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Author Spotlight: A Pharmacodissection Approach to Uncover Mechanisms in Cardiovascular Disease Risk Populations
Published on: July 21, 2023
Association of oral bisphosphonates with cardioembolic ischemic stroke: a nested case-control study
Sara Rodríguez-Martín1, Diana Barreira-Hernández1, Ramón Mazzucchelli2
1Department of Biomedical Sciences (Pharmacology), University of Alcalá (IRYCIS), Alcalá de Henares, Spain.
Insights
Oral bisphosphonates may increase the risk of cardioembolic ischemic stroke (IS). This risk appears to be duration-dependent and is mitigated by anticoagulants, suggesting a specific link to cardioembolic events.
Area of Science:
- Pharmacovigilance and Pharmacoepidemiology
- Cardiovascular Disease Epidemiology
- Bone Metabolism and Therapeutics
Background:
- Bisphosphonates are commonly used for osteoporosis and other bone conditions.
- Previous studies suggested a potential link between bisphosphonates and atrial fibrillation, raising concerns about cardioembolic risk.
- Existing research on bisphosphonates and ischemic stroke (IS) has not differentiated between cardioembolic and non-cardioembolic subtypes.
Purpose of the Study:
- To investigate whether oral bisphosphonates specifically increase the risk of cardioembolic ischemic stroke (IS).
- To explore the influence of oral bisphosphonate treatment duration on IS risk.
- To examine potential interactions between oral bisphosphonates, calcium supplements, and anticoagulants regarding IS risk.
Main Methods:
- A nested case-control study was conducted using the Spanish BIFAP primary healthcare database (2002-2015).
- Incident IS cases were identified and classified as cardioembolic or non-cardioembolic.
- Five controls per case were matched by age, sex, and index date; conditional logistic regression was used to assess associations.
Main Results:
- Oral bisphosphonate use was associated with an increased overall risk of IS (AOR=1.15).
- The risk was significantly higher for cardioembolic IS (AOR=1.35) compared to non-cardioembolic IS (AOR=1.03).
- Cardioembolic IS risk increased with treatment duration (p for trend=0.001) and was attenuated by anticoagulant use.
Conclusions:
- Oral bisphosphonates are specifically associated with an increased risk of cardioembolic ischemic stroke.
- This association is dependent on the duration of bisphosphonate treatment.
- Anticoagulant use appears to mitigate the bisphosphonate-associated risk of cardioembolic IS.
Abstract:
Background: Bisphosphonates have been reported to increase the risk of atrial fibrillation. Therefore, it is conceivable that they may increase the risk of cardioembolic ischemic stroke (IS). However, most epidemiological studies carried out thus far have not shown an increased risk of IS, though none separated by the main pathophysiologic IS subtype (cardioembolic and non-cardioembolic) which may be crucial. In this study, we tested the hypothesis that the use of oral bisphosphonates increases specifically the risk of cardioembolic IS, and explored the effect of treatment duration, as well as the potential interaction between oral bisphosphonates and calcium supplements and anticoagulants. Methods: We performed a case-control study nested in a cohort of patients aged 40-99 years, using the Spanish primary healthcare database BIFAP, over the period 2002-2015. Incident cases of IS were identified and classified as cardioembolic or non-cardioembolic. Five controls per case were randomly selected, matched for age, sex, and index date (first recording of IS) using an incidence-density sampling. The association of IS (overall and by subtype) with the use of oral bisphosphonates within the last year before index date was assessed by computing the adjusted odds ratios (AOR) and their 95% CI using a conditional logistic regression. Only initiators of oral bisphosphonates were considered. Results: A total of 13,781 incident cases of IS and 65,909 controls were included. The mean age was 74.5 (SD ± 12.4) years and 51.6% were male. Among cases, 3.15% were current users of oral bisphosphonates, while among controls they were 2.62%, yielding an AOR of 1.15 (95% CI:1.01-1.30). Of all cases, 4,568 (33.1%) were classified as cardioembolic IS (matched with 21,697 controls) and 9,213 (66.9%) as non-cardioembolic IS (matched with 44,212 controls) yielding an AOR of 1.35 (95% CI:1.10-1.66) and 1.03 (95% CI: 0.88-1.21), respectively. The association with cardioembolic IS was clearly duration-dependent (AOR≤1 year = 1.10; 95% CI:0.82-1.49; AOR>1-3 years = 1.41; 95% CI:1.01-1.97; AOR>3 years = 1.81; 95% CI:1.25-2.62; p for trend = 0.001) and completely blunted by anticoagulants, even in long-term users (AOR>1 year = 0.59; 0.30-1.16). An interaction between oral bisphosphonates and calcium supplements was suggested. Conclusion: The use of oral bisphosphonates increases specifically the odds of cardioembolic IS, in a duration-dependent manner, while leaves materially unaffected the odds of non-cardioembolic IS.
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