首页> 外文期刊>Therapeutic Drug Monitoring >Large variability of aripiprazole and dehydroaripiprazole serum concentrations in adolescent patients with schizophrenia.
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Large variability of aripiprazole and dehydroaripiprazole serum concentrations in adolescent patients with schizophrenia.

机译:青少年精神分裂症患者的阿立哌唑和脱氢阿立哌唑血清浓度差异较大。

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Aripiprazole is a fairly new atypical antipsychotic substance. It acts as a partial D2- and 5-HT1A-agonist and as a 5-HT2A-antagonist. To date, there are few data concerning the dose-serum concentration relationship in children and adolescent psychiatric patients. Also, there are only few data on the influence of age, sex, body mass index, smoking behavior, and comedication on aripiprazole serum concentrations. In 33 consecutively admitted patients of a child and adolescent psychiatric hospital [age (mean +/- standard deviation) 18.7 +/- 1.7 years (range, 13.5-21.6 years)], 117 steady-state serum concentrations (repeated samples from individuals) of aripiprazole and its metabolite dehydroaripiprazole were assessed using high-performance liquid chromatography. The aripiprazole (mean +/- standard deviation) daily dose was 12.9 +/- 6.4 mg (range, 5-30 mg); the aripiprazole serum concentration was 142.0 +/- 122.7 ng/mL (range, 40.0-648.3 ng/mL; interquartile range, 74.0-167.0 ng/mL). The mean dehydroaripiprazole serum concentration was 51.6 +/- 22.3 ng/mL (range, 30.0-111.6 ng/mL; interquartile range, 34.3-62.1 ng/mL). There was a positive correlation between oral dose and serum concentrations of aripiprazole (r = 0.548, P = 0.001) and dehydroaripiprazole (r = 0.740, P 0.0005). Aripiprazole serum concentrations showed high inter- and intraindividual variability. Intraindividual variability was one- to 9.3-fold (dehydroaripiprazole: one- to 8.6-fold) and maximum interindividual variability 6.4-fold (dehydroaripiprazole: 6.8-fold). No significant influence was detected for age, sex, body mass index, comedication, and smoking on concentration-to-dose aripiprazole serum concentrations. Further studies are required to obtain data on the relationship between serum concentrations and resulting clinical effects.
机译:阿立哌唑是一种相当新的非典型抗精神病药物。它充当部分D2-和5-HT1A激动剂以及5-HT2A拮抗剂。迄今为止,关于儿童和青少年精神病患者的剂量-血清浓度关系的数据很少。而且,关于年龄,性别,体重指数,吸烟行为和喜剧对阿立哌唑血清浓度的影响的数据很少。在儿童和青少年精神病医院的33例连续入院患者中[年龄(平均+/-标准偏差)18.7 +/- 1.7年(范围13.5-21.6岁)],稳态血药浓度为117(个体重复样本)使用高效液相色谱法评估阿立哌唑及其代谢产物脱氢阿立哌唑的含量。阿立哌唑(平均+/-标准偏差)日剂量为12.9 +/- 6.4 mg(范围5-30 mg);阿立哌唑血药浓度为142.0 +/- 122.7 ng / mL(范围40.0-648.3 ng / mL;四分位数范围74.0-167.0 ng / mL)。脱氢阿立哌唑血清平均浓度为51.6 +/- 22.3 ng / mL(范围30.0-111.6 ng / mL;四分位间距34.3-62.1 ng / mL)。口服剂量与阿立哌唑(r = 0.548,P = 0.001)和脱氢阿立哌唑(r = 0.740,P <0.0005)的血清浓度之间呈正相关。阿立哌唑血清浓度表现出较高的个体间和个体内变异性。个体间变异性为1到9.3倍(脱氢阿立哌唑:1到8.6倍),最大个体间变异性为6.4倍(脱氢阿立哌唑:6.8倍)。没有发现年龄,性别,体重指数,喜剧和吸烟对阿立哌唑血药浓度的显着影响。需要进一步的研究以获得有关血清浓度与临床效果之间关系的数据。

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