Lachmann HJ, Goodman HJ, Gilbertson JA, Gallimore JR, Sabin CA, Gillmore JD, et al. Natural history and outcome in systemic AA amyloidosis. N Engl J Med. 2007;356(23):2361–71. https://doi.org/10.1056/NEJMoa070265.
Article CAS PubMed Google Scholar
Papa R, Lachmann HJ. Secondary, AA, Amyloidosis. Rheum Dis Clin North Am. 2018;44(4):585–603. https://doi.org/10.1016/j.rdc.2018.06.004.
Hemminki K, Li X, Försti A, Sundquist J, Sundquist K. Incidence and survival in non-hereditary amyloidosis in Sweden. BMC Public Health. 2012;12:974. https://doi.org/10.1186/1471-2458-12-974.
Article PubMed PubMed Central Google Scholar
Aguirre MA, Boietti BR, Nucifora E, Sorroche PB, González Bernaldo de Quirós F, Giunta DH, et al. Incidence rate of amyloidosis in patients from a medical care program in Buenos Aires, Argentina: a prospective cohort. Amyloid. 2016;23(3):184–7. https://doi.org/10.1080/13506129.2016.1207626.
Karam S, Haidous M, Royal V, Leung N. Renal AA amyloidosis: presentation, diagnosis, and current therapeutic options: a review. Kidney Int. 2023;103(3):473–84. https://doi.org/10.1016/j.kint.2022.10.028.
Article CAS PubMed Google Scholar
Dasari S, Theis JD, Vrana JA, Rech KL, Dao LN, Howard MT, et al. Amyloid typing by mass spectrometry in clinical practice: a comprehensive review of 16,175 samples. Mayo Clin Proc. 2020;95(9):1852–64. https://doi.org/10.1016/j.mayocp.2020.06.029. A significant study addressing the clinical use of mass spectrometry in amyloidosis.
Article CAS PubMed Google Scholar
Real de Asúa D, Costa R, Galván JM, Filigheddu MT, Trujillo D, Cadiñanos J. Systemic AA amyloidosis: epidemiology, diagnosis, and management. Clin Epidemiol. 2014;6:369–77. https://doi.org/10.2147/clep.S39981.
Article PubMed PubMed Central Google Scholar
Bektas M, Koca N, Oguz E, Sari S, Dagci G, Ince B, et al. Characteristics and course of patients with AA amyloidosis: single centre experience with 174 patients from Turkey. Rheumatology (Oxford). 2024;63(2):319–28. https://doi.org/10.1093/rheumatology/kead465.
Delplanque M, Galicier L, Oziol E, Ducharme-Bénard S, Oksenhendler E, Buob D, et al. AA Amyloidosis secondary to primary immune deficiency: about 40 cases including 2 new French cases and a systematic literature review. J Allergy Clin Immunol Pract. 2021;9(2):745-52.e1. https://doi.org/10.1016/j.jaip.2020.09.023.
Article CAS PubMed Google Scholar
Lachmann HJ. Periodic fever syndromes. Best Pract Res Clin Rheumatol. 2017;31(4):596–609. https://doi.org/10.1016/j.berh.2017.12.001. A recent review of periodic fever syndromes that are known to result in AA amyloidosis if left untreated or undertreated.
Bunker D, Gorevic P. AA amyloidosis: Mount Sinai experience, 1997–2012. Mt Sinai J Med. 2012;79(6):749–56. https://doi.org/10.1002/msj.21342.
Blank N, Hegenbart U, Dietrich S, Brune M, Beimler J, Röcken C, et al. Obesity is a significant susceptibility factor for idiopathic AA amyloidosis. Amyloid. 2018;25(1):37–45. https://doi.org/10.1080/13506129.2018.1429391.
Article CAS PubMed Google Scholar
Westermark GT, Fändrich M, Westermark P. AA amyloidosis: pathogenesis and targeted therapy. Annu Rev Pathol. 2015;10:321–44. https://doi.org/10.1146/annurev-pathol-020712-163913.
Article CAS PubMed Google Scholar
Merlini G, Bellotti V. Molecular mechanisms of amyloidosis. N Engl J Med. 2003;349(6):583–96. https://doi.org/10.1056/NEJMra023144.
Article CAS PubMed Google Scholar
Benson MD, Buxbaum JN, Eisenberg DS, Merlini G, Saraiva MJM, Sekijima Y, et al. Amyloid nomenclature 2020: update and recommendations by the International Society of Amyloidosis (ISA) nomenclature committee. Amyloid. 2020;27(4):217–22. https://doi.org/10.1080/13506129.2020.1835263.
Article CAS PubMed Google Scholar
Sack GH Jr. Serum amyloid A (SAA) proteins. Subcell Biochem. 2020;94:421–36. https://doi.org/10.1007/978-3-030-41769-7_17.
Article CAS PubMed Google Scholar
Shah C, Hari-Dass R, Raynes JG. Serum amyloid A is an innate immune opsonin for Gram-negative bacteria. Blood. 2006;108(5):1751–7. https://doi.org/10.1182/blood-2005-11-011932.
Article CAS PubMed Google Scholar
Getz GS, Krishack PA, Reardon CA. Serum amyloid A and atherosclerosis. Curr Opin Lipidol. 2016;27(5):531–5. https://doi.org/10.1097/mol.0000000000000331.
Article CAS PubMed Google Scholar
Connolly M, Mullan RH, McCormick J, Matthews C, Sullivan O, Kennedy A, et al. Acute-phase serum amyloid A regulates tumor necrosis factor α and matrix turnover and predicts disease progression in patients with inflammatory arthritis before and after biologic therapy. Arthritis Rheum. 2012;64(4):1035–45. https://doi.org/10.1002/art.33455.
Article CAS PubMed Google Scholar
Malle E, Sodin-Semrl S, Kovacevic A. Serum amyloid A: an acute-phase protein involved in tumour pathogenesis. Cell Mol Life Sci. 2009;66(1):9–26. https://doi.org/10.1007/s00018-008-8321-x.
Article CAS PubMed PubMed Central Google Scholar
Uhlar CM, Whitehead AS. Serum amyloid A, the major vertebrate acute-phase reactant. Eur J Biochem. 1999;265(2):501–23. https://doi.org/10.1046/j.1432-1327.1999.00657.x.
Article CAS PubMed Google Scholar
Booth DR, Booth SE, Gillmore JD, Hawkins PN, Pepys MB. SAA1 alleles as risk factors in reactive systemic AA amyloidosis. Amyloid. 1998;5(4):262–5. https://doi.org/10.3109/13506129809007299.
Article CAS PubMed Google Scholar
Yilmaz E, Balci B, Kutlay S, Ozen S, Ertürk S, Oner A, et al. Analysis of the modifying effects of SAA1, SAA2 and TNF-alpha gene polymorphisms on development of amyloidosis in FMF patients. Turk J Pediatr. 2003;45(3):198–202.
Sikora J, Kmochová T, Mušálková D, Pohludka M, Přikryl P, Hartmannová H, et al. A mutation in the SAA1 promoter causes hereditary amyloid A amyloidosis. Kidney Int. 2022;101(2):349–59. https://doi.org/10.1016/j.kint.2021.09.007.
Article CAS PubMed Google Scholar
Baba S, Masago SA, Takahashi T, Kasama T, Sugimura H, Tsugane S, et al. A novel allelic variant of serum amyloid A, SAA1 gamma: genomic evidence, evolution, frequency, and implication as a risk factor for reactive systemic AA-amyloidosis. Hum Mol Genet. 1995;4(6):1083–7. https://doi.org/10.1093/hmg/4.6.1083.
Article CAS PubMed Google Scholar
van der Hilst JC, Yamada T, Op den Camp HJ, van der Meer JW, Drenth JP, Simon A. Increased susceptibility of serum amyloid A 1.1 to degradation by MMP-1: potential explanation for higher risk of type AA amyloidosis. Rheumatology (Oxford). 2008;47(11):1651–4. https://doi.org/10.1093/rheumatology/ken371.
Article CAS PubMed Google Scholar
Lu J, Yu Y, Zhu I, Cheng Y, Sun PD. Structural mechanism of serum amyloid A-mediated inflammatory amyloidosis. Proc Natl Acad Sci U S A. 2014;111(14):5189–94. https://doi.org/10.1073/pnas.1322357111.
Article CAS PubMed PubMed Central Google Scholar
Bansal A, Schmidt M, Rennegarbe M, Haupt C, Liberta F, Stecher S, et al. AA amyloid fibrils from diseased tissue are structurally different from in vitro formed SAA fibrils. Nat Commun. 2021;12(1):1013. https://doi.org/10.1038/s41467-021-21129-z.
Article CAS PubMed PubMed Central Google Scholar
Pepys MB. Amyloidosis. Annu Rev Med. 2006;57:223–41. https://doi.org/10.1146/annurev.med.57.121304.131243.
Article CAS PubMed Google Scholar
Gharibyan AL, Zamotin V, Yanamandra K, Moskaleva OS, Margulis BA, Kostanyan IA, et al. Lysozyme amyloid oligomers and fibrils induce cellular death via different apoptotic/necrotic pathways. J Mol Biol. 2007;365(5):1337–49. https://doi.org/10.1016/j.jmb.2006.10.101.
Article CAS PubMed Google Scholar
Migita K, Agematsu K, Masumoto J, Ida H, Honda S, Jiuchi Y, et al. The contribution of SAA1 polymorphisms to Familial Mediterranean fever susceptibility in the Japanese population. PLoS ONE. 2013;8(2):e55227. https://doi.org/10.1371/journal.pone.0055227.
Article CAS PubMed PubMed Central Google Scholar
Papa R, Doglio M, Lachmann HJ, Ozen S, Frenkel J, Simon A, et al. A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry. Orphanet J Rare Dis. 2017;12(1):167. https://doi.org/10.1186/s13023-017-0720-3.
Article PubMed PubMed Central Google Scholar
Atoyan S, Hayrapetyan H, Sarkisian T, Ben-Chetrit E. MEFV and SAA1 genotype associations with clinical features of familial Mediterranean fever and amyloidosis in Armenia. Clin Exp Rheumatol. 2016;34(6 Suppl 102):72–6.
Touitou I, Sarkisian T, Medlej-Hashim M, Tunca M, Livneh A, Cattan D, et al. Country as the primary risk factor for renal amyloidosis in familial Mediterranean fever. Arthritis Rheum. 2007;56(5):1706–12. https://doi.org/10.1002/art.22507.
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