Circulating miR-127-3p as a Potential Biomarker for Differential Diagnosis in Frontotemporal Dementia
Autor: | Michela A. Denti, Margherita Grasso, Rosa Campopiano, Paola Piscopo, Giuseppe Bruno, Marina Gasparini, Giuseppina Talarico, Emanuela D'Acunto, Maria Puopolo, Stefano Gambardella, Anna Elisa Castellano, Alessio Crestini, Annamaria Confaloni |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
Male
0301 basic medicine Oncology medicine.medical_specialty Central nervous system Disease Sensitivity and Specificity frontotemporal dementia Diagnosis Differential 03 medical and health sciences 0302 clinical medicine Alzheimer Disease Internal medicine mental disorders microRNA differential diagnosis Humans Medicine Circulating MicroRNA Biomarker miR-127-3p miRNA Aged Neuroscience (all) Receiver operating characteristic business.industry General Neuroscience General Medicine medicine.disease MicroRNAs Psychiatry and Mental health Clinical Psychology 030104 developmental biology medicine.anatomical_structure Psychiatry and Mental Health Frontotemporal Dementia Potential biomarkers Biomarker (medicine) Female Geriatrics and Gerontology Differential diagnosis business Frontotemporal dementia MiRNA Biomarkers 030217 neurology & neurosurgery |
Popis: | Given the heterogeneous nature of frontotemporal dementia (FTD), sensitive biomarkers are greatly needed for the accurate diagnosis of this neurodegenerative disorder. Circulating miRNAs have been reported as promising biomarkers for neurodegenerative disorders and processes affecting the central nervous system, especially in aging. The objective of the study was to evaluate if some circulating miRNAs linked with apoptosis (miR-29b-3p, miR-34a-5p, miR-16-5p, miR-17-5p, miR-107, miR-19b-3p, let-7b-5p, miR-26b-5p, and 127-3p) were able to distinguish between FTD patients and healthy controls. For this study, we enrolled 127 subjects, including 54 patients with FTD, 20 patients with Alzheimer's disease (AD), and 53 healthy controls. The qRT-PCR analysis showed a downregulation of miR-127-3p in FTD compared to controls, while the levels of other miRNAs remained unchanged. Then, miR-127-3p expression was also analyzed in AD patients, finding a different expression between two patient groups. A receiver operating characteristic curve was then created for miR-127-3p to discriminate FTD versus AD (AUC: 0.8986), and versus healthy controls (AUC: 0.8057). In conclusion, miR-127-3p could help to diagnose FTD and to distinguish it from AD. |
Databáze: | OpenAIRE |
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