4.3 Article

Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients

期刊

NEUROMOLECULAR MEDICINE
卷 18, 期 4, 页码 551-560

出版社

HUMANA PRESS INC
DOI: 10.1007/s12017-016-8396-8

关键词

Amyotrophic lateral sclerosis; Cerebrospinal fluid; microRNA; C9orf72 expansion; Biomarkers

资金

  1. Community's Health Seventh Framework Programme (FP7) [259867]
  2. Associazione Polisportiva Torrenieri a.s.d.- Ice Bucket Challenge [2268-2014-BS-CONTRLIB_001]
  3. Dottorato Toscano in Neuroscienze
  4. ESRC [ES/L008238/1] Funding Source: UKRI
  5. Economic and Social Research Council [ES/L008238/1] Funding Source: researchfish
  6. Medical Research Council [MR/L501529/1] Funding Source: researchfish
  7. Motor Neurone Disease Association [Jones/Oct15/958-799] Funding Source: researchfish

向作者/读者索取更多资源

Amyotrophic lateral sclerosis (ALS) is a progressive, fatal neurodegenerative disorder. Since no diagnostic laboratory test exists, the identification of specific biomarkers could be fundamental in clinical practice. microRNAs (miRNAs) are considered promising biomarkers for neurodegenerative diseases. The aim of the study was to identify a CSF miRNA set that could differentiate ALS from non-ALS condition. miRNA profiling in CSF from ALS patients (n = 24; eight with C9orf72 expansion) and unaffected control subjects (n = 24) by quantitative reverse transcription PCR identified fourteen deregulated miRNAs. Validation experiments confirmed eight miRNAs as significantly deregulated in ALS. No significant differences were observed between ALS patients with or without C9orf72 expansion. The receiver operator characteristic (ROC) curve analyses revealed the highest diagnostic accuracy for the upregulated miR181a-5p and the downregulated miR21-5p and miR15b-5p. The miR181a-5p/miR21-5p and miR181a-5p/miR15b-5p ratios detected ALS with 90 and 85 % sensitivity and 87 and 91 % specificity, respectively, confirming the application potential as disease biomarkers. These deregulated miRNAs are implicated in apoptotic way and provide insight into processes responsible for motor neuron degeneration.

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