Neonatal PBPK model of midazolam and its metabolites for perinatal asphyxia and therapeutic hypothermia

BACKGROUND AND PURPOSE: Therapeutic hypothermia (TH) decreases morbidity and mortality in neonates with perinatal asphyxia (PA) and moderate-to-severe hypoxic-ischaemic encephalopathy. Midazolam is an antiepileptic and substrate of CYP3A4. Drug metabolism during PA/TH remains partially characterized, and disentangling effects of PA and TH is difficult, making precision dosing challenging. The I-PREDICT project aims to develop a framework for drug disposition in PA/TH neonates, using physiologically based pharmacokinetic (PBPK) modelling. The predictive performance of the model was explored for midazolam and its active metabolites, 1'-hydroxymidazolam and 1'-hydroxymidazolam-O-glucuronide, in neonates with PA/TH. EXPERIMENTAL APPROACH: The model was established stepwise, starting with healthy adults, and extrapolated to paediatric (1 month-18 years) and neonatal (0-27 days, non-asphyxiated) populations. Finally, PA/TH-related physiological and metabolic changes were incorporated. For each population, performance was verified using clinical data. KEY RESULTS: Model predictive performance for midazolam and 1'-hydroxymidazolam was acceptable in adults and children, with AFE and AAFE values ranging from 0.87 to 1.22 and 1.15 to 1.23, respectively. The neonatal PA/TH PBPK model captured midazolam pharmacokinetics, with 71% of the observations within the 10th-90th percentiles and 46% within the 25th-75th percentiles of the prediction. Incorporating PA/TH physiology improved the neonatal PA/TH model by 6%-43% (within the 10th-90th percentiles), depending on the compound. CONCLUSIONS AND IMPLICATIONS: This PA/TH-adjusted neonatal PBPK model may support future midazolam dose optimization through mechanistic understanding and provides a framework for other drugs in neonates with PA/TH. Future knowledge on the impact of TH on protein binding and renal clearance of 1'-hydroxymidazolam-O-glucuronide would further improve the model.

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Publication Details

Journal
British Journal of Clinical Pharmacology
Published
2026-05-13
DOI
https://doi.org/10.1002/bcp.70601
Primary Topic
Neonatal and fetal brain pathology
Type
article
Field-Weighted Citation Impact
0.00

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article

Neonatal PBPK model of midazolam and its metabolites for perinatal asphyxia and therapeutic hypothermia

Marina‐Stefania Stroe, Julia Macente, Évelyne Jacqz-Aigrain, Miao‐Chan Huang et al.
British Journal of Clinical Pharmacology
Neonatal and fetal brain pathology
article

Neonatal PBPK model of midazolam and its metabolites for perinatal asphyxia and therapeutic hypothermia

Marina‐Stefania Stroe, Julia Macente, Évelyne Jacqz-Aigrain, Miao‐Chan Huang, Saskia N. de Wildt, Floris Groenendaal, Karen Leys, Timo Robert de Haan, A Smits, Agustos Ozbey, Pieter Annaert, Steven Van Cruchten, Karel Allegaert
article en

Abstract

BACKGROUND AND PURPOSE: Therapeutic hypothermia (TH) decreases morbidity and mortality in neonates with perinatal asphyxia (PA) and moderate-to-severe hypoxic-ischaemic encephalopathy. Midazolam is an antiepileptic and substrate of CYP3A4. Drug metabolism during PA/TH remains partially characterized, and disentangling effects of PA and TH is difficult, making precision dosing challenging. The I-PREDICT project aims to develop a framework for drug disposition in PA/TH neonates, using physiologically based pharmacokinetic (PBPK) modelling. The predictive performance of the model was explored for midazolam and its active metabolites, 1'-hydroxymidazolam and 1'-hydroxymidazolam-O-glucuronide, in neonates with PA/TH. EXPERIMENTAL APPROACH: The model was established stepwise, starting with healthy adults, and extrapolated to paediatric (1 month-18 years) and neonatal (0-27 days, non-asphyxiated) populations. Finally, PA/TH-related physiological and metabolic changes were incorporated. For each population, performance was verified using clinical data. KEY RESULTS: Model predictive performance for midazolam and 1'-hydroxymidazolam was acceptable in adults and children, with AFE and AAFE values ranging from 0.87 to 1.22 and 1.15 to 1.23, respectively. The neonatal PA/TH PBPK model captured midazolam pharmacokinetics, with 71% of the observations within the 10th-90th percentiles and 46% within the 25th-75th percentiles of the prediction. Incorporating PA/TH physiology improved the neonatal PA/TH model by 6%-43% (within the 10th-90th percentiles), depending on the compound. CONCLUSIONS AND IMPLICATIONS: This PA/TH-adjusted neonatal PBPK model may support future midazolam dose optimization through mechanistic understanding and provides a framework for other drugs in neonates with PA/TH. Future knowledge on the impact of TH on protein binding and renal clearance of 1'-hydroxymidazolam-O-glucuronide would further improve the model.

British Journal of Clinical Pharmacology
Radboud University Nijmegen (NL), University of Antwerp (BE), Erasmus MC (NL), Radboud University Medical Center (NL), Antwerp Management School (BE), Emma Kinderziekenhuis (NL), Idorsia (Switzerland) (CH), Erasmus MC - Sophia Children’s Hospital (NL), Hôpital Saint-Louis (FR), Wilhelmina Children's Hospital (NL), University of Amsterdam (NL), Erasmus University Rotterdam (NL), KU Leuven (BE)
Fonds Wetenschappelijk Onderzoek
Good health and well-being
Openalex Percentile: Top 5%
Neonatal and fetal brain pathology
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