High level of persistent liver injury is one of clinical characteristics in treatment-naïve acute onset autoimmune hepatitis: experience in a community hospital

J Hepatobiliary Pancreat Sci. 2016 Mar;23(3):174-80. doi: 10.1002/jhbp.319. Epub 2016 Feb 17.

Abstract

Background: There is, as yet, no gold standard for making the diagnosis of acute onset autoimmune hepatitis (A-AIH). Novel histological characteristics have been reported, but etiologies other than AIH could show similar histological pattern. We attempted to determine what clinical characteristics we should consider as A-AIH different from other etiologies, and to whom histological characteristics should be applied for the diagnosis.

Methods: Clinical, biochemical, immunological and pathological features of 46 patients (35 women, mean age 55.9 ± 14.2 years) with non-severe A-AIH admitted to a community hospital between 2001 and 2015 were analyzed.

Results: Immunoglobulin G level was normal in 28%, and anti-nuclear antibody titer was < × 80 in 28%. Liver histology of 49% showed acute form and 51% chronic one. Centrilobular necrosis/collapse and/or plasma cell accumulation, rosette formation were characteristic for A-AIH. High levels of alanine aminotransferase persisted in 21 patients who could be observed for equal to or more than 4 weeks before the start of treatment.

Conclusions: Long persistence of high levels of alanine aminotransferase would be one of clinical features for considering A-AIH along with conventional features. Histological diagnostic features should be applied for such patients. Guidelines for diagnosing A-AIH should be urgently drawn up.

Keywords: Acute presentation; Alanine aminotranferase; Autoimmune hepatitis; Non-severe.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / metabolism
  • Antibodies, Antinuclear / metabolism
  • Biomarkers / metabolism
  • Biopsy
  • Female
  • Hepatitis, Autoimmune / diagnosis*
  • Hepatitis, Autoimmune / metabolism*
  • Hepatitis, Autoimmune / pathology
  • Hospitals, Community
  • Humans
  • Immunoglobulin G / metabolism
  • Male
  • Middle Aged

Substances

  • Antibodies, Antinuclear
  • Biomarkers
  • Immunoglobulin G
  • Alanine Transaminase