Pharmacogenetic profiling via genome sequencing in children with medical complexity

Amy Pan1, Sierra Scodellaro2,3, Tayyaba Khan1

  • 1Genetics and Genome Biology, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.

Pediatric Research
|September 27, 2022
PubMed

Insights

Genome sequencing data in children with medical complexity can reveal pharmacogenetic insights for personalized medicine. Repurposing this data efficiently integrates precision prescribing into lifelong care.

Area of Science:

  • Pediatric Genomics
  • Pharmacogenetics
  • Precision Medicine

Background:

  • Children with medical complexity (CMC) are a high-need population with significant healthcare resource utilization.
  • As CMC age, polypharmacy (use of multiple medications) becomes common.
  • Genome-wide sequencing (GS) is increasingly used for CMC, and pharmacogenetic (PGx) information can be derived from this data.

Purpose of the Study:

  • To investigate the role and feasibility of genome sequencing-pharmacogenetic (GS-PGx) profiling in children with medical complexity.
  • To determine the prevalence of drug-gene associations among medications used by CMC.
  • To assess the utility of repurposing existing GS data for PGx profiling in this population.

Main Methods:

  • Medications were extracted from care plans of 802 CMC over 10 years.
  • Drug-gene associations were identified using Clinical Pharmacogenetics Implementation Consortium (CPIC) data.
  • GS-PGx profiling was performed on a subset of 50 CMC.

Main Results:

  • 68% of CMC were prescribed at least one medication with a known PGx association.
  • In the GS-PGx subgroup, 48% had pharmacogene variants relevant to their current medications.
  • Relevant findings included variants in CYP2C19 affecting proton-pump inhibitor metabolism in 64% of this subgroup.

Conclusions:

  • GS-PGx profiling can efficiently extract clinically relevant pharmacogenetic information from existing genome sequencing data in CMC.
  • Integrating GS-PGx profiling at the time of diagnostic genetic testing can support precision prescribing throughout the lifelong care of CMC.
Abstract

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