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Effect of CYP2D6 genetic variation on patient-reported symptom improvement and side effects among children and adolescents treated with amphetamines. | LitMetric

AI Article Synopsis

  • Amphetamine medications are often the first treatment choice for ADHD in kids and teens, but their effectiveness can differ greatly among individuals, possibly due to genetic differences in how these drugs are processed in the body.
  • A study involving 214 participants aged 6-24 analyzed how variations in the CYP2D6 gene affected treatment outcomes, collecting info on medication use, symptom improvement, and side effects.
  • Results showed that those with the poor metabolizer version of CYP2D6 had better odds of experiencing symptom improvement compared to intermediate metabolizers, with no significant link between the genotype and reported side effects.

Article Abstract

Objectives: Amphetamine-based medications are recommended as a first-line pharmacotherapy for the treatment of attention-deficit/hyperactivity disorder in children and adolescents. However, the efficacy and tolerability of these medications vary across individuals, which could be related to interindividual differences in amphetamine metabolism. This study examined if genotype-predicted phenotypes of the cytochrome P450 isozyme CYP2D6 were associated with self-reported side effects and symptom improvement in youth treated with amphetamines.

Methods: Two hundred fourteen participants aged 6-24 who had a history of past or current amphetamine treatment were enrolled from Western Canada. Amphetamine dose and duration information was collected from the participants along with questions regarding adherence, concomitant medications, symptom improvement and side effects. DNA was extracted from saliva samples and genotyped for CYP2D6 . Binomial logistic regression models were used to determine the effect of CYP2D6 metabolizer phenotype with and without correction for phenoconversion on self-reported symptom improvement and side effects.

Results: Genotype-predicted CYP2D6 poor metabolizers had significantly higher odds of reporting symptom improvement when compared to intermediate metabolizers (OR = 3.67, 95% CI = 1.15-11.7, P  = 0.029) after correction for phenoconversion and adjusting for sex, age, dose, duration, and adherence. There was no association between CYP2D6 metabolizer phenotype and self-reported side effects.

Conclusion: Our findings indicate that phenoconverted and genotype-predicted CYP2D6 poor metabolizer phenotype is significantly associated with higher odds of symptom improvement in children and adolescents treated with amphetamine. If replicated, these results could inform the development of future dosing guidelines for amphetamine treatment in children and adolescents.

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Source
http://dx.doi.org/10.1097/FPC.0000000000000529DOI Listing

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