Profile of plasma microRNAs as a potential biomarker of Wilson's disease.


Por: Sánchez-Monteagudo A, Ripollés E, Murillo O, Domènech S, Álvarez-Sauco M, Girona E, Sastre-Bataller I, Bono A, García-Villarreal L, Tugores A, García-García F, González-Aseguinolaza G, Berenguer M and Espinós C

Publicada: 26 jul 2024 Ahead of Print: 26 jul 2024
Resumen:
Wilson's disease (WD) is a rare condition resulting from autosomal recessive mutations in ATP7B, a copper transporter, manifesting with hepatic, neurological, and psychiatric symptoms. Timely diagnosis and appropriate treatment yield a positive prognosis, while delayed identification and/or insufficient therapy lead to a poor outcome. Our aim was to establish a prognostic method for WD by characterising biomarkers based on circulating microRNAs.

Filiaciones:
Sánchez-Monteagudo A:
 Unit of Rare Neurodegenerative Diseases, Valencia Biomedical Research Foundation-Centro de Investigación Príncipe Felipe (CIPF), Calle Eduardo Primo Yúfera No. 13, 46012, Valencia, Spain

Ripollés E:
 Unit of Rare Neurodegenerative Diseases, Valencia Biomedical Research Foundation-Centro de Investigación Príncipe Felipe (CIPF), Calle Eduardo Primo Yúfera No. 13, 46012, Valencia, Spain

 Rare Diseases Joint Unit, CIPF-IIS La Fe, Valencia, Spain

Murillo O:
 DNA@RNA Medicine Division, Centro de Investigación Médica Aplicada (CIMA), University of Navarra, Pamplona, Spain

Domènech S:
 Unit of Rare Neurodegenerative Diseases, Valencia Biomedical Research Foundation-Centro de Investigación Príncipe Felipe (CIPF), Calle Eduardo Primo Yúfera No. 13, 46012, Valencia, Spain

 Rare Diseases Joint Unit, CIPF-IIS La Fe, Valencia, Spain

Álvarez-Sauco M:
 Department of Neurology, Hospital General Universitari d'Elx, Alicante, Spain

Girona E:
 Department of Internal Medicine, Hospital General Universitari d'Elx, Alicante, Spain

Sastre-Bataller I:
 Rare Diseases Joint Unit, CIPF-IIS La Fe, Valencia, Spain

 Department of Neurology, Hospital Universitari I Politècnic La Fe, Valencia, Spain

Bono A:
 Rare Diseases Joint Unit, CIPF-IIS La Fe, Valencia, Spain

 Hepatology-Liver Transplantation Unit, Digestive Medicine Service, IIS La Fe and CIBER-EHD, Hospital Universitari i Politècnic La Fe, Valencia, Spain

García-Villarreal L:
 Research Unit, Complejo Hospitalario Universitario Insular Materno-Infantil, Las Palmas de Gran Canaria, Spain

Tugores A:
 Research Unit, Complejo Hospitalario Universitario Insular Materno-Infantil, Las Palmas de Gran Canaria, Spain

García-García F:
 Rare Diseases Joint Unit, CIPF-IIS La Fe, Valencia, Spain

 Unit of Bioinformatics and Biostatistics, Valencia Biomedical Research Foundation-Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain

González-Aseguinolaza G:
 DNA@RNA Medicine Division, Centro de Investigación Médica Aplicada (CIMA), University of Navarra, Pamplona, Spain

 Vivet Therapeutics S.L., Pamplona, Spain

Berenguer M:
 Rare Diseases Joint Unit, CIPF-IIS La Fe, Valencia, Spain

 Hepatology-Liver Transplantation Unit, Digestive Medicine Service, IIS La Fe and CIBER-EHD, Hospital Universitari i Politècnic La Fe, Valencia, Spain

 Department of Medicine, Universitat de València, Valencia, Spain

:
 Unit of Rare Neurodegenerative Diseases, Valencia Biomedical Research Foundation-Centro de Investigación Príncipe Felipe (CIPF), Calle Eduardo Primo Yúfera No. 13, 46012, Valencia, Spain.

 Rare Diseases Joint Unit, CIPF-IIS La Fe, Valencia, Spain.

 Biotechnology Department, Universitat Politècnica de València, Valencia, Spain.

 Rare Diseases Networking Biomedical Research Centre (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
ISSN: 09441174





JOURNAL OF GASTROENTEROLOGY
Editorial
SPRINGER JAPAN KK, SHIROYAMA TRUST TOWER 5F, 4-3-1 TORANOMON, MINATO-KU, TOKYO 105-6005, JAPAN, Japón
Tipo de documento: Article
Volumen: 59 Número: 10
Páginas: 921-931
WOS Id: 001278323500001
ID de PubMed: 39060521
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