Analysis of potential transcriptomic biomarkers for Huntington's disease in peripheral blood

被引:106
作者
Runne, Heike
Kuhn, Alexandre
Wild, Edward J.
Pratyaksha, Wirahpati
Kristiansen, Mark
Isaacs, Jeremy D.
Regulier, Etienne
Delorenzi, Mauro
Tabrizi, Sarah J.
Luthi-Carter, Ruth
机构
[1] Ecole Polytech Fed Lausanne, Brain Mind Inst, Lab Funct Neurogenom, CH-1015 Lausanne, Switzerland
[2] UCL, Inst Neurol, Dept Neurogenerat Dis, London WC1N 3BG, England
[3] Swiss Inst Expt Canc Res, Natl Ctr Competence Res Mol Oncol, CH-1066 Epalinges, Switzerland
[4] SIB, CH-1066 Epalinges, Switzerland
关键词
state biomarker; RNA biomarker; gene expression profiling; polyglutamine disease; neurodegenerative disease;
D O I
10.1073/pnas.0703652104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Highly quantitative biomarkers of neuroclegenerative disease remain an important need in the urgent quest for disease-modifying therapies. For Huntington's disease (HD), a genetic test is available (trait marker), but necessary state markers are still in development. in this report, we describe a large battery of transcriptomic tests explored as state biomarker candidates. In an attempt to exploit the known neuroinflarnmatory and transcriptional perturbations of disease, we measured relevant mRNAs in peripheral blood cells. The performance of these potential markers was weak overall, with only one mRNA, immediate early response 3 (IER3), showing a modest but significant increase of 32% in HD samples compared with controls. No statistically significant differences were found for any other mRNAs tested, including a panel of 12 RNA biomarkers identified in a previous report [Borovecki F, Lovrecic L, Zhou J, Jeong H, Then F, Rosas HID, Hersch SM, Hogarth P, Bouzou B, Jensen RV, et al. (2005) Proc Nad Acad Sci USA 102:11023-11028]. The present results may nonetheless inform the future design and testing of HD biomarker strategies.
引用
收藏
页码:14424 / 14429
页数:6
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