Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/124220
Title: Ykl-40 in the brain and cerebrospinal fluid of neurodegenerative dementias
Author: Llorens Torres, Franc
Thune, Katrin
Tahir, Waqas
Kanata, Eirini
Diaz Lucena, Daniela
Xanthopoulos, Konstantinos
Kovatsi, Eleni
Pleschka, Catharina
Garcia-Esparcia, Paula
Schmitz, Matthias
Ozbay, Duru
Correia, Susana
Correia, Ângela
Milosevic, Ira
Andreoletti, Olivier
Fernández Borges, Natalia
Vorberg, Ina M.
Glatzel, Markus
Sklaviadis, Theodoros
Torres, Juan Maria
Krasemann, Susanne
Sánchez Valle, Raquel
Ferrer, Isidro (Ferrer Abizanda)
Zerr, Inga
Keywords: Malalties neurodegeneratives
Glicoproteïnes
Neurodegenerative diseases
Glycoproteins
Issue Date: 10-Nov-2017
Publisher: BioMed Central
Abstract: Background: YKL-40 (also known as Chitinase 3-like 1) is a glycoprotein produced by inflammatory, cancer and stem cells. Its physiological role is not completely understood but YKL-40 is elevated in the brain and cerebrospinal fluid (CSF) in several neurological and neurodegenerative diseases associated with inflammatory processes. Yet the precise characterization of YKL-40 in dementia cases is missing. Methods: In the present study, we comparatively analysed YKL-40 levels in the brain and CSF samples from neurodegenerative dementias of different aetiologies characterized by the presence of cortical pathology and disease-specific neuroinflammatory signatures. Results: YKL-40 was normally expressed in fibrillar astrocytes in the white matter. Additionally YKL-40 was highly and widely expressed in reactive protoplasmic cortical and perivascular astrocytes, and fibrillar astrocytes in sporadic Creutzfeldt-Jakob disease (sCJD). Elevated YKL-40 levels were also detected in Alzheimer's disease (AD) but not in dementia with Lewy bodies (DLB). In AD, YKL-40-positive astrocytes were commonly found in clusters, often around beta-amyloid plaques, and surrounding vessels with beta-amyloid angiopathy; they were also distributed randomly in the cerebral cortex and white matter. YKL-40 overexpression appeared as a pre-clinical event as demonstrated in experimental models of prion diseases and AD pathology. CSF YKL-40 levels were measured in a cohort of 288 individuals, including neurological controls (NC) and patients diagnosed with different types of dementia. Compared to NC, increased YKL-40 levels were detected in sCJD (p < 0.001, AUC = 0.92) and AD (p < 0.001, AUC = 0.77) but not in vascular dementia (VaD) (p > 0.05, AUC = 0.71) or in DLB/Parkinson's disease dementia (PDD) (p > 0.05, AUC = 0.70). Further, two independent patient cohorts were used to validate the increased CSF YKL-40 levels in sCJD. Additionally, increased YKL-40 levels were found in genetic prion diseases associated with the PRNP-D178N (Fatal Familial Insomnia) and PRNP-E200K mutations. Conclusions: Our results unequivocally demonstrate that in neurodegenerative dementias, YKL-40 is a disease-specific marker of neuroinflammation showing its highest levels in prion diseases. Therefore, YKL-40 quantification might have a potential for application in the evaluation of therapeutic intervention in dementias with a neuroinflammatory component.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1186/s13024-017-0226-4
It is part of: Molecular Neurodegeneration, 2017, vol. 12, num. 83
URI: http://hdl.handle.net/2445/124220
Related resource: http://dx.doi.org/10.1186/s13024-017-0226-4
Appears in Collections:Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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