Howard Katherine L, Filley Christopher M
Department of Neurology, University of Colorado at Denver School of Medicine, Aurora, CO, USA.
Rev Neurol Dis. 2009 Winter;6(1):26-32.
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.
随着老年人群中最常见的痴呆症——阿尔茨海默病(AD)的患病率持续上升,神经科医生将会面对越来越多关于痴呆症患者、其亲属以及除年龄增长外无明显风险但担心记忆力或认知功能的人群进行基因检测的问题。直到最近,临床基因检测仅包括载脂蛋白E基因分型和早老素1突变检测。2008年,检测范围扩大到包括早老素2和淀粉样前体蛋白基因。尽管有这些进展,但基因检测目前并不适用于大多数被诊断为AD的个体,且用于预测目的的效用有限。然而,进一步的研究可能会扩大这种检测对痴呆症患者及其亲属的有用性。如果进行基因检测,无论是由医生还是合格的基因咨询师进行全面的咨询,都是受影响个体及其家庭检测过程中不可或缺的一部分。