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Plasma microRNA biomarkers for detection of mild cognitive impairment: Biomarker Validation Study

A minimally invasive test for early detection and monitoring of Alzheimer's and other neurodegenerative diseases is a highly unmet need for drug development and planning of patient care. Mild Cognitive Impairment (MCI) is a syndrome characteristic of early stages of many neurodegenerative disea...

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Autores principales: Sheinerman, Kira S., Tsivinsky, Vladimir G., Abdullah, Laila, Crawford, Fiona, Umansky, Samuil R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883708/
https://www.ncbi.nlm.nih.gov/pubmed/24368295
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author Sheinerman, Kira S.
Tsivinsky, Vladimir G.
Abdullah, Laila
Crawford, Fiona
Umansky, Samuil R.
author_facet Sheinerman, Kira S.
Tsivinsky, Vladimir G.
Abdullah, Laila
Crawford, Fiona
Umansky, Samuil R.
author_sort Sheinerman, Kira S.
collection PubMed
description A minimally invasive test for early detection and monitoring of Alzheimer's and other neurodegenerative diseases is a highly unmet need for drug development and planning of patient care. Mild Cognitive Impairment (MCI) is a syndrome characteristic of early stages of many neurodegenerative diseases. Recently, we have identified two sets of circulating brain-enriched miRNAs, the miR-132 family (miR-128, miR-132, miR-874) normalized per miR-491-5p and the miR-134 family (miR-134, miR-323-3p, miR-382) normalized per miR-370, capable of differentiating MCI from age-matched control (AMC) with high accuracy. Here we report a biomarker validation study of the identified miRNA pairs using larger independent sets of age- and gender- matched plasma samples. The biomarker pairs detected MCI with sensitivity, specificity and overall accuracy similar to those obtained in the first study. The miR-132 family biomarkers differentiated MCI from AMC with 84%-94% sensitivity and 96%-98% specificity, and the miR-134 family biomarkers demonstrated 74%-88% sensitivity and 80-92% specificity. When miRNAs of the same family were combined, miR-132 and miR-134 family biomarkers demonstrated 96% and 87% overall accuracy, respectively. No statistically significant differences in the biomarker concentrations in samples obtained from male and female subjects were observed for either MCI or AMC. The present study also demonstrated that the highest sensitivity and specificity are achieved with pairs of miRNAs whose concentrations in plasma are highly correlated.
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spelling pubmed-38837082014-01-13 Plasma microRNA biomarkers for detection of mild cognitive impairment: Biomarker Validation Study Sheinerman, Kira S. Tsivinsky, Vladimir G. Abdullah, Laila Crawford, Fiona Umansky, Samuil R. Aging (Albany NY) Research Paper A minimally invasive test for early detection and monitoring of Alzheimer's and other neurodegenerative diseases is a highly unmet need for drug development and planning of patient care. Mild Cognitive Impairment (MCI) is a syndrome characteristic of early stages of many neurodegenerative diseases. Recently, we have identified two sets of circulating brain-enriched miRNAs, the miR-132 family (miR-128, miR-132, miR-874) normalized per miR-491-5p and the miR-134 family (miR-134, miR-323-3p, miR-382) normalized per miR-370, capable of differentiating MCI from age-matched control (AMC) with high accuracy. Here we report a biomarker validation study of the identified miRNA pairs using larger independent sets of age- and gender- matched plasma samples. The biomarker pairs detected MCI with sensitivity, specificity and overall accuracy similar to those obtained in the first study. The miR-132 family biomarkers differentiated MCI from AMC with 84%-94% sensitivity and 96%-98% specificity, and the miR-134 family biomarkers demonstrated 74%-88% sensitivity and 80-92% specificity. When miRNAs of the same family were combined, miR-132 and miR-134 family biomarkers demonstrated 96% and 87% overall accuracy, respectively. No statistically significant differences in the biomarker concentrations in samples obtained from male and female subjects were observed for either MCI or AMC. The present study also demonstrated that the highest sensitivity and specificity are achieved with pairs of miRNAs whose concentrations in plasma are highly correlated. Impact Journals LLC 2013-12-22 /pmc/articles/PMC3883708/ /pubmed/24368295 Text en Copyright: © 2013 Sheinerman et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Research Paper
Sheinerman, Kira S.
Tsivinsky, Vladimir G.
Abdullah, Laila
Crawford, Fiona
Umansky, Samuil R.
Plasma microRNA biomarkers for detection of mild cognitive impairment: Biomarker Validation Study
title Plasma microRNA biomarkers for detection of mild cognitive impairment: Biomarker Validation Study
title_full Plasma microRNA biomarkers for detection of mild cognitive impairment: Biomarker Validation Study
title_fullStr Plasma microRNA biomarkers for detection of mild cognitive impairment: Biomarker Validation Study
title_full_unstemmed Plasma microRNA biomarkers for detection of mild cognitive impairment: Biomarker Validation Study
title_short Plasma microRNA biomarkers for detection of mild cognitive impairment: Biomarker Validation Study
title_sort plasma microrna biomarkers for detection of mild cognitive impairment: biomarker validation study
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883708/
https://www.ncbi.nlm.nih.gov/pubmed/24368295
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