早老素
发病机制
医学
痴呆
阿尔茨海默病
疾病
淀粉样蛋白(真菌学)
遗传学
神经科学
生物信息学
生物
病理
作者
Kaj Blennow,Mony J. de Leon,Henrik Zetterberg
出处
期刊:The Lancet
[Elsevier]
日期:2006-07-01
卷期号:368 (9533): 387-403
被引量:2936
标识
DOI:10.1016/s0140-6736(06)69113-7
摘要
Alzheimer's disease is the most common cause of dementia. Research advances have enabled detailed understanding of the molecular pathogenesis of the hallmarks of the disease—ie, plaques, composed of amyloid β (Aβ), and tangles, composed of hyperphosphorylated tau. However, as our knowledge increases so does our appreciation for the pathogenic complexity of the disorder. Familial Alzheimer's disease is a very rare autosomal dominant disease with early onset, caused by mutations in the amyloid precursor protein and presenilin genes, both linked to Aβ metabolism. By contrast with familial disease, sporadic Alzheimer's disease is very common with more than 15 million people affected worldwide. The cause of the sporadic form of the disease is unknown, probably because the disease is heterogeneous, caused by ageing in concert with a complex interaction of both genetic and environmental risk factors. This seminar reviews the key aspects of the disease, including epidemiology, genetics, pathogenesis, diagnosis, and treatment, as well as recent developments and controversies.
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