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Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
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.
Introduction:
Hereditary fibrinogen Aα-chain (AFib) amyloidosis is a relatively uncommon renal disease associated with a small number of pathogenic fibrinogen Aα (FibA) variants; wild-type FibA normally does not result in amyloid deposition. Proteomics is now routinely used to identify the amyloid type in clinical samples, and we report here our algorithm for identification of FibA in amyloid.
Methods:
Proteomics data from 1001 Congo red-positive patient samples were examined using the Mascot search engine to interrogate the Swiss-Prot database and generate protein identity scores. An algorithm was applied to identify FibA as the amyloid protein based on Mascot scores. FibA variants were identified by appending the known amyloidogenic variant sequences to the Swiss-Prot database.
Results:
AFib amyloid was identified by proteomics in 64 renal samples based on the Mascot scores relative to other amyloid proteins, the presence of a pathogenic variant, and coverage of the p.449-621 sequence. Contamination by blood could be excluded from a comparison of the FibA score with that of the fibrinogen β and γ chains. The proteomics results were consistent with the clinical diagnosis. Four additional renal samples did not fulfill all the criteria using the algorithm but were adjudged as AFib amyloid based on a full assessment of the clinical and biochemical results.
Conclusion:
AFib amyloid can be identified reliably in glomerular amyloid by proteomics using a score-based algorithm. Proteomics data should be used as a guide to AFib diagnosis, with the results considered together with all available clinical and laboratory information.
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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