Department of Pharmacy, Children's Hospital Colorado, Aurora, Colorado, USA.
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado, Aurora, Colorado, USA.
J Child Adolesc Psychopharmacol. 2024 Feb;34(1):52-60. doi: 10.1089/cap.2023.0087.
Evidence for pharmacogenomic (PGx) guided treatment in child and adolescent psychiatry is growing. This study evaluated the impact of PGx testing on psychotropic medication prescribing in an ambulatory child and adolescent psychiatry and a developmental pediatrics clinic. This was a single-center, retrospective, descriptive analysis of patients who underwent PGx testing between January 2015 and October 2022 at a child and adolescent psychiatry clinic or developmental pediatrics clinic. The primary outcome was the proportion of patients with at least one psychotropic medication modification made 6-month posttesting that could be attributed to CYP2C19, CYP2D6, HLA-B15:02, or HLA-A31:01. Secondary outcomes included reason for testing, types of therapeutic modifications made, and whether the therapeutic modifications concorded with PGx guidelines. A total of 193 patients were analyzed. The average age was 10 ± 4 years old, 60% were male, 78% were Caucasian. Sixty-eight percent had a primary diagnosis of a neurodevelopmental disorder, namely autism spectrum disorder (51%), and attention-deficit/hyperactivity disorder (14%). The reasons for PGx testing included medication inefficacy (34%), medication intolerance (20%), and family request (19%). At the time of PGx testing, 37% of patients were taking ≥1 psychotropic medication with PGx annotation. Overall, 35 PGx-related therapeutic modifications were made in 32 (17%) patients. These included continuing current PGx medication (6.2%) and starting PGx medication (5.2%). These modifications mainly involved antidepressants. Out of these 35 PGx-related therapeutic modifications, 94% were concordant with PGx guidelines. Among 29 patients who were prescribed at least one CYP2D6 inhibitor, 25 (86%) underwent CYP2D6 phenoconversion. It is critical to apply pediatric age-specific considerations when utilizing PGx testing in child and adolescent psychiatry. PGx testing stewardship could provide a framework to guide the clinical utility of PGx in a pediatric population with mental health conditions, including neurodevelopmental disorders.
越来越多的证据表明,药物基因组学(PGx)指导治疗在儿童和青少年精神病学中是有效的。本研究评估了 PGx 测试对门诊儿童和青少年精神病学和发育儿科诊所中精神药物处方的影响。这是一项单中心、回顾性、描述性分析,对 2015 年 1 月至 2022 年 10 月期间在儿童和青少年精神病学诊所或发育儿科诊所进行 PGx 测试的患者进行了分析。主要结果是 6 个月后测试后至少有一种精神药物修改,可归因于 CYP2C19、CYP2D6、HLA-B15:02 或 HLA-A31:01 的患者比例。次要结果包括测试的原因、进行的治疗修改类型以及治疗修改是否符合 PGx 指南。共分析了 193 名患者。平均年龄为 10±4 岁,60%为男性,78%为白种人。68%的患者有神经发育障碍的主要诊断,即自闭症谱系障碍(51%)和注意缺陷/多动障碍(14%)。PGx 测试的原因包括药物无效(34%)、药物不耐受(20%)和家庭要求(19%)。在进行 PGx 测试时,37%的患者正在服用具有 PGx 注释的≥1 种精神药物。总体而言,32 名(17%)患者进行了 35 次与 PGx 相关的治疗修改。这些包括继续当前的 PGx 药物(6.2%)和开始 PGx 药物(5.2%)。这些修改主要涉及抗抑郁药。在这 35 次与 PGx 相关的治疗修改中,94%与 PGx 指南一致。在 29 名服用至少一种 CYP2D6 抑制剂的患者中,25 名(86%)进行了 CYP2D6 表型转化。在儿童和青少年精神病学中使用 PGx 测试时,应用儿科特定年龄段的注意事项至关重要。PGx 测试管理可以为指导儿科人群的 PGx 临床应用提供一个框架,包括神经发育障碍等精神健康状况。