Decreased plasma gelsolin concentrations in acute liver failure, myocardial infarction, septic shock, and myonecrosis

OBJECTIVE To quantitate gelsolin concentrations in serum of patients with a variety of conditions involving actin release into the circulation. DESIGN Prospective evaluation of sera on consecutive patients. SETTING Metropolitan county hospital. PATIENTS Ninety hospital patients with a variety of wel...

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Veröffentlicht in:Critical care medicine 1997-04, Vol.25 (4), p.594-598
Hauptverfasser: Suhler, Eric, Lin, Weng, Yin, Helen L, Lee, William M
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Sprache:eng
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Zusammenfassung:OBJECTIVE To quantitate gelsolin concentrations in serum of patients with a variety of conditions involving actin release into the circulation. DESIGN Prospective evaluation of sera on consecutive patients. SETTING Metropolitan county hospital. PATIENTS Ninety hospital patients with a variety of well-characterized diseases. INTERVENTIONS None. MEASUREMENTS AND MAIN RESULTS Sera were studied from patients with acute liver failure (n = 18), chronic hepatitis (n = 17), cirrhosis of varying etiology (n = 17), pancreatitis (n = 10), acute myocardial infarction (n = 10), myonecrosis due either to polymyositis or crush injuries (n = 12), and septic shock (n = 6); results were compared with sera from healthy individuals (n = 25). Gelsolin was quantified by Western blotting with monoclonal anti-gelsolin and laser densitometry.Significant reductions in mean gelsolin concentrations compared with healthy controls were observed in patients with acute liver failure (47%), myocardial infarction (69%), sepsis (51%), and myonecrosis (66%). An inverse correlation was observed between gelsolin concentration and severity of illness, as indicated by the magnitude of serum enzyme concentrations. CONCLUSIONS Gelsolin depletion occurs in a variety of tissue injury syndromes. Depletion of actin-scavenger capacity in the presence of continued actin release may affect outcome in situations of severe organ damage. (Crit Care Med 1997; 25:594-598)
ISSN:0090-3493
1530-0293
DOI:10.1097/00003246-199704000-00007