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首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >Increased expression of NDEL1 and MBP genes in the peripheral blood of antipsychotic-naive patients with first-episode psychosis
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Increased expression of NDEL1 and MBP genes in the peripheral blood of antipsychotic-naive patients with first-episode psychosis

机译:抗精神病药患者外周血中NDEL1和MBP基因的表达增加了一集精神病

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Schizophrenia is a multifactorial neurodevelopmental disorder with high heritability. First-episode psychosis (FEP) is a critical period for determining the disease prognosis and is especially helpful for identifying potential biomarkers associated with the onset and progression of the disorder. We investigated the mRNA expression of 12 schizophrenia-related genes in the blood of antipsychotic-naive FEP patients (N=73) and healthy controls (N=73). To evaluate the influences of antipsychotic treatment and progression of the disorder, we compared the gene expression within patients before and after two months of treatment with risperidone (N=64). We observed a significantly increased myelin basic protein (MBP) and nuclear distribution protein nudE-like 1 (NDEL1) mRNA levels in FEP patients compared with controls. Comparing FEP before and after risperidone treatment, no significant differences were identified; however; a trend of relatively low NDEL1 expression was observed after risperidone treatment. Animals chronically treated with saline or risperidone exhibited no significant change in Ndel1 expression levels in the blood or the prefrontal cortex (PFC), suggesting that the trend of low NDEL1 expression observed in FEP patients after treatment is likely due to factors other than risperidone treatment (Le., disease progression). In addition to the recognized association with schizophrenia, MBP and NDEL1 gene products also play an essential role in the functions that are deregulated in schizophrenia, such as neurodevelopment. Our data strengthen the importance of these biological processes in psychotic disorders, indicating that these changes can be detected peripherally and potentially represent putative novel blood biomarkers of susceptibility and disorder progression. (C) 2015 Elsevier B.V. and ECNP. All rights reserved.
机译:精神分裂症是具有高遗传性的多因素神经发育障碍。第一集集精神病(FEP)是确定疾病预后的关键时期,并且特别有助于鉴定与疾病发病和进展相关的潜在生物标志物。我们研究了在抗精神病药物 - 幼稚FEP患者(n = 73)和健康对照的血液中12种精神分裂症相关基因的mRNA表达(n = 73)。为了评估抗精神病药治疗和疾病进展的影响,我们将患者的基因表达与Risperidone治疗(n = 64)进行了两次和之后。与对照相比,我们观察到FEP患者中显着增加的髓鞘基本蛋白(MBP)和核分布蛋白裸样1(NDEL1)mRNA水平。比较FEP在锂碘酮治疗之前和之后,没有确定显着差异;然而;在Risperidone治疗后观察到相对低的NDEL1表达的趋势。用盐水或立牛酮慢性处理的动物表现出血液或前额定皮层(PFC)中NDEL1表达水平的显着变化,表明在治疗后,在FEP患者中观察到的低NDEL1表达的趋势可能是由于Risperidone治疗以外的因素( le。,疾病进展)。除了与精神分裂症的公认联合外,MBP和NDEL1基因产品还在精神分裂症中解毒的功能中起重要作用,例如神经发育。我们的数据增强了这些生物过程在精神病疾病中的重要性,表明这些变化可以在外围检测到,并且可能代表易感性和紊乱进展的推定新型血液生物标志物。 (c)2015 Elsevier B.V.和ECNP。版权所有。

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