Olanzapine-Induced Weight Gain and Glycolipid Metabolism Aberrations in First-Episode and Antipsychotic-Naïve Schizophrenia Patients: A Longitudinal Study.

IF 4.8 2区 医学 Q1 NEUROSCIENCES Current Neuropharmacology Pub Date : 2024-09-20 DOI:10.2174/1570159X23666240918103730
Shen Li, Doudou Zheng, Wanyao Wang, Nannan Liu, Yanzhe Li, Chenghao Lu, Yeqing Dong, Xinxu Wang, Wei-Dong Li, Jie Li
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Abstract

Objective: Limited research has delved into the comprehensive impact of monotherapy on weight and glycolipid metabolism in schizophrenia (SCZ) patients. Our study aims to longitudinally investigate the multidimensional effects of olanzapine (OLA) monotherapy on weight and glycolipid metabolism in first-episode and antipsychotic-naïve (FEAN) SCZ patients.

Methods: A total of 74 FEAN-SCZ patients were recruited, as well as 58 sex- and age-matched healthy controls. Eligible patients underwent a 4-week OLA treatment regimen, with weight assessments conducted at baseline and week 4. Moreover, lipid profiles and fasting plasma glucose (FPG) were measured at baseline and week 4. Insulin, leptin (LEP), and adiponectin (APN) levels were determined using enzyme-linked immunosorbent assay (ELISA) kits.

Results: At baseline, FEAN-SCZ patients showed elevated levels of insulin, low-density lipoprotein (LDL), impaired insulin sensitivity, and reduced levels of APN compared to the healthy controls. Following 4-week OLA treatment, patients showed an increase in body mass index (BMI) of 0.96 kg/m2. Additionally, FPG, quantitative insulin sensitivity check index (QUICKI), HOMA-insulin sensitivity index (HOMA-ISI), and fasting plasma glucose to insulin ratio (G/I) displayed significant decreases, while insulin, HOMA-IR, and LEP levels showed significant increases. Stepwise regression analysis revealed that baseline FPG independently predicted the change in BMI after 4 weeks of OLA treatment.

Conclusion: FEAN-SCZ patients exhibited pre-existing alterations in glucose homeostasis. After 4 weeks of OLA treatment, SCZ patients experienced significant weight gain, deteriorating insulin resistance, and increased LEP levels. In addition, baseline FPG emerged as a predictor of BMI changes after 4 weeks of OLA treatment.

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奥氮平诱发首发和抗精神病药物无效的精神分裂症患者体重增加和糖脂代谢异常:一项纵向研究。
目的:有关单一疗法对精神分裂症(SCZ)患者体重和糖脂代谢的综合影响的研究有限。我们的研究旨在纵向调查奥氮平(OLA)单一疗法对首发和抗精神病药物无效(FEAN)SCZ患者体重和糖脂代谢的多维影响:共招募了74名FEAN-SCZ患者以及58名性别和年龄匹配的健康对照者。符合条件的患者接受了为期4周的OLA治疗,并在基线和第4周进行了体重评估。此外,还在基线和第 4 周测量了血脂概况和空腹血浆葡萄糖 (FPG)。使用酶联免疫吸附试验(ELISA)试剂盒测定胰岛素、瘦素(LEP)和脂肪连通素(APN)水平:与健康对照组相比,FEAN-SCZ 患者基线时胰岛素和低密度脂蛋白(LDL)水平升高,胰岛素敏感性受损,而 APN 水平降低。经过 4 周的 OLA 治疗后,患者的体重指数(BMI)增加了 0.96 kg/m2。此外,FPG、胰岛素敏感性定量检查指数(QUICKI)、HOMA-胰岛素敏感性指数(HOMA-ISI)和空腹血浆葡萄糖与胰岛素比值(G/I)显著下降,而胰岛素、HOMA-IR和LEP水平显著上升。逐步回归分析显示,基线 FPG 可独立预测 OLA 治疗 4 周后 BMI 的变化:结论:FEAN-SCZ 患者的血糖平衡发生了改变。经过 4 周的 OLA 治疗后,SCZ 患者的体重明显增加,胰岛素抵抗恶化,LEP 水平升高。此外,在接受 4 周的 OLA 治疗后,基线 FPG 成为 BMI 变化的预测因子。
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来源期刊
Current Neuropharmacology
Current Neuropharmacology 医学-神经科学
CiteScore
8.70
自引率
1.90%
发文量
369
审稿时长
>12 weeks
期刊介绍: Current Neuropharmacology aims to provide current, comprehensive/mini reviews and guest edited issues of all areas of neuropharmacology and related matters of neuroscience. The reviews cover the fields of molecular, cellular, and systems/behavioural aspects of neuropharmacology and neuroscience. The journal serves as a comprehensive, multidisciplinary expert forum for neuropharmacologists and neuroscientists.
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Olanzapine-Induced Weight Gain and Glycolipid Metabolism Aberrations in First-Episode and Antipsychotic-Naïve Schizophrenia Patients: A Longitudinal Study. Exploring the Confluence of Animal Medicine and its Implications for Human Health: A Systematic Literature Review Disease-Modifying Symptomatic Treatment (DMST) Potential of Cannabinoids in Patients with Multiple Sclerosis. Disease-Modifying Symptomatic Treatment (DMST): The Potential Role of Vortioxetine in the Treatment of Depression in Patients with Multiple Sclerosis. Pharmacological Strategies and Surgical Management of Posthemorrhagic Hydrocephalus Following Germinal Matrix-Intraventricular Hemorrhage in Preterm Infants.
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