Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN 46285, USA.
Curr Med Res Opin. 2011;27 Suppl 2:45-52. doi: 10.1185/03007995.2011.599372.
To determine the effects of long-term atomoxetine treatment on sexual development in children and adolescents with attention-deficit/hyperactivity disorder (ADHD) as compared with placebo and with a national US survey in non-Hispanic white children and adolescents.
This double-blind, placebo-controlled, relapse prevention, multicenter trial was conducted in pediatric patients (6-15 years) with DSM-IV diagnosed ADHD and lasting for ∼ 18 months. All patients received 10 weeks of open-label atomoxetine treatment (0.5-1.8 mg/kg/day). Patients responding in the last 2 weeks of treatment were randomized to double-blind treatment with either placebo or atomoxetine for up to 9 months, after which atomoxetine patients were re-randomized to either continued atomoxetine treatment or to placebo for up to another 6 months. Patients randomized to placebo at first randomization remained on placebo. The Tanner stage was assessed by the investigator at baseline and at approximately 6, 12, and 18 months, and the rate of sexual development (change in the Tanner stage) was compared between treatment groups.
No statistically significant differences were observed between treatment groups either in sexual development (mean time, in days, to the first Tanner stage change: atomoxetine, 464.3 ± 23.0; placebo, 433.1 ± 14.4; p = 0.33) or in the duration of treatment exposure (atomoxetine, 315.3 days; placebo, 315.1 days; p = 0.90). Similar proportions of patients had at least one Tanner stage increase (atomoxetine: 27.1%; placebo: 31.9%; p = 0.39). Proportions of patients in each baseline Tanner stage group moving to higher stages were not statistically significantly different (p = 0.88, p = 0.18, p > 0.99, p = 0.68 for baseline Tanner stages 1-4, respectively). The puberty onset age was similar across treatment groups and consistent with US normative data.
Long-term atomoxetine treatment was not associated with any appreciable impact on or delay in sexual maturation in children with ADHD compared with US normative data.
Study limitations include the relatively short duration of exposure to atomoxetine treatment, and the fact that half of the patients had been previously treated with stimulants. In addition, the Tanner stage data were collected as a secondary measure.
与安慰剂相比,并与美国非西班牙裔白人儿童和青少年的全国性调查相比,确定长期服用阿托西汀对注意缺陷多动障碍(ADHD)儿童和青少年性发育的影响。
本双盲、安慰剂对照、复发预防、多中心试验纳入了符合 DSM-IV 诊断的 ADHD 且持续时间约为 18 个月的儿科患者(6-15 岁)。所有患者均接受了 10 周的开放标签阿托西汀治疗(0.5-1.8mg/kg/天)。对治疗最后 2 周有反应的患者被随机分为双盲安慰剂或阿托西汀治疗组,最长可达 9 个月,然后将阿托西汀患者重新随机分为继续接受阿托西汀治疗或安慰剂治疗,最长可达另 6 个月。首次随机分组时接受安慰剂的患者继续接受安慰剂治疗。研究者在基线时和大约 6、12 和 18 个月时评估 Tanner 分期,比较治疗组之间的性发育(Tanner 分期变化率)。
治疗组之间在性发育方面(首次 Tanner 分期变化的平均时间,天:阿托西汀,464.3±23.0;安慰剂,433.1±14.4;p=0.33)或治疗暴露持续时间(阿托西汀,315.3 天;安慰剂,315.1 天;p=0.90)方面均未观察到统计学显著差异。至少有一次 Tanner 分期增加的患者比例相似(阿托西汀:27.1%;安慰剂:31.9%;p=0.39)。各基线 Tanner 分期组中进展到更高分期的患者比例无统计学显著差异(p=0.88、p=0.18、p>0.99、p=0.68,分别对应基线 Tanner 分期 1-4)。治疗组的青春期起始年龄相似,与美国参考数据一致。
与美国参考数据相比,长期阿托西汀治疗与 ADHD 儿童性成熟的任何明显影响或延迟无关。
研究局限性包括暴露于阿托西汀治疗的相对较短时间,以及一半的患者之前曾接受过兴奋剂治疗。此外,Tanner 分期数据是作为次要措施收集的。