首页> 外文期刊>JAMA: the Journal of the American Medical Association >Cardiometabolic risk of second-generation antipsychotic medications during first-time use in children and adolescents.
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Cardiometabolic risk of second-generation antipsychotic medications during first-time use in children and adolescents.

机译:儿童和青少年初次使用第二代抗精神病药物的心脏代谢风险。

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CONTEXT: Cardiometabolic effects of second-generation antipsychotic medications are concerning but have not been sufficiently studied in pediatric and adolescent patients naive to antipsychotic medication. OBJECTIVE: To study the association of second-generation antipsychotic medications with body composition and metabolic parameters in patients without prior antipsychotic medication exposure. DESIGN, SETTING, AND PATIENTS: Nonrandomized Second-Generation Antipsychotic Treatment Indications, Effectiveness and Tolerability in Youth (SATIETY) cohort study, conducted between December 2001 and September 2007 at semi-urban, tertiary care, academic inpatient and outpatient clinics in Queens, New York, with a catchment area of 4.5-million individuals. Of 505 youth aged 4 to 19 years with 1 week or less of antipsychotic medication exposure, 338 were enrolled (66.9%). Of these patients, 272 had at least 1 postbaseline assessment (80.5%), and 205 patients [corrected] completed the study (60.7%). Patients had mood spectrum (n = 130; 47.8%), schizophrenia spectrum (n = 82; 30.1%), and disruptive or aggressive behavior spectrum (n = 60; 22.1%) disorders. Fifteen patients who refused participation or were nonadherent served as a comparison group. INTERVENTION: Treatment with aripiprazole, olanzapine, quetiapine, or risperidone for 12 weeks. MAIN OUTCOME MEASURES: Weight gain and changes in lipid and metabolic parameters. RESULTS: After a median of 10.8 weeks (interquartile range, 10.5-11.2 weeks) of treatment, weight increased by 8.5 kg (95% confidence interval [CI], 7.4 to 9.7 kg) with olanzapine (n = 45), by 6.1 kg (95% CI, 4.9 to 7.2 kg) with quetiapine (n = 36), by 5.3 kg (95% CI, 4.8 to 5.9 kg) with risperidone (n = 135), and by 4.4 kg (95% CI, 3.7 to 5.2 kg) with aripiprazole (n = 41) compared with the minimal weight change of 0.2 kg (95% CI, -1.0 to 1.4 kg) in the untreated comparison group (n = 15). With olanzapine and quetiapine, respectively, mean levels increased significantly for total cholesterol (15.6 mg/dL [95% CI, 6.9 to 24.3 mg/dL] P < .001 and 9.1 mg/dL [95% CI, 0.4 to 17.7 mg/dL] P = .046), triglycerides (24.3 mg/dL [95% CI, 9.8 to 38.9 mg/dL] P = .002 and 37.0 mg/dL [95% CI, 10.1 to 63.8 mg/dL] P = .01), non-high-density lipoprotein (HDL) cholesterol (16.8 mg/dL [95% CI, 9.3 to 24.3 mg/dL] P < .001 and 9.9 mg/dL [95% CI, 1.4 to 18.4 mg/dL] P = .03), and ratio of triglycerides to HDL cholesterol (0.6 [95% CI, 0.2 to 0.9] P = .002 and (1.2 [95% CI, 0.4 to 2.0] P = .004). With risperidone, triglycerides increased significantly (mean level, 9.7 mg/dL [95% CI, 0.5 to 19.0 mg/dL]; P = .04). Metabolic baseline-to-end-point changes were not significant with aripiprazole or in the untreated comparison group. CONCLUSIONS: First-time second-generation antipsychotic medication use was associated with significant weight gain with each medication. Metabolic changes varied among the 4 antipsychotic medications.
机译:语境:第二代抗精神病药物的心脏代谢作用值得关注,但尚未对未使用抗精神病药物的儿童和青少年患者进行充分研究。目的:研究未接触抗精神病药物的患者中第二代抗精神病药物与身体成分和代谢参数的关系。设计,地点和患者:2001年12月至2007年9月在纽约市皇后区的半城市,三级医疗,学术住院和门诊进行的非随机第二代抗精神病药物治疗适应症,青少年的有效性和耐受性(SATIETY)队列研究。约克,集水区有450万人。在505位4至19岁的年轻人中,服用抗精神病药物1周或更短的时间,其中338位(66.9%)被纳入研究。这些患者中,有272位接受了至少1次基线后评估(占80.5%),有205位患者(校正后)完成了研究(占60.7%)。患者有情绪频谱(n = 130; 47.8%),精神分裂症频谱(n = 82; 30.1%)和破坏性或攻击行为频谱(n = 60; 22.1%)。十五名拒绝参加或未坚持治疗的患者作为对照组。干预:用阿立哌唑,奥氮平,喹硫平或利培酮治疗12周。主要观察指标:体重增加以及脂质和代谢参数的变化。结果:在接受中位治疗10.8周(四分位间距为10.5-11.2周)后,奥氮平(n = 45)使体重增加8.5千克(95%置信区间[CI]为7.4至9.7千克),增加6.1千克(95%CI,4.9至7.2千克)与喹硫平(n = 36),5.3千克(95%CI,4.8至5.9千克)与利培酮(n = 135)和4.4千克(95%CI,3.7至3.7千克) 5.2公斤)与阿立哌唑(n = 41)相比,未治疗的对照组(n = 15)的最小体重变化为0.2公斤(95%CI,-1.0至1.4公斤)。分别使用奥氮平和喹硫平后,总胆固醇的平均水平显着增加(15.6 mg / dL [95%CI,6.9至24.3 mg / dL] P <.001和9.1 mg / dL [95%CI,0.4至17.7 mg / d dL] P = .046),甘油三酸酯(24.3 mg / dL [95%CI,9.8至38.9 mg / dL] P = .002和37.0 mg / dL [95%CI,10.1至63.8 mg / dL] P =。 01),非高密度脂蛋白(HDL)胆固醇(16.8 mg / dL [95%CI,9.3至24.3 mg / dL] P <.001和9.9 mg / dL [95%CI,1.4至18.4 mg / dL ] P = .03),以及甘油三酸酯与HDL胆固醇的比率(0.6 [95%CI,0.2至0.9] P = .002和(1.2 [95%CI,0.4至2.0] P = .004)。甘油三酸酯显着增加(平均水平,9.7 mg / dL [95%CI,0.5至19.0 mg / dL]; P = .04)。阿立哌唑或未经治疗的对照组的代谢基线至终点变化不明显结论:第一次使用第二代抗精神病药物与每种药物的体重显着增加有关,代谢变化在不同的药物中有所不同。 4种抗精神病药。

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