Suppr超能文献

儿童和青少年使用抗精神病药物相关的体重增加及代谢风险。

Weight gain and metabolic risks associated with antipsychotic medications in children and adolescents.

作者信息

Maayan Lawrence, Correll Christoph U

机构信息

Nathan Kline Institute for Psychiatric Research, Orangeburg, New York, USA.

出版信息

J Child Adolesc Psychopharmacol. 2011 Dec;21(6):517-35. doi: 10.1089/cap.2011.0015. Epub 2011 Dec 13.

Abstract

BACKGROUND

Antipsychotic-related weight gain and metabolic adverse effects have become a major focus, especially in youth.

METHODS

Review of randomized, cohort, and pharmacoepidemiologic studies of antipsychotic-related weight gain and metabolic adverse effects and of interventions for their reduction in youth.

RESULTS

Across 34 published head-to-head and placebo-controlled studies in youth with psychotic and bipolar disorders, weight gain ranged from 3.8 to 16.2 kg with olanzapine (n=353), 0.9-9.5 kg with clozapine (n=97), 1.9-7.2 kg with risperidone (n=571), 2.3-6.1 kg with quetiapine (n=133), and 0-4.4 kg with aripiprazole (n=451). In 24 placebo-controlled trials, the numbers-needed-to-harm for weight gain ≥7% in youth with bipolar disorder and schizophrenia were 39 (confidence interval [CI]: -1 to +6, not significant) for aripiprazole, 36 (CI: -1 to +7, not significant) for ziprasidone, 9 (CI: 7-14) for quetiapine, 6 (CI: 5-8) for risperidone, and 3 (CI: 3-4) for olanzapine. Data in youth with autism and disruptive behavior disorders, available only for some antipsychotics, suggest greater weight gain, possibly due to less prior antipsychotic exposure. Three-month results from a large cohort study in antipsychotic-naïve youth indicated that metabolic effects differ among second-generation antipsychotics, despite significant weight gain with all studied agents, suggesting additional, weight-independent effects. Further, pharmacoepidemiologic work indicates that antipsychotic polypharmacy increases the risk for obesity (odds ratio [OR]: 2.28 [CI: 1.49-3.65]) or any cardiovascular, cerebrovascular, or hypertensive adverse event (OR: 1.72 [CI: 1.10-2.69]). However, despite marked weight gain and its greater impact on youth, monitoring rates are low and studies of pharmacologic and behavioral interventions are extremely limited.

CONCLUSIONS

More research is needed to develop strategies to minimize antipsychotic-related weight gain and metabolic effects in youth and to discover treatments with lower risk potential.

摘要

背景

抗精神病药物相关的体重增加和代谢不良反应已成为主要关注点,尤其是在青少年中。

方法

回顾关于抗精神病药物相关体重增加和代谢不良反应以及减少青少年此类不良反应干预措施的随机、队列和药物流行病学研究。

结果

在34项已发表的针对患有精神病性和双相情感障碍青少年的头对头及安慰剂对照研究中,使用奥氮平(n = 353)时体重增加范围为3.8至16.2千克,使用氯氮平(n = 97)时为0.9至9.5千克,使用利培酮(n = 571)时为1.9至7.2千克,使用喹硫平(n = 133)时为2.3至6.1千克,使用阿立哌唑(n = 451)时为0至4.4千克。在24项安慰剂对照试验中,双相情感障碍和精神分裂症青少年体重增加≥7%的伤害性需治数,阿立哌唑为39(置信区间[CI]:-1至+6,无显著性差异),齐拉西酮为36(CI:-1至+7,无显著性差异),喹硫平为9(CI:7 - 14),利培酮为6(CI:5 - 8),奥氮平为3(CI:3 - 4)。在患有自闭症和破坏性行为障碍的青少年中,仅部分抗精神病药物有相关数据,提示体重增加更多,可能是因为之前使用抗精神病药物较少。一项针对未使用过抗精神病药物青少年的大型队列研究的三个月结果表明,尽管所有研究药物均导致显著体重增加,但第二代抗精神病药物的代谢效应存在差异,提示存在其他与体重无关的效应。此外,药物流行病学研究表明,联合使用多种抗精神病药物会增加肥胖风险(比值比[OR]:2.28 [CI:1.49 - 3.65])或任何心血管、脑血管或高血压不良事件的风险(OR:1.72 [CI:1.10 - 2.69])。然而,尽管体重显著增加且对青少年影响更大,但监测率较低,关于药物和行为干预的研究极为有限。

结论

需要开展更多研究,以制定策略将青少年抗精神病药物相关体重增加和代谢效应降至最低,并发现潜在风险较低的治疗方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验