Gentile S
Mental Health Center N. 4, ASL Salerno 1, Italy.
Obes Rev. 2009 Sep;10(5):527-42. doi: 10.1111/j.1467-789X.2009.00589.x. Epub 2009 May 12.
The increased rates of both overweight and obesity reported in severely mentally-ill patients are prevalently due to the use of second-generation antipsychotics (SGAs). Hence, the main purpose of this article is to analyze systematically potential patient- and drug-related factors which may increase the risk of weight gain during long-term treatment with such medications. Literature information published in English since 1966 and last updated on 17 January 2009 was identified through different databases and using various combinations of search terms. Searches provided 242 articles, whereas 6 additional references were identified manually. Peer-reviewed articles focusing on the risk of weight gain during SGA-chronic treatment (at least 52 weeks, N = 81) were acquired. Data were extracted from the 39 peer-reviewed articles which investigated factors potentially associated with an increased risk of this event. Evidence-based information suggests that a number of factors, either patient- (age, baseline BMI/bodyweight, recent onset of psychotic episodes, need of concomitant psychotropic medications) or drug-specific (relative receptorial affinity, timing of weight changes plateau, daily dose, iatrogenic concomitant changes in biochemical metabolic parameters) may contribute to increase either rates and/or magnitude of this effect during long-term treatments with specific SGAs. All contributors and their relationship with specific drugs should be taken into consideration when designing a long-term therapy with SGAs. Among the best studied agents (clozapine, olanzapine, and risperidone) of this class, the latter seems to be the most susceptible drug to the amplifying effects of both patient- and drug-related factors on the risk of inducing weight changes during chronic treatments.
据报道,重症精神病患者超重和肥胖率的上升主要归因于第二代抗精神病药物(SGA)的使用。因此,本文的主要目的是系统分析可能增加此类药物长期治疗期间体重增加风险的潜在患者因素和药物相关因素。通过不同数据库并使用各种搜索词组合,确定了自1966年以来以英文发表并于2009年1月17日最后更新的文献信息。搜索共得到242篇文章,另外还手动识别出6篇参考文献。获取了专注于SGA长期治疗(至少52周,N = 81)期间体重增加风险的同行评审文章。从39篇同行评审文章中提取数据,这些文章调查了可能与此事件风险增加相关的因素。循证信息表明,一些因素,无论是患者相关因素(年龄、基线BMI/体重、近期精神病发作、需要同时使用精神药物)还是药物特异性因素(相对受体亲和力、体重变化平稳期的时间、每日剂量、生化代谢参数的医源性伴随变化),都可能在使用特定SGA进行长期治疗期间导致这种影响的发生率和/或程度增加。在设计SGA长期治疗方案时,应考虑所有促成因素及其与特定药物的关系。在这类研究最多的药物(氯氮平、奥氮平和利培酮)中,利培酮似乎是在慢性治疗期间患者相关因素和药物相关因素对诱发体重变化风险放大作用最敏感的药物。