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Exosomal MicroRNAs as Potential Biomarkers of Hepatic Injury and Kidney Disease in Glycogen Storage Disease Type Ia Patients

Glycogen storage disease type Ia (GSDIa) is an inherited metabolic disorder caused by mutations in the enzyme glucose-6-phosphatase-α (G6Pase-α). Affected individuals develop renal and liver complications, including the development of hepatocellular adenoma/carcinoma and kidney failure. The purpose...

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Autores principales: Resaz, Roberta, Cangelosi, Davide, Segalerba, Daniela, Morini, Martina, Uva, Paolo, Bosco, Maria Carla, Banderali, Giuseppe, Estrella, Ana, Wanner, Corbinian, Weinstein, David A., Sechi, Annalisa, Paci, Sabrina, Melis, Daniela, Di Rocco, Maja, Lee, Young Mok, Eva, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745197/
https://www.ncbi.nlm.nih.gov/pubmed/35008754
http://dx.doi.org/10.3390/ijms23010328
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author Resaz, Roberta
Cangelosi, Davide
Segalerba, Daniela
Morini, Martina
Uva, Paolo
Bosco, Maria Carla
Banderali, Giuseppe
Estrella, Ana
Wanner, Corbinian
Weinstein, David A.
Sechi, Annalisa
Paci, Sabrina
Melis, Daniela
Di Rocco, Maja
Lee, Young Mok
Eva, Alessandra
author_facet Resaz, Roberta
Cangelosi, Davide
Segalerba, Daniela
Morini, Martina
Uva, Paolo
Bosco, Maria Carla
Banderali, Giuseppe
Estrella, Ana
Wanner, Corbinian
Weinstein, David A.
Sechi, Annalisa
Paci, Sabrina
Melis, Daniela
Di Rocco, Maja
Lee, Young Mok
Eva, Alessandra
author_sort Resaz, Roberta
collection PubMed
description Glycogen storage disease type Ia (GSDIa) is an inherited metabolic disorder caused by mutations in the enzyme glucose-6-phosphatase-α (G6Pase-α). Affected individuals develop renal and liver complications, including the development of hepatocellular adenoma/carcinoma and kidney failure. The purpose of this study was to identify potential biomarkers of the evolution of the disease in GSDIa patients. To this end, we analyzed the expression of exosomal microRNAs (Exo-miRs) in the plasma exosomes of 45 patients aged 6 to 63 years. Plasma from age-matched normal individuals were used as controls. We found that the altered expression of several Exo-miRs correlates with the pathologic state of the patients and might help to monitor the progression of the disease and the development of late GSDIa-associated complications.
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spelling pubmed-87451972022-01-11 Exosomal MicroRNAs as Potential Biomarkers of Hepatic Injury and Kidney Disease in Glycogen Storage Disease Type Ia Patients Resaz, Roberta Cangelosi, Davide Segalerba, Daniela Morini, Martina Uva, Paolo Bosco, Maria Carla Banderali, Giuseppe Estrella, Ana Wanner, Corbinian Weinstein, David A. Sechi, Annalisa Paci, Sabrina Melis, Daniela Di Rocco, Maja Lee, Young Mok Eva, Alessandra Int J Mol Sci Article Glycogen storage disease type Ia (GSDIa) is an inherited metabolic disorder caused by mutations in the enzyme glucose-6-phosphatase-α (G6Pase-α). Affected individuals develop renal and liver complications, including the development of hepatocellular adenoma/carcinoma and kidney failure. The purpose of this study was to identify potential biomarkers of the evolution of the disease in GSDIa patients. To this end, we analyzed the expression of exosomal microRNAs (Exo-miRs) in the plasma exosomes of 45 patients aged 6 to 63 years. Plasma from age-matched normal individuals were used as controls. We found that the altered expression of several Exo-miRs correlates with the pathologic state of the patients and might help to monitor the progression of the disease and the development of late GSDIa-associated complications. MDPI 2021-12-28 /pmc/articles/PMC8745197/ /pubmed/35008754 http://dx.doi.org/10.3390/ijms23010328 Text en © 2021 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
Resaz, Roberta
Cangelosi, Davide
Segalerba, Daniela
Morini, Martina
Uva, Paolo
Bosco, Maria Carla
Banderali, Giuseppe
Estrella, Ana
Wanner, Corbinian
Weinstein, David A.
Sechi, Annalisa
Paci, Sabrina
Melis, Daniela
Di Rocco, Maja
Lee, Young Mok
Eva, Alessandra
Exosomal MicroRNAs as Potential Biomarkers of Hepatic Injury and Kidney Disease in Glycogen Storage Disease Type Ia Patients
title Exosomal MicroRNAs as Potential Biomarkers of Hepatic Injury and Kidney Disease in Glycogen Storage Disease Type Ia Patients
title_full Exosomal MicroRNAs as Potential Biomarkers of Hepatic Injury and Kidney Disease in Glycogen Storage Disease Type Ia Patients
title_fullStr Exosomal MicroRNAs as Potential Biomarkers of Hepatic Injury and Kidney Disease in Glycogen Storage Disease Type Ia Patients
title_full_unstemmed Exosomal MicroRNAs as Potential Biomarkers of Hepatic Injury and Kidney Disease in Glycogen Storage Disease Type Ia Patients
title_short Exosomal MicroRNAs as Potential Biomarkers of Hepatic Injury and Kidney Disease in Glycogen Storage Disease Type Ia Patients
title_sort exosomal micrornas as potential biomarkers of hepatic injury and kidney disease in glycogen storage disease type ia patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745197/
https://www.ncbi.nlm.nih.gov/pubmed/35008754
http://dx.doi.org/10.3390/ijms23010328
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