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Translational Research in Genomics of Alzheimer's Disease: A Review of Current Practice and Future Perspectives

机译:阿尔茨海默氏病基因组学的转化研究:当前实践和未来展望的回顾

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摘要

Alzheimer's disease (AD) is the most prevalent form of dementia and the number of cases is expected to increase exponentially worldwide. Three highly penetrant genes (AβPP, PSEN1, and PSEN2) explain only a small number of AD cases with a Mendelian transmission pattern. Many genes have been analyzed for association with non-Mendelian AD, but the only consistently replicated finding is APOE. At present, possibilities for prevention, early detection, and treatment of the disease are limited. Predictive and diagnostic genetic testing is available only in Mendelian forms of AD. Currently, APOE genotyping is not considered clinically useful for screening, presymptomatic testing, or clinical diagnosis of non-Mendelian AD. However, clinical management of the disease is expected to benefit from the rapid pace of discoveries in the genomics of AD. Following a recently developed framework for the continuum of translation research that is needed to move genetic discoveries to health applications, this paper reviews recent genetic discoveries as well as translational research on genomic applications in the prevention, early detection, and treatment of AD. The four phases of translation research include: 1) translation of basic genomics research into a potential health care application; 2) evaluation of the application for the development of evidence-based guidelines; 3) evaluation of the implementation and use of the application in health care practice; and 4) evaluation of the achieved population health impact. Most research on genome-based applications in AD is still in the first phase of the translational research framework, which means that further research is still needed before their implementation can be considered. © 2010 - IOS Press and the authors. All rights reserved.
机译:阿尔茨海默氏病(AD)是痴呆症最普遍的形式,预计全世界的病例数将呈指数增长。三种高度渗透性的基因(AβPP,PSEN1和PSEN2)仅解释了少数具有孟德尔传播模式的AD病例。已经分析了许多基因与非孟德尔AD的关联,但是唯一持续复制的发现是APOE。目前,预防,早期发现和治疗该疾病的可能性是有限的。预测和诊断性基因检测仅在孟德尔形式的AD中可用。目前,APOE基因分型不被认为对非孟德尔AD的筛查,症状前测试或临床诊断具有临床意义。但是,预计该疾病的临床治疗将受益于AD基因组学研究的迅速发展。根据最近开发的将遗传发现应用于健康应用所需的翻译研究连续性框架,本文回顾了最近的遗传发现以及基因组在预防,早期发现和治疗中的应用的翻译研究。翻译研究的四个阶段包括:1)将基本基因组学研究转化为潜在的医疗保健应用; 2)评估制定循证指南的申请; 3)在卫生保健实践中评估该应用程序的实施和使用情况; 4)评估对人口健康的影响。 AD中基于基因组的应用程序的大多数研究仍处于翻译研究框架的第一阶段,这意味着在考虑将其实施之前仍需要进一步的研究。 ©2010-IOS Press和作者。版权所有。

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