Martinez Nicko C, Bharani Krishna L, Hasan Saadia, Hayes Cellas A
University of California, Riverside.
Stanford University School of Medicine.
Res Sq. 2025 Jul 14:rs.3.rs-7036276. doi: 10.21203/rs.3.rs-7036276/v1.
A growing number of older adults exhibit neurofibrillary tangle pathology without significant amyloid deposition, a biomarker profile consistent with suspected non-Alzheimer's pathophysiology or primary age-related tauopathy. The cognitive consequences within this subgroup remain poorly characterized, particularly with respect to vascular comorbidity. This study investigates whether vascular neuropathologies are associated with pre-mortem cognitive decline among individuals with predominately neurofibrillary tangles and low to none neuritic plaque pathology detected post-mortem.
The sample included autopsy-confirmed data from 579 participants in the National Alzheimer's Coordinating Center (NACC) cohort with intermediate-to-high Braak stage (B2-B3) and absent or minimal neuritic plaques (C0-C1). Vascular neuropathologies included arteriolosclerosis, atherosclerosis of the circle of Willis, gross infarcts/ lacunes, and microinfarcts were assessed for associations with global cognition (Clinical Dementia Rating Sum of Boxes, CDR-SOB) and harmonized cognitive domain specific performance (memory, executive function, and language) using multivariable regression adjusted for age, sex, education, and apolipoprotein ε4 status. Sensitivity analyses further controlled for cardiovascular risk, excluded individuals with any neuritic plaques, and controlling for individual neuritic plaque and Braak staging.
Cross-sectionally, microinfarcts were consistently associated with poorer memory (β = - 0.28, p = 0.02), executive function (β = - 0.24, p = 0.02), and language (β = - 0.21, p = 0.02) approximate to death. Gross infarcts were associated with language impairment and higher CDR scores. These associations remained significant after adjusting for cardiovascular risk and were even stronger when restricted to strictly neuritic amyloid negative individuals.
Microinfarcts may represent a key driver of cognitive impairment in neurofibrillary tangle predominant individuals. These findings highlight a vascular-neurodegenerative pathway that warrants consideration in non-neuritic plaque models of cognitive decline and may inform targeted prevention strategies.
越来越多的老年人表现出神经纤维缠结病理改变,但无明显淀粉样蛋白沉积,这种生物标志物特征与疑似非阿尔茨海默病病理生理学或原发性年龄相关性tau病一致。该亚组内的认知后果仍未得到充分描述,尤其是在血管合并症方面。本研究调查了血管神经病理学是否与死后检测到以神经纤维缠结为主且神经炎性斑块病理改变低或无的个体生前认知衰退相关。
样本包括来自国家阿尔茨海默病协调中心(NACC)队列的579名参与者的尸检确诊数据,这些参与者处于中高Braak分期(B2 - B3)且无或有极少神经炎性斑块(C0 - C1)。评估血管神经病理学,包括小动脉硬化、 Willis环动脉粥样硬化、大体梗死灶/腔隙和微梗死灶,与总体认知(临床痴呆评定框总和,CDR - SOB)以及经年龄、性别、教育程度和载脂蛋白ε4状态校正的多变量回归分析得出的协调认知领域特定表现(记忆、执行功能和语言)之间的关联。敏感性分析进一步控制了心血管风险,排除了有任何神经炎性斑块的个体,并控制了个体神经炎性斑块和Braak分期。
横断面分析显示,微梗死灶与接近死亡时较差的记忆(β = - 0.28,p = 0.02)、执行功能(β = - 0.24,p = 0.02)和语言(β = - 0.21,p = 0.02)持续相关。大体梗死灶与语言障碍和更高的CDR评分相关。在调整心血管风险后,这些关联仍然显著,并且在严格限制为神经炎性淀粉样蛋白阴性个体时更强。
微梗死灶可能是神经纤维缠结为主的个体认知障碍的关键驱动因素。这些发现突出了一条血管 - 神经退行性途径,在认知衰退的非神经炎性斑块模型中值得考虑,并且可能为有针对性的预防策略提供信息。