Ruud H J Verstegen, Iris Cohn, Mark E Feldman, Daniel Gorman, Shinya Ito
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Practice guidelines have been developed for variants in pharmacogenes encoding cytochrome P450 drug-metabolizing enzymes (e.g., <i>CYP2C19</i>, <i>CYP2D6</i>, <i>CYP2C9</i>) as one determinant of drug concentrations in blood, which can support both drug choice and dosing strategy for certain anti-psychotics, anti-depressants, and anti-epileptics. Adverse drug reactions to some anti-epileptic drugs (e.g., carbamazepine and phenytoin) have been associated with certain human leukocyte antigen types and variants in DNA polymerase gamma (<i>POLG</i>; valproic acid). 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引用次数: 0
摘要
越来越多的精神药物被用于治疗患有精神疾病的儿童和青少年,但个体反应的差异凸显了精准医疗的必要性。药物基因(PGx)检测是精准医疗的关键组成部分。近年来,推广 PGx 的商业药物基因检测公司数量急剧增加,它们承诺实现精神疾病的个体化有效治疗。支持使用 PGx 治疗精神疾病的科学证据有限,尤其是在儿科人群中。本实践要点概述了在临床环境中使用和解释精神活性药物 PGx 检测的指导步骤,以及主要的支持资源。药物基因编码细胞色素P450药物代谢酶(如CYP2C19、CYP2D6、CYP2C9)的变异是血液中药物浓度的决定因素之一,已针对这些变异制定了实践指南,可为某些抗精神病药、抗抑郁药和抗癫痫药的药物选择和剂量策略提供支持。某些抗癫痫药物(如卡马西平和苯妥英)的药物不良反应与某些人类白细胞抗原类型和 DNA 聚合酶伽马(POLG;丙戊酸)变异有关。有关药物靶蛋白基因变异的证据仍然有限,这使得确定在治疗血药浓度下治疗反应发生改变的患者具有挑战性。
Gene-based drug therapy for children and youth treated with psychoactive medications.
Psychoactive medications are increasingly used to treat children and youth with mental health conditions, but individual variations in response highlight the need for precision medicine. Pharmacogenetic (PGx) testing is a key component of precision medicine. The number of commercial pharmacogenetic testing companies promoting PGx, with the promise of achieving individualized and effective treatment of mental health conditions, has grown exponentially in recent years. Scientific evidence supporting the use of PGx to manage mental health conditions is limited, especially for paediatric populations. This practice point outlines steps guiding the use and interpretation of PGx testing for psychoactive medications in clinical settings, along with key supportive resources. Practice guidelines have been developed for variants in pharmacogenes encoding cytochrome P450 drug-metabolizing enzymes (e.g., CYP2C19, CYP2D6, CYP2C9) as one determinant of drug concentrations in blood, which can support both drug choice and dosing strategy for certain anti-psychotics, anti-depressants, and anti-epileptics. Adverse drug reactions to some anti-epileptic drugs (e.g., carbamazepine and phenytoin) have been associated with certain human leukocyte antigen types and variants in DNA polymerase gamma (POLG; valproic acid). Evidence remains limited for genetic variants of drug target proteins, making it challenging to identify patients with altered treatment responses at a therapeutic blood concentration.
期刊介绍:
Paediatrics & Child Health (PCH) is the official journal of the Canadian Paediatric Society, and the only peer-reviewed paediatric journal in Canada. Its mission is to advocate for the health and well-being of all Canadian children and youth and to educate child and youth health professionals across the country.
PCH reaches 8,000 paediatricians, family physicians and other child and youth health professionals, as well as ministers and officials in various levels of government who are involved with child and youth health policy in Canada.