Meltzer Herbert Y, Perry Edward, Jayathilake Karuna
Department of Psychiatry, Psychiatric Hospital at Vanderbilt, Vanderbilt University School of Medicine, 1601 23rd Avenue South 306, Nashville, TN 37215, USA.
Schizophr Res. 2003 Jan 1;59(1):19-27. doi: 10.1016/s0920-9964(01)00326-7.
Some, but not all, previous studies have indicated that weight gain is associated with greater improvement in psychopathology during clozapine treatment. Possible reasons for the inconsistent results include failure to adjust for initial body weight and level of psychopathology, differences in trial duration, outcome measures, reliability of assessment, concomitant medications and clozapine dosage. The purpose of this study was to test the hypothesis that clozapine-induced weight gain is related to antipsychotic efficacy at 6 weeks and 6 months after adjusting for initial body weight and severity of illness.
Weight and psychopathology were determined in 74 patients with schizophrenia or schizoaffective disorder at baseline and after 6 weeks and 6 months of open treatment with clozapine monotherapy. The primary measures of psychopathology were the Brief Psychiatric Rating Scale (BPRS) Total and Positive symptoms subscales, Schedule for Assessment of Negative Symptoms (SANS), Schedule for Assessment of Positive Symptoms (SAPS) and Global Assessment of Function Scale (GAFS).
Significant improvement in the key measures of psychopathology was noted at 6 weeks and 6 months. Mean weight gains at 6 weeks and 6 months were 3.7+/-5.7 S.D. and 7.3+/-7.9 S.D. kg, respectively, with the increase between 6 weeks and 6 months being significant. Age, but not gender, initial body weight, clozapine dosage or plasma levels predicted weight gain at both time points. At 6 weeks and 6 months, after adjustment for age, initial weight and level of psychopathology, the percentage change in weight significantly predicted the improvement in the BPRS Total and Positive symptoms subscale, the SANS Global score, as well as other measures of psychopathology.
Increase in weight with clozapine predicted improvement in psychopathology. This suggests that effects of clozapine on neurotransmitters which influence weight gain, e.g. 5-HT(2C) and 5-HT(1a) antagonism, in association with individual variations in these receptors and others molecules, e.g. peptides and transporters, due to polymorphisms or post-translational editing of mRNAs, may also contribute to the improvement in psychopathology.
先前的一些研究(但并非全部)表明,在氯氮平治疗期间体重增加与精神病理学的更大改善相关。结果不一致的可能原因包括未对初始体重和精神病理学水平进行调整、试验持续时间、结果测量、评估的可靠性、合并用药以及氯氮平剂量的差异。本研究的目的是检验这样一个假设:在调整初始体重和疾病严重程度后,氯氮平引起的体重增加与6周和6个月时的抗精神病疗效相关。
对74例精神分裂症或分裂情感性障碍患者在基线时以及接受氯氮平单一疗法开放治疗6周和6个月后测定体重和精神病理学情况。精神病理学的主要测量指标为简明精神病评定量表(BPRS)总分及阳性症状分量表、阴性症状评定量表(SANS)、阳性症状评定量表(SAPS)以及功能总体评定量表(GAFS)。
在6周和6个月时,精神病理学的关键测量指标有显著改善。6周和6个月时的平均体重增加分别为3.7±5.7标准差和7.3±7.9标准差千克,6周和6个月之间的增加具有显著性。年龄而非性别、初始体重、氯氮平剂量或血浆水平在两个时间点均预测了体重增加。在6周和6个月时,在调整年龄、初始体重和精神病理学水平后,体重的百分比变化显著预测了BPRS总分及阳性症状分量表、SANS总体评分以及其他精神病理学测量指标的改善情况。
氯氮平导致的体重增加预示着精神病理学的改善。这表明氯氮平对影响体重增加的神经递质(例如5-HT(2C)和5-HT(1a)拮抗作用)的作用,与这些受体以及其他分子(例如肽和转运体)由于多态性或mRNA的翻译后编辑导致的个体差异相关,也可能有助于精神病理学的改善。