Medullary amyloidosis associated with apolipoprotein A-IV deposition

Sanjeev Sethi, Jason D. Theis, Shirley M. Shiller, Cynthia C. Nast, David Harrison, Helmut G. Rennke, Julie A. Vrana, Ahmet Dogan

Research output: Contribution to journalArticlepeer-review

40 Scopus citations

Abstract

Amyloidosis is caused by extracellular deposition of proteins in an insoluble manner within tissues. In hereditary forms of amyloidosis, transthyretin, fibrinogen A-α, lysozyme, gelsolin, apolipoprotein A-I, and A-II accumulate in the tissue plaques. Here we describe a 52-year-old man with no family history of renal disease who presented with increased urinary frequency, gradual loss of renal function but no significant proteinuria. Renal biopsy found large amounts of amyloid restricted to the medulla with no involvement of glomeruli or vessels. Immunohistochemical analysis for transthyretin or serum amyloid A and tests for an underlying monoclonal gammopathy were negative. Although initially suspected to be amyloid light chain amyloidosis, laser microdissection and mass spectrometry showed that the amyloid was composed of large amounts of apolipoprotein A-IV. This was based on mass spectrometry studies that showed 100, 96, and 73 spectra in three microdissected samples that matched to apolipoprotein A-IV with 100% probability. DNA analyses detected three sequence variants representing common polymorphisms of the apolipoprotein A-IV gene. Thus, in this case, apolipoprotein A-IV deposition and renal involvement appear to be restricted to the medulla. A high degree of suspicion is required for the diagnosis of apolipoprotein A-IV amyloidosis as it may be missed if a renal biopsy consists only of cortex.

Original languageEnglish (US)
Pages (from-to)201-206
Number of pages6
JournalKidney international
Volume81
Issue number2
DOIs
StatePublished - Jan 2 2012

Keywords

  • amyloid
  • apolipoprotein A-IV
  • laser microdissection
  • mass spectrometry
  • medulla
  • proteomics

ASJC Scopus subject areas

  • Nephrology

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