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Course and Prognosis of AA Amyloidosis in Patients with Psoriatic Arthritis: Report of Three Cases from a Single Center Cohort and Review of the Literature

OBJECTIVE: Herein, we aimed to evaluate the frequency and clinical features of AA amyloidosis in patients with PsA followed up in our tertiary referral clinic. METHODS: We retrospectively evaluated PsA patients classified according to CASPAR classification criteria followed-up in our tertiary referr...

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Autores principales: Bektaş, Murat, Koca, Nevzat, Ince, Burak, Yalçınkaya, Yasemin, Esen, Bahar Artım, Öcal, M. Lale, Gül, Ahmet, Inanç, Murat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Mediterranean Journal of Rheumatology (MJR) 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450196/
https://www.ncbi.nlm.nih.gov/pubmed/36128216
http://dx.doi.org/10.31138/mjr.33.2.185
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author Bektaş, Murat
Koca, Nevzat
Ince, Burak
Yalçınkaya, Yasemin
Esen, Bahar Artım
Öcal, M. Lale
Gül, Ahmet
Inanç, Murat
author_facet Bektaş, Murat
Koca, Nevzat
Ince, Burak
Yalçınkaya, Yasemin
Esen, Bahar Artım
Öcal, M. Lale
Gül, Ahmet
Inanç, Murat
author_sort Bektaş, Murat
collection PubMed
description OBJECTIVE: Herein, we aimed to evaluate the frequency and clinical features of AA amyloidosis in patients with PsA followed up in our tertiary referral clinic. METHODS: We retrospectively evaluated PsA patients classified according to CASPAR classification criteria followed-up in our tertiary referral clinic for AA amyloidosis. The literature search was also done by three independent researchers using the keywords “psoriatic arthritis AND amyloidosis”, “spondyloarthritis AND amyloidosis”, “AA amyloidosis”, “secondary amyloidosis”. RESULTS AND CONCLUSIONS: A total of 253 patients were included into the analysis. Two thirds of (n=162; 64%) the patients were women, and the mean age of the patients was 50.6 ± 13.4 (range, 20–90). We identified three patients with AA amyloidosis in 253 patients with PsA (1.2 %). The frequency of PsA-related amyloidosis in our AA amyloidosis cohort (n=165) was 1.8 %. Literature search revealed only a retrospective cohort study and 17 case reports, and we analysed these 31 cases. Nearly half of the cases were male, mean age of the patients was 50.7±15.3 and mean age of amyloidosis diagnosis was 47.2±16.7 years. Most of these patients had both polyarticular and axial involvement (81.3%). AA amyloidosis is a rare in patients with PsA. It should be kept in mind that patients with PsA who have not received appropriate treatment for a long time and/or have refractory disease may develop AA amyloidosis.
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spelling pubmed-94501962022-09-19 Course and Prognosis of AA Amyloidosis in Patients with Psoriatic Arthritis: Report of Three Cases from a Single Center Cohort and Review of the Literature Bektaş, Murat Koca, Nevzat Ince, Burak Yalçınkaya, Yasemin Esen, Bahar Artım Öcal, M. Lale Gül, Ahmet Inanç, Murat Mediterr J Rheumatol Review OBJECTIVE: Herein, we aimed to evaluate the frequency and clinical features of AA amyloidosis in patients with PsA followed up in our tertiary referral clinic. METHODS: We retrospectively evaluated PsA patients classified according to CASPAR classification criteria followed-up in our tertiary referral clinic for AA amyloidosis. The literature search was also done by three independent researchers using the keywords “psoriatic arthritis AND amyloidosis”, “spondyloarthritis AND amyloidosis”, “AA amyloidosis”, “secondary amyloidosis”. RESULTS AND CONCLUSIONS: A total of 253 patients were included into the analysis. Two thirds of (n=162; 64%) the patients were women, and the mean age of the patients was 50.6 ± 13.4 (range, 20–90). We identified three patients with AA amyloidosis in 253 patients with PsA (1.2 %). The frequency of PsA-related amyloidosis in our AA amyloidosis cohort (n=165) was 1.8 %. Literature search revealed only a retrospective cohort study and 17 case reports, and we analysed these 31 cases. Nearly half of the cases were male, mean age of the patients was 50.7±15.3 and mean age of amyloidosis diagnosis was 47.2±16.7 years. Most of these patients had both polyarticular and axial involvement (81.3%). AA amyloidosis is a rare in patients with PsA. It should be kept in mind that patients with PsA who have not received appropriate treatment for a long time and/or have refractory disease may develop AA amyloidosis. The Mediterranean Journal of Rheumatology (MJR) 2022-06-30 /pmc/articles/PMC9450196/ /pubmed/36128216 http://dx.doi.org/10.31138/mjr.33.2.185 Text en © 2022 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 Review
Bektaş, Murat
Koca, Nevzat
Ince, Burak
Yalçınkaya, Yasemin
Esen, Bahar Artım
Öcal, M. Lale
Gül, Ahmet
Inanç, Murat
Course and Prognosis of AA Amyloidosis in Patients with Psoriatic Arthritis: Report of Three Cases from a Single Center Cohort and Review of the Literature
title Course and Prognosis of AA Amyloidosis in Patients with Psoriatic Arthritis: Report of Three Cases from a Single Center Cohort and Review of the Literature
title_full Course and Prognosis of AA Amyloidosis in Patients with Psoriatic Arthritis: Report of Three Cases from a Single Center Cohort and Review of the Literature
title_fullStr Course and Prognosis of AA Amyloidosis in Patients with Psoriatic Arthritis: Report of Three Cases from a Single Center Cohort and Review of the Literature
title_full_unstemmed Course and Prognosis of AA Amyloidosis in Patients with Psoriatic Arthritis: Report of Three Cases from a Single Center Cohort and Review of the Literature
title_short Course and Prognosis of AA Amyloidosis in Patients with Psoriatic Arthritis: Report of Three Cases from a Single Center Cohort and Review of the Literature
title_sort course and prognosis of aa amyloidosis in patients with psoriatic arthritis: report of three cases from a single center cohort and review of the literature
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450196/
https://www.ncbi.nlm.nih.gov/pubmed/36128216
http://dx.doi.org/10.31138/mjr.33.2.185
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