Biomarkers for physical frailty and sarcopenia

Riccardo Calvani, Federico Marini, Matteo Cesari, Matteo Tosato, Anna Picca, Stefan D. Anker, Stephan Von Haehling, Ram R. Miller, Roberto Bernabei, Francesco Landi, Emanuele Marzetti

Research output: Contribution to journalArticle

Abstract

Physical frailty (PF) and sarcopenia are major health issues in geriatric populations, given their high prevalence and association with several adverse outcomes. Nevertheless, the lack of an univocal operational definition for the two conditions has so far hampered their clinical implementation. Existing definitional ambiguities of PF and sarcopenia, together with their complex underlying pathophysiology, also account for the absence of robust biomarkers that can be used for screening, diagnostic and/or prognostication purposes. This review provides an overview of currently available biological markers for PF and sarcopenia, as well as a critical appraisal of strengths and weaknesses of traditional procedures for biomarker development in the field. A novel approach for biomarker identification and validation, based on multivariate methodologies, is also discussed. This strategy relies on the multidimensional modeling of complementary biomarkers to cope with the phenotypical and pathophysiological complexity of PF and sarcopenia. Biomarkers identified through the implementation of multivariate strategies may be used to support the detection of the two conditions, track their progression over time or in response to interventions, and reveal the onset of complications (e.g., mobility disability) at a very early stage.
Original languageEnglish
Pages (from-to)29-34
Number of pages6
JournalAging clinical and experimental research
Volume29
DOIs
Publication statusPublished - 2017

Keywords

  • Aging
  • Disability
  • Markers
  • Multivariate analysis
  • Physical performance
  • Skeletal muscle

Fingerprint

Dive into the research topics of 'Biomarkers for physical frailty and sarcopenia'. Together they form a unique fingerprint.

Cite this