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Post-COVID-19 arthritis: is it hyperinflammation or autoimmunity?

BACKGROUND: Various musculoskeletal and autoimmune manifestations have been described in patients with coronavirus disease 2019 (COVID-19). OBJECTIVES: This study aims to investigate the prevalence and etiology of arthritis in post-COVID Egyptian patients. METHODS: We included 100 post-COVID Egyptia...

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Autores principales: Taha, Sara Ibrahim, Samaan, Sara Farid, Ibrahim, Rehab Ali, El-Sehsah, Eman Mousa, Youssef, Mariam Karam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Libbey Eurotext 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831681/
https://www.ncbi.nlm.nih.gov/pubmed/35118946
http://dx.doi.org/10.1684/ecn.2021.0471
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author Taha, Sara Ibrahim
Samaan, Sara Farid
Ibrahim, Rehab Ali
El-Sehsah, Eman Mousa
Youssef, Mariam Karam
author_facet Taha, Sara Ibrahim
Samaan, Sara Farid
Ibrahim, Rehab Ali
El-Sehsah, Eman Mousa
Youssef, Mariam Karam
author_sort Taha, Sara Ibrahim
collection PubMed
description BACKGROUND: Various musculoskeletal and autoimmune manifestations have been described in patients with coronavirus disease 2019 (COVID-19). OBJECTIVES: This study aims to investigate the prevalence and etiology of arthritis in post-COVID Egyptian patients. METHODS: We included 100 post-COVID Egyptian patients who recovered 6 months ago and assessed several inflammatory and autoimmune markers. RESULTS: The prevalence of post-COVID arthritis was 37%. Ankle, knee, and wrist were the most commonly affected joints. Old age (P = 0.010), smoking (P = 0.001), and arthralgia (P = 0.049) were all linked with post-COVID arthritis. Levels of pretreatment (baseline) interleukin (IL)-6 (46.41 ± 3.67 vs. 24.03 ± 2.46; P = 0.001), as well as 6-month post-COVID C-reactive protein (CRP; 98.49 ± 67.55 vs. 54.32 ± 65.73; P = 0.002), and erythrocyte sedimentation rate (ESR; 109.08 ± 174.91 vs. 58.35 ± 37.87; P = 0.029) were significantly higher in patients with arthritis compared to those without. On the other hand, complement C3 (P = 0.558) and C4 (P = 0.192), anti-nuclear antibodies (P = 0.709), and anti-cyclic citrullinated peptides (anti-CCP; P = 0.855) did not show significant differences. Only pretreatment IL-6 level was the significant single predictor of post-COVID arthritis with an odds ratio (95% confidence interval) of 3.988 (1.460–10.892) and a P-value of 0.007. CONCLUSION: The strong association observed with inflammatory markers (ESR and CRP) and the insignificant association with serologic markers of autoimmunity (ANA and anti-CCP) in our study support the notion that the underlying mechanism of post-COVID-19 arthritis is primarily due to the hyperinflammatory process associated with COVID-19 infection, and not the result of an autoimmune reaction. IL-6 levels before therapy can predict post-COVID arthritis allowing for early management.
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spelling pubmed-88316812022-02-18 Post-COVID-19 arthritis: is it hyperinflammation or autoimmunity? Taha, Sara Ibrahim Samaan, Sara Farid Ibrahim, Rehab Ali El-Sehsah, Eman Mousa Youssef, Mariam Karam Eur Cytokine Netw Research Article BACKGROUND: Various musculoskeletal and autoimmune manifestations have been described in patients with coronavirus disease 2019 (COVID-19). OBJECTIVES: This study aims to investigate the prevalence and etiology of arthritis in post-COVID Egyptian patients. METHODS: We included 100 post-COVID Egyptian patients who recovered 6 months ago and assessed several inflammatory and autoimmune markers. RESULTS: The prevalence of post-COVID arthritis was 37%. Ankle, knee, and wrist were the most commonly affected joints. Old age (P = 0.010), smoking (P = 0.001), and arthralgia (P = 0.049) were all linked with post-COVID arthritis. Levels of pretreatment (baseline) interleukin (IL)-6 (46.41 ± 3.67 vs. 24.03 ± 2.46; P = 0.001), as well as 6-month post-COVID C-reactive protein (CRP; 98.49 ± 67.55 vs. 54.32 ± 65.73; P = 0.002), and erythrocyte sedimentation rate (ESR; 109.08 ± 174.91 vs. 58.35 ± 37.87; P = 0.029) were significantly higher in patients with arthritis compared to those without. On the other hand, complement C3 (P = 0.558) and C4 (P = 0.192), anti-nuclear antibodies (P = 0.709), and anti-cyclic citrullinated peptides (anti-CCP; P = 0.855) did not show significant differences. Only pretreatment IL-6 level was the significant single predictor of post-COVID arthritis with an odds ratio (95% confidence interval) of 3.988 (1.460–10.892) and a P-value of 0.007. CONCLUSION: The strong association observed with inflammatory markers (ESR and CRP) and the insignificant association with serologic markers of autoimmunity (ANA and anti-CCP) in our study support the notion that the underlying mechanism of post-COVID-19 arthritis is primarily due to the hyperinflammatory process associated with COVID-19 infection, and not the result of an autoimmune reaction. IL-6 levels before therapy can predict post-COVID arthritis allowing for early management. John Libbey Eurotext 2022-02-11 2021 /pmc/articles/PMC8831681/ /pubmed/35118946 http://dx.doi.org/10.1684/ecn.2021.0471 Text en © JLE/Springer 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Research Article
Taha, Sara Ibrahim
Samaan, Sara Farid
Ibrahim, Rehab Ali
El-Sehsah, Eman Mousa
Youssef, Mariam Karam
Post-COVID-19 arthritis: is it hyperinflammation or autoimmunity?
title Post-COVID-19 arthritis: is it hyperinflammation or autoimmunity?
title_full Post-COVID-19 arthritis: is it hyperinflammation or autoimmunity?
title_fullStr Post-COVID-19 arthritis: is it hyperinflammation or autoimmunity?
title_full_unstemmed Post-COVID-19 arthritis: is it hyperinflammation or autoimmunity?
title_short Post-COVID-19 arthritis: is it hyperinflammation or autoimmunity?
title_sort post-covid-19 arthritis: is it hyperinflammation or autoimmunity?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831681/
https://www.ncbi.nlm.nih.gov/pubmed/35118946
http://dx.doi.org/10.1684/ecn.2021.0471
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