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Epidemiology and risk factors associated with avascular necrosis in patients with autoimmune diseases: a nationwide study

BACKGROUND/AIMS: Avascular necrosis (AVN) is a clinical condition characterized by the death of bone components due to interruption in the blood supply. This study aimed to investigate the epidemiology and determine the risk factors for AVN in patients with autoimmune diseases. METHODS: We conducted...

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Autores principales: Tsai, Hsin-Lin, Chang, Jei-Wen, Lu, Jen-Her, Liu, Chin-Su
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271726/
https://www.ncbi.nlm.nih.gov/pubmed/35236014
http://dx.doi.org/10.3904/kjim.2020.098
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author Tsai, Hsin-Lin
Chang, Jei-Wen
Lu, Jen-Her
Liu, Chin-Su
author_facet Tsai, Hsin-Lin
Chang, Jei-Wen
Lu, Jen-Her
Liu, Chin-Su
author_sort Tsai, Hsin-Lin
collection PubMed
description BACKGROUND/AIMS: Avascular necrosis (AVN) is a clinical condition characterized by the death of bone components due to interruption in the blood supply. This study aimed to investigate the epidemiology and determine the risk factors for AVN in patients with autoimmune diseases. METHODS: We conducted a population-based retrospective cohort analysis using claims data from the Taiwan National Health Insurance Research Database. A total of 49,636 patients with autoimmune diseases between January 1, 2005 and December 31, 2013 were included. Cox regression analysis was used to identify associated risk factors for the development of AVN. RESULTS: A total of 490/49,636 patients (1.0%) developed symptomatic AVN. The systemic lupus erythematosus patients had a higher risk of AVN compared to other autoimmune diseases. AVN was positively correlated with male sex (p < 0.001), alcoholism (p < 0.001), mean daily prednisolone dosage 7.51 to 30 mg (p < 0.001) and > 30 mg (p < 0.001), and total cumulative prednisolone dose 0 g to 5 g (p = 0.002). However, AVN was inversely correlated with cumulative duration of hydroxychloroquine exposure > 0.6 years (p < 0.001). CONCLUSIONS: Male sex, systemic lupus erythematosus, alcoholism, mean daily corticosteroid > 7.5 mg and a total cumulative dose of corticosteroid 0 to 5 g were independently associated with the development of AVN in autoimmune patients. While hydroxychloroquine use > 0.6 years conferred significant protection against the development of AVN. Clinicians should regularly assess patients with risk factors to enable the early diagnosis of AVN.
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spelling pubmed-92717262022-07-13 Epidemiology and risk factors associated with avascular necrosis in patients with autoimmune diseases: a nationwide study Tsai, Hsin-Lin Chang, Jei-Wen Lu, Jen-Her Liu, Chin-Su Korean J Intern Med Original Article BACKGROUND/AIMS: Avascular necrosis (AVN) is a clinical condition characterized by the death of bone components due to interruption in the blood supply. This study aimed to investigate the epidemiology and determine the risk factors for AVN in patients with autoimmune diseases. METHODS: We conducted a population-based retrospective cohort analysis using claims data from the Taiwan National Health Insurance Research Database. A total of 49,636 patients with autoimmune diseases between January 1, 2005 and December 31, 2013 were included. Cox regression analysis was used to identify associated risk factors for the development of AVN. RESULTS: A total of 490/49,636 patients (1.0%) developed symptomatic AVN. The systemic lupus erythematosus patients had a higher risk of AVN compared to other autoimmune diseases. AVN was positively correlated with male sex (p < 0.001), alcoholism (p < 0.001), mean daily prednisolone dosage 7.51 to 30 mg (p < 0.001) and > 30 mg (p < 0.001), and total cumulative prednisolone dose 0 g to 5 g (p = 0.002). However, AVN was inversely correlated with cumulative duration of hydroxychloroquine exposure > 0.6 years (p < 0.001). CONCLUSIONS: Male sex, systemic lupus erythematosus, alcoholism, mean daily corticosteroid > 7.5 mg and a total cumulative dose of corticosteroid 0 to 5 g were independently associated with the development of AVN in autoimmune patients. While hydroxychloroquine use > 0.6 years conferred significant protection against the development of AVN. Clinicians should regularly assess patients with risk factors to enable the early diagnosis of AVN. Korean Association of Internal Medicine 2022-07 2022-03-03 /pmc/articles/PMC9271726/ /pubmed/35236014 http://dx.doi.org/10.3904/kjim.2020.098 Text en Copyright © 2022 The Korean Association of Internal Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Tsai, Hsin-Lin
Chang, Jei-Wen
Lu, Jen-Her
Liu, Chin-Su
Epidemiology and risk factors associated with avascular necrosis in patients with autoimmune diseases: a nationwide study
title Epidemiology and risk factors associated with avascular necrosis in patients with autoimmune diseases: a nationwide study
title_full Epidemiology and risk factors associated with avascular necrosis in patients with autoimmune diseases: a nationwide study
title_fullStr Epidemiology and risk factors associated with avascular necrosis in patients with autoimmune diseases: a nationwide study
title_full_unstemmed Epidemiology and risk factors associated with avascular necrosis in patients with autoimmune diseases: a nationwide study
title_short Epidemiology and risk factors associated with avascular necrosis in patients with autoimmune diseases: a nationwide study
title_sort epidemiology and risk factors associated with avascular necrosis in patients with autoimmune diseases: a nationwide study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271726/
https://www.ncbi.nlm.nih.gov/pubmed/35236014
http://dx.doi.org/10.3904/kjim.2020.098
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