Elevated Plasma microRNA-206 Levels Predict Cognitive Decline and Progression to Dementia from Mild Cognitive Impairment

被引:52
|
作者
Kenny, Aidan [1 ]
McArdle, Hazel [2 ]
Calero, Miguel [3 ,4 ]
Rabano, Alberto [3 ,5 ]
Madden, Stephen F. [6 ]
Adamson, Kellie [2 ]
Forster, Robert [7 ,8 ]
Spain, Elaine [2 ]
Prehn, Jochen H. M. [1 ,8 ]
Henshall, David C. [1 ,8 ]
Medina, Miguel [3 ,5 ]
Jimenez-Mateos, Eva M. [9 ]
Engel, Tobias [1 ,8 ]
机构
[1] Royal Coll Surgeons Ireland, Dept Physiol & Med Phys, Dublin D02 YN77, Ireland
[2] Dublin City Univ, Sch Chem Sci, Dublin 9, Ireland
[3] Ctr Invest Biomed Red Enfermedades Neurodegenerat, Madrid 28031, Spain
[4] Carlos III Inst Hlth, Madrid 28220, Spain
[5] Queen Sofia Fdn Alzheimer Ctr, Ctr Invest Enfermedades Neurol CIEN Fdn, Madrid 28031, Spain
[6] Royal Coll Surgeons Ireland, Data Sci Ctr, Dublin D02 YN77, Ireland
[7] Dublin City Univ, Natl Ctr Sensor Res, Sch Chem Sci, Dublin 9, Ireland
[8] FutureNeuro SFI Res Ctr, Dublin D02 YN77, Ireland
[9] Univ Dublin, Trinity Coll Dublin, Sch Med, Discipline Physiol, Dublin D02 PN40, Ireland
基金
爱尔兰科学基金会;
关键词
Alzheimer's disease; prodromal; prognosis; microRNA; microfluidic device; PRECLINICAL ALZHEIMERS-DISEASE; BRAIN-BARRIER BREAKDOWN; NEUROTROPHIC FACTOR; BIOMARKERS; DIAGNOSIS; MARKERS; TRIALS; MEMORY;
D O I
10.3390/biom9110734
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The need for practical biomarkers for early diagnosis of Alzheimer's disease (AD) remains largely unmet. Here we investigated the use of blood-based microRNAs as prognostic biomarkers for AD and their application in a novel electrochemical microfluidic device for microRNA detection. MicroRNA transcriptome was profiled in plasma from patients with mild cognitive impairment (MCI) and AD. MicroRNAs Let-7b and microRNA-206 were validated at elevated levels in MCI and AD, respectively. MicroRNA-206 displayed a strong correlation with cognitive decline and memory deficits. Longitudinal follow-ups over five years identified microRNA-206 increases preceding the onset of dementia. MicroRNA-206 was increased in unprocessed plasma of AD and MCI subjects, detected by our microfluidic device. While increased Let-7b levels in plasma may be used to identify patients with MCI, changes in plasma levels of microRNA-206 may be used to predict cognitive decline and progression towards dementia at an MCI stage. MicroRNA quantification via a microfluidic device could provide a practical cost-effective tool for the stratification of patients with MCI according to risk of developing AD.
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页数:16
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