Abstract

Autoimmune hepatitis (AIH) is a chronic hepatitis with an increasing incidence. The majority of patients require life-long immunosuppression and incomplete treatment response is associated with a disease progression. An abnormal iron homeostasis or hyperferritinemia is associated with worse outcome in other chronic liver diseases and after liver transplantation. We assessed the capacity of baseline parameters including the iron status to predict the treatment response upon standard therapy in 109 patients with untreated AIH type 1 (AIH-1) in a retrospective single center study. Thereby, a hyperferritinemia (> 2.09 times upper limit of normal; Odds ratio (OR) = 8.82; 95% confidence interval (CI): 2.25–34.52) and lower immunoglobulins (<1.89 times upper limit of normal; OR = 6.78; CI: 1.87–24.59) at baseline were independently associated with the achievement of complete biochemical remission upon standard therapy. The predictive value increased when both variables were combined to a single treatment response score, when the cohort was randomly split into a training (area under the curve (AUC) = 0.749; CI 0.635–0.863) and internal validation cohort (AUC = 0.741; CI 0.558–0.924). Patients with a low treatment response score (<1) had significantly higher cumulative remission rates in the training (p<0.001) and the validation cohort (p = 0.024). The baseline hyperferritinemia was accompanied by a high serum iron, elevated transferrin saturations and mild hepatic iron depositions in the majority of patients. However, the abnormal iron status was quickly reversible under therapy. Mechanistically, the iron parameters were not stringently related to a hepatocellular damage. Ferritin rather seems deregulated from the master regulator hepcidin, which was down regulated, potentially mediated by the elevated hepatocyte growth factor. In conclusion, baseline levels of serum ferritin and immunoglobulins, which are part of the diagnostic work-up of AIH, can be used to predict the treatment response upon standard therapy in AIH-1, although confirmation from larger multicenter studies is pending.

Highlights

  • Autoimmune hepatitis (AIH) is an autoimmune disorder that affects all age groups and shows an increasing incidence [1]

  • Baseline parameters related to the subsequent treatment response in AIH type 1 (AIH-1)

  • immunoglobulin G (IgG), serum iron (SI) and serum ferritin (SF) were significantly different and AST showed a trend to be different between patients with subsequent biochemical remission (BR) and incomplete biochemical response (IR) (Table 1)

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Summary

Introduction

Autoimmune hepatitis (AIH) is an autoimmune disorder that affects all age groups and shows an increasing incidence [1]. Associations of genetic factors like MHC class II molecules [2] and external triggers like e.g. hepatitis A or Epstein-Barr virus infections [3] led to the hypothesis of an externally triggered break of tolerance in genetically predisposed individuals. Complete biochemical remission (BR) can be achieved in about 80% of patients, a relapse after the withdrawal of immunosuppression is common, even in patients with a complete histological remission (CR) [8]. As patients with incomplete biochemical response (IR) have worse prognosis a predictive identification of those patients could lead to a stronger immunosuppressive salvage therapy. Several studies described factors that are associated with worse outcome [12,13,14], none of those led to a practical risk stratification approach to predict the treatment response upon standard therapy

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