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miRNA in Circulating Microvesicles as Biomarkers for Age-Related Cognitive Decline

Community dwelling older individuals from the North Florida region were examined for health status and a comprehensive neuropsychological battery, including the Montreal Cognitive Assessment (MoCA), was performed on each participant. A subpopulation (58 females and 39 males) met the criteria for age...

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Autores principales: Rani, Asha, O’Shea, Andrew, Ianov, Lara, Cohen, Ronald A., Woods, Adam J., Foster, Thomas C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632661/
https://www.ncbi.nlm.nih.gov/pubmed/29046635
http://dx.doi.org/10.3389/fnagi.2017.00323
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author Rani, Asha
O’Shea, Andrew
Ianov, Lara
Cohen, Ronald A.
Woods, Adam J.
Foster, Thomas C.
author_facet Rani, Asha
O’Shea, Andrew
Ianov, Lara
Cohen, Ronald A.
Woods, Adam J.
Foster, Thomas C.
author_sort Rani, Asha
collection PubMed
description Community dwelling older individuals from the North Florida region were examined for health status and a comprehensive neuropsychological battery, including the Montreal Cognitive Assessment (MoCA), was performed on each participant. A subpopulation (58 females and 39 males) met the criteria for age (60–89) and no evidence of mild cognitive impairment, with a MoCA score ≥23. Despite the stringent criteria for participation, MoCA scores were negatively correlated within the limited age range. Extracellular microvesicles were isolated from the plasma and samples were found to be positive for the exosome marker CD63, with an enrichment of particles within the size range for exosomes. miRNA was extracted and examined using next generation sequencing with a stringent criterion (average of ≥10 counts per million reads) resulting in 117 miRNA for subsequent analysis. Characterization of expression confirmed pervious work concerning the relative abundance and overall pattern of expression of miRNA in plasma. Correlation analysis indicated that most of the miRNAs (74 miRNAs) were positively correlated with age (p <0.01). Multiple regression was employed to identify the relationship of miRNA expression and MoCA score, accounting for age. MoCA scores were negatively correlated with 13 miRNAs. The pattern of expression for cognition-related miRNA did not match that previously described for Alzheimer’s disease. Enrichment analysis was employed to identify miRNA–gene interactions to reveal possible links to brain function.
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spelling pubmed-56326612017-10-18 miRNA in Circulating Microvesicles as Biomarkers for Age-Related Cognitive Decline Rani, Asha O’Shea, Andrew Ianov, Lara Cohen, Ronald A. Woods, Adam J. Foster, Thomas C. Front Aging Neurosci Neuroscience Community dwelling older individuals from the North Florida region were examined for health status and a comprehensive neuropsychological battery, including the Montreal Cognitive Assessment (MoCA), was performed on each participant. A subpopulation (58 females and 39 males) met the criteria for age (60–89) and no evidence of mild cognitive impairment, with a MoCA score ≥23. Despite the stringent criteria for participation, MoCA scores were negatively correlated within the limited age range. Extracellular microvesicles were isolated from the plasma and samples were found to be positive for the exosome marker CD63, with an enrichment of particles within the size range for exosomes. miRNA was extracted and examined using next generation sequencing with a stringent criterion (average of ≥10 counts per million reads) resulting in 117 miRNA for subsequent analysis. Characterization of expression confirmed pervious work concerning the relative abundance and overall pattern of expression of miRNA in plasma. Correlation analysis indicated that most of the miRNAs (74 miRNAs) were positively correlated with age (p <0.01). Multiple regression was employed to identify the relationship of miRNA expression and MoCA score, accounting for age. MoCA scores were negatively correlated with 13 miRNAs. The pattern of expression for cognition-related miRNA did not match that previously described for Alzheimer’s disease. Enrichment analysis was employed to identify miRNA–gene interactions to reveal possible links to brain function. Frontiers Media S.A. 2017-10-04 /pmc/articles/PMC5632661/ /pubmed/29046635 http://dx.doi.org/10.3389/fnagi.2017.00323 Text en Copyright © 2017 Rani, O’Shea, Ianov, Cohen, Woods and Foster. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Rani, Asha
O’Shea, Andrew
Ianov, Lara
Cohen, Ronald A.
Woods, Adam J.
Foster, Thomas C.
miRNA in Circulating Microvesicles as Biomarkers for Age-Related Cognitive Decline
title miRNA in Circulating Microvesicles as Biomarkers for Age-Related Cognitive Decline
title_full miRNA in Circulating Microvesicles as Biomarkers for Age-Related Cognitive Decline
title_fullStr miRNA in Circulating Microvesicles as Biomarkers for Age-Related Cognitive Decline
title_full_unstemmed miRNA in Circulating Microvesicles as Biomarkers for Age-Related Cognitive Decline
title_short miRNA in Circulating Microvesicles as Biomarkers for Age-Related Cognitive Decline
title_sort mirna in circulating microvesicles as biomarkers for age-related cognitive decline
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632661/
https://www.ncbi.nlm.nih.gov/pubmed/29046635
http://dx.doi.org/10.3389/fnagi.2017.00323
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