# The effects on clinical characteristics, potential factors and outcomes in SAPHO patients during the COVID-19 epidemic

**Authors:** Minhui Su, Haixu Jiang, Shengyan Liu, Pengfei Shen, Dinghua Zhou, Keqiang Zhu, Zixi Huang, Chen Li, Meiling Li

PMC · DOI: 10.3389/fmed.2025.1580989 · Frontiers in Medicine · 2025-07-16

## TL;DR

This study examines how the COVID-19 pandemic affected SAPHO syndrome patients, finding that JAK inhibitors may protect against severe symptoms while tonsillectomy might increase risks.

## Contribution

The study identifies JAK inhibitors as potentially protective and highlights tonsillectomy as a risk factor for adverse outcomes in SAPHO patients during the pandemic.

## Key findings

- Infected SAPHO patients had higher disease activity, but JAK inhibitor use was lower in infected cases.
- Tonsillectomized patients showed a higher prevalence of pneumonia during the pandemic.
- JAK inhibitors were inversely correlated with disease activity and showed protective effects against new symptoms.

## Abstract

The coronavirus disease (COVID-19) pandemic has potentially impacted the care of patients with rheumatic diseases, including Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis (SAPHO) syndrome. We investigates the effects on clinical characteristics, potential factors, and outcomes in SAPHO patients during the COVID-19 pandemic.

SAPHO patients were recruited for this cross-sectional study from Fangshan Hospital of Beijing University of Chinese Medicine. In total, 375 patients (mean age, 47.5 years, 72.53% females) were asked about demographic data, disease status, current treatments, and clinical manifestations during the epidemic, and potential relationships were analyzed.

Among 375 included patients, 329 were infected with coronavirus 2019. Compared with non-infected patients, infected ones were more likely to have higher disease activity (p = 0.006). However, Janus kinase (JAK) inhibitor use was lower in detected COVID-19 cases than in non-infected cases in our cohort. Disease symptoms during COVID-19 were more commonly present in the non-JAK group than JAK groups, including rhinorrhea (p = 0.030), nasal congestion (p = 0.023), sore throat (p = 0.042), pneumonia (p = 0.044), headache (p = 0.023), and prevalence of palpitation (p = 0.015). In this study, 29 participants underwent tonsillectomy. Tonsillectomized patients showed a significantly higher prevalence of pneumonia than patients who did not undergo tonsillectomy (p = 0.009). The associated effect factors were displayed in the case of previous tonsillectomy using multivariate analysis and Firth’s penalized likelihood. JAK inhibitor use (p = 0.025) and pneumonia (p = 0.011) were more likely to develop in patients with a history of tonsillectomy.

Disease activity was inversely correlated with JAK inhibitor use in SAPHO patients with COVID-19 during the pandemic. Thus, JAK antagonists have protective effects on SAPHO patients with infections and can significantly mitigate new clinical crown symptoms. However, there was a significant negative correlation between tonsillectomy and the prevalence of SAPHO with COVID-19, which demonstrates that tonsillectomy may be associated with an increased risk of COVID-19 adverse outcomes, especially in cases of taste disorders and pneumonia.

## Linked entities

- **Diseases:** SAPHO syndrome (MONDO:0019266), pneumonia (MONDO:0005249)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** diarrhea (MESH:D003967), sore throat (MESH:D010612), dysgeusia (MESH:D004408), COVID-19 (MESH:D000086382), rheumatoid arthritis (MESH:D001172), headache (MESH:D006261), autoimmune conditions (MESH:D001327), nasal congestion (MESH:D009668), bone and skin symptoms (MESH:D001847), shortness of breath (MESH:D004417), dizziness (MESH:D004244), tonsillitis (MESH:D014069), nausea (MESH:D009325), appetite disturbance (MESH:D001068), cognitive impairment (MESH:D003072), depression (MESH:D003866), Acne, Pustulosis, Hyperostosis, and Osteitis (SAPHO) syndrome (MESH:D010000), rheumatic diseases (MESH:D012216), rhinorrhea (MESH:D012818), coronavirus disease (MESH:D018352), cough (MESH:D003371), myalgia (MESH:D063806), anxiety (MESH:D001007), viral infections (MESH:D014777), allergy (MESH:D004342), Pneumonia (MESH:D011014), deaths (MESH:D003643), COPD (MESH:D029424), coagulation abnormalities (MESH:D001778), taste disorders (MESH:D013651), inflammatory (MESH:D007249), insomnia (MESH:D007319), infected (MESH:D007239), Synovitis (MESH:D013585), chills (MESH:D023341), palpitation (MESH:D006331), arthralgia (MESH:D018771), fever (MESH:D005334)
- **Chemicals:** CS (MESH:D002586), Zn (MESH:D015032), tofacitinib (MESH:C479163), JAK blocker (-), alcohol (MESH:D000438), Infliximab (MESH:D000069285), Adalimumab (MESH:D000068879)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12307422/full.md

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Source: https://tomesphere.com/paper/PMC12307422