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Pré-Publication, Document De Travail Année : 2021

Neurofunctional and neuroimaging readouts for designing a preclinical stem-cell therapy trial in experimental stroke

Chrystelle Po
  • Fonction : Auteur
Lucille Capin
  • Fonction : Auteur
Radu Bolbos
Camille Amaz
Céline Auxenfans
  • Fonction : Auteur
Claire Rome

Résumé

Abstract With the aim of designing a preclinical study evaluating an intracerebral cell-based therapy for stroke, an observational study was performed in the rat suture model of ischemic stroke. Objectives were threefold: (i) to characterize neurofunctional and imaging readouts in the first weeks following transient ischemic stroke, according to lesion subtype (hypothalamic, striatal, corticostriatal); (ii) to confirm that intracerebral administration does not negatively impact these readouts; and (iii) to calculate sample sizes for a future therapeutic trial using these readouts as endpoints. Our results suggested that the most relevant endpoints were side bias (staircase test) and axial diffusivity (AD) (diffusion tensor imaging). Hypothalamic-only lesions did not affect those parameters, which were close to normal. Side bias in striatal lesions reached near-normal levels within 2 weeks, while rats with corticostriatal lesions remained impaired until week 14. AD values were decreased at 4 days and increased at 5 weeks post-surgery, with a subtype gradient: hypothalamic < striatal < corticostriatal. Intracerebral administration did not impact these readouts. After sample size calculation (18-147 rats per group according to the endpoint considered), we conclude that a therapeutic trial based on both readouts would be feasible only in the framework of a multicenter trial.

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Dates et versions

hal-03451443 , version 1 (26-11-2021)
hal-03451443 , version 2 (01-04-2022)

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Chloé Dumot, Chrystelle Po, Lucille Capin, Violaine Hubert, Elodie Ong, et al.. Neurofunctional and neuroimaging readouts for designing a preclinical stem-cell therapy trial in experimental stroke. 2021. ⟨hal-03451443v1⟩
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