Proteomic Analysis for the Diagnosis of Fibrinogen Aα-chain Amyloidosis

Graham W Taylor1, Janet A Gilbertson1, Rabya Sayed1,2

  • 1National Amyloidosis Centre and Wolfson Drug Discovery Unit, Centre for Amyloidosis and Acute Phase Proteins, University College London, London, UK.

Abstract

Insights

Hereditary fibrinogen Aα-chain amyloidosis can be reliably identified in kidney samples using a proteomics-based algorithm. This method aids in diagnosing this rare renal disease by analyzing amyloid protein composition.

Area of Science:

  • Nephrology
  • Biochemistry
  • Proteomics

Background:

  • Hereditary fibrinogen Aα-chain (AFib) amyloidosis is a rare kidney disease caused by specific fibrinogen Aα (FibA) variants.
  • Wild-type FibA does not typically cause amyloid deposition, distinguishing it from pathogenic variants.

Purpose of the Study:

  • To develop and validate a proteomics-based algorithm for identifying FibA in amyloid deposits.
  • To establish a reliable method for diagnosing AFib amyloidosis in clinical renal samples.

Main Methods:

  • Proteomics data from 1001 Congo red-positive samples were analyzed using Mascot search engine against the Swiss-Prot database.
  • A scoring algorithm was developed to identify FibA, incorporating known pathogenic variant sequences.
  • FibA identification was confirmed by comparing its score to other fibrinogen chains to exclude blood contamination.

Main Results:

  • The algorithm successfully identified AFib amyloid in 64 renal samples based on specific criteria, including Mascot scores and sequence coverage.
  • Proteomics results correlated well with clinical diagnoses, confirming the algorithm's accuracy.
  • Four additional samples were diagnosed as AFib amyloid after comprehensive clinical and biochemical assessment, despite not fully meeting algorithmic criteria.

Conclusions:

  • Proteomics, utilizing a score-based algorithm, reliably identifies AFib amyloid in glomerular deposits.
  • Proteomics data serves as a valuable guide for AFib diagnosis when integrated with clinical and laboratory findings.

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