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MiR-93-5p is a novel predictor of coronary in-stent restenosis

AIMS: MicroRNAs (miRNAs), small non-coding RNAs, have been implicated as regulators of multiple phases of atherothrombosis, and some reports have suggested altered levels in coronary artery in-stent restenosis (ISR). We recently demonstrated that miR-93-5 p was able to discriminate between patients...

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Autores principales: O'Sullivan, John F, Neylon, Antoinette, Fahy, Eoin F, Yang, Pengyi, McGorrian, Catherine, Blake, Gavin J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454319/
https://www.ncbi.nlm.nih.gov/pubmed/31031831
http://dx.doi.org/10.1136/heartasia-2018-011134
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author O'Sullivan, John F
Neylon, Antoinette
Fahy, Eoin F
Yang, Pengyi
McGorrian, Catherine
Blake, Gavin J
author_facet O'Sullivan, John F
Neylon, Antoinette
Fahy, Eoin F
Yang, Pengyi
McGorrian, Catherine
Blake, Gavin J
author_sort O'Sullivan, John F
collection PubMed
description AIMS: MicroRNAs (miRNAs), small non-coding RNAs, have been implicated as regulators of multiple phases of atherothrombosis, and some reports have suggested altered levels in coronary artery in-stent restenosis (ISR). We recently demonstrated that miR-93-5 p was able to discriminate between patients with stable coronary artery disease (CAD) and those with no CAD, after adjusting for traditional risk factors (RFs). Thus, we wanted to determine if circulating miRNAs could predict coronary ISR. OBJECTIVE: To determine if circulating miRNAs have diagnostic capability for determining ISR in a cohort of matched patients with and without ISR. APPROACH AND RESULTS: To determine if miRNA plasma levels are elevated in coronary ISR, we conducted a study comprising 78 patients (39 with no ISR and 39 with ISR) and measured plasma miRNAs in each. We then determined the predictive ability of differential miRNAs, adjusting for Framingham Heart Study (FHS) RFs, and stent length and diameter, to discriminate between ISR and no ISR. After correction for multiple testing, two miRNAs—miR425-5p and miR-93-5 p—were differential between patients with ISR and patients without ISR. Only miR-93-5 p remained a strong independent predictor of ISR after correction for FHS RFs (OR 6.30, p=0.008) and FHS RFs plus stent length and diameter (OR 4.80, p=0.02) and improved discriminatory power for ISR over FHS RFs alone in receiver operator characteristic curve analysis. CONCLUSION: This novel finding that miR-93-5 p independently predicts ISR extends our recent observation that miR-93-5 p predicted CAD after adjustment for traditional CAD RFs. These data suggest further potential diagnostic utility.
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spelling pubmed-64543192019-04-26 MiR-93-5p is a novel predictor of coronary in-stent restenosis O'Sullivan, John F Neylon, Antoinette Fahy, Eoin F Yang, Pengyi McGorrian, Catherine Blake, Gavin J Heart Asia Original Research AIMS: MicroRNAs (miRNAs), small non-coding RNAs, have been implicated as regulators of multiple phases of atherothrombosis, and some reports have suggested altered levels in coronary artery in-stent restenosis (ISR). We recently demonstrated that miR-93-5 p was able to discriminate between patients with stable coronary artery disease (CAD) and those with no CAD, after adjusting for traditional risk factors (RFs). Thus, we wanted to determine if circulating miRNAs could predict coronary ISR. OBJECTIVE: To determine if circulating miRNAs have diagnostic capability for determining ISR in a cohort of matched patients with and without ISR. APPROACH AND RESULTS: To determine if miRNA plasma levels are elevated in coronary ISR, we conducted a study comprising 78 patients (39 with no ISR and 39 with ISR) and measured plasma miRNAs in each. We then determined the predictive ability of differential miRNAs, adjusting for Framingham Heart Study (FHS) RFs, and stent length and diameter, to discriminate between ISR and no ISR. After correction for multiple testing, two miRNAs—miR425-5p and miR-93-5 p—were differential between patients with ISR and patients without ISR. Only miR-93-5 p remained a strong independent predictor of ISR after correction for FHS RFs (OR 6.30, p=0.008) and FHS RFs plus stent length and diameter (OR 4.80, p=0.02) and improved discriminatory power for ISR over FHS RFs alone in receiver operator characteristic curve analysis. CONCLUSION: This novel finding that miR-93-5 p independently predicts ISR extends our recent observation that miR-93-5 p predicted CAD after adjustment for traditional CAD RFs. These data suggest further potential diagnostic utility. BMJ Publishing Group 2019-02-22 /pmc/articles/PMC6454319/ /pubmed/31031831 http://dx.doi.org/10.1136/heartasia-2018-011134 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Original Research
O'Sullivan, John F
Neylon, Antoinette
Fahy, Eoin F
Yang, Pengyi
McGorrian, Catherine
Blake, Gavin J
MiR-93-5p is a novel predictor of coronary in-stent restenosis
title MiR-93-5p is a novel predictor of coronary in-stent restenosis
title_full MiR-93-5p is a novel predictor of coronary in-stent restenosis
title_fullStr MiR-93-5p is a novel predictor of coronary in-stent restenosis
title_full_unstemmed MiR-93-5p is a novel predictor of coronary in-stent restenosis
title_short MiR-93-5p is a novel predictor of coronary in-stent restenosis
title_sort mir-93-5p is a novel predictor of coronary in-stent restenosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454319/
https://www.ncbi.nlm.nih.gov/pubmed/31031831
http://dx.doi.org/10.1136/heartasia-2018-011134
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