Department of Endocrinology, Wuyi County First People's Hospital, 321200 Wuyi, Zhejiang, China.
Department of Mental Health, Wuyi County First People's Hospital, 321200 Wuyi, Zhejiang, China.
Actas Esp Psiquiatr. 2024 Aug;52(4):412-419. doi: 10.62641/aep.v52i4.1681.
Treatment with different antipsychotics can lead to various metabolic side effects in patients with psychosis, impacting long-term prognosis. This study aimed to compare the changes and clinical efficacy of insulin resistance in patients treated with olanzapine and ziprasidone.
A retrospective analysis was conducted on the clinical data of 80 patients with schizophrenia. The patients were divided into olanzapine treatment group and ziprasidone treatment group. Parameters including body weight, body mass index (BMI), fasting plasma glucose (FPG), fasting plasma insulin (FPI), cholesterol (CHO), triglyceride (TG), high-density lipoprotein (HDL), low-density lipoprotein (LDL), insulin resistance index, and Positive and Negative Syndrome Scale (PANSS) scores were recorded and compared before and after treatment.
BMI, FPG, FPI, homeostatic model assessment of insulin resistance (HOMA-IR), CHO, TG and LDL in both groups were significantly higher than before treatment (p < 0.05). These parameters were significantly higher in the olanzapine group than in the ziprasidone group (p < 0.05). The level of HDL in both groups was significantly decreased after treatment, and the level of HDL in the olanzapine group was significantly lower than that in the ziprasidone group after treatment (p < 0.05). After treatment, the total score and score of PANSS in both groups were significantly lower than before treatment (p < 0.05). After treatment, there was no significant difference in total score and PANSS score between both groups (p > 0.05). The incidence of insulin resistance (IR) was significantly higher in the olanzapine group compared to the ziprasidone group (χ2 = 4.021, p < 0.05). In the IR group, BMI, FPG, FPI, TG, and LDL levels were higher than in the non-IR group (p < 0.05). Multivariate analysis indicated that BMI, FPG, FPI, TG, and LDL were independent risk factors for IR (odd ratio (OR) >1, p < 0.05).
Treatment with olanzapine and ziprasidone improves clinical symptoms in patients with schizophrenia, but increases the risk of insulin resistance. The metabolic side effects of olanzapine are more pronounced.
不同的抗精神病药物治疗会导致精神病患者出现各种代谢副作用,影响长期预后。本研究旨在比较奥氮平和齐拉西酮治疗患者胰岛素抵抗的变化和临床疗效。
对 80 例精神分裂症患者的临床资料进行回顾性分析,将患者分为奥氮平治疗组和齐拉西酮治疗组。记录并比较两组患者治疗前后的体重、体重指数(BMI)、空腹血糖(FPG)、空腹胰岛素(FPI)、胆固醇(CHO)、甘油三酯(TG)、高密度脂蛋白(HDL)、低密度脂蛋白(LDL)、胰岛素抵抗指数及阳性与阴性症状量表(PANSS)评分。
两组患者的 BMI、FPG、FPI、稳态模型评估的胰岛素抵抗(HOMA-IR)、CHO、TG 和 LDL 均明显高于治疗前(p<0.05),奥氮平组明显高于齐拉西酮组(p<0.05)。两组患者的 HDL 水平治疗后均明显降低,奥氮平组明显低于齐拉西酮组(p<0.05)。两组患者治疗后 PANSS 总分及各因子分均明显低于治疗前(p<0.05),两组间治疗后 PANSS 总分及各因子分比较差异均无统计学意义(p>0.05)。奥氮平组的胰岛素抵抗(IR)发生率明显高于齐拉西酮组(χ2=4.021,p<0.05)。IR 组患者的 BMI、FPG、FPI、TG 和 LDL 水平均高于非 IR 组(p<0.05)。多因素分析表明,BMI、FPG、FPI、TG 和 LDL 是 IR 的独立危险因素(OR>1,p<0.05)。
奥氮平和齐拉西酮治疗精神分裂症患者可改善临床症状,但增加了发生胰岛素抵抗的风险,奥氮平的代谢副作用更为明显。