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Detecting Circulating MicroRNAs as Biomarkers in Alzheimer’s Disease

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Amyloid Proteins

Part of the book series: Methods in Molecular Biology ((MIMB,volume 1779))

Abstract

Alzheimer’s disease is the most common form of dementia and is characterized by a progressive loss of cognitive functions. As the result of predicted demographic changes over the next decades, Alzheimer’s disease is expected to be one of the most pressing medical and social challenges facing our generation. Current treatment strategies remain symptomatic. However, new approaches have shown promise in clinical trials, particularly in patients with only mild or moderate symptoms. Early detection of Alzheimer’s disease is therefore of critical importance. Currently available diagnostic approaches (such as protein analysis in cerebrospinal fluid or neuroimaging), however, are expensive and invasive and therefore unsuitable for the screening of a large population. Consequently, Alzheimer’s disease is generally diagnosed too late for effective intervention. MicroRNAs—readily measurable in biofluids and resistant to freeze-thaw and pH changes, have shown encouraging diagnostic potential in Alzheimer’s disease. Several studies have attempted to correlate changes of specific microRNAs to disease progression using different approaches and profiling platforms including micro-arrays, RNA sequencing, and qPCR-based systems. In the present book chapter, we will describe the different steps involved in how to determine the microRNA profile in plasma samples from patients using the OpenArray platform.

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Abbreviations

AD:

Alzheimer’s disease

Ago2:

Argonaute-2

APP:

Amyloid precursor protein

Aβ:

Amyloid β

CSF:

Cerebrospinal fluid

Ct:

Cycle threshold

GMN:

Global mean normalization

MCI:

Mild cognitive impairment

miRNA:

MicroRNA

NC:

Normal cognition

NFT:

Neurofibrillary tangles

NTC:

No template controls (negative control)

PHF:

Paired helical filaments

PreAmp:

Pre-amplification

qPCR:

Quantitative polymerase chain reaction

RT:

Reverse transcription

TE:

Tris + EDTA

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Acknowledgments

This work was supported by funding from Science Foundation Ireland (13/SIRG/2114 to E.M.J.-M. and 12/COEN/18 and 13/SIRG/2098 to T.E.), from the Health Research Board Ireland (HRA-POR-2015-1243 to T.E.), and from Carlos III Institute of Health (SAF2016-78603-R to M.M. and M.C.).

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Correspondence to Tobias Engel .

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Kenny, A., Jimenez-Mateos, E.M., Calero, M., Medina, M., Engel, T. (2018). Detecting Circulating MicroRNAs as Biomarkers in Alzheimer’s Disease. In: Sigurdsson, E., Calero, M., Gasset, M. (eds) Amyloid Proteins. Methods in Molecular Biology, vol 1779. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7816-8_29

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  • DOI: https://doi.org/10.1007/978-1-4939-7816-8_29

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  • Publisher Name: Humana Press, New York, NY

  • Print ISBN: 978-1-4939-7815-1

  • Online ISBN: 978-1-4939-7816-8

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