# Comparative efficacy and safety of anti-osteoporotic therapies for kidney transplant recipients: a systematic review and network meta-analysis

**Authors:** Xiaopei Liu, Xingyao Li, Yanhong Zhao, Qi Gao, Yuan Xue, Zhongheng Wu, Xingmin Shi, Xili Wu

PMC · DOI: 10.3389/fendo.2025.1689233 · Frontiers in Endocrinology · 2025-11-03

## TL;DR

This study compares the effectiveness and safety of osteoporosis treatments in kidney transplant patients, finding denosumab most effective for spine bone density.

## Contribution

The study provides a network meta-analysis comparing anti-osteoporotic therapies specifically for kidney transplant recipients, identifying denosumab as a potentially superior option.

## Key findings

- Denosumab significantly improved lumbar spine bone mineral density compared to bisphosphonates, calcitonin, and calcium.
- Calcitonin showed better results than calcium for femoral neck bone mineral density.
- No significant safety differences were found between the treatments.

## Abstract

Kidney transplant recipients (KTRs) are at an increased risk of osteoporosis, which negatively impacts their quality of life and transplant outcomes. However, the efficacy and safety of anti-osteoporosis treatments in this group remain uncertain.

We conducted a systematic search of PubMed, Embase, Web of Science, and the Cochrane Central Register of Controlled Trials up to August 1, 2024. Randomized controlled trials (RCTs) examining anti-osteoporotic medications in KTRs were included. Primary outcomes were changes in bone mineral density (BMD) at femoral neck and lumbar spine, and adverse events. We performed a frequentist network meta-analysis using random-effects models. Evidence certainty was assessed using the GRADE approach.

Twenty-one RCTs involving 1,066 participants were included, published between 2000 and 2021. For femoral neck BMD, bisphosphonates significantly improved BMD compared to control (MD = 0.04, 95%CI=0.00-0.09, p<0.05) based on low certainty evidence, while calcitonin was significantly superior to calcium (MD=-0.14, 95%CI=-0.28 to -0.01). Most other comparisons showed no statistically significant differences based on very low to moderate certainty evidence. For lumbar spine BMD, bisphosphonates, calcitonin, and calcium demonstrated statistically significant inferiority compared to denosumab, with bisphosphonates showing MD=-4.98 (95%CI=-6.84 to -3.13), calcitonin showing MD=-4.35 (95%CI=-6.24 to -2.47), and calcium showing MD=-5.85 (95%CI=-7.72 to -3.98), while denosumab was superior to control (MD = 5.10, 95%CI=3.25-6.95), based on low to very low certainty evidence from one RCT. Calcitonin was also significantly superior to calcium (MD = 0.60, 95%CI=0.07-1.12). For safety outcomes, no statistically significant differences were observed between interventions based on low to moderate certainty evidence.

Denosumab appears most effective for improving lumbar spine BMD in KTRs, while calcitonin shows promise for femoral neck BMD improvement. However, the low to moderate certainty of evidence necessitates individualized treatment approaches considering patient-specific factors including renal function and safety profiles. These findings suggest current guidelines emphasizing bisphosphonates as first-line therapy may require revision, though larger long-term studies with fracture endpoints are needed to confirm these results.

https://www.crd.york.ac.uk/prospero/?utm_source=chatgpt.com, identifier PROSPERO CRD42024587203.

## Linked entities

- **Chemicals:** calcitonin (PubChem CID 118984394), calcium (PubChem CID 5460341)
- **Diseases:** osteoporosis (MONDO:0005298)

## Full-text entities

- **Diseases:** fracture (MESH:D050723), osteoporosis (MESH:D010024), osteoporotic (MESH:D058866)
- **Chemicals:** calcium (MESH:D002118), bisphosphonates (MESH:D004164), Denosumab (MESH:D000069448)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12620273/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12620273/full.md

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Source: https://tomesphere.com/paper/PMC12620273