Plasma microRNA profiling distinguishes patients with frontotemporal dementia from healthy subjects

被引:37
作者
Grasso, Margherita [1 ]
Piscopo, Paola [2 ]
Talarico, Giuseppina [3 ]
Ricci, Leonardo [4 ,5 ]
Crestini, Alessio [2 ]
Tosto, Giuseppe [6 ]
Gasparini, Marina [3 ]
Bruno, Giuseppe [3 ]
Denti, Michela A. [1 ]
Confaloni, Annamaria [2 ]
机构
[1] Dept Cellular Computat & Integrat Biol CIBIO, Trento, Italy
[2] Ist Super Sanita, Dept Neurosci, Viale Regina Elena 299, I-00161 Rome, Italy
[3] Sapienza Univ Rome, Dept Neurol & Psychiat, Rome, Italy
[4] Univ Trento, Dept Phys, Trento, Italy
[5] Univ Trento, Ctr Mind Brain Sci, CIMeC, Rovereto, Italy
[6] Columbia Univ Coll Phys & Surg, Taub Inst Res Alzheimers Dis & Aging Brain, 630 W 168th St, New York, NY 10032 USA
关键词
Frontotemporal dementia; Biomarkers; MicroRNAs; Gender; RT-qPCR; LOBAR DEGENERATION; NEUROTROPHIC FACTOR; ALZHEIMERS-DISEASE; REFERENCE GENES; COLON-CANCER; MIR-206; BIOMARKERS; TDP-43; PROLIFERATION; NORMALIZATION;
D O I
10.1016/j.neurobiolaging.2019.01.024
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The purpose of this study was to develop an easy and minimally invasive assay to detect a plasma miRNA profile in frontotemporal dementia (FTD) patients, with the final aim of discriminating between FTD patients and healthy controls (HCs). After a global miRNA profiling, significant downregulation of miR-663a, miR-502-3p, and miR-206 (p = 0.0001, p = 0.0002, and p = 0.02 respectively) in FTD patients was confirmed when compared with HCs in a larger case-control sample. Moreover, miR-663a and miR-502-3p showed significant differences in both genders, whereas miR-206, only in male subjects. To obtain a discriminating measure between FTD patients and HCs, we calculated a combined score of the 3 miRNAs by applying a Bayesian approach and obtaining a classifier with an accuracy of 84.4%. Moreover, for men, combined miRNA levels showed an excellent sensitivity (100%) and a good specificity (87.5%) in distinguishing FTD patients from HCs. All these findings open new hypotheses in the pathophysiology and new perspectives in the diagnosis of a complex pathology as FTD. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:240.e1 / 240.e12
页数:12
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