首页> 外文期刊>CNS drugs >Lower IQ is associated with decreased clinical response to atomoxetine in children and adolescents with attention-deficit hyperactivity disorder.
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Lower IQ is associated with decreased clinical response to atomoxetine in children and adolescents with attention-deficit hyperactivity disorder.

机译:智商低与患有注意力缺陷多动障碍的儿童和青少年对阿托西汀的临床反应降低有关。

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OBJECTIVES: Atomoxetine is commonly used to treat attention-deficit hyperactivity disorder (ADHD) in children with a broad range of cognitive abilities. We examined the association between level of cognitive functioning as determined by IQ and clinical response during treatment with atomoxetine. METHODS: The records of all the children and adolescents treated with atomoxetine at a university clinic in Catania, Italy, over a 3-year period were examined. A total of 55 clinically referred children and adolescents (aged 5-15 years, 53 males) with ADHD were treated with atomoxetine (10-110 mg/day; mean: 1.28 mg/kg/day) for a period ranging from 2 to 168 weeks (mean: 57.3 +/- SD 39.4, median: 56). The IQ was assessed as part of the diagnostic evaluation prior to starting treatment. During treatment, clinical outcome was rated on the Clinical Global Impression-Improvement (CGI-I) and CGI-Severity (CGI-S) scales. RESULTS: The IQ ranged from 43 to 117 (mean: 80.6 +/- SD 18.6, median: 84). The IQ and final CGI-I scores were negatively correlated (r = -0.68; p < 0.01). Children and adolescents with an IQ <85 were less likely to be responders (defined as a final CGI-I score of 1 or 2) than children and adolescents with an IQ >/=85 (20.71% vs 76.9%; p < 0.001). None of the patients discontinued atomoxetine due to adverse effects, while treatment was discontinued in 20 subjects due to a lack of efficacy or ambivalence of parents about pharmacological treatment. CONCLUSIONS: Atomoxetine appears to be less effective in children and adolescents with an IQ <85 than in children and adolescents in the average range of cognitive functioning. This difference is not accounted for by differences in the severity of ADHD symptoms, co-morbidity or reduced tolerability to the medication. These findings suggest that, in order to be fully informative, clinical trials of medications for ADHD should also include children and adolescents functioning in the borderline and cognitive disability range.
机译:目的:阿托莫西汀通常用于治疗具有广泛认知能力的儿童的注意力缺陷多动障碍(ADHD)。我们检查了由智商决定的认知功能水平与阿托西汀治疗期间的临床反应之间的关联。方法:检查了在意大利卡塔尼亚的一家大学诊所接受阿托西汀治疗的所有儿童和青少年在3年期间的记录。共有55名临床上转诊的ADHD儿童和青少年(5-15岁,男53名)接受阿托西汀(10-110 mg /天;平均:1.28 mg / kg /天)治疗,时间从2至168周(平均值:57.3 +/- SD 39.4,中位数:56)。在开始治疗之前,将智商作为诊断评估的一部分进行评估。在治疗期间,根据临床总体印象改善(CGI-1)和CGI严重程度(CGI-S)量表对临床结局进行评估。结果:智商范围从43到117(平均值:80.6 +/- SD 18.6,中位数:84)。智商和最终CGI-I得分呈负相关(r = -0.68; p <0.01)。与智商> / = 85的儿童和青少年相比,智商<85的儿童和青少年的响应者(定义为最终CGI-I得分为1或2)的可能性较小(20.71%对76.9%; p <0.001) 。没有一例患者因不良反应而停用阿托西汀,而由于缺乏疗效或父母对药理学的态度不明确,终止了20名受试者的治疗。结论:在平均认知功能范围内,智商低于85的儿童和青少年看来,阿托莫西汀的疗效不及儿童和青少年。 ADHD症状的严重程度,并存症或对药物的耐受性降低无法解释这种差异。这些发现表明,为了提供充分的信息,多动症药物的临床试验还应包括在临界和认知障碍范围内起作用的儿童和青少年。

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