The role of plasma concentrations and drug characteristics of beta‐blockers in fall risk of older persons

Author:

Ploegmakers K. J.12ORCID,van Poelgeest E. P.12,Seppala L. J.12,van Dijk S. C.3,de Groot L. C. P. G. M.4,Oliai Araghi S.5,van Schoor N. M.26,Stricker B.5,Swart K. M. A.7,Uitterlinden A. G.58,Mathôt R. A. A.9,van der Velde N.12

Affiliation:

1. Amsterdam UMC Location University of Amsterdam Internal Medicine, Section of Geriatric Medicine Amsterdam The Netherlands

2. Amsterdam Public Health Aging and Later Life Amsterdam The Netherlands

3. Department of Geriatrics, Franciscus Gasthuis & Vlietland Rotterdam the Netherlands

4. Division of Human Nutrition and Health Wageningen University Wageningen the Netherlands

5. Department of Epidemiology Erasmus University Medical Center Rotterdam the Netherlands

6. Amsterdam UMC Location Vrije Universiteit Amsterdam Epidemiology and Data Science Amsterdam Netherlands

7. Amsterdam UMC Location Vrije Universiteit Amsterdam General Practice Amsterdam The Netherlands

8. Department of Internal Medicine Erasmus University Medical Center Rotterdam the Netherlands

9. Amsterdam UMC Location University of Amsterdam Hospital Pharmacy—Clinical Pharmacology Amsterdam The Netherlands

Abstract

AbstractBeta‐blocker usage is inconsistently associated with increased fall risk in the literature. However, due to age‐related changes and interindividual heterogeneity in pharmacokinetics and dynamics, it is difficult to predict which older adults are more at risk for falls. Therefore, we wanted to explore whether elevated plasma concentrations of selective and nonselective beta‐blockers are associated with an increased risk of falls in older beta‐blocker users. To answer our research question, we analyzed samples of selective (metoprolol, n = 316) and nonselective beta‐blockers (sotalol, timolol, propranolol, and carvedilol, n = 179) users from the B‐PROOF cohort. The associations between the beta‐blocker concentration and time to first fall were assessed using Cox proportional hazard models. Change of concentration over time in relation to fall risk was assessed with logistic regression models. Models were adjusted for potential confounders. Our results showed that above the median concentration of metoprolol was associated with an increased fall risk (HR 1.55 [1.11–2.16], p = .01). No association was found for nonselective beta‐blocker concentrations. Also, changes in concentration over time were not associated with increased fall risk. To conclude, metoprolol plasma concentrations were associated with an increased risk of falls in metoprolol users while no associations were found for nonselective beta‐blockers users. This might be caused by a decreased β1‐selectivity in high plasma concentrations. In the future, beta‐blocker concentrations could potentially help clinicians estimate fall risk in older beta‐blockers users and personalize treatment.

Funder

Nederlandse Zuivel Organisatie

ZonMw

Publisher

Wiley

Subject

General Pharmacology, Toxicology and Pharmaceutics,Neurology

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