000 02466nam a22003617a 4500
008 240723s20242024 xxu||||| |||| 00| 0 eng d
022 _a1523-3774
024 _a10.1007/s11926-024-01147-8 [pii]
040 _aOvid MEDLINE(R)
099 _a38568326
245 _aAA Amyloidosis: A Contemporary View. [Review]
251 _aCurrent Rheumatology Reports. 2024 Apr 03
252 _aCurr Rheumatol Rep. 2024 Apr 03
253 _aCurrent rheumatology reports
260 _c2024
260 _p2024 Apr 03
265 _saheadofprint
265 _tPublisher
266 _d2024-07-23
520 _aPURPOSE OF REVIEW: Amyloid A (AA) amyloidosis is an organ- or life-threatening complication of chronic inflammatory disorders. Here, we review the epidemiology, causes, pathogenesis, clinical features, and diagnostic and therapeutic strategies of AA amyloidosis.
520 _aRECENT FINDINGS: The incidence of AA amyloidosis has declined due to better treatment of the underlying diseases. Histopathological examination is the gold standard of diagnosis, but magnetic resonance imaging can be used to detect cardiac involvement. There is yet no treatment option for the clearance of amyloid fibril deposits; therefore, the management strategy primarily aims to reduce serum amyloid A protein. Anti-inflammatory biologic agents have drastically expanded our therapeutic armamentarium. Kidney transplantation is preferred in patients with kidney failure, and the recurrence of amyloidosis in the allograft has become rare as transplant recipients have started to benefit from the new agents. The management of AA amyloidosis has been considerably changed over the recent years due to the novel therapeutic options aiming to control inflammatory activity. New agents capable of clearing amyloid deposits from the tissues are still needed. Copyright © 2024. The Author(s).
546 _aEnglish
650 _zAutomated
650 _aIN PROCESS -- NOT YET INDEXED
656 _aInternal Medicine Residency
656 _aMedStar Georgetown University Hospital/MedStar Washington Hospital Center
657 _aJournal Article
657 _aReview
700 _aDoumas, Stavros
_bMGUH
_cInternal Medicine Residency
_dMD
790 _aMirioglu S, Uludag O, Hurdogan O, Kumru G, Berke I, Doumas SA, Frangou E, Gul A
856 _uhttps://dx.doi.org/10.1007/s11926-024-01147-8
_zhttps://dx.doi.org/10.1007/s11926-024-01147-8
942 _cART
_dArticle
999 _c14194
_d14194