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Oral Bisphosphonate use Reduces Cardiovascular Events in a Cohort of Danish Patients Referred for Bone Mineral Density
Author(s) -
Alexander J. Rodríguez,
Martin Ernst,
Mads Nybo,
Daniel PrietoAlhambra,
Peter R. Ebeling,
Anne Pernille Hermann,
Bo Abrahamsen
Publication year - 2020
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/clinem/dgaa481
Subject(s) - medicine , hazard ratio , context (archaeology) , confounding , bone mineral , atrial fibrillation , proportional hazards model , propensity score matching , rate ratio , confidence interval , cohort study , cohort , danish , osteoporosis , paleontology , biology , linguistics , philosophy
Context The cardiovascular (CV) safety of oral bisphosphonates (oBPs) is uncertain. Objective Determine the risk of CV events in oBP users referred for bone mineral density (BMD) testing compared with matched controls. Design Cohort study. Setting Danish national prescription registry enriched with local hospital data from Odense. Participants Individuals aged ≥45 years referred for BMD testing. Exposure oBP. Outcomes Hospitalization for any CV event. Secondary study outcomes were specific CV events. Negative (inguinal hernia surgery and ingrown toenail) and positive (fragility fracture) control outcomes assessed systemic bias. Cox proportional hazards models were fitted to estimate hazard ratio (HR) and 95% confidence intervals. Results There were 2565 oBP users (82.6% women) and 4568 (82.3% women) propensity score–matched controls. Alendronate accounted for 96% of oBP prescription. A total of 406 (15.8%) CV events occurred in oBP users (rate = 73.48 [66.67-80.98]); rate = events divided by person-time; and 837 (18.3%) events in controls (rate = 104.73 [97.87-112.07]) with an adjusted HR of 0.68 (95% CI 0.60-0.77). Additional adjustment for BMD did not attenuate estimates (HR 0.67; 95% CI 0.58-0.78]. Similar results were seen for secondary outcomes where risk reductions were seen regarding atrial fibrillation, stroke, heart failure, and aneurysms. Positive and negative control outcome analyses identified minimal residual confounding. Conclusion Oral BP users experienced a 33% reduced risk of CV events. This observational real-world study adds to a growing body of evidence for cardioprotection by oBP that warrants testing in a randomized setting.

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