Scopus: 4 citas, Google Scholar: citas,
CSF progranulin increases in the course of Alzheimer's disease and is associated with sTREM2, neurodegeneration and cognitive decline
Suárez‐Calvet, Marc (Ludwig Maximilians Universität München)
Capell, Anja (Ludwig Maximilians Universität München)
Araque Caballero, Miguel Ángel (Ludwig Maximilians Universität München)
Morenas‐Rodríguez, Estrella (Universitat Autònoma de Barcelona)
Fellerer, Katrin (Ludwig Maximilians Universität München)
Franzmeier, Nicolai (Ludwig Maximilians Universität München)
Kleinberger, Gernot (Munich Cluster for Systems Neurology (SyNergy))
Eren, Erden (Dokuz Eylul University, Turkey)
Deming, Yuetiva (Washington University School of Medicine)
Piccio, Laura (Washington University School of Medicine)
Karch, Celeste M (Washington University School of Medicine)
Cruchaga, Carlos (Washington University School of Medicine)
Paumier, Katrina (Washington University School of Medicine)
Bateman, Randall J (Washington University School of Medicine)
Fagan, Anne M (Washington University School of Medicine)
Morris, John C (Washington University School of Medicine)
Levin, Johannes (Ludwig Maximilians Universität München)
Danek, Adrian (Ludwig Maximilians Universität München)
Jucker, Mathias (University of Tübingen)
Masters, Colin L (University of Melbourne)
Rossor, Martin N (UCL Institute of Neurology)
Ringman, John M (University of Southern California)
Shaw, Leslie M (University of Pennsylvania)
Trojanowski, John Q (University of Pennsylvania)
Weiner, Michael (University of California at San Francisco)
Ewers, Michael (Ludwig Maximilians Universität München)
Haass, Christian (Munich Cluster for Systems Neurology (SyNergy))

Fecha: 2018
Resumen: Progranulin (PGRN) is predominantly expressed by microglia in the brain, and genetic and experimental evidence suggests a critical role in Alzheimer's disease (AD). We asked whether expression is changed in a disease severity‐specific manner in . We measured in cerebrospinal fluid (CSF) in two of the best‐characterized patient cohorts, namely the Dominant Inherited Alzheimer's Disease Network (DIAN) and the Alzheimer's Disease Neuroimaging Initiative (ADNI). In carriers of causing dominant mutations, cross‐sectionally assessed increased over the course of the disease and significantly differed from non‐carriers 10 years before the expected symptom onset. In late‐onset , higher was associated with more advanced disease stages and cognitive impairment. Higher was associated with higher soluble 2 (triggering receptor expressed on myeloid cells 2) only when there was underlying pathology, but not in controls. In conclusion, we demonstrate that, although is not a diagnostic biomarker for , it may together with 2 reflect microglial activation during the disease.
Derechos: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Lengua: Anglès.
Documento: article ; recerca ; publishedVersion
Materia: Alzheimer's disease ; Biomarker ; Microglia ; Progranulin ; TREM2 ; Diagnostic Imaging ; Neuroscience
Publicado en: EMBO Molecular Medicine, Vol. 10 (november 2018) , ISSN 1757-4684

PMID: 30482868
DOI: 10.15252/emmm.201809712


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 Registro creado el 2019-08-12, última modificación el 2019-09-30



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