Altered microRNAs related to synaptic function as potential plasma biomarkers for Alzheimer's disease

Several evidences suggest that failure of synaptic function occurs at preclinical stages of Alzheimer's disease (AD) preceding neuronal loss and the classical AD pathological hallmarks. Nowadays, there is an urgent need to identify reliable biomarkers that could be obtained with non-invasive me...

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Detalhes bibliográficos
Autores: Siedlecki-Wullich, Dolores|||0000-0002-9099-9406, Català-Solsona, Judit|||0000-0002-2927-9135, Fábregas Ordóñez, Cristina, Hernández, Isabel|||0000-0001-8119-393X, Clarimón, Jordi|||0000-0002-6824-6942, Lleó, Alberto|||0000-0002-2568-5478, Boada, Mercè|||0000-0003-2617-3009, Saura Antolín, Carlos|||0000-0003-3692-5657, Rodríguez Álvarez, José|||0000-0001-8582-8082, Miñano Molina, Alfredo Jesús|||0000-0002-7761-5682
Formato: artículo
Fecha de publicación:2019
País:España
Recursos:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:226464
Acesso em linha:https://ddd.uab.cat/record/226464
https://dx.doi.org/urn:doi:10.1186/s13195-019-0501-4
Access Level:acceso abierto
Palavra-chave:Alzheimer's disease
Mild cognitive impairment
Synapses
Mirnas
Plasma
Human
Biomarker
Frontotemporal dementia
Descrição
Resumo:Several evidences suggest that failure of synaptic function occurs at preclinical stages of Alzheimer's disease (AD) preceding neuronal loss and the classical AD pathological hallmarks. Nowadays, there is an urgent need to identify reliable biomarkers that could be obtained with non-invasive methods to improve AD diagnosis at early stages. Here, we have examined plasma levels of a group of miRNAs related to synaptic proteins in a cohort composed of cognitive healthy controls (HC), mild cognitive impairment (MCI) and AD subjects. Plasma and brain levels of miRNAs were analysed in two different cohorts including 38 HC, 26 MCI, 56 AD dementia patients and 27 frontotemporal dementia (FTD) patients. D'Agostino and Pearson and Shapiro-Wilk tests were used to evaluate data normality. miRNA levels between groups were compared using a two-sided nonparametric Mann-Whitney test and sensitivity and specificity was determined by receiver operating characteristic curve analysis. Significant upregulation of miR-92a-3p, miR-181c-5p and miR-210-3p was found in the plasma of both MCI and AD subjects. MCI patients that progress to AD showed higher plasma levels of these miRNAs. By contrast, no changes in miR-92a-3p, miR-181c-5p or miR-210-3p levels were observed in plasma obtained from a cohort of FTD. Our study shows that plasma miR-92a-3p, miR-181c-5p and miR-210-3p constitute a specific molecular signature potentially useful as a potential biomarker for AD. The online version of this article (10.1186/s13195-019-0501-4) contains supplementary material, which is available to authorized users.