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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
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.
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.
Background:
Children with medical complexity (CMC) are a priority pediatric population, with high resource use and associated costs. Genome-wide sequencing is increasingly organized for CMC early in life as a diagnostic test. Polypharmacy becomes common as CMC age. Clinically relevant pharmacogenetic (PGx) information can be extracted from existing genome sequencing (GS) data via GS-PGx profiling. The role of GS-PGx profiling in the CMC population is unclear.
Methods:
Prescribed medications were extracted from care plans of 802 eligible CMC enrolled in a structured Complex Care Program over a 10-year period. Drug-gene associations were annotated using curated Clinical Pharmacogenetics Implementation Consortium data. GS-PGx profiling was then performed for a subset of 50 CMC.
Results:
Overall, 546 CMC (68%) were prescribed at least one medication with an established PGx association. In the GS-PGx subgroup, 24 (48%) carried variants in pharmacogenes with drug-gene guidelines for one or more of their current medications. All had findings of potential relevance to some medications, including 32 (64%) with variants in CYP2C19 that could affect their metabolism of proton-pump inhibitors.
Conclusion:
GS-PGx profiling at the time of diagnostics-focused genetic testing could be an efficient way to incorporate precision prescribing practices into the lifelong care of CMC.
Impact:
Polypharmacy and genetic test utilization are both common in children with medical complexity. The role of repurposing genome sequencing data for pharmacogenetic profiling in children with medical complexity was previously unclear. We identified a high rate of medication use with clinically relevant drug-gene associations in this priority pediatric population and demonstrated that relevant pharmacogenetic information can be extracted from their existing genome sequencing data. Pharmacogenetic profiling at the time of diagnostics-focused genetic testing could be an efficient way to incorporate precision prescribing practices into the lifelong care of children with medical complexity.
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