Kang Dongyu, Lu Jinjun, Liu Wenqing, Shao Ping, Wu Renrong
Department of Psychiatry, and National Clinical Research Center for Mental Disorders, The Second Xiangya Hospital of Central South University, Changsha, 410011, Hunan, China.
Department of Psychiatry, Jiangyin No.3 People's hospital, Jiangyin, 214400, Jiangsu, China.
Schizophrenia (Heidelb). 2022 Feb 28;8(1):9. doi: 10.1038/s41537-022-00211-5.
Second-generation antipsychotics are widely used to treat schizophrenia but their use could induce metabolic dysfunction. To balance efficacy and side effects, various guidelines recommend the use of therapeutic drug monitoring. Given the controversial relationship between olanzapine serum concentration and metabolic dysfunction, its use in clinical practice is still debated. To address this issue, we conducted a prospective cohort study to explore the associations in patients with schizophrenia. Specifically, first-episode drug-naive patients and patients with chronic schizophrenia were recruited. All participants received olanzapine monotherapy for 8 weeks. Anthropometric parameters and metabolic indices were tested at baseline and at week 8, and olanzapine serum concentration was tested at week 4. After 8 weeks of observation, body weight and BMI increased significantly in drug-naive patients. Moreover, triglycerides and LDL increased significantly in both drug-naive and chronic patients. Among chronic patients, those who have never used olanzapine/clozapine before had a significantly higher increase in weight and BMI than those who have previously used olanzapine/clozapine. Furthermore, olanzapine concentration was associated with changes in weight, BMI, and LDL levels in the drug-naive group and glucose, triglyceride and LDL levels in chronic patients who have not used olanzapine/clozapine previously. In conclusion, the metabolic dysfunction induced by olanzapine is more severe and dose-dependent in drug-naive patients but independent in patients with chronic schizophrenia. Future studies with a longer period of observation and a larger sample are warranted.
第二代抗精神病药物被广泛用于治疗精神分裂症,但其使用可能会诱发代谢功能障碍。为了平衡疗效和副作用,各种指南推荐使用治疗药物监测。鉴于奥氮平血清浓度与代谢功能障碍之间存在争议性的关系,其在临床实践中的应用仍存在争议。为了解决这个问题,我们进行了一项前瞻性队列研究,以探讨精神分裂症患者中的相关性。具体而言,招募了首发未用药患者和慢性精神分裂症患者。所有参与者接受奥氮平单药治疗8周。在基线和第8周时测试人体测量参数和代谢指标,并在第4周时测试奥氮平血清浓度。经过8周的观察,未用药患者的体重和BMI显著增加。此外,未用药患者和慢性患者的甘油三酯和低密度脂蛋白均显著增加。在慢性患者中,之前从未使用过奥氮平/氯氮平的患者体重和BMI的增加显著高于之前使用过奥氮平/氯氮平的患者。此外,在未用药组中,奥氮平浓度与体重、BMI和低密度脂蛋白水平的变化相关,在之前未使用过奥氮平/氯氮平的慢性患者中,奥氮平浓度与血糖、甘油三酯和低密度脂蛋白水平相关。总之,奥氮平诱发的代谢功能障碍在未用药患者中更严重且呈剂量依赖性,但在慢性精神分裂症患者中则与之无关。有必要开展观察期更长、样本量更大的未来研究。