对精神分裂症患者的脑源性神经营养因子研究

Partik Kaur, V. Pal, Vijay Niranjan, V. Mudgal
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摘要

脑源性神经营养因子(BDNF)是一种被广泛研究的神经营养素,据说它参与了许多神经元过程的调节,包括神经发生、神经元分化、成熟和存活。多年来,研究表明精神分裂症患者的血清 BDNF 水平存在显著差异,但尚未达成广泛一致。在此,我们报告了未服药的精神分裂症患者与健康对照组(HC)的血清 BDNF 水平对比,以及精神分裂症患者 BDNF 水平的相关性。 研究样本由 120 名参与者组成,其中包括 60 名精神分裂症患者和 60 名健康对照组。研究人员采集了研究对象的血样,并使用酶联免疫吸附试剂盒对血清中的 BDNF 水平进行了分析。研究人员使用阳性和阴性综合征量表(PANSS)和蒙特利尔认知评估对患者进行了临床评估。 与年龄和性别匹配的HC相比,未服药的精神分裂症患者血清BDNF水平明显较低(P - 0.024)。PANSS 总分和阳性分量表得分与血清 BDNF 水平呈负相关,分别为 P = 0.005 和 P = 0.001,具有统计学意义。 索引研究发现,精神分裂症患者的 BDNF 水平降低,而且 BDNF 与病情严重程度,尤其是阳性症状相关。因此,开发能够激活 BDNF 信号的治疗策略可能会有利于改善精神分裂症的临床疗效。
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Study of Brain-derived Neurotrophic Factor in Drug-naive Patients with Schizophrenia
Brain-derived neurotrophic factor (BDNF) is a widely studied neurotrophin and is said to be involved in the regulation of many neuronal processes, including neurogenesis, neuronal differentiation, maturation, and survival. Over the years, research has shown a significant variation of serum BDNF levels in schizophrenia with no widespread agreement. Herein, we report on serum BDNF levels in drug-naive patients of schizophrenia in comparison to healthy controls (HC) and correlates of BDNF levels in patients of schizophrenia. The study sample consisted of 120 participants with 60 drug-naive patients of schizophrenia and 60 HC. The blood sample of the study subjects was collected and processed serum was analyzed using an enzyme-linked immunosorbent assay kit for BDNF levels. Clinical assessment of patients was done using the Positive and Negative Syndrome Scale (PANSS) and Montreal Cognitive Assessment. Serum BDNF levels were significantly lower in drug-naive patients of schizophrenia as compared to age and sex-matched HC (P – 0.024). The PANSS total score and positive subscale score were negatively correlated with serum BDNF levels which were statistically significant with P = 0.005 and P = 0.001, respectively. The index study found BDNF levels to be reduced in patients of schizophrenia and BDNF was found to correlate with severity of illness, especially positive symptoms. Thus, developing therapeutic strategies that can activate BDNF signaling may prove beneficial in improving the clinical outcome of schizophrenia.
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