Defining and diagnosing sarcopenia: Is the glass now half full?

Metabolism. 2023 Jun:143:155558. doi: 10.1016/j.metabol.2023.155558. Epub 2023 Apr 7.

Abstract

Low muscle mass and function exert a substantial negative impact on quality of life, health and ultimately survival, but their definition, identification and combination to define sarcopenia have suffered from lack of universal consensus. Methodological issues have also contributed to incomplete agreement, as different approaches, techniques and potential surrogate measures inevitably lead to partly different conclusions. As a consequence: 1) awareness of sarcopenia and implementation of diagnostic procedures in clinical practice have been limited; 2) patient identification and evaluation of therapeutic strategies is largely incomplete. Significant progress has however recently occurred after major diagnostic algorithms have been developed, with common features and promising perspectives for growing consensus. At the same time, the need for further refinement of the sarcopenia concept has emerged, to address its increasingly recognized clinical heterogeneity. This includes potential differential underlying mechanisms and clinical features for age- and disease-driven sarcopenia, and the emerging challenge of sarcopenia in persons with obesity. Here, we will review existing algorithms to diagnose sarcopenia, and major open methodological issues to assess skeletal muscle mass and function under different clinical conditions, in order to highlight similarities and differences. Potential for consensus on sarcopenia diagnosis as well as emerging new challenges will be discussed.

Keywords: Algorithm; Diagnostic criteria; Sarcopenia.

Publication types

  • Review

MeSH terms

  • Algorithms
  • Anthropometry
  • Consensus*
  • Humans
  • Muscle Strength
  • Muscle, Skeletal / pathology
  • Muscle, Skeletal / physiopathology
  • Obesity / complications
  • Obesity / pathology
  • Obesity / physiopathology
  • Organ Size
  • Sarcopenia* / diagnosis
  • Sarcopenia* / etiology
  • Sarcopenia* / pathology
  • Sarcopenia* / physiopathology