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The interactive walkway provides fit-for-purpose fall-risk biomarkers in the elderly: Comparison of zolpidem and suvorexant.
Koopmans, Ingrid; Geerse, Daphne; de Ridder, Lara; Roerdink, Melvyn; Juachon, Maria Joanna; Muehlan, Clemens; Dingemanse, Jasper; van Gerven, Joop; Groeneveld, Geert Jan; Zuiker, Rob.
Afiliação
  • Koopmans I; Centre for Human Drug Research, Leiden, The Netherlands.
  • Geerse D; Leiden University Medical Center, Leiden, The Netherlands.
  • de Ridder L; Leiden University Medical Center, Leiden, The Netherlands.
  • Roerdink M; Department of Human Movement Sciences, Faculty of Behavioural and Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam Movement Sciences, Amsterdam, Netherlands.
  • Juachon MJ; Centre for Human Drug Research, Leiden, The Netherlands.
  • Muehlan C; Department of Human Movement Sciences, Faculty of Behavioural and Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam Movement Sciences, Amsterdam, Netherlands.
  • Dingemanse J; Centre for Human Drug Research, Leiden, The Netherlands.
  • van Gerven J; Department of Clinical Pharmacology, Idorsia Pharmaceuticals Ltd., Allschwil, Switzerland.
  • Groeneveld GJ; Department of Clinical Pharmacology, Idorsia Pharmaceuticals Ltd., Allschwil, Switzerland.
  • Zuiker R; Centre for Human Drug Research, Leiden, The Netherlands.
Clin Transl Sci ; 17(7): e13875, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38978326
ABSTRACT
Dynamic balance assessments such as walking adaptability may yield a more realistic prediction of drug-induced falls compared with postural stability measurements, as falls often result from limited gait adjustments when walking. The Interactive Walkway (IWW) measures walking adaptability but sensitivity to medication effects is unknown. If proven sensitive and specific, IWW could serve as a biomarker for targeted fall-risk assessments in early clinical drug development. In this three-way crossover study, 18 healthy elderly (age 65-80 years) subjects received 5 mg zolpidem, 10 mg suvorexant, or placebo in the morning. Assessments were performed pre-dose and approximately hourly until 9 h post-dose. IWW assessments included an 8-meter walking test, goal-directed stepping, obstacle-avoidance, and tandem-walking. Other pharmacodynamic measurements were the Timed-Up-and-Go (TUG) test at a comfortable and fast pace, adaptive tracking, and body sway. A decline in performance was observed for zolpidem compared with placebo for 3 h post-dose in IWW walking adaptability outcome measures, TUG, adaptive tracking, and body sway. For the IWW tasks, a decrease in walking speed (among others) was observed. IWW parameters were not affected by suvorexant compared with placebo at any timepoint. However, an increase of 9.8% (95%CI 1.8%, 18.5%) in body sway was observed for suvorexant compared with placebo up to 3 h post-dose. The IWW successfully quantified drug effects of two hypnotic drugs and distinguished between zolpidem and suvorexant regarding their effects on walking. As a biomarker, the IWW demonstrated sensitivity in assessing dynamic balance and potential fall risk in early phase clinical drug development.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Azepinas / Triazóis / Acidentes por Quedas / Caminhada / Estudos Cross-Over / Equilíbrio Postural / Zolpidem Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Azepinas / Triazóis / Acidentes por Quedas / Caminhada / Estudos Cross-Over / Equilíbrio Postural / Zolpidem Idioma: En Ano de publicação: 2024 Tipo de documento: Article