MicroRNA Expression Levels Are Altered in the Cerebrospinal Fluid of Patients with Young-Onset Alzheimer's Disease

被引:143
作者
McKeever, Paul M. [1 ,2 ]
Schneider, Raphael [1 ,2 ]
Taghdiri, Foad [1 ,3 ]
Weichert, Anna [1 ]
Multani, Namita [1 ,4 ]
Brown, Robert A. [5 ]
Boxer, Adam L. [6 ]
Karydas, Anna [6 ]
Miller, Bruce [6 ]
Robertson, Janice [1 ,2 ]
Tartaglia, Maria Carmela [1 ,3 ,4 ]
机构
[1] Tanz Ctr Res Neurodegenerat Dis, Krembil Discovery Tower,60 Leonard Ave,4KD-481, Toronto, ON M5T 2S8, Canada
[2] Univ Toronto, Lab Med & Pathobiol, Toronto, ON, Canada
[3] Univ Toronto, Inst Med Sci, Toronto, ON, Canada
[4] Univ Hlth Network, Toronto, ON, Canada
[5] McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada
[6] Univ Calif San Francisco, Memory & Aging Ctr, San Francisco, CA 94143 USA
关键词
Alzheimer's disease; Young-onset; Cerebrospinal fluid; Exosomes; MicroRNA; NEURODEGENERATIVE DISEASE; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; MISSENSE MUTATIONS; TUMOR-SUPPRESSOR; QUANTITATIVE PCR; GENE; BIOMARKERS; EXOSOMES;
D O I
10.1007/s12035-018-1032-x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Clinical diagnosis of Alzheimer's disease (AD) prior to the age of 65years is classified as young-onset (YOAD), whereas diagnosis after the age of 65years is considered late-onset (LOAD). Although rare autosomal mutations more commonly associate with YOAD, most YOAD and LOAD cases are sporadic. YOAD and LOAD share amyloid and tau pathology, but many YOAD patients show increased disease severity and rate of progression. The current study examined the microRNA (miRNA) expression profile from exosomes isolated from the cerebrospinal fluid (CSF) of YOAD patients with biomarker-confirmed AD. Results uncovered miR-16-5p, miR-125b-5p, miR-451a, and miR-605-5p as differentially expressed in the CSF-derived exosomes of YOAD patients when compared with healthy controls (HC). In a cohort of LOAD patients, miR-125b-5p, miR-451a, and miR-605-5p were similarly altered in expression, but miR-16-5p showed similar expression to control. Analysis of the mRNA targets of these miRNAs revealed transcripts enriched in biological processes relevant to the post-mortem posterior cingulate cortex transcriptome in YOAD from a previously published microarray study, including those related to neuron projections, synaptic signaling, metabolism, apoptosis, and the immune system. Hence, these miRNAs represent novel targets for uncovering disease mechanisms and for biomarker development in both YOAD and LOAD.
引用
收藏
页码:8826 / 8841
页数:16
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