Pharmacopsychiatry
DOI: 10.1055/a-2764-4939
Original Paper

The Effect of Kidney Function and Cardiovascular and Anti-Inflammatory Comedications on the Serum Concentration of Risperidone under Naturalistic Conditions

Authors

  • Meike Kohler

    1   Department of Psychiatry, Psychosomatics and Psychotherapy, Centre of Mental Health, University Hospital of Würzburg, Würzburg, Germany
  • Jürgen Deckert

    1   Department of Psychiatry, Psychosomatics and Psychotherapy, Centre of Mental Health, University Hospital of Würzburg, Würzburg, Germany
    2   Institute of Clinical Epidemiology and Biometry, Julius-Maximilians-Universität Würzburg, Würzburg, Germany
  • Sebastian Walther

    1   Department of Psychiatry, Psychosomatics and Psychotherapy, Centre of Mental Health, University Hospital of Würzburg, Würzburg, Germany
  • Stefan Unterecker

    1   Department of Psychiatry, Psychosomatics and Psychotherapy, Centre of Mental Health, University Hospital of Würzburg, Würzburg, Germany
    3   Department of Psychiatry and Psychotherapy, Social Foundation Bamberg, Teaching Hospital of the University of Erlangen, Bamberg, Germany
  • Maike Scherf-Clavel

    1   Department of Psychiatry, Psychosomatics and Psychotherapy, Centre of Mental Health, University Hospital of Würzburg, Würzburg, Germany

Abstract

Introduction

Polypharmacy has an important role in psychiatry, as the kidney function can be affected by medication. Risperidone is metabolized hepatically to 9-hydroxyrisperidone and excreted renally. Here, we study how serum concentrations of risperidone, 9-hydroxyrisperidone and active moiety (risperidone+9-hydroxyrisperidone) are related to impairment of kidney function and potentially interacting comedications that affect renal functions ((1) nonsteroidal anti-inflammatory drugs, (2) angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers, and (3) diuretics).

Methods

In this retrospective study, data from risperidone-treated inpatients (2015–2020, n=517) at the University Hospital of Würzburg were analyzed. Routine therapeutic drug monitoring was performed at trough levels at a steady-state. Groups were compared by means of the Kruskal–Wallis test. To correct for confounding parameters, additional multiple linear regression modeling was performed.

Results

After correction for age, sex, body mass index and the respective interaction between the estimated glomerular filtration rate and the number of interacting drugs, the dose-corrected serum concentration of 9-hydroxyrisperidone and the active moiety of risperidone were positively associated with the number of interacting drugs. The active moiety was negatively associated with the estimated glomerular filtration rate.

Discussion

Our data suggest that renal functions and the number of interacting drugs influence the pharmacokinetics of risperidone. Previous studies often explained the increasing serum concentration with age as a surrogate, whereas our results suggest that the kidney function and comedication affecting kidney function might be more relevant. When prescribing risperidone, especially in patients with renal impairment or co-medicated with interacting drugs, we suggest to start with lower starting doses and recommend monitoring serum concentrations to prevent overdosing.



Publication History

Received: 23 April 2025

Accepted after revision: 03 November 2025

Article published online:
19 December 2025

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