评估精神分裂症患者胰岛素抵抗与抗精神病药物治疗之间的临床相关性。

IF 1 4区 医学 Q4 NEUROSCIENCES
Fang Wang, Faya Wang, Xiaoqing Tao, Wenxian Ni, Wenxin Li, Jiao Lin
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引用次数: 0

摘要

背景:使用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:方法:对80名精神分裂症患者的临床数据进行回顾性分析。将患者分为奥氮平治疗组和齐拉西酮治疗组。记录并比较了治疗前后的体重、体重指数(BMI)、空腹血浆葡萄糖(FPG)、空腹血浆胰岛素(FPI)、胆固醇(CHO)、甘油三酯(TG)、高密度脂蛋白(HDL)、低密度脂蛋白(LDL)、胰岛素抵抗指数以及阳性和阴性综合征量表(PANSS)评分等参数:结果:两组患者的体重指数(BMI)、血脂饱和值(FPG)、血脂指数(FPI)、胰岛素抵抗的稳态模型评估(HOMA-IR)、胆固醇(CHO)、总胆固醇(TG)和低密度脂蛋白(LDL)均显著高于治疗前(P < 0.05)。奥氮平组的这些参数明显高于齐拉西酮组(P < 0.05)。两组患者治疗后高密度脂蛋白水平均明显下降,奥氮平组治疗后高密度脂蛋白水平明显低于齐拉西酮组(P<0.05)。治疗后,两组患者的 PANSS 总分和得分均明显低于治疗前(P < 0.05)。治疗后,两组的总分和 PANSS 评分无明显差异(P > 0.05)。与齐拉西酮组相比,奥氮平组的胰岛素抵抗(IR)发生率明显更高(χ2 = 4.021,P < 0.05)。在 IR 组中,BMI、FPG、FPI、TG 和 LDL 水平均高于非 IR 组(P < 0.05)。多变量分析表明,BMI、FPG、FPI、TG和LDL是导致IR的独立危险因素(奇数比(OR)>1,P<0.05):结论:使用奥氮平和齐拉西酮治疗可改善精神分裂症患者的临床症状,但会增加胰岛素抵抗的风险。奥氮平的代谢副作用更为明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Clinical Correlation between Insulin Resistance and Antipsychotic Drug Therapy in Patients with Schizophrenia.

Background: 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.

Method: 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.

Results: 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).

Conclusions: 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.

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来源期刊
Actas espanolas de psiquiatria
Actas espanolas de psiquiatria 医学-精神病学
CiteScore
1.70
自引率
6.70%
发文量
46
审稿时长
>12 weeks
期刊介绍: Actas Españolas de Psiquiatría publicará de manera preferente trabajos relacionados con investigación clínica en el área de la Psiquiatría, la Psicología Clínica y la Salud Mental.
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