To develop a pharmacokinetic-pharmacogenomic population model of midazolam in critically ill children with primary respiratory failure.
Prospective pharmacokinetic-pharmacogenomic observational study.
Thirteen PICUs across the United States.
Pediatric subjects mechanically ventilated for acute respiratory failure, weight greater than or equal to 7 kg, receiving morphine and/or midazolam continuous infusions.
Serial blood sampling for drug quantification and a single blood collection for genomic evaluation.
Concentrations of midazolam, the 1’ (1`-hydroxymidazolam metabolite) and 4’ (4`-hydroxymidazolam metabolite) hydroxyl, and the 1’ and 4’ glucuronide metabolites were measured. Subjects were genotyped using the Illumina HumanOmniExpress genome-wide single nucleotide polymorphism chip. Nonlinear mixed effects modeling was performed to develop the pharmacokinetic-pharmacogenomic model. Body weight, age, hepatic and renal functions, and the UGT2B7 rs62298861 polymorphism are relevant predictors of midazolam pharmacokinetic variables. The estimated midazolam clearance was 0.61 L/min/70kg. Time to reach 50% complete mature midazolam and 1`-hydroxymidazolam metabolite/4`-hydroxymidazolam metabolite clearances was 1.0 and 0.97 years postmenstrual age. The final model suggested a decrease in midazolam clearance with increase in alanine transaminase and a lower clearance of the glucuronide metabolites with a renal dysfunction. In the pharmacogenomic analysis, rs62298861 and rs28365062 in the UGT2B7 gene were in high linkage disequilibrium. Minor alleles were associated with a higher 1`-hydroxymidazolam metabolite clearance in Caucasians. In the pharmacokinetic-pharmacogenomic model, clearance was expected to increase by 10% in heterozygous and 20% in homozygous for the minor allele with respect to homozygous for the major allele.
This work leveraged available knowledge on nonheritable and heritable factors affecting midazolam pharmacokinetic in pediatric subjects with primary respiratory failure requiring mechanical ventilation, providing the basis for a future implementation of an individual-based approach to sedation.
1Department of Pediatric Anesthesia and Critical Care Medicine, Children’s Hospital of Philadelphia, Philadelphia, PA.
2Children’s Hospital of Philadelphia, Center for Clinical Pharmacology, Philadelphia, PA.
3Metrum Research Group, Tariffville, CT.
4Family and Community Heath, University of Pennsylvania School of Nursing, Philadelphia, PA.
5Anesthesia and Critical Care Medicine, Perelman School of Medicine, Philadelphia, PA.
6Research Institute, Children’s Hospital of Philadelphia, PA.
7Quantinuum Research LLC, San Diego CA.
8Children’s Hospital of Philadelphia, Center for Applied Genomics, Philadelphia, PA.
9Department of Pediatrics, Children’s Hospital of Philadelphia, Perelman School of Medicine, Philadelphia, PA.
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Dr. Zuppa is supported by 1 R01 HL098087-01—Impact of Pharmacology on the Duration of Ventilation in Pediatric Patients with Respiratory Failure National Heart, Lung, and Blood Institute. Dr. Zane is supported by a National Institute of General Medicine Sciences T32 Clinical Pharmacology Fellowship (2T32GM008562-21). Dr. Hakonarson received Electronic Medical Records and Genomics consortium grant 1U01HG006830 from the National Human Genome Research Institute. The remaining authors have not disclosed any potential conflicts of interest.
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