Combination of circulating antilipoprotein lipase (Anti-LPL) antibody and heterozygous S172 fsX179 mutation of LPL gene leading to chronic hyperchylomicronemia

J Clin Endocrinol Metab. 2005 Jul;90(7):3995-8. doi: 10.1210/jc.2005-0205. Epub 2005 Apr 19.

Abstract

Context: Sporadic hyperchylomicronemia (type V hyperlipoproteinemia) results from complex interactions between genetic and environmental factors that often remain unknown.

Design: Upon investigation of a patient suffering from recurrent hypertriglyceridemic pancreatitis without family history or conventional secondary cause of dyslipidemia, we identified a previously unreported nonsense heterozygous lipoprotein lipase (LPL) gene mutation S172fsX179 associated with an antihuman LPL IgG.

Results: This autoantibody partially inhibited wild-type LPL activity in vitro. Furthermore, the patient's plasma triglyceride concentrations were efficiently decreased under immunosuppressive treatment, and this was confirmed by sequential withdrawal/reintroduction tests.

Conclusions: We consider that this unique combination of a genetic defect and an autoimmune disease results in chronic major hypertriglyceridemia. Because immunosuppressive treatment can improve this dyslipidemia, assessment of anti-LPL autoantibody is worthwhile in unmanageable chronic major hypertriglyceridemia, even in the presence of a heterozygous LPL deficiency.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autoantibodies / blood*
  • Chronic Disease
  • Chylomicrons / blood*
  • Heterozygote
  • Humans
  • Hyperlipidemias / etiology
  • Lipoprotein Lipase / antagonists & inhibitors
  • Lipoprotein Lipase / genetics*
  • Lipoprotein Lipase / immunology*
  • Male
  • Middle Aged
  • Mutation*

Substances

  • Autoantibodies
  • Chylomicrons
  • Lipoprotein Lipase