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Article type: Research Article
Authors: Kiko, Takehiroa | Nakagawa, Kiyotakaa; * | Tsuduki, Tsuyoshib | Furukawa, Katsutoshic | Arai, Hiroyukic | Miyazawa, Teruoa
Affiliations: [a] Food & Biodynamic Chemistry Laboratory, Graduate School of Agricultural Science, Tohoku University, Sendai, Japan | [b] Laboratory of Food and Biomolecular Science, Graduate School of Agricultural Science, Tohoku University, Sendai, Japan | [c] Department of Geriatrics and Gerontology, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan
Correspondence: [*] Correspondence to: Kiyotaka Nakagawa, PhD, Food & Biodynamic Chemistry Laboratory, Graduate School of Agricultural Science, Tohoku University, 1-1 Tsutsumidori-Amamiyamachi, Aobaku, Sendai 981-8555, Japan. Tel.: +81 22 717 8904; Fax: +81 22 717 8905; E-mail: nkgw@biochem.tohoku.ac.jp.
Abstract: The development of Alzheimer's disease (AD) biomarkers remains an unmet challenge, and new approaches that can improve current AD biomarker strategies are needed. Recent reports suggested that microRNA (miRNA) profiling of biological fluids has emerged as a diagnostic tool for several pathologic conditions. In this study, we measured six candidate miRNAs (miR-9, miR-29a, miR-29b, miR-34a, miR-125b, and miR-146a) in plasma and cerebrospinal fluid (CSF) of AD and normal subjects by using quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) to evaluate their potential usability as AD biomarkers. The qRT-PCR results showed that plasma miR-34a and miR-146a levels, and CSF miR-34a, miR-125b, and miR-146a levels in AD patients were significantly lower than in control subjects. On the other hand, CSF miR-29a and miR-29b levels were significantly higher than in control subjects. Our results provide a possibility that miRNAs detected in plasma and CSF can serve as biomarkers for AD.
Keywords: Alzheimer's disease, cerebrospinal fluid, miRNA, plasma
DOI: 10.3233/JAD-130932
Journal: Journal of Alzheimer's Disease, vol. 39, no. 2, pp. 253-259, 2014
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