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

被引:0
作者
Paul M. McKeever
Raphael Schneider
Foad Taghdiri
Anna Weichert
Namita Multani
Robert A. Brown
Adam L. Boxer
Anna Karydas
Bruce Miller
Janice Robertson
Maria Carmela Tartaglia
机构
[1] Tanz Centre for Research in Neurodegenerative Diseases,Laboratory Medicine and Pathobiology
[2] University of Toronto,Institute for Medical Sciences
[3] University of Toronto,Montreal Neurological Institute
[4] University Health Network,Memory and Aging Center
[5] McGill University,undefined
[6] University of California,undefined
[7] San Francisco,undefined
来源
Molecular Neurobiology | 2018年 / 55卷
关键词
Alzheimer’s disease; Young-onset; Cerebrospinal fluid; Exosomes; MicroRNA;
D O I
暂无
中图分类号
学科分类号
摘要
Clinical diagnosis of Alzheimer’s disease (AD) prior to the age of 65 years is classified as young-onset (YOAD), whereas diagnosis after the age of 65 years 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:15
相关论文
共 852 条
[1]  
Goate A(1991)Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer’s disease Nature 349 704-706
[2]  
Chartier-Harlin M-C(1995)Familial Alzheimer’s disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer’s disease type 3 gene Nature 376 775-778
[3]  
Mullan M(1995)Cloning of a gene bearing missense mutations in early-onset familial Alzheimer’s disease Nature 375 754-760
[4]  
Brown J(1999)Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum Am J Hum Genet 65 664-670
[5]  
Crawford F(2003)Early onset familial Alzheimer’s disease: mutation frequency in 31 families Neurology 60 235-239
[6]  
Fidani L(2014)Differences in routine clinical practice between early and late onset Alzheimer’s disease: data from the Swedish Dementia Registry (SveDem) J Alzheimers Dis 41 411-419
[7]  
Giuffra L(2005)Structural correlates of early and late onset Alzheimer’s disease: voxel based morphometric study J Neurol Neurosurg Psychiatry 76 112-114
[8]  
Haynes A(2013)Rate of progression of Alzheimer’s disease in younger versus older patients: a longitudinal single photon emission computed tomography study: effect of age on AD progression Geriatr Gerontol Int 13 555-562
[9]  
Irving N(1993)Comparison of the severity of neuropathologic changes in familial and sporadic Alzheimer’s disease Alzheimer Dis Assoc Disord 7 212-222
[10]  
James L(1996)Clinical and neuropsychological differences between patients with earlier and later onset of Alzheimer’s disease: a CERAD analysis, part XII Neurology 46 136-141