Zhang Chen, Fang Xinyu, Yao Peifen, Mao Yemeng, Cai Jun, Zhang Yi, Chen Meijuan, Fan Weixing, Tang Wei, Song Lisheng
Schizophrenia Program, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Schizophrenia Program, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Psychoneuroendocrinology. 2017 Jul;81:138-143. doi: 10.1016/j.psyneuen.2017.04.014. Epub 2017 Apr 27.
There is accumulating evidence indicating that long-term treatment with second-generation antipsychotics (SGAs) results in metabolic syndrome (MetS) and cognitive impairment. This evidence suggests an intrinsic link between antipsychotic-induced MetS and cognitive dysfunction in schizophrenia patients. Olanzapine is a commonly prescribed SGA with a significantly higher MetS risk than that of most antipsychotics. In this study, we hypothesized that olanzapine-induced MetS may exacerbate cognitive dysfunction in patients with schizophrenia.
A sample of 216 schizophrenia patients receiving long-term olanzapine monotherapy were divided into two groups, MetS and non-MetS, based on the diagnostic criteria of the National Cholesterol Education Program's Adult Treatment Panel III. We also recruited 72 healthy individuals for a control group. Cognitive function was evaluated using the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS). Plasma brain-derived neurotrophic factor (BDNF) and tumor necrosis factor-alpha (TNF-alpha) were measured by an enzyme-linked immunosorbent assay for 108 patients and 47 controls.
Among the 216 schizophrenia patients receiving olanzapine monotherapy, MetS was found in 95/216 (44%). Patients with MetS had more negative symptoms, higher total scores in PANSS (Ps<0.05) and lower immediate memory, attention, delayed memory and total scores in RBANS (Ps<0.01). Stepwise multivariate linear regression analysis revealed that increased glucose was the independent risk factor for cognitive dysfunction (t=-2.57, P=0.01). Patients with MetS had significantly lower BDNF (F=6.49, P=0.012) and higher TNF-alpha (F=5.08, P=0.026) levels than those without MetS. There was a negative correlation between the BDNF and TNF-alpha levels in the patients (r=-0.196, P=0.042).
Our findings provide evidence suggesting that the metabolic adverse effects of olanzapine may aggravate cognitive dysfunction in patients with schizophrenia through an interaction between BDNF and TNF-alpha.
越来越多的证据表明,第二代抗精神病药物(SGA)的长期治疗会导致代谢综合征(MetS)和认知障碍。这一证据表明,抗精神病药物诱发的MetS与精神分裂症患者的认知功能障碍之间存在内在联系。奥氮平是一种常用的SGA,其导致MetS的风险明显高于大多数抗精神病药物。在本研究中,我们假设奥氮平诱发的MetS可能会加重精神分裂症患者的认知功能障碍。
根据美国国家胆固醇教育计划成人治疗专家组III的诊断标准,将216例接受长期奥氮平单一疗法的精神分裂症患者分为两组,即MetS组和非MetS组。我们还招募了72名健康个体作为对照组。使用可重复使用的神经心理状态评估量表(RBANS)评估认知功能。通过酶联免疫吸附测定法对108例患者和47例对照者测量血浆脑源性神经营养因子(BDNF)和肿瘤坏死因子-α(TNF-α)。
在216例接受奥氮平单一疗法的精神分裂症患者中,95/216(44%)患有MetS。患有MetS的患者有更多的阴性症状,PANSS总分更高(P<0.05),并且在RBANS中的即时记忆、注意力、延迟记忆和总分更低(P<0.01)。逐步多元线性回归分析显示,血糖升高是认知功能障碍的独立危险因素(t=-2.57,P=0.01)。患有MetS的患者的BDNF水平显著低于未患MetS的患者(F=6.49,P=0.012),而TNF-α水平更高(F=5.08,P=0.026)。患者的BDNF和TNF-α水平之间存在负相关(r=-0.196,P=0.042)。
我们的研究结果提供了证据,表明奥氮平的代谢不良反应可能通过BDNF和TNF-α之间的相互作用加重精神分裂症患者的认知功能障碍。