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  • Derde, Sarah (author)

Muscle atrophy and preferential loss of myosin in prolonged critically ill patients

  • Article/chapterEnglish2012

Publisher, publication year, extent ...

  • 2012
  • printrdacarrier

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  • LIBRIS-ID:oai:DiVA.org:uu-163421
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-163421URI
  • https://doi.org/10.1097/CCM.0b013e31822d7c18DOI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • OBJECTIVE: Muscle weakness contributes to prolonged rehabilitation and adverse outcome of critically ill patients. Distinction between a neurogenic and/or myogenic underlying problem is difficult using routine diagnostic tools. Preferential loss of myosin has been suggested to point to a myogenic component. We evaluated markers of muscle atrophy and denervation, and the myosin/actin ratio in limb and abdominal wall skeletal muscle, of prolonged critically ill patients and matched controls in relation to insulin therapy and known risk factors for intensive care unit-acquired weakness. DESIGN: Secondary analysis of two large, prospective, single-center randomized clinical studies. SETTING: University hospital surgical and medical intensive care unit. PATIENTS: Critically ill patients and matched controls. INTERVENTIONS: Intensive care unit patients had been randomized to blood glucose control to 80-110 mg/dL with insulin infusion or conventional glucose management, where insulin was only administered when glucose levels rose above 215 mg/dL. MEASUREMENTS AND MAIN RESULTS: As compared with controls, rectus abdominis and vastus lateralis muscle of critically ill patients showed smaller myofiber size, decreased mRNA levels for myofibrillar proteins, increased proteolytic enzyme activities, and a lower myosin/actin ratio, virtually irrespective of insulin therapy. Increased forkhead box protein O1 action may have played a role. Most alterations were more severe in patients treated with corticosteroids. Duration of corticosteroid treatment, independent of duration of intensive care unit stay or other risk factors, was a dominant risk factor for a low myosin/actin ratio. The immature acetylcholine receptor subunit γ mRNA expression was elevated in vastus lateralis, independent of the myosin/actin ratio. CONCLUSIONS: Both limb and abdominal wall skeletal muscles of prolonged critically ill patients showed downregulation of protein synthesis at the gene expression level as well as increased proteolysis. This affected myosin to a greater extent than actin, resulting in a decreased myosin/actin ratio. Muscle atrophy was not ameliorated by intensive insulin therapy, but possibly aggravated by corticosteroids.

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Added entries (persons, corporate bodies, meetings, titles ...)

  • Hermans, Greet (author)
  • Derese, Inge (author)
  • Güiza, Fabian (author)
  • Hedström, YvetteUppsala universitet,Klinisk neurofysiologi(Swepub:uu)yvhed466 (author)
  • Wouters, Pieter J (author)
  • Bruyninckx, Frans (author)
  • Dʼhoore, André (author)
  • Larsson, LarsUppsala universitet,Klinisk neurofysiologi(Swepub:uu)lalar021 (author)
  • Van den Berghe, Greet (author)
  • Vanhorebeek, Ilse (author)
  • Uppsala universitetKlinisk neurofysiologi (creator_code:org_t)

Related titles

  • In:Critical Care Medicine40:1, s. 79-890090-34931530-0293

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