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Gout and AA-Amyloidosis: A Case-Based Review

BACKGROUND: AA-amyloidosis complicates many chronic infections and inflammatory diseases, including rheumatoid arthritis, ankylosing spondylitis, and psoriatic arthritis, but its relationship to gout is extremely rare. As it is unknown definitely what the pathophysiological connections between gout...

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Autores principales: Gromova, Margarita Aleksandrovna, Tsurko, Vladimir Viktorovich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Mediterranean Journal of Rheumatology (MJR) 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314881/
https://www.ncbi.nlm.nih.gov/pubmed/34386704
http://dx.doi.org/10.31138/mjr.32.1.74
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author Gromova, Margarita Aleksandrovna
Tsurko, Vladimir Viktorovich
author_facet Gromova, Margarita Aleksandrovna
Tsurko, Vladimir Viktorovich
author_sort Gromova, Margarita Aleksandrovna
collection PubMed
description BACKGROUND: AA-amyloidosis complicates many chronic infections and inflammatory diseases, including rheumatoid arthritis, ankylosing spondylitis, and psoriatic arthritis, but its relationship to gout is extremely rare. As it is unknown definitely what the pathophysiological connections between gout and amyloidosis are, treatment issues of the diseases are open for discussion. AIM: To establish a link between gout and AA-amyloidosis, and to improve the quality of treatment in patients suffering from gout and AA-amyloidosis. METHODS: We reviewed the English-language literature sources, searching not only for rare cases of the combination of gout and AA amyloidosis, but also detailed descriptions of the medical treatments for the two pathologies. RESULTS: By July 2020, we had identified 14 cases describing AA amyloidosis in patients with gout. Most of those patients had been suffering tophaceous gout for at least 10 years, and were prescribed various methods of treatment; however, not all patients took colchicine regularly. In some cases, therapy with allopurinol and colchicine was effective against attacks of gouty arthritis, although amyloidogenic inflammation was not controlled sufficiently. However, there were no cases that described in detail the successful treatment of both diseases. Besides those 14 patients described in literature, we examined one more patient with amyloidosis that is secondary to gout, in whom the protein of amyloid A (AA) had affected the kidneys, intestines, and adrenal glands. The patient has been successfully treated with the combination of canakinumab, prednisone, colchicine and allopurinol. CONCLUSION: Clinicians should be aware that patients may have atypical combinations of diseases like gout and amyloidosis. The obtained results help to explain some pathogenic processes associated with AA-amyloidosis. Further research is necessary to confirm the effectiveness of different treatment options such as lifestyle biologic agents or other medicines with anti-inflammatory properties.
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spelling pubmed-83148812021-08-11 Gout and AA-Amyloidosis: A Case-Based Review Gromova, Margarita Aleksandrovna Tsurko, Vladimir Viktorovich Mediterr J Rheumatol Case-Based Review BACKGROUND: AA-amyloidosis complicates many chronic infections and inflammatory diseases, including rheumatoid arthritis, ankylosing spondylitis, and psoriatic arthritis, but its relationship to gout is extremely rare. As it is unknown definitely what the pathophysiological connections between gout and amyloidosis are, treatment issues of the diseases are open for discussion. AIM: To establish a link between gout and AA-amyloidosis, and to improve the quality of treatment in patients suffering from gout and AA-amyloidosis. METHODS: We reviewed the English-language literature sources, searching not only for rare cases of the combination of gout and AA amyloidosis, but also detailed descriptions of the medical treatments for the two pathologies. RESULTS: By July 2020, we had identified 14 cases describing AA amyloidosis in patients with gout. Most of those patients had been suffering tophaceous gout for at least 10 years, and were prescribed various methods of treatment; however, not all patients took colchicine regularly. In some cases, therapy with allopurinol and colchicine was effective against attacks of gouty arthritis, although amyloidogenic inflammation was not controlled sufficiently. However, there were no cases that described in detail the successful treatment of both diseases. Besides those 14 patients described in literature, we examined one more patient with amyloidosis that is secondary to gout, in whom the protein of amyloid A (AA) had affected the kidneys, intestines, and adrenal glands. The patient has been successfully treated with the combination of canakinumab, prednisone, colchicine and allopurinol. CONCLUSION: Clinicians should be aware that patients may have atypical combinations of diseases like gout and amyloidosis. The obtained results help to explain some pathogenic processes associated with AA-amyloidosis. Further research is necessary to confirm the effectiveness of different treatment options such as lifestyle biologic agents or other medicines with anti-inflammatory properties. The Mediterranean Journal of Rheumatology (MJR) 2021-02-15 /pmc/articles/PMC8314881/ /pubmed/34386704 http://dx.doi.org/10.31138/mjr.32.1.74 Text en © 2021 The Mediterranean Journal of Rheumatology (MJR) https://creativecommons.org/licenses/by/4.0/This work is licensed under and Creative Commons Attribution-NonCommercial 4.0 International License.
spellingShingle Case-Based Review
Gromova, Margarita Aleksandrovna
Tsurko, Vladimir Viktorovich
Gout and AA-Amyloidosis: A Case-Based Review
title Gout and AA-Amyloidosis: A Case-Based Review
title_full Gout and AA-Amyloidosis: A Case-Based Review
title_fullStr Gout and AA-Amyloidosis: A Case-Based Review
title_full_unstemmed Gout and AA-Amyloidosis: A Case-Based Review
title_short Gout and AA-Amyloidosis: A Case-Based Review
title_sort gout and aa-amyloidosis: a case-based review
topic Case-Based Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314881/
https://www.ncbi.nlm.nih.gov/pubmed/34386704
http://dx.doi.org/10.31138/mjr.32.1.74
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