Advances in genetic testing for Alzheimer's disease.

Reviews in neurological diseases Pub Date : 2009-01-01
Katherine L Howard, Christopher M Filley
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Abstract

As the prevalence of Alzheimer's disease (AD), the most common dementia in the elderly, continues to increase, neurologists will encounter a growing number of questions about genetic testing for dementia patients, their relatives, and people concerned about memory or cognitive function who have no apparent risk except advancing age. Until recently, clinical gene testing only included apolipoprotein E genotyping and testing for presenilin 1 mutations. In 2008, testing expanded to include the presenilin 2 and amyloid precursor protein genes. Despite these advances, genetic testing is currently not appropriate for most individuals diagnosed with AD and has limited utility for predictive purposes. Further research, however, is likely to expand the usefulness of this testing for both dementia patients and their relatives. If genetic testing is undertaken, thorough counseling, whether by the physician or a qualified genetic counselor, is an integral component of the testing process for both affected individuals and their families.

阿尔茨海默病基因检测的进展。
老年痴呆症(Alzheimer's disease, AD)是老年人中最常见的痴呆症,随着其患病率的不断增加,神经科医生将会遇到越来越多的关于痴呆症患者、他们的亲属以及关注记忆或认知功能的人的基因检测的问题,这些人除了年龄增长之外没有明显的风险。直到最近,临床基因检测只包括载脂蛋白E基因分型和早老素1突变检测。2008年,检测范围扩大到早老素2和淀粉样蛋白前体基因。尽管取得了这些进展,但基因检测目前并不适合大多数被诊断患有阿尔茨海默病的个体,并且在预测目的方面的效用有限。然而,进一步的研究可能会扩大这种测试对痴呆症患者及其亲属的有用性。如果进行基因检测,彻底的咨询,无论是由医生还是合格的遗传咨询师,都是受影响个人及其家庭检测过程中不可或缺的组成部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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