Ronsley Rebecca, Nguyen Duc, Davidson Jana, Panagiotopoulos Constadina
Pediatrics Resident, Department of Pediatrics, University of British Columbia, British Columbia Children's Hospital, Vancouver, British Columbia.
Research Coordinator and Statistical Analyst, Department of Pediatrics, University of British Columbia, British Columbia Children's Hospital, Vancouver, British Columbia.
Can J Psychiatry. 2015 Oct;60(10):441-50. doi: 10.1177/070674371506001005.
To determine the risk of developing obesity and related metabolic complications in children following long-term treatment with risperidone or quetiapine.
This was a 1-year naturalistic longitudinal study conducted between February 2009 and March 2012. A total of 130 children aged 2 to 18 years without prior exposure to second-generation antipsychotics (SGAs) were enrolled at initiation of treatment with either risperidone or quetiapine. Metabolic parameters were measured at baseline and months 6 and 12. Data of 37 participants (20 treated with risperidone and 17 treated with quetiapine) who completed 12-month monitoring were used in the analysis.
After 1 year of SGA treatment, mean weight increased significantly by 10.8 kg (95% CI 7.9 kg to 13.7 kg) for risperidone and 9.7 kg (95% CI 6.5 kg to 12.8 kg) for quetiapine. Body mass index z score also increased significantly in both groups (P < 0.001). There was a high incidence of children becoming overweight or obese (6/15 [40.0%] for risperidone-treated and 7/14 [50.0%] for quetiapine-treated). The mean levels of fasting glucose (for risperidone-treated) and ratio of total cholesterol to high-density lipoprotein cholesterol (for quetiapine-treated) increased significantly by 0.23 mmol/L (95% CI 0.03 mmol/L to 0.42 mmol/L) and 0.48 mmol/L (95% CI 0.15 mmol/L to 0.80 mmol/L), respectively.
Children treated with risperidone or quetiapine are at a significant risk for developing obesity, elevated waist circumference, and dyslipidemia during 12 months of treatment. These data emphasize the importance of regular monitoring for early identification and treatment of metabolic side effects.
确定接受利培酮或喹硫平长期治疗的儿童发生肥胖及相关代谢并发症的风险。
这是一项于2009年2月至2012年3月期间进行的为期1年的自然纵向研究。共有130名年龄在2至18岁、未曾接触过第二代抗精神病药物(SGA)的儿童在开始使用利培酮或喹硫平治疗时入组。在基线、第6个月和第12个月时测量代谢参数。分析使用了37名完成12个月监测的参与者的数据(20名接受利培酮治疗,17名接受喹硫平治疗)。
在SGA治疗1年后,利培酮组平均体重显著增加10.8 kg(95%可信区间7.9 kg至13.7 kg),喹硫平组平均体重显著增加9.7 kg(95%可信区间6.5 kg至12.8 kg)。两组的体重指数z评分也均显著增加(P<0.001)。儿童超重或肥胖的发生率较高(利培酮治疗组为6/15 [40.0%],喹硫平治疗组为7/14 [50.0%])。空腹血糖平均水平(利培酮治疗组)和总胆固醇与高密度脂蛋白胆固醇之比(喹硫平治疗组)分别显著增加0.23 mmol/L(95%可信区间0.03 mmol/L至0.42 mmol/L)和0.48 mmol/L(95%可信区间0.15 mmol/L至0.80 mmol/L)。
接受利培酮或喹硫平治疗的儿童在12个月治疗期间发生肥胖、腰围增加和血脂异常的风险显著。这些数据强调了定期监测以早期识别和治疗代谢副作用的重要性。