Rush Alzheimer's Disease Center, Chicago, Illinois, USA.
University of Rochester Center for Translational Neuromedicine, Rochester, NY, USA.
Curr Opin Neurol. 2021 Apr 1;34(2):237-245. doi: 10.1097/WCO.0000000000000912.
Beta-amyloid with paired helical filaments (PHF)-tau neurofibrillary tangles define hallmark Alzheimer's disease neuropathologic changes (AD-NC). Yet persons with Alzheimer's dementia, defined broadly as an amnestic multidomain progressive dementia, often exhibit postmortem evidence of other neuropathologies including other neurodegenerative (Lewy body disease and transactive response DNA-binding protein disease) and vascular-related brain lesions. Clinicopathologic and epidemiologic analyses demonstrate the significance of these substrates, as coinciding neuropathologies mitigate the threshold for diagnosis of Alzheimer's dementia. In addition, other biologic processes may also independently underlie a progressive amnestic dementia. Advances in research on the relationship between age-related cognitive decline and the underlying neuropathologic substrates indicate that consensus neuropathologic criteria or disease nomenclature may need new considerations or refinement. This review appraises seminal literature as well as mixed pathologies and biological factors that may be determinants of clinical and pathologic disease.
Cognition in aging (spanning from normal cognition to dementia) represents a clinical continuum. Traditional neuropathologic substrates of dementia however do not explain the variability of cognitive decline. Conversely, not all patients with AD-NC exhibit symptomatology of Alzheimer's dementia. In addition to diagnostic plaques and tangles, other neurodegenerative, cerebrovascular, and perivascular substrates manifest through discrete tissue lesions. Factors related to energetics, neurogenetics, neuroimmunology, resilience, proteinopathies, and waste clearance are increasingly suggested to be general drivers of disease. Recognition of novel neuroimmune pathways and brain-body connections further suggest there may be broader extracranial determinants of person-specific disease.
Alzheimer's dementia is a pathologically heterogeneous and biologically multilayered disease. Recent studies and exercises in nomenclature reveal shortcomings in existing terminologies. Recognizing and overcoming these limitations is required for experts to effectively communicate about and ultimately prevent and treat Alzheimer's dementia.
β-淀粉样蛋白伴双螺旋丝(PHF)-tau 神经原纤维缠结定义了阿尔茨海默病神经病理改变的标志性特征(AD-NC)。然而,阿尔茨海默病痴呆症的定义很广泛,包括一种遗忘型多领域进行性痴呆症,患者通常在死后会出现其他神经病理学改变的证据,包括其他神经退行性疾病(路易体病和转染反应 DNA 结合蛋白病)和血管相关的脑损伤。临床病理和流行病学分析表明这些病变的重要性,因为同时存在的神经病理学改变降低了阿尔茨海默病痴呆症的诊断阈值。此外,其他生物学过程也可能独立导致进行性遗忘性痴呆。关于与年龄相关的认知能力下降和潜在神经病理学基础之间关系的研究进展表明,共识性神经病理学标准或疾病命名法可能需要新的考虑或改进。本综述评估了开创性文献以及可能决定临床和病理疾病的混合病理学和生物学因素。
衰老过程中的认知(从正常认知到痴呆)代表了一个临床连续体。然而,传统的痴呆症神经病理学基础并不能解释认知能力下降的可变性。相反,并非所有 AD-NC 患者都表现出阿尔茨海默病痴呆的症状。除了诊断性斑块和缠结外,其他神经退行性、脑血管和血管周围病变也通过离散的组织损伤表现出来。与能量学、神经遗传学、神经免疫学、弹性、蛋白病和废物清除有关的因素越来越被认为是疾病的一般驱动因素。对新的神经免疫途径和脑-体连接的认识进一步表明,可能存在更广泛的颅外决定因素来影响特定个体的疾病。
阿尔茨海默病痴呆症是一种病理异质性和生物学多层次的疾病。最近的研究和命名法练习揭示了现有术语的局限性。专家需要认识并克服这些局限性,以便有效地交流,并最终预防和治疗阿尔茨海默病痴呆症。