Cao Hailing, Meng Yajing, Li Xiaojing, Ma Xiaohong, Deng Wei, Guo Wanjun, Li Tao
Mental Health Center and Psychiatric Laboratory, The State Key Laboratory of Biotherapy, West China Hospital of Sichuan University, Chengdu, Sichuan, 610041, China; West China Brain Research Center, West China Hospital of Sichuan University, Chengdu, Sichuan, 610041, China.
Mental Health Center and Psychiatric Laboratory, The State Key Laboratory of Biotherapy, West China Hospital of Sichuan University, Chengdu, Sichuan, 610041, China; West China Brain Research Center, West China Hospital of Sichuan University, Chengdu, Sichuan, 610041, China.
J Psychiatr Res. 2020 Oct;129:265-271. doi: 10.1016/j.jpsychires.2020.07.038. Epub 2020 Aug 10.
This study aims to better characterize the metabolic effects of antipsychotics in the early stage of treatment in first-episode patients with schizophrenia.
We performed a retrospective real-world study in a naturalistic setting that included inpatients with first-episode drug-naïve schizophrenia; metabolic profiles were measured at baseline and 2 weeks and 4 weeks after antipsychotic treatment. The metabolic profiles of medicated patients with first-episode schizophrenia were also included.
Insulin resistance, based on the ratio of triglycerides to high-density lipoprotein cholesterol (TG/HDL-C), increased significantly after 2 weeks of antipsychotic treatment, whereas fasting glucose (FG) decreased significantly. Regarding lipid metabolism, triglycerides (TG), cholesterol (CHOL) and low-density lipoprotein cholesterol (LDL-C) increased significantly after 2 weeks of antipsychotic treatment; however, high-density lipoprotein cholesterol (HDL-C) decreased significantly after 4 weeks of antipsychotic treatment. There were no statistically significant differences between the antipsychotic groups in any of the metabolic parameters evaluated.
Our study revealed that insulin resistance and lipid metabolic abnormalities occurred as early as two weeks after the initiation of antipsychotic treatment. Our findings suggest that metabolic profiles should been monitored in the early stage of antipsychotics treatment in clinical practice. Further research is needed to explore the underlying mechanisms of the short-term effects of antipsychotics on metabolic parameters.
本研究旨在更好地描述抗精神病药物对首发精神分裂症患者治疗早期的代谢影响。
我们在自然环境中进行了一项回顾性现实世界研究,纳入初发未用药的精神分裂症住院患者;在基线以及抗精神病药物治疗后2周和4周测量代谢指标。还纳入了初发精神分裂症用药患者的代谢指标。
基于甘油三酯与高密度脂蛋白胆固醇比值(TG/HDL-C)的胰岛素抵抗在抗精神病药物治疗2周后显著增加,而空腹血糖(FG)显著降低。关于脂质代谢,抗精神病药物治疗2周后甘油三酯(TG)、胆固醇(CHOL)和低密度脂蛋白胆固醇(LDL-C)显著增加;然而,抗精神病药物治疗4周后高密度脂蛋白胆固醇(HDL-C)显著降低。在评估的任何代谢参数中,抗精神病药物组之间均无统计学显著差异。
我们的研究表明,抗精神病药物治疗开始后两周就出现了胰岛素抵抗和脂质代谢异常。我们的研究结果表明,在临床实践中,抗精神病药物治疗早期应监测代谢指标。需要进一步研究以探索抗精神病药物对代谢参数短期影响的潜在机制。