Serum activin A and B levels predict outcome in patients with acute respiratory failure: a prospective cohort study

30 day mortality in patients with Acute Respiratory Failure (ARF) is approximately 30%, defined as patients requiring ventilator support for more than 6 hours. Novel biomarkers are needed to predict patient outcomes and to guide potential future therapies. The activins A and B, members of the Transf...

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Veröffentlicht in:Critical care (London, England) England), 2013-10, Vol.17 (5), p.R263-R263, Article R263
Hauptverfasser: de Kretser, David Morritz, Bensley, Jonathan Guy, Pettilä, Ville, Linko, Rita, Hedger, Mark Peter, Hayward, Susan, Allan, Carolyn Anne, McLachlan, Robert Ian, Ludlow, Helen, Phillips, David James
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Sprache:eng
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Zusammenfassung:30 day mortality in patients with Acute Respiratory Failure (ARF) is approximately 30%, defined as patients requiring ventilator support for more than 6 hours. Novel biomarkers are needed to predict patient outcomes and to guide potential future therapies. The activins A and B, members of the Transforming Growth Factor β family of proteins, and their binding protein, follistatin, have recently been shown to be important regulators of inflammation and fibrosis but no substantial data are available concerning their roles in ARF. Specific assays for activin A, B and follistatin were used and the results analyzed according to diagnostic groups as well as according to standard measures in intensive care. Multivariable logistic regression was used to create a model to predict death at 90 days and 12 months from the onset of the ARF. Serum activin A and B were significantly elevated in most patients and in most of the diagnostic groups. Patients who had activin A and/or B concentrations above the reference maximum were significantly more likely to die in the 12 months following admission [either activin A or B above reference maximum: Positive Likelihood Ratio [LR+] 1.65 [95% CI 1.28-2.12, P = 0.00013]; both activin A and B above reference maximum: LR + 2.78 [95% CI 1.96-3.95, P 
ISSN:1364-8535
1466-609X
1364-8535
DOI:10.1186/cc13093