Blacker D, Tanzi R E
Department of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, USA.
Arch Neurol. 1998 Mar;55(3):294-6. doi: 10.1001/archneur.55.3.294.
Four genes involved in the development of Alzheimer disease have been identified. Three fully penetrant (deterministic) genes lead to the development of Alzheimer disease in patients younger than 60 years: the amyloid beta-protein precursor on chromosome 21, presenilin 1 on chromosome 14, and presenilin 2 on chromosome 1. Together, they account for about half of this early-onset form of the disease. One genetic risk factor--apolipoprotein E-4--is associated with late-onset Alzheimer disease. It accounts for a substantial fraction of disease burden but seems to act primarily to lower the age of disease onset. In general, none of these genes can be easily adapted for use as a diagnostic or predictive test for Alzheimer disease. Research activity includes searching for additional genes, especially for late-onset disease, and elucidating the mechanism of action of all identified genes as part of a long-term effort to develop more effective therapeutic and preventive strategies.
已确定了与阿尔茨海默病发展相关的四个基因。三个完全显性(决定性)基因会导致60岁以下患者患上阿尔茨海默病:位于21号染色体上的淀粉样β蛋白前体、位于14号染色体上的早老素1和位于1号染色体上的早老素2。它们共同构成了这种早发型疾病的约一半病例。一个遗传风险因素——载脂蛋白E-4——与晚发型阿尔茨海默病相关。它占疾病负担的很大一部分,但似乎主要作用是降低疾病发病年龄。一般来说,这些基因都不容易被轻易用作阿尔茨海默病的诊断或预测检测。研究活动包括寻找其他基因,特别是针对晚发型疾病的基因,并阐明所有已确定基因的作用机制,这是开发更有效治疗和预防策略的长期努力的一部分。