Cummings J L, Vinters H V, Cole G M, Khachaturian Z S
Department of Neurology, University of California at Los Angeles School of Medicine, 90095-1769, USA.
Neurology. 1998 Jul;51(1 Suppl 1):S2-17; discussion S65-7. doi: 10.1212/wnl.51.1_suppl_1.s2.
Alzheimer's disease (AD) can be diagnosed with a considerable degree of accuracy. In some centers, clinical diagnosis predicts the autopsy diagnosis with 90% certainty in series reported from academic centers. The characteristic histopathologic changes at autopsy include neurofibrillary tangles, neuritic plaques, neuronal loss, and amyloid angiopathy. Mutations on chromosomes 21, 14, and 1 cause familial AD. Risk factors for AD include advanced age, lower intelligence, small head size, and history of head trauma; female gender may confer additional risks. Susceptibility genes do not cause the disease by themselves but, in combination with other genes or epigenetic factors, modulate the age of onset and increase the probability of developing AD. Among several putative susceptibility genes (on chromosomes 19, 12, and 6), the role of apolipoprotein E (ApoE) on chromosome 19 has been repeatedly confirmed. Protective factors include ApoE-2 genotype, history of estrogen replacement therapy in postmenopausal women, higher educational level, and history of use of nonsteroidal anti-inflammatory agents. The most proximal brain events associated with the clinical expression of dementia are progressive neuronal dysfunction and loss of neurons in specific regions of the brain. Although the cascade of antecedent events leading to the final common path of neurodegeneration must be determined in greater detail, the accumulation of stable amyloid is increasingly widely accepted as a central pathogenetic event. All mutations known to cause AD increase the production of beta-amyloid peptide. This protein is derived from amyloid precursor protein and, when aggregated in a beta-pleated sheet configuration, is neurotoxic and forms the core of neuritic plaques. Nerve cell loss in selected nuclei leads to neurochemical deficiencies, and the combination of neuronal loss and neurotransmitter deficits leads to the appearance of the dementia syndrome. The destructive aspects include neurochemical deficits that disrupt cell-to-cell communications, abnormal synthesis and accumulation of cytoskeletal proteins (e.g., tau), loss of synapses, pruning of dendrites, damage through oxidative metabolism, and cell death. The concepts of cognitive reserve and symptom thresholds may explain the effects of education, intelligence, and brain size on the occurrence and timing of AD symptoms. Advances in understanding the pathogenetic cascade of events that characterize AD provide a framework for early detection and therapeutic interventions, including transmitter replacement therapies, antioxidants, anti-inflammatory agents, estrogens, nerve growth factor, and drugs that prevent amyloid formation in the brain.
阿尔茨海默病(AD)能够在相当程度上准确诊断。在一些中心,临床诊断在学术中心报告的系列研究中对尸检诊断的预测准确率达90%。尸检时特征性的组织病理学改变包括神经原纤维缠结、神经炎性斑块、神经元丢失及淀粉样血管病。21号、14号和1号染色体上的突变导致家族性AD。AD的危险因素包括高龄、低智力、小头围及头部外伤史;女性可能有额外风险。易感基因本身不会引发该病,但与其他基因或表观遗传因素共同作用时,会调节发病年龄并增加患AD的可能性。在几个假定的易感基因(位于19号、12号和6号染色体上)中,19号染色体上载脂蛋白E(ApoE)的作用已得到反复证实。保护因素包括ApoE-2基因型、绝经后女性的雌激素替代治疗史、较高的教育水平及使用非甾体抗炎药的历史。与痴呆临床症状相关的最直接脑内事件是进行性神经元功能障碍及脑特定区域的神经元丢失。尽管导致神经退行性变最终共同途径的一系列先前事件必须更详细地确定,但稳定淀粉样蛋白的积累越来越被广泛认为是一个核心致病事件。所有已知导致AD的突变都会增加β-淀粉样肽的产生。这种蛋白质源自淀粉样前体蛋白,当以β折叠片层结构聚集时具有神经毒性,并形成神经炎性斑块的核心。特定核团中的神经细胞丢失导致神经化学物质缺乏,神经元丢失和神经递质缺乏共同作用导致痴呆综合征的出现。破坏性方面包括破坏细胞间通讯的神经化学物质缺乏、细胞骨架蛋白(如tau)的异常合成和积累、突触丢失、树突修剪、氧化代谢损伤及细胞死亡。认知储备和症状阈值的概念可以解释教育、智力和脑容量对AD症状发生及时间的影响。对AD特征性致病事件级联反应理解的进展为早期检测和治疗干预提供了框架,包括递质替代疗法、抗氧化剂、抗炎药、雌激素、神经生长因子以及预防脑内淀粉样蛋白形成的药物。