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Cited by 441

The DOI matches its Crossref record; 52 of the 52 references it cites were found in a registry or an index.

Survival in Critical Illness Is Associated with Early Activation of Mitochondrial Biogenesis

Open access
Carré, Jane E., Orban, Jean-Christophe, Re, Lorenza, Felsmann, Karen, Iffert, Wiebke, Bauer, Michael, Suliman, Hagir B., Piantadosi, Claude A., Mayhew, Terry M., Breen, Patrick, Stotz, Martin, Singer, Mervyn·2010·American Journal of Respiratory and Critical Care Medicine

Abstract

RATIONALE: We previously reported outcome-associated decreases in muscle energetic status and mitochondrial dysfunction in septic patients with multiorgan failure. We postulate that survivors have a greater ability to maintain or recover normal mitochondrial functionality. OBJECTIVES: To determine whether mitochondrial biogenesis, the process promoting mitochondrial capacity, is affected in critically ill patients. METHODS: Muscle biopsies were taken from 16 critically ill patients recently admitted to intensive care (average 1-2 d) and from 10 healthy, age-matched patients undergoing elective hip surgery. MEASUREMENTS AND MAIN RESULTS: Survival, mitochondrial morphology, mitochondrial protein content and enzyme activity, mitochondrial biogenesis factor mRNA, microarray analysis, and phosphorylated (energy) metabolites were determined. Ten of 16 critically ill patients survived intensive care. Mitochondrial size increased with worsening outcome, suggestive of swelling. Respiratory protein subunits and transcripts were depleted in critically ill patients and to a greater extent in nonsurvivors. The mRNA content of peroxisome proliferator-activated receptor γ coactivator 1-α (transcriptional coactivator of mitochondrial biogenesis) was only elevated in survivors, as was the mitochondrial oxidative stress protein manganese superoxide dismutase. Eventual survivors demonstrated elevated muscle ATP and a decreased phosphocreatine/ATP ratio. CONCLUSIONS: Eventual survivors responded early to critical illness with mitochondrial biogenesis and antioxidant defense responses. These responses may partially counteract mitochondrial protein depletion, helping to maintain functionality and energetic status. Impaired responses, as suggested in nonsurvivors, could increase susceptibility to mitochondrial damage and cellular energetic failure or impede the ability to recover normal function. Clinical trial registered with clinical trials.gov (NCT00187824).

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Metadata

Authors
Carré, J. E., Orban, J.-C., Re, L., Felsmann, K., Iffert, W., Bauer, M., Suliman, H. B., Piantadosi, C. A., Mayhew, T. M., Breen, P., Stotz, M., & Singer, M.
Venue
American Journal of Respiratory and Critical Care Medicine
Published
2010-09-15
Volume
182
Issue
6
Pages
745-751
ISSN
  • 1073-449X (ISSN-L)
  • 1535-4970
OpenAlex
W2133037534
Cited by
441
References
52
FWCI
7.68
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Survival in Critical Illness Is Associated with Early Activation of Mitochondrial Biogenesis. https://app.cochat.ai/papers/10.1164/rccm.201003-0326oc
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Carré, J. E., Orban, J.-C., Re, L., Felsmann, K., Iffert, W., Bauer, M., Suliman, H. B., Piantadosi, C. A., Mayhew, T. M., Breen, P., Stotz, M., & Singer, M. (2010). Survival in Critical Illness Is Associated with Early Activation of Mitochondrial Biogenesis. American Journal of Respiratory and Critical Care Medicine. https://doi.org/10.1164/rccm.201003-0326oc

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