Center for Memory and Brain Health, The Sandra and Malcolm Berman Brain & Spine Institute, Baltimore, MD 21209,, USA.
Nat Rev Neurol. 2009 Dec;5(12):649-58. doi: 10.1038/nrneurol.2009.175. Epub 2009 Nov 17.
Individuals over 80 years of age represent the most rapidly growing segment of the population, and late-life dementia has become a major public health concern worldwide. Development of effective preventive and treatment strategies for late-life dementia relies on a deep understanding of all the processes involved. In the centuries since the Greek philosopher Pythagoras described the inevitable loss of higher cognitive functions with advanced age, various theories regarding the potential culprits have dominated the field, ranging from demonic possession, through 'hardening of blood vessels', to Alzheimer disease (AD). Recent studies suggest that atrophy in the cortex and hippocampus-now considered to be the best determinant of cognitive decline with aging-results from a combination of AD pathology, inflammation, Lewy bodies, and vascular lesions. A specific constellation of genetic and environmental factors (including apolipoprotein E genotype, obesity, diabetes, hypertension, head trauma, systemic illnesses, and obstructive sleep apnea) contributes to late-life brain atrophy and dementia in each individual. Only a small percentage of people beyond the age of 80 years have 'pure AD' or 'pure vascular dementia'. These concepts, formulated as the dynamic polygon hypothesis, have major implications for clinical trials, as any given drug might not be ideal for all elderly people with dementia.
80 岁以上的人群代表了人口中增长最快的部分,而老年痴呆症已成为全球主要的公共卫生关注点。开发针对老年痴呆症的有效预防和治疗策略依赖于对所有涉及过程的深入理解。自希腊哲学家毕达哥拉斯(Pythagoras)在几个世纪前描述了随着年龄的增长,高级认知功能不可避免地丧失以来,各种关于潜在罪魁祸首的理论一直主导着该领域,从恶魔附身到血管硬化,再到阿尔茨海默病(AD)。最近的研究表明,大脑皮层和海马体的萎缩(现在被认为是衰老导致认知能力下降的最佳决定因素)是 AD 病理、炎症、路易体和血管病变的综合作用所致。特定的遗传和环境因素组合(包括载脂蛋白 E 基因型、肥胖、糖尿病、高血压、头部创伤、全身性疾病和阻塞性睡眠呼吸暂停)导致了每个人的晚年大脑萎缩和痴呆。只有一小部分 80 岁以上的人患有“单纯 AD”或“单纯血管性痴呆”。这些概念以动态多边形假说的形式提出,对临床试验具有重大意义,因为任何特定的药物可能并不适合所有患有痴呆症的老年人。