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Identification of serum microRNAs as potential biomarkers in Pompe disease

OBJECTIVE: To analyze the microRNA profile in serum of patients with Adult Onset Pompe disease (AOPD). METHODS: We analyzed the expression of 185 microRNAs in serum of 15 AOPD patients and five controls using microRNA PCR Panels. The expression levels of microRNAs that were deregulated were further...

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Autores principales: Carrasco‐Rozas, Ana, Fernández‐Simón, Esther, Lleixà, Maria Cinta, Belmonte, Izaskun, Pedrosa-Hernandez, Irene, Montiel-Morillo, Elena, Nuñez‐Peralta, Claudia, Llauger Rossello, Jaume, Segovia, Sonia, De Luna, Noemí, Suarez‐Calvet, Xavier, Illa, Isabel, Díaz‐Manera, Jordi, Gallardo, Eduard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649638/
https://www.ncbi.nlm.nih.gov/pubmed/31353854
http://dx.doi.org/10.1002/acn3.50800
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author Carrasco‐Rozas, Ana
Fernández‐Simón, Esther
Lleixà, Maria Cinta
Belmonte, Izaskun
Pedrosa-Hernandez, Irene
Montiel-Morillo, Elena
Nuñez‐Peralta, Claudia
Llauger Rossello, Jaume
Segovia, Sonia
De Luna, Noemí
Suarez‐Calvet, Xavier
Illa, Isabel
Díaz‐Manera, Jordi
Gallardo, Eduard
author_facet Carrasco‐Rozas, Ana
Fernández‐Simón, Esther
Lleixà, Maria Cinta
Belmonte, Izaskun
Pedrosa-Hernandez, Irene
Montiel-Morillo, Elena
Nuñez‐Peralta, Claudia
Llauger Rossello, Jaume
Segovia, Sonia
De Luna, Noemí
Suarez‐Calvet, Xavier
Illa, Isabel
Díaz‐Manera, Jordi
Gallardo, Eduard
author_sort Carrasco‐Rozas, Ana
collection PubMed
description OBJECTIVE: To analyze the microRNA profile in serum of patients with Adult Onset Pompe disease (AOPD). METHODS: We analyzed the expression of 185 microRNAs in serum of 15 AOPD patients and five controls using microRNA PCR Panels. The expression levels of microRNAs that were deregulated were further studied in 35 AOPD patients and 10 controls using Real‐Time PCR. Additionally, the skeletal muscle expression of microRNAs which showed significant increase levels in serum samples was also studied. Correlations between microRNA serum levels and muscle function test, spirometry, and quantitative muscle MRI were performed (these data correspond to the study NCT01914536 at ClinicalTrials.gov). RESULTS: We identified 14 microRNAs that showed different expression levels in serum samples of AOPD patients compared to controls. We validated these results in a larger cohort of patients and we found increased levels of three microRNAs, the so called dystromirs: miR‐1‐3p, miR‐133a‐3p, and miR‐206. These microRNAs are involved in muscle regeneration and the expression of these was increased in patients' muscle biopsies. Significant correlations between microRNA levels and muscle function test were found. INTERPRETATION: Serum expression levels of dystromirs may represent additional biomarkers for the follow‐up of AOPD patients.
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spelling pubmed-66496382019-07-31 Identification of serum microRNAs as potential biomarkers in Pompe disease Carrasco‐Rozas, Ana Fernández‐Simón, Esther Lleixà, Maria Cinta Belmonte, Izaskun Pedrosa-Hernandez, Irene Montiel-Morillo, Elena Nuñez‐Peralta, Claudia Llauger Rossello, Jaume Segovia, Sonia De Luna, Noemí Suarez‐Calvet, Xavier Illa, Isabel Díaz‐Manera, Jordi Gallardo, Eduard Ann Clin Transl Neurol Research Articles OBJECTIVE: To analyze the microRNA profile in serum of patients with Adult Onset Pompe disease (AOPD). METHODS: We analyzed the expression of 185 microRNAs in serum of 15 AOPD patients and five controls using microRNA PCR Panels. The expression levels of microRNAs that were deregulated were further studied in 35 AOPD patients and 10 controls using Real‐Time PCR. Additionally, the skeletal muscle expression of microRNAs which showed significant increase levels in serum samples was also studied. Correlations between microRNA serum levels and muscle function test, spirometry, and quantitative muscle MRI were performed (these data correspond to the study NCT01914536 at ClinicalTrials.gov). RESULTS: We identified 14 microRNAs that showed different expression levels in serum samples of AOPD patients compared to controls. We validated these results in a larger cohort of patients and we found increased levels of three microRNAs, the so called dystromirs: miR‐1‐3p, miR‐133a‐3p, and miR‐206. These microRNAs are involved in muscle regeneration and the expression of these was increased in patients' muscle biopsies. Significant correlations between microRNA levels and muscle function test were found. INTERPRETATION: Serum expression levels of dystromirs may represent additional biomarkers for the follow‐up of AOPD patients. John Wiley and Sons Inc. 2019-06-12 /pmc/articles/PMC6649638/ /pubmed/31353854 http://dx.doi.org/10.1002/acn3.50800 Text en © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Carrasco‐Rozas, Ana
Fernández‐Simón, Esther
Lleixà, Maria Cinta
Belmonte, Izaskun
Pedrosa-Hernandez, Irene
Montiel-Morillo, Elena
Nuñez‐Peralta, Claudia
Llauger Rossello, Jaume
Segovia, Sonia
De Luna, Noemí
Suarez‐Calvet, Xavier
Illa, Isabel
Díaz‐Manera, Jordi
Gallardo, Eduard
Identification of serum microRNAs as potential biomarkers in Pompe disease
title Identification of serum microRNAs as potential biomarkers in Pompe disease
title_full Identification of serum microRNAs as potential biomarkers in Pompe disease
title_fullStr Identification of serum microRNAs as potential biomarkers in Pompe disease
title_full_unstemmed Identification of serum microRNAs as potential biomarkers in Pompe disease
title_short Identification of serum microRNAs as potential biomarkers in Pompe disease
title_sort identification of serum micrornas as potential biomarkers in pompe disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649638/
https://www.ncbi.nlm.nih.gov/pubmed/31353854
http://dx.doi.org/10.1002/acn3.50800
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