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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8745197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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