氨酸受体-4(GluR4)的基线浓度,以及使用线性混合模型的认知轨迹差异。通过TBI特征(时间、严重程度、次数)在分层的TBI组内重复进行探索性分析。我们发现AD患者与无TBI病史的AD患者之间,脑脊液生物标志物基线浓度和认知轨迹均无差异。与5年及以内的TBI相比,5年以前的TBI与更高的NPTX2以及更高的SNAP25浓度趋势相关,这表明仅当TBI发生在AD发病前或临床前期疾病阶段时,可能与长期突触功能障碍有关。