Ascher-Svanum Haya, Stensland Michael, Zhao Zhongyun, Kinon Bruce J
Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana.
BMC Psychiatry. 2005 Jan 13;5:3. doi: 10.1186/1471-244X-5-3.
Previous research indicated that women are more vulnerable than men to adverse psychological consequences of weight gain. Other research has suggested that weight gain experienced during antipsychotic therapy may also psychologically impact women more negatively. This study assessed the impact of acute treatment-emergent weight gain on clinical and functional outcomes of patients with schizophrenia by patient gender and antipsychotic treatment (olanzapine or haloperidol).
Data were drawn from the acute phase (first 6-weeks) of a double-blind randomized clinical trial of olanzapine versus haloperidol in the treatment of 1296 men and 700 women with schizophrenia-spectrum disorders. The associations between weight change and change in core schizophrenia symptoms, depressive symptoms, and functional status were examined post-hoc for men and women and for each medication group. Core schizophrenia symptoms (positive and negative) were measured with the Brief Psychiatric Rating Scale (BPRS), depressive symptoms with the BPRS Anxiety/Depression Scale and the Montgomery-Asberg Depression Rating Scale, and functional status with the mental and physical component scores on the Medical Outcome Survey-Short Form 36. Statistical analysis included methods that controlled for treatment duration.
Weight gain during 6-week treatment with olanzapine and haloperidol was significantly associated with improvements in core schizophrenia symptoms, depressive symptoms, mental functioning, and physical functioning for men and women alike. The conditional probability of clinical response (20% reduction in core schizophrenia symptom), given a clinically significant weight gain (at least 7% of baseline weight), showed that about half of the patients who lost weight responded to treatment, whereas three-quarters of the patients who had a clinically significant weight gain responded to treatment. The positive associations between therapeutic response and weight gain were similar for the olanzapine and haloperidol treatment groups. Improved outcomes were, however, more pronounced for the olanzapine-treated patients, and more olanzapine-treated patients gained weight.
The findings of significant relationships between treatment-emergent weight gain and improvements in clinical and functional status at 6-weeks suggest that patients who have greater treatment-emergent weight gain are more likely to benefit from treatment with olanzapine or haloperidol regardless of gender.
先前的研究表明,在体重增加的不良心理后果方面,女性比男性更脆弱。其他研究表明,在抗精神病药物治疗期间体重增加对女性的心理影响可能也更负面。本研究按患者性别和抗精神病药物治疗(奥氮平或氟哌啶醇)评估了急性治疗期出现的体重增加对精神分裂症患者临床和功能结局的影响。
数据取自一项奥氮平与氟哌啶醇治疗1296名男性和700名精神分裂症谱系障碍女性的双盲随机临床试验的急性期(前6周)。对男性和女性以及每个药物治疗组,事后检验体重变化与精神分裂症核心症状、抑郁症状和功能状态变化之间的关联。精神分裂症核心症状(阳性和阴性)用简明精神病评定量表(BPRS)测量,抑郁症状用BPRS焦虑/抑郁量表和蒙哥马利-阿斯伯格抑郁评定量表测量,功能状态用医学结局调查简表36的心理和生理成分得分测量。统计分析包括控制治疗持续时间的方法。
奥氮平和氟哌啶醇治疗6周期间体重增加与男性和女性精神分裂症核心症状、抑郁症状、心理功能和生理功能的改善均显著相关。在临床显著体重增加(至少为基线体重的7%)的情况下,临床反应(核心精神分裂症症状减少20%)的条件概率表明,约一半体重减轻的患者对治疗有反应,而四分之三临床显著体重增加的患者对治疗有反应。奥氮平和氟哌啶醇治疗组治疗反应与体重增加之间的正相关相似。然而,奥氮平治疗的患者结局改善更明显,且更多接受奥氮平治疗的患者体重增加。
治疗期出现的体重增加与6周时临床和功能状态改善之间存在显著关系的研究结果表明,无论性别,治疗期体重增加较多的患者更有可能从奥氮平或氟哌啶醇治疗中获益。