2024 · Drug metabolism and personalized therapy · paywalled
Pediatric pharmacogenetics: profiling CYP2C8 polymorphisms at King Abdulaziz University Dental Clinic
Bagher et al.
The finding, in our words
Using the Oragene saliva device, this study identified elevated CYP2C8 allele frequencies in a Saudi paediatric cohort compared to other Asian populations, suggesting potential variability in ibuprofen metabolism and drug response.
A paraphrase to the Library’s standard, never the abstract. The source is one link away and is always the authority.
Using the Oragene Discovery 500 series for decentralised saliva collection in 524 African American adolescents, this study found that positive neighbourhood conditions relate to fewer behavioural difficulties, despite genetic risk. The authors note that most gene-environment studies of behaviour use European ancestry samples, limiting generalisability to African American youth.
This proof-of-principle study found that baseline salivary DNA methylation, collected using the Oragene DNA kit, predicted childhood obesity three years later. A child at the 75th percentile of NRF1 methylation had a 48% chance of obesity versus 30% at the 25th percentile, showing the value of salivary microsampling for paediatric screening.
A study of 307 youth aged 10 to 14 years found that DNA extracted from saliva collected with Oragene kits was suitable for genotyping the OXTR rs53576 variant. This supports decentralised paediatric genetic testing, although the study was limited by its reliance on a community sample.
Saliva self-collection with Oragene tubes enabled genotyping of COMT polymorphisms in children, revealing that the AA genotype buffers the negative effect of authoritarian parenting on long-term executive dysfunction after early childhood traumatic brain injury. This demonstrates how decentralised genetic sampling can support longitudinal neurodevelopmental studies in paediatric populations.
DNA concentration from whole saliva correlates positively with age, so children yield significantly less DNA than adults. This means saliva collection protocols for genetic studies must be adjusted for paediatric populations to ensure adequate DNA quantity for genotyping.