# Influence of SARS-CoV-2 reinfection on bone health in the population over 55 years old in Beijing, China: a cross-sectional study

**Authors:** Qian Qiu, Tong Wu, Yuyong Jiang, Zimeng Shang, Wanxin Shi, Xiaohui Zhang, Xu Han, Zhiyun Yang, Xieyuan Jiang, Xiuying Liu

PMC · DOI: 10.3389/fpubh.2026.1758835 · Frontiers in Public Health · 2026-02-19

## TL;DR

This study finds that older adults in Beijing who experienced SARS-CoV-2 reinfection had a significantly higher risk of osteoporosis compared to those with a single infection.

## Contribution

The study is the first to demonstrate a strong association between SARS-CoV-2 reinfection and increased osteoporosis risk in individuals over 55 years old.

## Key findings

- Individuals with SARS-CoV-2 reinfection had a 48.3% prevalence of osteoporosis compared to 17.3% in those with a single infection.
- Reinfection was significantly linked to higher osteoporosis rates at the hip and lumbar spine after adjusting for confounding factors.
- The odds ratio for osteoporosis in reinfection cases was 3.08, indicating a strong independent association.

## Abstract

Despite the global prevalence of SARS-CoV-2 reinfection, relatively little is known regarding its association with osteoporosis in older adults. This study investigated the potential impact of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection on bone health or osteoporosis risk in adults aged 55 years and older in Beijing, China, while also exploring additional factors that may influence this association.

This cross-sectional study was conducted at Beijing Ditan Hospital, Beijing, China, between August and December 2024. Patients aged ≥ 55 years with SARS-CoV-2 infections were included. Data on demographic characteristics, lifestyle habits, diet, serum contents of 25-hydroxyvitamin D (25-OH-VD), and other potential risk factors for osteoporosis were collected through structured questionnaires. Bone mineral density (BMD) was assessed using dual-energy X-ray absorptiometry (DXA). To identify the variables associated with osteoporosis, logistic regression analysis was employed.

Three hundred and eighty-eight patients were enrolled, comprising 272 individuals with a single SARS-CoV-2 infection and 116 with two or more infections. The results revealed that individuals who had reinfection revealed a considerably higher prevalence of osteoporosis (48.3% vs. 17.3%, p < 0.0001). This trend was consistent across different skeletal sites: 33.6% vs. 7.4% at the left hip, 37.9% vs. 5.5% at the right hip (p < 0.0001), and 30.2% vs. 12.9% at the lumbar spine (L1–L4) (p < 0.0001). SARS-CoV-2 reinfection remained substantially associated with osteoporosis after controlling for con-founding variables, with an OR of 3.08 (95% CI: 1.696–5.593).

In summary, the risk of osteoporosis among individuals with SARS-CoV-2 reinfection should be carefully monitored, and greater emphasis should be placed on early, individualized prevention and treatment strategies.

## Linked entities

- **Chemicals:** 25-hydroxyvitamin D (PubChem CID 5353325)
- **Diseases:** osteoporosis (MONDO:0005298)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** TNFRSF11B (TNF receptor superfamily member 11b) [NCBI Gene 4982] {aka OCIF, OPG, PDB5, TR1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, TNFSF11 (TNF superfamily member 11) [NCBI Gene 8600] {aka CD254, ODF, OPGL, OPTB2, RANKL, TNLG6B}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** thoracic wedge deformities (MESH:C537350), Vitamin D deficiency (MESH:D014808), skeletal abnormalities (MESH:D009139), bone metabolism disorders (MESH:D001851), spinal stenosis (MESH:D013130), 25-OH-VD deficiency (MESH:C565301), secondary hyperparathyroidism (MESH:D006962), multiple myeloma (MESH:D009101), osteonecrosis (MESH:D010020), malignancies (MESH:D009369), fracture (MESH:D050723), parathyroid, gonadal, adrenal, or thyroid diseases (MESH:D010279), degenerative changes (MESH:D019636), inflammation (MESH:D007249), storm (MESH:C566109), neuromuscular diseases (MESH:D009468), estrogen deficiency (MESH:D056828), musculoskeletal health (MESH:D009140), bone loss (MESH:D001847), Osteoporosis (MESH:D010024), digestive or renal disorders (MESH:D004066), infected (MESH:D007239), immune-related diseases (MESH:D007154), COVID-19 (MESH:D000086382), endocrine disorders (MESH:D004700), lumbar scoliosis (MESH:D012600), rheumatoid arthritis (MESH:D001172)
- **Chemicals:** vitamin D (MESH:D014807), Calcium (MESH:D002118), 25-hydroxyvitamin D (MESH:C104450), 25-OH-VD (-)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12960145/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12960145/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960145/full.md

---
Source: https://tomesphere.com/paper/PMC12960145