Riegger Jessica, Egberts Karin Maria, Clement Hans-Willi, Schneider-Momm Katja, Taurines Regina, Fekete Stefanie, Wewetzer Christoph, Karwautz Andreas, Correll Christoph U, Plener Paul L, Malzahn Uwe, Heuschmann Peter, Unterecker Stefan, Scherf-Clavel Maike, Rock Hans, Antony Gisela, Briegel Wolfgang, Banaschewski Tobias, Hellenschmidt Tobias, Kaess Michael, Kölch Michael, Renner Tobias, Rexroth Christian, Schulte-Körne Gerd, Walitza Susanne, Gerlach Manfred, Romanos Marcel, Fleischhaker Christian
Department of Child and Adolescent Psychiatry and Psychotherapy, University Medical Center Freiburg, Freiburg, Germany.
Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Center for Mental Health, University Hospital of Wuerzburg, Wuerzburg, Germany.
J Neural Transm (Vienna). 2025 Feb;132(2):295-312. doi: 10.1007/s00702-024-02819-6. Epub 2024 Nov 2.
Aripiprazole is approved for various severe mental disorders in adults and adolescents. However, off-label prescribing is common, especially in children and adolescents (youth) in whom aripiprazole therapeutic serum level reference ranges are lacking for any disorders. The aim of the study was to evaluate the relationship between aripiprazole dose and serum concentrations and provide further knowledge on the use of aripiprazole in order to improve drug safety and effectiveness in the treatment of minors. The clinical course of youth treated with aripiprazole in the multicentre pharmacovigilance study TDM-VIGIL was systematically followed and serum concentrations measured. Sex, age, weight and comedications were analysed to identify possible effect modifiers. A preliminary therapeutic reference range was estimated for youth with schizophrenia-spectrum disorders, affective disorders and behavioural/emotional/tic disorders coded as treatment responders based on a Clinical-Global Impressions-Improvement (CGI-I) score of much or very much improved. In 93 youth (mean age = 15.2 ± 2.6, range = 7.4-18.2 years, females = 53%, CGI-Severity = 4.4 ± 1.1, responders = 64%), a positive, moderate correlation between the weight-normalized daily dose (WNDD) and aripiprazole serum concentration (=0.791, p < 0.0001) was found. The WNDD and co-medications that interact with CYP2D6 and CYP3A4 affected aripiprazole serum levels, explaining 64% of the variance. In patients within the preliminary therapeutic ranges determined by interquartile ranges (IQRs), slightly better outcomes and fewer adverse drug reactions were found versus patients within preliminary therapeutic ranges determined by the mean ± SD. The preliminary reference range for paediatric patients with schizophrenia-spectrum disorders calculated by the IQR showed an identical lower threshold (100-230 ng/ml) compared to adult schizophrenia-spectrum disorders patients (100-350 ng/ml). The preliminary therapeutic ranges for patients with affective disorders was: 60-160 ng/ml and for patients with behavioural/tic disorders 60-140 ng/ml. The therapeutic reference ranges for aripiprazole in youth estimated via the 25th and 75th IQRs may result in more clinically relevant therapeutic windows. Further studies need to confirm these results, especially in patients with affective and behavioural/tic disorder diagnoses.
阿立哌唑被批准用于治疗成人和青少年的各种严重精神障碍。然而,超说明书用药很常见,尤其是在儿童和青少年(青年)中,目前尚无任何疾病的阿立哌唑治疗血清水平参考范围。本研究的目的是评估阿立哌唑剂量与血清浓度之间的关系,并提供关于阿立哌唑使用的更多知识,以提高其在治疗未成年人中的药物安全性和有效性。在多中心药物警戒研究TDM-VIGIL中,系统地跟踪了接受阿立哌唑治疗的青年的临床病程,并测量了血清浓度。分析了性别、年龄、体重和合并用药情况,以确定可能的效应修饰因素。根据临床总体印象改善(CGI-I)评分为“明显改善”或“非常明显改善”,将精神分裂症谱系障碍、情感障碍和行为/情绪/抽动障碍的青年患者编码为治疗反应者,并估计其初步治疗参考范围。在93名青年患者中(平均年龄=15.2±2.6岁,范围=7.4-18.2岁,女性=53%,CGI严重程度=4.4±1.1,反应者=64%),发现体重标准化日剂量(WNDD)与阿立哌唑血清浓度之间存在正性、中度相关性(r=0.791,p<0.0001)。与CYP2D6和CYP3A4相互作用的WNDD和合并用药影响阿立哌唑血清水平,解释了64%的变异。与根据均值±标准差确定的初步治疗范围内的患者相比,在由四分位数间距(IQR)确定的初步治疗范围内的患者中,发现结局略好且药物不良反应较少。通过IQR计算的精神分裂症谱系障碍儿科患者的初步参考范围显示,其下限(100-230 ng/ml)与成人精神分裂症谱系障碍患者(100-350 ng/ml)相同。情感障碍患者的初步治疗范围为:60-160 ng/ml,行为/抽动障碍患者为60-140 ng/ml。通过第25和第75四分位数间距估计的青年阿立哌唑治疗参考范围可能会产生更具临床相关性的治疗窗。需要进一步研究来证实这些结果,尤其是在情感障碍和行为/抽动障碍诊断的患者中。