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Analytical Validation of a Novel MicroRNA Panel for Risk Stratification of Cognitive Impairment
We have been developing a novel approach to identify cognitive impairment-related biomarkers by profiling brain-enriched and inflammation-associated microRNA (miRNA) in plasma specimens of cognitively unimpaired and cognitively impaired patients. Here, we present an analytical validation of the nove...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340136/ https://www.ncbi.nlm.nih.gov/pubmed/37443567 http://dx.doi.org/10.3390/diagnostics13132170 |
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author | Kunwar, Arzu Ablordeppey, Kenny Kwabena Mireskandari, Alidad Sheinerman, Kira Kiefer, Michael Umansky, Samuil Kumar, Gyanendra |
author_facet | Kunwar, Arzu Ablordeppey, Kenny Kwabena Mireskandari, Alidad Sheinerman, Kira Kiefer, Michael Umansky, Samuil Kumar, Gyanendra |
author_sort | Kunwar, Arzu |
collection | PubMed |
description | We have been developing a novel approach to identify cognitive impairment-related biomarkers by profiling brain-enriched and inflammation-associated microRNA (miRNA) in plasma specimens of cognitively unimpaired and cognitively impaired patients. Here, we present an analytical validation of the novel miRNA panel, CogniMIR(®), using two competing quantitative PCR technologies for the expression analysis of 24 target miRNAs. Total RNA from the plasma specimens was isolated using the MagMAX mirVana Kit, and RT-qPCR was performed using stem-loop-based TaqMan and LNA-based qPCR assays. Evaluation of RNA dilution series for our target 24 miRNAs, performed by two operators on two different days, demonstrated that all CogniMIR(®) panel miRNAs can be reliably and consistently detected by both qPCR technologies, with sample input as low as 20 copies in a qPCR reaction. Intra-run and inter-run repeatability and reproducibility analyses using RNA specimens demonstrated that both operators generated repeatable and consistent Cts, with R(2) values of 0.94 to 0.99 and 0.96 to 0.97, respectively. The study results clearly indicate the suitability of miRNA profiling of plasma specimens using either of the qPCR technologies. However, the LNA-based qPCR technology appears to be more operationally friendly and better suited for a CAP/CLIA-certified clinical laboratory. |
format | Online Article Text |
id | pubmed-10340136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103401362023-07-14 Analytical Validation of a Novel MicroRNA Panel for Risk Stratification of Cognitive Impairment Kunwar, Arzu Ablordeppey, Kenny Kwabena Mireskandari, Alidad Sheinerman, Kira Kiefer, Michael Umansky, Samuil Kumar, Gyanendra Diagnostics (Basel) Article We have been developing a novel approach to identify cognitive impairment-related biomarkers by profiling brain-enriched and inflammation-associated microRNA (miRNA) in plasma specimens of cognitively unimpaired and cognitively impaired patients. Here, we present an analytical validation of the novel miRNA panel, CogniMIR(®), using two competing quantitative PCR technologies for the expression analysis of 24 target miRNAs. Total RNA from the plasma specimens was isolated using the MagMAX mirVana Kit, and RT-qPCR was performed using stem-loop-based TaqMan and LNA-based qPCR assays. Evaluation of RNA dilution series for our target 24 miRNAs, performed by two operators on two different days, demonstrated that all CogniMIR(®) panel miRNAs can be reliably and consistently detected by both qPCR technologies, with sample input as low as 20 copies in a qPCR reaction. Intra-run and inter-run repeatability and reproducibility analyses using RNA specimens demonstrated that both operators generated repeatable and consistent Cts, with R(2) values of 0.94 to 0.99 and 0.96 to 0.97, respectively. The study results clearly indicate the suitability of miRNA profiling of plasma specimens using either of the qPCR technologies. However, the LNA-based qPCR technology appears to be more operationally friendly and better suited for a CAP/CLIA-certified clinical laboratory. MDPI 2023-06-26 /pmc/articles/PMC10340136/ /pubmed/37443567 http://dx.doi.org/10.3390/diagnostics13132170 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kunwar, Arzu Ablordeppey, Kenny Kwabena Mireskandari, Alidad Sheinerman, Kira Kiefer, Michael Umansky, Samuil Kumar, Gyanendra Analytical Validation of a Novel MicroRNA Panel for Risk Stratification of Cognitive Impairment |
title | Analytical Validation of a Novel MicroRNA Panel for Risk Stratification of Cognitive Impairment |
title_full | Analytical Validation of a Novel MicroRNA Panel for Risk Stratification of Cognitive Impairment |
title_fullStr | Analytical Validation of a Novel MicroRNA Panel for Risk Stratification of Cognitive Impairment |
title_full_unstemmed | Analytical Validation of a Novel MicroRNA Panel for Risk Stratification of Cognitive Impairment |
title_short | Analytical Validation of a Novel MicroRNA Panel for Risk Stratification of Cognitive Impairment |
title_sort | analytical validation of a novel microrna panel for risk stratification of cognitive impairment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340136/ https://www.ncbi.nlm.nih.gov/pubmed/37443567 http://dx.doi.org/10.3390/diagnostics13132170 |
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