The Use of Oral Amino-Bisphosphonates and Coronavirus Disease 2019 (COVID-19) Outcomes.


Journal

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
ISSN: 1523-4681
Titre abrégé: J Bone Miner Res
Pays: United States
ID NLM: 8610640

Informations de publication

Date de publication:
11 2021
Historique:
revised: 24 07 2021
received: 30 03 2021
accepted: 03 08 2021
pubmed: 19 8 2021
medline: 19 11 2021
entrez: 18 8 2021
Statut: ppublish

Résumé

The determinants of the susceptibility to severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) infection and severe coronavirus disease 2019 (COVID-19) manifestations are yet not fully understood. Amino-bisphosphonates (N-BPs) have anti-inflammatory properties and have been shown to reduce the incidence of lower respiratory infections, cardiovascular events, and cancer. We conducted a population-based retrospective observational cohort study with the primary objective of determining if oral N-BPs treatment can play a role in the susceptibility to development of severe COVID-19. Administrative International Classification of Diseases, Ninth Revision, Clinical ModificationI (ICD-9-CM) and anatomical-therapeutic chemical (ATC) code data, representative of Italian population (9% sample of the overall population), were analyzed. Oral N-BPs (mainly alendronate and risedronate) were included in the analysis, zoledronic acid was excluded because of the low number of patients at risk. Incidence of COVID-19 hospitalization was 12.32 (95% confidence interval [CI], 9.61-15.04) and 11.55 (95% CI, 8.91-14.20), of intensive care unit (ICU) utilization because of COVID-19 was 1.25 (95% CI, 0.38-2.11) and 1.42 (95% CI, 0.49-2.36), and of all-cause death was 4.06 (95% CI, 2.50-5.61) and 3.96 (95% CI, 2.41-5.51) for oral N-BPs users and nonusers, respectively. Sensitivity analyses that excluded patients with prevalent vertebral or hip fragility fractures and without concomitant glucocorticoid treatment yielded similar results. In conclusion, we found that the incidence of COVID-19 hospitalization, intensive care unit (ICU) utilization, and COVID-19 potentially related mortality were similar in N-BPs-treated and nontreated subjects. Similar results were found in N-BPs versus other anti-osteoporotic drugs. We provide real-life data on the safety of oral N-BPs in terms of severe COVID-19 risk on a population-based cohort. Our results do not support the hypothesis that oral N-BPs can prevent COVID-19 infection and/or severe COVID-19; however, they do not seem to increase the risk. © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

Identifiants

pubmed: 34405441
doi: 10.1002/jbmr.4419
pmc: PMC8420492
doi:

Substances chimiques

Diphosphonates 0
Risedronic Acid KM2Z91756Z

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2177-2183

Subventions

Organisme : Open Access Funding provided by Universita degli Studi di Verona within the CRUI-CARE Agreement. WOA Institution: Universita degli Studi di Verona Blended DEAL: CARE

Informations de copyright

© 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

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Auteurs

Luca Degli Esposti (L)

CliCon S.r.l. Health, Economics & Outcomes Research, Bologna, Italy.

Valentina Perrone (V)

CliCon S.r.l. Health, Economics & Outcomes Research, Bologna, Italy.

Diego Sangiorgi (D)

CliCon S.r.l. Health, Economics & Outcomes Research, Bologna, Italy.

Margherita Andretta (M)

UOC Assistenza Farmaceutica Territoriale, Azienda ULSS 8 Berica, Vicenza, Italy.

Fausto Bartolini (F)

Dipartimento Farmaceutico, USL Umbria 2, Perugia, Italy.

Arturo Cavaliere (A)

UOC Farmacia Aziendale, ASL, Viterbo, Italy.

Andrea Ciaccia (A)

Dipartimento Farmaceutico, ASL, Foggia, Italy.

Stefania Dell'orco (S)

UOC Farmaceutica Territoriale, ASL Roma 6, Rome, Italy.

Stefano Grego (S)

Dipartimento Tecnico-Amministrativo, ASL 3 Genovese, Genova, Italy.

Sara Salzano (S)

UOC Farmacia Territoriale, ASL Roma 4, Rome, Italy.

Loredana Ubertazzo (L)

UOC Farmacia Territoriale, ASL Roma 4, Rome, Italy.

Adriano Vercellone (A)

Dipartimento Farmaceutico, ASL Naples 3 Sud, Naples, Italy.

Davide Gatti (D)

Rheumatology Unit, University of Verona, Verona, Italy.

Angelo Fassio (A)

Rheumatology Unit, University of Verona, Verona, Italy.

Ombretta Viapiana (O)

Rheumatology Unit, University of Verona, Verona, Italy.

Maurizio Rossini (M)

Rheumatology Unit, University of Verona, Verona, Italy.

Giovanni Adami (G)

Rheumatology Unit, University of Verona, Verona, Italy.

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Classifications MeSH