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

IF 1.7 3区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pharmacogenetics and genomics Pub Date : 2024-07-01 Epub Date: 2024-03-20 DOI:10.1097/FPC.0000000000000529
Samuel Gerlach, Abdullah Al Maruf, Sarker M Shaheen, Ryden McCloud, Madison Heintz, Laina McAusland, Paul D Arnold, Chad A Bousman
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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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CYP2D6 基因变异对接受苯丙胺类药物治疗的儿童和青少年中患者报告的症状改善和副作用的影响。
目的:苯丙胺类药物被推荐为治疗儿童和青少年注意力缺陷/多动症的一线药物疗法。然而,这些药物的疗效和耐受性因人而异,这可能与苯丙胺代谢的个体差异有关。本研究探讨了细胞色素 P450 同工酶 CYP2D6 的基因型预测表型是否与接受苯丙胺治疗的青少年自我报告的副作用和症状改善有关:方法: 从加拿大西部招募了 214 名年龄在 6-24 岁、过去或现在接受过苯丙胺治疗的参与者。收集了参与者的苯丙胺剂量和持续时间信息,以及有关坚持治疗、伴随药物、症状改善和副作用的问题。从唾液样本中提取 DNA 并进行 CYP2D6 基因分型。采用二项式逻辑回归模型来确定 CYP2D6 代谢物表型对自我报告的症状改善和副作用的影响,并对表型转换进行校正:在校正表型转换并调整性别、年龄、剂量、疗程和依从性后,基因型预测的 CYP2D6 差代谢者报告症状改善的几率明显高于中等代谢者(OR = 3.67,95% CI = 1.15-11.7,P = 0.029)。CYP2D6代谢物表型与自我报告的副作用之间没有关联:我们的研究结果表明,表型转换和基因型预测的 CYP2D6 不良代谢者表型与苯丙胺治疗的儿童和青少年症状改善的几率显著相关。这些结果如能得到证实,可为今后制定儿童和青少年苯丙胺治疗剂量指南提供参考。
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来源期刊
Pharmacogenetics and genomics
Pharmacogenetics and genomics 医学-生物工程与应用微生物
CiteScore
3.20
自引率
3.80%
发文量
47
审稿时长
3 months
期刊介绍: ​​​​Pharmacogenetics and Genomics is devoted to the rapid publication of research papers, brief review articles and short communications on genetic determinants in response to drugs and other chemicals in humans and animals. The Journal brings together papers from the entire spectrum of biomedical research and science, including biochemistry, bioinformatics, clinical pharmacology, clinical pharmacy, epidemiology, genetics, genomics, molecular biology, pharmacology, pharmaceutical sciences, and toxicology. Under a single cover, the Journal provides a forum for all aspects of the genetics and genomics of host response to exogenous chemicals: from the gene to the clinic.
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