Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetics

Lancet. 1993 Aug 28;342(8870):527-8. doi: 10.1016/0140-6736(93)91649-7.

Abstract

Autoimmunity is thought to lead to islet-cell-antibody (ICA) formation in diabetes mellitus. However, we found a mitochondrial gene mutation at nucleotide pair 3243 in 3 of 27 Japanese ICA-positive, initially non-insulin-dependent diabetic patients. All 3 progressed to insulin-dependency within 13-31 months, whereas 5 of the other 24 are non-insulin-dependent after 54-90 months. ICA, at least in these 3 patients, may follow gradual beta-cell destruction due to mitochondrial gene mutation, although the possibility of beta-cells with the mutation being susceptible to autoimmune destruction cannot be excluded.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Autoantibodies / biosynthesis*
  • DNA, Mitochondrial / genetics*
  • Diabetes Mellitus, Type 1 / genetics*
  • Diabetes Mellitus, Type 1 / immunology
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetes Mellitus, Type 2 / immunology
  • Female
  • Humans
  • Islets of Langerhans / immunology*
  • Male
  • Middle Aged
  • Point Mutation*
  • Prospective Studies

Substances

  • Autoantibodies
  • DNA, Mitochondrial