Physiopathological mechanisms of diaphragmatic dysfunction associated with mechanical ventilation

Rev Esp Anestesiol Reanim (Engl Ed). 2020 Apr;67(4):195-203. doi: 10.1016/j.redar.2019.12.002. Epub 2020 Jan 22.
[Article in English, Spanish]

Abstract

Ventilator-induced diaphragm dysfunction (VIDD) is the loss of diaphragmatic muscle strength'related to of mechanical ventilation, noticed during the first day or 48hours after initiating controlled mechanical ventilation. This alteration has been related to disruption on the insulin growth factor/phosphoinositol 3-kinase/kinase B protein pathway (IGF/PI3K/AKT), in addition to an overexpression of FOXO, expression of NF-kB signaling, increase function of muscular ubiquitin ligase and activation of caspasa-3. VIDD has a negative impact on quality of life, duration of mechanical ventilation, and hospitalization stance and cost. More studies are necessary to understated the process and impact of VIDD. This is a narrative review of non-systematic literature, aiming to explain the molecular pathways involved in VIDD.

Keywords: Biotrauma; Diaphragm dysfunction; Disfunción diafragmática; Factores de riego; Mechanically ventilated; Proteolysis; Proteólisis; Risk factors; Ventilación mecánica.

Publication types

  • Review

MeSH terms

  • Age Factors
  • Caspase 3 / metabolism
  • Diaphragm* / injuries
  • Forkhead Transcription Factors / metabolism
  • Glucocorticoids / adverse effects
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Muscular Diseases / etiology*
  • Muscular Diseases / metabolism
  • NF-kappa B / metabolism
  • Nutritional Status
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Quality of Life
  • Respiration, Artificial / adverse effects*
  • Sarcopenia / etiology
  • Sarcopenia / metabolism
  • Time Factors
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • Forkhead Transcription Factors
  • Glucocorticoids
  • NF-kappa B
  • Insulin-Like Growth Factor I
  • Ubiquitin-Protein Ligases
  • Proto-Oncogene Proteins c-akt
  • Caspase 3