Kidins220 Correlates with Tau in Alzheimer’s Disease Brain and Cerebrospinal Fluid
Autor: | Isidro Ferrer, Andrea Gamir-Morralla, Teresa Iglesias, Daniel Alcolea, A. Lleo, Juan Fortea, Olivia Belbin |
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Přispěvatelé: | Universitat de Barcelona, Ministerio de Economía y Competitividad (España), Comunidad de Madrid, Instituto de Salud Carlos III, European Commission |
Rok vydání: | 2016 |
Předmět: |
Male
0301 basic medicine Kidins220 Statistics as Topic Cohort Studies ARMS 0302 clinical medicine antibody Membrane proteins Pathology Medicine Phosphorylation Cervell Aged 80 and over Calpain General Neuroscience Proteïnes de membrana Brain General Medicine Middle Aged Alzheimer's disease Patologia Metabolisme Psychiatry and Mental health Clinical Psychology Cerebrospinal fluid Female Alzheimer’s disease Adult Amyloid Nerve Tissue Proteins tau Proteins tau protein Antibodies Necrosis Young Adult 03 medical and health sciences Regional development Alzheimer Disease mental disorders Humans Excitotoxicity Aged Tau protei Amyloid beta-Peptides business.industry Líquid cefalorraquidi Membrane Proteins Peptide Fragments Malaltia d'Alzheimer Metabolism 030104 developmental biology Phosphopyruvate Hydratase Postmortem Changes Geriatrics and Gerontology business Humanities Biomarkers 030217 neurology & neurosurgery |
Zdroj: | Dipòsit Digital de la UB Universidad de Barcelona Recercat. Dipósit de la Recerca de Catalunya instname Digital.CSIC. Repositorio Institucional del CSIC JOURNAL OF ALZHEIMERS DISEASE r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau |
ISSN: | 1875-8908 1387-2877 |
DOI: | 10.3233/jad-160639 |
Popis: | Identification of neurodegeneration-monitoring biomarkers would be of great clinical value for Alzheimer's disease (AD) diagnosis. Using N- or C-terminal antibodies, we studied the pro-survival synaptic effector, Kidins220, in the brain and cerebrospinal fluid (CSF) of controls and AD patients. Only the N-terminal antibody showed a positive correlation between Kidins220 and phosphorylated tau in AD brains. Using this antibody, Kidins220 was detected in CSF from AD patients where it positively correlated with CSF phosphorylated tau and tau. This study highlights the potential of Kidins220 as a CSF biomarker in AD. T.I. is funded by SAF2014-52737-P (Ministerio de Economía y Competitividad, Spain), P2010/BMD-2331-Neurodegmodels (Comunidad de Madrid, Madrid, Spain); A.L. is funded by PI11/3035 and PI14/1561 provided by FEDER (European Funds for Regional Development) and Instituto de Salud Carlos III (Ministerio de Economía y Competitividad, Spain). T.I. and A.L. are also funded by Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED) and CIBERNED cooperarive project 2013/07 (Instituto de Salud Carlos III, Ministerio de Economía y Competitividad, Spain). A.G.M is funded by a contract from CIBERNED-2013/07; O.B. is funded by the Miguel Servet Associate Investigator Project Grant (CP13/0091) and FIS (PI15/00058) provided by FEDER and Instituto de Salud Carlos III (Ministerio de Economía y Competitividad, Spain). The cost of this publication has been paid in part by FEDER funds. |
Databáze: | OpenAIRE |
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