# Sarcopenia as a Potential Risk Factor for Denosumab-Related Osteonecrosis of the Jaw in Asian Prostate Cancer Patients with Bone Metastases

**Authors:** Shinobu Mizushima, Daisuke Watanabe, Kazuki Yanagida, Norikazu Kawae, Kashia Goto, Tatsuya Takagi, Hajime Kajihara, Akio Mizushima

PMC · DOI: 10.3390/diagnostics15202635 · Diagnostics · 2025-10-19

## TL;DR

This study suggests that low muscle mass (sarcopenia) may increase the risk of jaw bone death in Asian prostate cancer patients taking denosumab for bone metastases.

## Contribution

The study identifies sarcopenia as a novel risk factor for DRONJ in prostate cancer patients receiving denosumab.

## Key findings

- Sarcopenia was significantly more common in patients who developed DRONJ.
- Inflammatory biomarker NLR correlated with reduced muscle mass but not directly with DRONJ.
- Body composition factors like fat distribution and BMI were not significant predictors of DRONJ.

## Abstract

Background/Objectives: Denosumab-related osteonecrosis of the jaw (DRONJ) is a serious complication in patients receiving long-term antiresorptive therapy for bone metastases from prostate cancer. While established risk factors include invasive dental procedures and poor oral health, the role of body composition, with a particular focus on sarcopenia and inflammatory biomarkers, remains unclear. This study aims to evaluate the association between skeletal muscle mass, fat distribution, and systemic inflammatory biomarkers with DRONJ risk in Asian prostate cancer patients with bone metastases. Methods: This retrospective study reviewed 64 patients who received denosumab between 2014 and 2023. Baseline CT scans were used to measure total psoas muscle index (TPI), visceral fat area (VFA), subcutaneous fat area (SFA), and body mass index (BMI). Neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) were calculated from blood counts. Group comparisons used the Wilcoxon rank-sum or chi-squared test, and correlations were assessed using Spearman’s coefficient. Results: Twelve patients (18.8%) developed DRONJ, with a mean onset time of 20.3 months. The prevalence of sarcopenia was significantly higher in the DRONJ group compared to the non-DRONJ group (p = 0.0331). VFA, SFA, BMI, diabetes, and visceral obesity were not significant predictors. NLR, but not PLR, showed a significant negative correlation with TPI (ρ = −0.2487, p = 0.0475), but no direct association with DRONJ, suggesting an indirect effect via sarcopenia. Conclusions: Sarcopenia may be an independent risk factor for DRONJ. Inflammatory biomarkers, particularly NLR, may contribute indirectly through reduced muscle mass. Body composition assessment may improve DRONJ risk stratification.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159), osteonecrosis of the jaw (MONDO:0018378), diabetes (MONDO:0005015)

## Full-text entities

- **Diseases:** Sarcopenia (MESH:D055948), diabetes (MESH:D003920), Bone Metastases (MESH:D009362), Inflammatory (MESH:D007249), reduced muscle mass (MESH:D009135), Prostate Cancer (MESH:D011471), visceral obesity (MESH:D056128), Osteonecrosis of the Jaw (MESH:D059266)
- **Chemicals:** Denosumab (MESH:D000069448)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12563517/full.md

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Source: https://tomesphere.com/paper/PMC12563517