Runne, H; Kuhn, A; Wild, EJ; Pratyaksha, W; Kristiansen, M; Isaacs, JD; Regulier, E; ... Luthi-Carter, R; + view all Runne, H; Kuhn, A; Wild, EJ; Pratyaksha, W; Kristiansen, M; Isaacs, JD; Regulier, E; Delorenzi, M; Tabrizi, SJ; Luthi-Carter, R; - view fewer (2007) Analysis of potential transcriptomic biomarkers for Huntington's disease in peripheral blood. Proceedings of the National Academy of Sciences , 104 (36) 14424 - 14429. 10.1073/pnas.0703652104.

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Abstract

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.

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