Article Text


Liver failure
PTU-004 Extreme hyperferritinaemia following paracetamol-induced human acute liver injury
  1. D G Craig1,
  2. A Pryde2,
  3. A Conway-Morris3,
  4. J Simpson3,
  5. S W Walker4,
  6. G J Beckett4,
  7. C O Bellamy5,
  8. P C Hayes2,
  9. K J Simpson2
  1. 1Scottish Liver Transplantation Unit, Royal Infirmary of Edinburgh, Edinburgh, UK
  2. 2Division of Clinical and Surgical Sciences, University of Edinburgh, Edinburgh, UK
  3. 3MRC Centre for Inflammation Research, University of Edinburgh, Edinburgh, UK
  4. 4Department of Clinical Biochemistry, Royal Infirmary of Edinburgh, Edinburgh, UK
  5. 5Department of Pathology, Royal Infirmary of Edinburgh, Edinburgh, UK


Introduction Activated macrophages may play a critical role in the pathogenesis of acute liver failure (ALF). Serum ferritin (SF) is a circulating marker of macrophage activation, and heavy (H) isoforms of ferritin may have immunostimulatory effects. However, ferritin may be released from necrotic liver, confounding SF interpretation in ALF. The SF/ALT ratio may have prognostic value in non-paracetamol ALF, but has not been examined in patients with paracetamol (POD)-ALF.

Methods Analysis of SF levels in acute liver injury patients admitted to a tertiary liver center, with western blotting and immunohistochemistry for ferritin isoforms.

Results Retrospective database analysis revealed elevated admission SF (>300 μg/l) in 109/124 (87.9%) of acute liver injury patients. Extreme SF elevations (>10000 μg/l) were more common in POD (36/71, 50.7%) compared with non-POD patients (5/53, 9.4%, p<0.001). Extremely elevated admission SF was confirmed in a prospective cohort of 47 POD cases (22/47, 46.8%). In both POD cohorts, admission SF was significantly higher in patients who died/were transplanted compared with spontaneous survivors (p=0.001, AUC 0.722 (95% CI 0.614 to 0.831) and in patients who developed hepatic encephalopathy (p=0.038) or the systemic inflammatory response syndrome (SIRS, p=0.008). Hyperferritinaemia correlated with proinflammatory (IL-6, Spearman's r=0.442, p=0.006; IL-8, r=0.502, p=0.001) and antiinflammatory (IL-10; r=0.349, p=0.030) cytokine release following POD, and with organ dysfunction (SOFA; r=0.529, p<0.001), but not with serum ALT (r=0.113, p=0.227). The ferritin/ALT ratio did not improve prognostic accuracy in PODs (AUC 0.706 (95% CI 0.595 to 0.817). Immunohistochemistry confirmed H and light (L) ferritin isoform expression in both normal liver tissue and explanted tissue from ALF patients. Immunoblotting of serum from POD patients with elevated SF revealed significant amounts of circulating H-ferritin, with no circulating H-ferritin observed in healthy controls.

Conclusion Extreme elevations of SF are common following POD, and are associated with adverse outcomes. SF is a widely available biomarker that may have prognostic value in patients with POD-ALF and merits further evaluation in larger, prospective studies. The correlation with SIRS, organ failure and cytokinaemia and the observation of circulating H ferritin also suggests that SF may be a mediator of adverse outcome.

Competing interests None declared.

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