Risk of Ischemic Stroke Associated with Calcium Supplements and Interaction with Oral Bisphosphonates: A Nested Case-Control Study

Author:

Barreira-Hernández Diana1ORCID,Rodríguez-Martín Sara1,Gil Miguel2,Mazzucchelli Ramón3ORCID,Izquierdo-Esteban Laura4,García-Lledó Alberto56ORCID,Pérez-Gómez Ana67,Rodríguez-Miguel Antonio1ORCID,de Abajo Francisco J.18ORCID

Affiliation:

1. Department of Biomedical Sciences (Pharmacology), University of Alcalá (IRYCIS), 28805 Alcalá de Henares, Spain

2. Division of Pharmacoepidemiology and Pharmacovigilance, Spanish Agency on Medicines and Medical Devices (AEMPS), 28022 Madrid, Spain

3. Rheumatology Department, University Hospital “Fundación Alcorcón”, 28922 Alcorcón, Spain

4. Stroke Unit, Department of Neurology, University Hospital “Príncipe de Asturias”, 28805 Alcalá de Henares, Spain

5. Department of Cardiology, University Hospital “Príncipe de Asturias”, 28805 Alcalá de Henares, Spain

6. Department of Medicine, University of Alcalá, 28805 Alcalá de Henares, Spain

7. Department of Rheumatology, University Hospital “Príncipe de Asturias”, 28805 Alcalá de Henares, Spain

8. Clinical Pharmacology Unit, University Hospital “Príncipe de Asturias”, 28805 Alcalá de Henares, Spain

Abstract

Conflicting results about the association of calcium supplements (CS) with ischemic stroke (IS) have been reported. We tested this hypothesis by differentiating between CS alone (CaM) and CS with vitamin D (CaD) and between cardioembolic and non-cardioembolic IS. We examined the potential interaction with oral bisphosphonates (oBs). A nested case-control study was carried out. We identified incident IS cases aged 40–90 and randomly sampled five controls per case matched by age, sex, and index date. Current users were compared to non-users. An adjusted odds ratios (AOR) and 95% CI were computed through conditional logistic regression. Only new users were considered. We included 13,267 cases (4400 cardioembolic, 8867 non-cardioembolic) and 61,378 controls (20,147 and 41,231, respectively). CaM use was associated with an increased risk of cardioembolic IS (AOR = 1.88; 95% CI: 1.21–2.90) in a duration-dependent manner, while it showed no association with non-cardioembolic IS (AOR = 1.05; 95% CI: 0.74–1.50); its combination with oBs increased the risk of cardioembolic IS considerably (AOR = 2.54; 95% CI: 1.28–5.04), showing no effect on non-cardioembolic. CaD use was not associated with either cardioembolic (AOR = 1.08; 95% CI: 0.88–1.31) or non-cardioembolic IS (AOR = 0.98; 95% CI: 0.84–1.13) but showed a small association with cardioembolic IS when combined with oBs (AOR = 1.35; 95% CI: 1.03–1.76). The results support the hypothesis that CS increases the risk of cardioembolic IS, primarily when used concomitantly with oBs.

Funder

Biomedical Research Foundation of the University Hospital Principe de Asturias

Spanish Agency for Medicines and Medical Devices

Publisher

MDPI AG

Subject

General Medicine

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