Secondary, AA, Amyloidosis

Key Information
Source
Rheumatic Diseases Clinics of North America
Year
2018
summary/abstract

Secondary, AA, amyloidosis is a rare systemic complication that can develop in any long-term inflammatory disorder, and is characterized by the extracellular deposition of fibrils derived from serum amyloid A (SAA) protein. SAA is an acute-phase reactant synthetized largely by hepatocytes under the transcriptional regulation of proinflammatory cytokines. The kidney is the major involved organ with proteinuria as first clinical manifestation; renal biopsy is the commonest diagnostic investigation.

Targeted anti-inflammatory treatment promotes normalization of circulating SAA levels preventing amyloid deposition and renal damage. Novel therapies aimed at promoting clearance of existing amyloid deposits soon may be an effective treatment approach.

Abstract Source
https://www.ncbi.nlm.nih.gov/pubmed/30274625
DOI
10.1016/j.rdc.2018.06.004
Authors
Papa R, Lachmann HJ
Organisation
University of Genoa, Italy; University College Medical School, UK