Kravitz Efrat, Schmeidler James, Beeri Michal Schnaider
The Joseph Sagol Neuroscience Center, Sheba Medical Center, Ramat Gan, Israel; ; Parkinson's Disease and Movement Disorders Clinic, Department of Neurology, Sheba Medical Center, Ramat Gan, Israel; and.
Rambam Maimonides Med J. 2012 Oct 31;3(4):e0026. doi: 10.5041/RMMJ.10092. Print 2012 Oct.
The oldest-old are the fastest growing segment of the Western population. Over half of the oldest-old will have dementia, but the etiology is yet unknown. Age is the only risk factor consistently associated with dementia in the oldest-old. Many of the risk and protective factors for dementia in the young elderly, such as ApoE genotype, physical activity, and healthy lifestyle, are not relevant for the oldest-old. Neuropathology is abundant in the oldest-old brains, but specific pathologies of Alzheimer's disease (AD) or vascular dementia are not necessarily correlated with cognition, as in younger persons. It has been suggested that accumulation of both AD-like and vascular pathologies, loss of synaptic proteins, and neuronal loss contribute to the cognitive decline observed in the oldest-old. Several characteristics of the oldest-old may confound the diagnosis of dementia in this age group. A gradual age-related cognitive decline, particularly in executive function and mental speed, is evident even in non-demented oldest-old. Hearing and vision losses, which are also prevalent in the oldest-old and found in some cases to precede/predict cognitive decline, may mechanically interfere in neuropsychological evaluations. Difficulties in carrying out everyday activities, observed in the majority of the oldest-old, may be the result of motor or physical dysfunction and of neurodegenerative processes. The oldest-old appear to be a select population, who escapes major illnesses or delays their onset and duration toward the end of life. Dementia in the oldest-old may be manifested when a substantial amount of pathology is accumulated, or with a composition of a variety of pathologies. Investigating the clinical and pathological features of dementia in the oldest-old is of great importance in order to develop therapeutic strategies and to provide the most elderly of our population with good quality of life.
高龄老人是西方人口中增长最快的群体。超过半数的高龄老人会患痴呆症,但其病因尚不清楚。年龄是唯一始终与高龄老人痴呆症相关的风险因素。许多在年轻老年人中与痴呆症相关的风险和保护因素,如载脂蛋白E基因型、身体活动和健康的生活方式,对高龄老人并不适用。高龄老人的大脑中神经病理学现象普遍存在,但与年轻人不同,阿尔茨海默病(AD)或血管性痴呆的特定病理学现象不一定与认知相关。有人提出,AD样和血管性病理学现象的积累、突触蛋白的丧失以及神经元的丧失,共同导致了高龄老人中观察到的认知能力下降。高龄老人的一些特征可能会混淆该年龄组痴呆症的诊断。即使在未患痴呆症的高龄老人中,与年龄相关的认知能力逐渐下降,尤其是执行功能和思维速度方面的下降也很明显。听力和视力丧失在高龄老人中也很普遍,在某些情况下被发现先于/预测认知能力下降,可能会在神经心理学评估中产生机械干扰。在大多数高龄老人中观察到的日常生活活动困难,可能是运动或身体功能障碍以及神经退行性过程的结果。高龄老人似乎是一个特殊群体,他们能避免重大疾病,或在生命末期延迟疾病的发作和病程。高龄老人的痴呆症可能在积累了大量病理学现象时出现,或者由多种病理学现象共同导致。研究高龄老人痴呆症的临床和病理特征对于制定治疗策略以及为我们最年长的人群提供高质量生活至关重要。