PLoS ONE (Jan 2014)

Low levels of blood lipids are associated with etiology and lethal outcome in acute liver failure.

  • Paul Manka,
  • Verena Olliges,
  • Lars P Bechmann,
  • Martin Schlattjan,
  • Christoph Jochum,
  • Jürgen W Treckmann,
  • Fuat H Saner,
  • Guido Gerken,
  • Wing-Kin Syn,
  • Ali Canbay

DOI
https://doi.org/10.1371/journal.pone.0102351
Journal volume & issue
Vol. 9, no. 7
p. e102351

Abstract

Read online

BACKGROUND/AIMS:Emerging data links different aspects of lipid metabolism to liver regeneration. In patients with acute liver failure (ALF), low levels of lipids may correlate with disease severity. Thus, we determined whether there is an etiology-specific link between lipid levels in patients suffering from ALF and aimed to investigate an effect of lipid levels on the prognosis of ALF. METHODS:In this retrospective single center study, we reviewed 89 consecutive ALF patients, who met the criteria of the "Acute Liver Failure Study Group". Patient characteristics, clinical data and laboratory parameters were individually analyzed at admission and correlated with the patients' outcome after a four week follow up. Possible endpoints were either discharge, or death or liver transplantation. RESULTS:High-density lipoprotein (HDL), cholesterol and triglyceride levels were significantly lower in patients who died or required a liver transplant. HDL levels were significantly higher in patients with ALF caused by acetaminophen intoxication, compared to fulminant HBV infection or drug induced liver injury. HDL levels correlated with hepatic injury by ALT levels, and Albumin, and inversely correlated with the MELD score, INR, and bilirubin. CONCLUSION:In our cohort of patients with ALF, we could show that HDL and cholesterol are suppressed. In addition novel etiology specific patterns between acteminophen and non-acteminophen induced liver failure were detected for serum lipid components. Further studies are needed to address the role of cholesterol and lipid metabolism and the according pathways in different etiologies of ALF.