Novel biomarkers in Alzheimer's disease using high resolution proteomics and metabolomics: miRNAS, proteins and metabolites.

Alzheimer's disease (AD) is the most common form of dementia. It affects approximately 6% of people over the age of 65 years. It is a clinicopathological, degenerative, chronical and progressive disease that exhibits a deterioration of memory, orientation, speech and other functions. Factors contrib...

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Published in:Critical Reviews in Clinical Laboratory Sciences Vol. 58; no. 3; pp. 167 - 180
Main Authors: Navas-Carrillo, Diana, Rivera-Caravaca, José Miguel, Sampedro-Andrada, Arturo, Orenes-Piñero, Esteban
Format: pictorial review tables/charts Journal Article
Published: Taylor & Francis Ltd May2021
Online Access:View this record in EBSCOhost
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      issn: 10408363
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      dt: May2021
      vid: 58
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      pub: Taylor & Francis Ltd
      place: Philadelphia, Pennsylvania
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        10.1080/10408363.2020.1833298
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      tig:
        atl: Novel biomarkers in Alzheimer's disease using high resolution proteomics and metabolomics: miRNAS, proteins and metabolites.
      aug:
        au:
          Navas-Carrillo, Diana
          Rivera-Caravaca, José Miguel
          Sampedro-Andrada, Arturo
          Orenes-Piñero, Esteban
        affil: Department of Surgery, Hospital HLA La Vega, Murcia, Spain
      sug:
        subj:
          Biological Markers
          Alzheimer's Disease Diagnosis
          Proteomics
          Metabolomics
          MicroRNA
          Proteins
          Metabolites
          Amyloid beta-Peptides
          tau Proteins
          Alzheimer's Disease Physiopathology
          Alzheimer's Disease Prevention and Control
          Alzheimer's Disease Familial and Genetic
      ab: Alzheimer's disease (AD) is the most common form of dementia. It affects approximately 6% of people over the age of 65 years. It is a clinicopathological, degenerative, chronical and progressive disease that exhibits a deterioration of memory, orientation, speech and other functions. Factors contributing to the pathogenesis of the disease are the presence of extracellular amyloid deposits, called neuritic senile plaques, and fibrillary protein deposits inside neurons, known as neurofibrillary bundles, that appear mainly in the frontal and temporal lobes. AD has a long preclinical latency and is difficult to diagnose and prevent at early stages. Despite the advent of novel high-throughput technologies, it is a great challenge to identify precise biomarkers to understand the progression of the disease and the development of new treatments. In this sense, important knowledge is emerging regarding novel molecular and biological candidates with diagnostic potential, including microRNAs that have a key role in gene repression. On the other hand, proteomic approaches offer a platform for the comprehensive analysis of the whole proteome in a certain physiological time. Proteomic technology investigates protein expression directly and reveals post-translational modifications known to be determinant for many human diseases. Clinically, there is growing evidence for the role of proteomic and metabolomic technologies in AD biomarker discovery. This review discusses the role of several miRNAs identified using genomic technologies, and the importance of novel proteomic and metabolomic approaches to identify new proteins and metabolites that may be useful as biomarkers for monitoring the progression and treatment of AD.
      pubtype: Academic Journal
      doctype:
        pictorial
        review
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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