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The metabolomics side of frailty: Toward personalized medicine for the aged.

Abstract
Frailty encompasses several domains (i.e., metabolic, physical, cognitive). The multisystem derangements underlying frailty pathophysiology, its phenotypic heterogeneity, and the fluctuations of individuals across severity states have hampered a comprehensive appraisal of the condition. Circulating biomarkers emerged as an alleged tool for capturing this complexity and, as proxies for organismal metabolic changes, may hold the advantages of: 1) supporting diagnosis, 2) tracking the progression, 3) assisting healthcare professionals in clinical and therapeutic decision-making, and 4) verifying the efficacy of an intervention before measurable clinical manifestations occur. Among available analytical tools, metabolomics are able to identify and quantify the (ideally) whole repertoire of small molecules in biological matrices (i.e., cells, tissues, and biological fluids). Results of metabolomics analysis may define the final output of genome-environment interactions at the individual level. This entire collection of metabolites is called "metabolome" and is highly dynamic. Here, we discuss how monitoring the dynamics of metabolic profiles may provide a read-out of the environmental and clinical disturbances affecting cell homeostasis in frailty-associated conditions.
AuthorsAnna Picca, Hélio José Coelho-Junior, Matteo Cesari, Federico Marini, Alfredo Miccheli, Jacopo Gervasoni, Maurizio Bossola, Francesco Landi, Roberto Bernabei, Emanuele Marzetti, Riccardo Calvani
JournalExperimental gerontology (Exp Gerontol) Vol. 126 Pg. 110692 (10 15 2019) ISSN: 1873-6815 [Electronic] England
PMID31421185 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
CopyrightCopyright © 2019 Elsevier Inc. All rights reserved.
Chemical References
  • Biomarkers
Topics
  • Aged
  • Biomarkers (blood)
  • Cognition Disorders (metabolism)
  • Frailty (diagnosis, metabolism)
  • Humans
  • Metabolomics (methods)
  • Precision Medicine (methods)
  • Sarcopenia (metabolism)

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