Platelet miRNA Biosignature Discriminates between Dementia with Lewy Bodies and Alzheimer's Disease

被引:12
作者
Gamez-Valero, Ana [1 ,2 ,7 ]
Campdelacreu, Jaume [3 ]
Vilas, Dolores [4 ]
Ispierto, Lourdes [4 ]
Gascon-Bayarri, Jordi [3 ]
Rene, Ramon [3 ]
Alvarez, Ramiro [4 ]
Armengol, Maria P. [5 ]
Borras, Francesc E. [2 ,6 ]
Beyer, Katrin [1 ]
机构
[1] Univ Autonoma Barcelona UAB, Germans Trias & Pujol Res Inst IGTP, Dept Pathol, Barcelona 08193, Spain
[2] Germans Trias & Pujol Res Inst IGTP, REMAR IVECAT Grp, Barcelona 08916, Spain
[3] Hosp Univ Bellvitge, Serv Neurol, Barcelona, Spain
[4] Hosp Badalona Germans Trias & Pujol, Serv Neurol, Badalona 08916, Spain
[5] Germans Trias & Pujol Res Inst IGTP, Genom & Microscopy Facil, Barcelona 08916, Spain
[6] Hosp Badalona Germans Trias & Pujol, Nephrol Serv, Barcelona 08916, Spain
[7] Univ Barcelona, Fac Med & Ciencies Salut, Inst Neurociencies, Dept Biomed, Barcelona 08036, Spain
关键词
Alzheimer disease; dementia with Lewy bodies; miRNA; peripheral biomarkers; platelets; synucleinopathies; PARKINSONS-DISEASE; DIAGNOSIS; MICRORNA; BIOMARKERS; MANAGEMENT; SIGNATURES; PATHWAY; QUALITY; CELLS;
D O I
10.3390/biomedicines9091272
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
Dementia with Lewy bodies (DLB) is one of the most common causes of degenerative dementia, after Alzheimer's disease (AD), and presents pathological and clinical overlap with both AD and Parkinson's disease (PD). Consequently, only one in three DLB cases is diagnosed correctly. Platelets, previously related to neurodegeneration, contain microRNAs (miRNAs) whose analysis may provide disease biomarkers. Here, we profiled the whole platelet miRNA transcriptome from DLB patients and healthy controls. Differentially expressed miRNAs were further validated in three consecutive studies from 2017 to 2019 enrolling 162 individuals, including DLB, AD, and PD patients, and healthy controls. Results comprised a seven-miRNA biosignature, showing the highest diagnostic potential for the differentiation between DLB and AD. Additionally, compared to controls, two miRNAs were down-regulated in DLB, four miRNAs were up-regulated in AD, and two miRNAs were down-regulated in PD. Predictive target analysis identified three disease-specific clusters of pathways as a result of platelet-miRNA deregulation. Our cross-sectional study assesses the identification of a novel, highly specific and sensitive platelet-associated miRNA-based biosignature, which distinguishes DLB from AD.
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页数:19
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