DIAGNOSTICO DE LA ENFERMEDAD DE ALZHEIMER MEDIANTE BIOPSIA LIQUIDA

PI20/01701

Nombre agencia financiadora Instituto de Salud Carlos III
Acrónimo agencia financiadora ISCIII
Programa Programa Estatal de Generación de Conocimiento y Fortalecimiento del Sistema Español de I+D+I
Subprograma Subprograma Estatal de Generación de Conocimiento
Convocatoria Proyectos de investigación en salud
Año convocatoria 2020
Unidad de gestión Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020 (ISCIII)
Centro beneficiario FUNDACION INSTITUTO DE INVESTIGACION SANITARIA DE NAVARRA
Centro realización INSTITUTO DE INVESTIGACION SANITARIA DE NAVARRA (IdISNA)
Identificador persistente https://doi.org/10.13039/501100004587

Publicaciones

Resultados totales (Incluyendo duplicados): 1
Encontrada(s) 1 página(s)

Liquid biopsy in alzheimer's disease patients reveals epigenetic changes in the PRLHR gene

Academica-e. Repositorio Institucional de la Universidad Pública de Navarra
  • Macías, Mónica
  • Acha Santamaría, Blanca
  • Corroza, Jon
  • Urdánoz Casado, Amaya
  • Roldán, Miren
  • Robles Solano, Maitane
  • Sánchez Ruiz de Gordoa, Javier
  • Erro Aguirre, María Elena
  • Jericó Pascual, Ivonne
  • Blanco Luquin, Idoia
  • Mendióroz Iriarte, Maite
In recent years, new DNA methylation variants have been reported in genes biologically relevant to Alzheimer’s disease (AD) in human brain tissue. However, this AD-specific epigenetic information remains brain-locked and unreachable during patients’ lifetimes. In a previous methylome performed in the hippocampus of 26 AD patients and 12 controls, we found higher methylation levels in AD patients in the promoter region of PRLHR, a gene involved in energy balance regulation. Our aim was to further characterize PRLHR’s role in AD and to evaluate if the liquid biopsy technique would provide life access to this brain information in a non-invasive way. First, we extended the methylation mapping of PRLHR and validated previous methylome results via bisulfite cloning sequencing. Next, we observed a positive correlation between PRLHR methylation levels and AD-related neuropathological changes and a decreased expression of PRLHR in AD hippocampus. Then, we managed to replicate the hippocampal methylation differences in plasma cfDNA from an additional cohort of 35 AD patients and 35 controls. The isolation of cfDNA from the plasma of AD patients may constitute a source of potential epigenetic biomarkers to aid AD clinical management., The authors sincerely appreciate funding support by the Government of Navarra [G°Na 36/18], by the Spanish Government through a grant from the Institute of Health Carlos III (FIS PI20/01701), jointly funded by the European Regional Development Fund (ERDF), European Union, A way of shaping Europe. The project leading to these results has received funding from “la Caixa” Foundation (ID 100010434) co-funded by Fundación Luzón (HR20-01109_BIOP-ALS). In addition, B.A. is supported by a PFIS fellowship from the Spanish Government (FI18/00150), M.M. (Mónica Macías) is beneficiary of a grant “Río Hortega” from the Spanish Government (CM20/00240), A.U.-C. received a grant Doctorandos industriales 2018–2020 and a Predoctoral grant (2019) funded by the Department of Industry and Health of the Government of Navarra, M.M. (Maite Mendioroz) received a grant Contrato de intensificación from the Institute of Health Carlos III (INT19/00029) and a grant (LCF/PR/PR15/51100006) funded by LaCaixa Foundation.