Using Genetics to Enable Studies on the Prevention of Alzheimer's Disease

被引:52
作者
Crenshaw, D. G. [1 ]
Gottschalk, W. K. [1 ]
Lutz, M. W. [1 ]
Grossman, I. [2 ]
Saunders, A. M. [1 ]
Burke, J. R. [1 ,3 ]
Welsh-Bohmer, K. A. [1 ,3 ]
Brannan, S. K. [4 ]
Burns, D. K. [5 ]
Roses, A. D. [1 ,5 ]
机构
[1] Duke Univ, Med Ctr, Dept Neurol, Joseph & Kathleen Bryan Alzheimers Dis Res Ctr, Durham, NC 27710 USA
[2] IsraGene Ltd, Rosh Haayin, Israel
[3] Duke Univ, Med Ctr, Dept Psychiat, Durham, NC 27710 USA
[4] Takeda Pharmaceut Int Inc, Pharmaceut Dev Div, Deerfield, IL USA
[5] Zinfandel Pharmaceut Inc, Durham, NC USA
基金
美国国家卫生研究院;
关键词
MILD COGNITIVE IMPAIRMENT; CONJUGATED EQUINE ESTROGENS; APOLIPOPROTEIN-E GENOTYPE; DATA SET UDS; POSTMENOPAUSAL WOMEN; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; GINKGO-BILOBA; DOUBLE-BLIND;
D O I
10.1038/clpt.2012.222
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Curing Alzheimer's disease (AD) remains an elusive goal; indeed, it may even prove to be impossible, given the nature of the disease. Although modulating disease progression is an attractive target and will alleviate the burden of the most severe stages, this strategy will not reduce the prevalence of the disease itself. Preventing or (as described in this article) delaying the onset of cognitive impairment and AD will provide the greatest benefit to individuals and society by pushing the onset of disease into the later years of life. Because of the high variability in the age of onset of the disease, AD prevention studies that do not stratify participants by age-dependent disease risk will be operationally challenging, being large in size and of long duration. We present a composite genetic biomarker to stratify disease risk so as to facilitate clinical studies in high-risk populations. In addition, we discuss the rationale for the use of pioglitazone to delay the onset of AD in individuals at high risk.
引用
收藏
页码:177 / 185
页数:9
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