Abstract
Aim. To investigate an influence of the currently changed etiologic structure of AA-amyloidosis on the diagnosis and treatment tactics.
Materials and methods. In 110 patients with АА-amyloidosis followed during full disease duration (1 month 29 years) etiology, clinical manyfestations and approaches to diagnose and treatment of AA-amyloidosis were evaluated. With ELISA levels of amyloid precursor acute phase inflammation reactant SAA and neutrophil activity marker S100A12 were measured.
Results. Among the most common causes of AA-amyloidosis at the present stage, in addition to RA (40.3%), a significant place is occupied by a group of diseases with a predominantly autoinflammatory mechanism (53.73%). To confirm the autoinflammatory mechanism of the predisposing disease it is recommended to study a highly sensitive parameter serum protein S100A12. An effective marker of the risk of AA-amyloidosis progression, especially in patients with subclinical activity of inflammatory disease, is a high level of production of amyloidogenic protein-a precursor of SAA.
Subject
General Medicine,Endocrinology, Diabetes and Metabolism,History,Family Practice
Reference13 articles.
1. Amyloid fibril proteins and amyloidosis: chemical identification and clinical classification International Society of Amyloidosis 2016 Nomenclature Guidelines
2. Серов В.В., Шамов И.А. Амилоидоз. М.: Медицина, 1977 [Serov VV, Shamov IA. Amyloidosis. Moscow: Medicine, 1977 (in Russian)].
3. Мухин Н.А. Амилоидоз почек: вопросы клиники и патогенеза: автореф. дис. … д-ра мед. наук. М., 1981; с. 41 [Mukhin NA. Amiloidoz pochek: voprosy kliniki i patogeneza: avtoref. dis. … d-ra med. nauk. Moscow: 1981; p. 41 (in Russian)].
4. Natural History and Outcome in Systemic AA Amyloidosis
5. Systemic Amyloidosis in England: an epidemiological study
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