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非典型抗精神病药物的长期治疗与体重增加风险:一项文献分析。

Long-term treatment with atypical antipsychotics and the risk of weight gain : a literature analysis.

作者信息

Gentile Salvatore

机构信息

Department of Mental Health ASL Salerno 1, Mental Health Center n. 4, Cava de' Tirreni, Salerno, Italy.

出版信息

Drug Saf. 2006;29(4):303-19. doi: 10.2165/00002018-200629040-00002.

Abstract

The aim of this review is to analyse and summarise the literature data about the incidence of weight gain in patients exposed to atypical antipsychotics during long-term (>or=1 year) treatment regimens. Despite the clinical relevance of the topic, the vast majority of reviewed studies showed methodological limitations. Some trials had retrospective analysis, and concomitant medications also associated with an increased risk of weight gain, such as antidepressants and mood stabilisers, were often prescribed. Results were obtained from clinical trials conducted using flexible dosages; thus, the relationship between dosage and weight change was not explored adequately. Also, in a large number of studies, the average antipsychotic daily dose was lower than the usual dosage in clinical practice. Moreover, weight gain was evaluated by different measures, such as mean weight gain in the enrolled population, percentage of patients who gained >7% of basal weight or body mass index (BMI) variations from baseline. In short-term studies, a definite rank order of weight-gain potential among atypical antipsychotics has been demonstrated: clozapine is related to the highest risk of weight gain, followed in decreasing order of magnitude by olanzapine, quetiapine, risperidone, amisulpride, aripiprazole and ziprasidone. However, in long-term studies, except for clozapine at one end of the scale and ziprasidone at the other, the differences in weight-gain liability showed by the other atypical antipsychotics became less intense. Differences between short-term and long-term treatment could be due to a complex overlapping of different factors, both drug-specific (relative receptorial affinity; timing of weight change plateau; and drug-specific/dose-dependent weight gain), and patient-specific (genetic vulnerability; sex; age; BMI; weight before starting antipsychotic treatment; type of psychiatric disorder; and individual lifestyle). There is an urgent need for well designed, randomised controlled trials to assess firmly both the differential effects of atypical antipsychotics on weight and the role of other factors in contributing to iatrogenic unwanted weight changes. Meanwhile, the well known benefits shown by some atypical antipsychotics in reducing akathisia and other extrapyramidal adverse effects and improving cognition should be carefully balanced with the problems of weight gain, other metabolic complications and higher health care costs.

摘要

本综述的目的是分析和总结有关长期(≥1年)治疗方案中使用非典型抗精神病药物的患者体重增加发生率的文献数据。尽管该主题具有临床相关性,但绝大多数综述研究显示出方法学上的局限性。一些试验采用回顾性分析,并且经常开具也与体重增加风险增加相关的伴随药物,如抗抑郁药和心境稳定剂。结果来自使用灵活剂量进行的临床试验;因此,未充分探讨剂量与体重变化之间的关系。此外,在大量研究中,抗精神病药物的平均每日剂量低于临床实践中的常用剂量。而且,体重增加通过不同的测量方法进行评估,如纳入人群的平均体重增加、体重增加超过基础体重7%的患者百分比或体重指数(BMI)相对于基线的变化。在短期研究中,已证明非典型抗精神病药物之间体重增加潜力存在明确的排序:氯氮平与体重增加风险最高相关,其次按风险程度递减依次为奥氮平、喹硫平、利培酮、氨磺必利、阿立哌唑和齐拉西酮。然而,在长期研究中,除了一端的氯氮平和另一端的齐拉西酮外,其他非典型抗精神病药物显示出的体重增加倾向差异变得不那么明显。短期和长期治疗之间的差异可能归因于不同因素的复杂重叠,包括药物特异性因素(相对受体亲和力;体重变化平台期的时间;以及药物特异性/剂量依赖性体重增加)和患者特异性因素(遗传易感性;性别;年龄;BMI;开始抗精神病药物治疗前的体重;精神疾病类型;以及个人生活方式)。迫切需要设计良好的随机对照试验,以确切评估非典型抗精神病药物对体重的不同影响以及其他因素在导致医源性不良体重变化中的作用。同时,一些非典型抗精神病药物在减轻静坐不能和其他锥体外系不良反应以及改善认知方面所显示的众所周知的益处,应与体重增加问题、其他代谢并发症和更高的医疗保健成本仔细权衡。

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