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DOI 10.1016/j.medcli.2024.07.020

Медицинская библиотека · Medicina clinica · 2024

Hyperparathyroidism in patients with low bone mineral density treated with zoledronic acid or denosumab.

Riesco-Bárcena Carmen, Ivorra-Cortés José, Grau-García Elena, González-Puig Luis, Leal Samuel, Huaylla Anderson, Román-Ivorra José

СтатьяНаблюдательное исследованиеПеревод в очереди

Аннотация

OBJECTIVE

To analyze the prevalence of hyperparathyroidism in patients treated with zoledronic acid (ZA) or denosumab, its relationship with other parameters and how it affects on bone mineral density (BMD) evolution.

METHODS

Retrospective observational study in patients with osteoporosis or osteopenia and high risk of fracture, who have received denosumab or ZA for at least two years. Patients diagnosed with hyperparathyroidism or glomerular filtration rate <30ml/min at baseline visit were excluded from the study.

RESULTS

Ninety patients (ZA: 54.44%) were included. 18.36% of ZA-treated patients had elevated PTH levels at some time compared to 36.58% denosumab-treated patients (p>0.05). Patients with persistently elevated PTH were 6.13% in the AZ group and 19.51% in the denosumab group (p<0.04). We found a statistically significant inverse association between elevated PTH levels, glomerular filtration rate (p=0.007), and albumin-corrected calcium (p <0.001). We did not find an association between hyperparathyroidism and BMD evolution.

CONCLUSIONS

A high incidence of hyperparathyroidism was observed in patients treated with AZ and especially denosumab. Hyperparathyroidism correlated inversely with glomerular filtration rate and albumin-corrected calcium. Elevated PTH does not appear to affect short-term bone mineral density evolution.

Для цитирования: Riesco-Bárcena Carmen, Ivorra-Cortés José, Grau-García Elena, González-Puig Luis, Leal Samuel, Huaylla Anderson, Román-Ivorra José. Hyperparathyroidism in patients with low bone mineral density treated with zoledronic acid or denosumab.. Medicina clinica. 2024. DOI: 10.1016/j.medcli.2024.07.020.

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