Wetterling T
Department of Psychiatry and Psychotherapy I, Johann Wolfgang Goethe University, Frankfurt, Germany.
Drug Saf. 2001 Jan;24(1):59-73. doi: 10.2165/00002018-200124010-00005.
The atypical antipsychotics have been shown to have superior efficacy compared with typical antipsychotics such as haloperidol, particularly in the treatment of negative symptoms of schizophrenia. Furthermore, they induce less extrapyramidal effects. However, following clinical use, marked bodyweight gain has been frequently observed with some of the atypical antipsychotic drugs. In order to examine and compare the frequency, amount and conditions of bodyweight gain during treatment with atypical antipsychotics, studies concerning bodyweight gain with these agents were identified through a MEDLINE search from 1966 to March 2000. Although comparison is limited by the different designs and recruitment procedures of the reviewed studies, the available data support the notion that the frequency as well as the amount of bodyweight gain is high in patients treated with olanzapine (average bodyweight gain 2.3 kg/month), clozapine (1.7 kg/month), quetiapine (1.8 kg/month), and possibly also zotepine (2.3 kg/month). Moderate changes in bodyweight have been observed in the treatment with risperidone (average bodyweight gain 1.0 kg/month). Ziprasidone seems to induce only slight bodyweight changes (0.8 kg/month). Bodyweight gain most frequently occurs in the first 12 weeks of treatment. Patients who were underweight at the beginning of treatment are at highest risk of gaining bodyweight. The underlying pathomechanism still remains largely unclear. The relative receptor affinities of the atypical antipsychotics for histamine H1 receptors as well as the ratio of their affinity for serotonin 5-HT2 and dopamine D2 receptors appear to be the most robust correlate of bodyweight gain. Furthermore, the induction of leptin secretion may have an important impact on bodyweight gain in patients treated with atypical antipsychotics. Although many questions concerning the pathogenesis of bodyweight gain remain unresolved, this adverse effect has to be taken into consideration when prescribing the atypical antipsychotics, particularly in view its affect on compliance during long term treatment and the long term effects of obesity on mortality and morbidity.
与氟哌啶醇等典型抗精神病药物相比,非典型抗精神病药物已显示出更高的疗效,尤其是在治疗精神分裂症的阴性症状方面。此外,它们引起的锥体外系反应较少。然而,在临床应用后,经常观察到一些非典型抗精神病药物会导致明显的体重增加。为了研究和比较使用非典型抗精神病药物治疗期间体重增加的频率、幅度和情况,通过对1966年至2000年3月的MEDLINE数据库检索,确定了有关这些药物导致体重增加的研究。尽管由于所审查研究的设计和招募程序不同,比较受到限制,但现有数据支持这样一种观点,即使用奥氮平(平均体重增加2.3千克/月)、氯氮平(1.7千克/月)、喹硫平(1.8千克/月)以及可能还有佐替平(2.3千克/月)治疗的患者体重增加的频率和幅度都很高。使用利培酮治疗时观察到体重有中度变化(平均体重增加1.0千克/月)。齐拉西酮似乎仅引起轻微的体重变化(0.8千克/月)。体重增加最常发生在治疗的前12周。治疗开始时体重过轻的患者体重增加的风险最高。其潜在的发病机制在很大程度上仍不清楚。非典型抗精神病药物对组胺H1受体的相对受体亲和力以及它们对5-羟色胺5-HT2和多巴胺D2受体的亲和力之比似乎是体重增加最密切的相关因素。此外,瘦素分泌的诱导可能对使用非典型抗精神病药物治疗的患者的体重增加有重要影响。尽管关于体重增加的发病机制仍有许多问题未得到解决,但在开具非典型抗精神病药物处方时必须考虑到这种不良反应,特别是鉴于其对长期治疗依从性的影响以及肥胖对死亡率和发病率的长期影响。