Drug treatment of Alzheimer's disease patients leads to expression changes in peripheral blood cells

被引:10
作者
Calciano, Margaret A. [1 ]
Zhou, Weiyin [1 ]
Snyder, Peter J. [2 ,3 ]
Einstein, Richard [1 ]
机构
[1] ExonHit Therapeut Inc, Gaithersburg, MD USA
[2] Brown Univ, Lifespan Affiliated Hosp, Providence, RI 02912 USA
[3] Brown Univ, Alpert Med Sch, Providence, RI 02912 USA
关键词
Alzheimer's disease; Cholinesterase inhibitors; Acetylcholinesterase; Donepezil; Galantamine; Rivastigmine; Expression profiling; Microarray; Genome-wide SpliceArray; Pharmacogenomics; Peripheral blood; BUTYRYLCHOLINESTERASE K-VARIANT; MILD COGNITIVE IMPAIRMENT; DONEPEZIL; RIVASTIGMINE; NEUROPROTECTION; GALANTAMINE; PROGRESSION; EFFICACY; PREDICTION; INHIBITOR;
D O I
10.1016/j.jalz.2009.12.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Background: Increasing cholinergic activity has been the primary mechanism for treating dementia clue to Alzheimer's disease. However, the effectiveness of cholinesterase inhibitors (ChEIs) is still widely debated. The identification of specific biomarkers capable of identifying patients more likely to respond to these treatments could potentially provide specific evidence to clearly address this controversy through patient stratification. The goal of this study was to determine the feasibility of discovering biomarkers specific for the treatment of Alzheimer's disease. Methods: Peripheral blood was collected from a cohort of patients treated with different ChEIs. Total RNA was isolated and profiled on the human Genome-Wide SpliceArray (GWSA) to test the feasibility of discriminating the different treatment subgroups of subjects based on the expression patterns generated from the Genome-Wide SpliceArray. Results: Specific expression differences were identified for the various treatment groups that lead to a clear separation between patients treated with ChEIs versus naive patients when Principal Component Analysis was performed on probe sets selected for differential expression. In addition, specific probe sets were identified to be dependent on the inhibitor used among the treated patients. Conclusions: Distinct separation between non-treated, galantamine, donepezil, and rivastigmine-treated patients was clearly identified based on small sets of expression probes. The ability to identify drug-specific treatment expression differences strengthens the potential for using peripheral gene signatures for the identification of individuals responding to drug treatment. (c) 2010 The Alzheimer's Association. All rights reserved.
引用
收藏
页码:386 / 393
页数:8
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