Serum nerve growth factor beta, brain- and glial-derived neurotrophic factor levels and psychopathology in unmedicated patients with schizophrenia

未接受药物治疗的精神分裂症患者血清神经生长因子β、脑源性神经营养因子和神经胶质细胞源性神经营养因子水平与精神病理学

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作者:Che-Sheng Chu, Chin-Liang Chu, Chih-Ching Wu, Ti Lu

Background

There is accumulating evidence that neurotrophic factors may be involved in the pathophysiology of patients with schizophrenia. This study aimed to explore the relationship between serum nerve growth factor beta (NGF-beta), brain-derived neurotrophic factor (BDNF), and glial-derived neurotrophic factor (GDNF) levels and psychopathology in unmedicated patients with schizophrenia.

Conclusion

Neurotrophic factors play a vital role in the regulation of neuroplasticity and neurogenesis in humans. This study suggests that BDNF and GDNF may be contributing to the pathological mechanisms involved in unmedicated patients with schizophrenia.

Methods

Serum NGF-beta, BDNF, and GDNF levels were determined using enzyme-linked-immunosorbent assay (ELISA) in the serum of 30 unmedicated patients with schizophrenia. Symptomatology was assessed with the expanded version of the 24-items brief psychiatric rating scale (BPRS-E), which was divided into four conceptual domains: manic excitement/disorganization, depression/anxiety, negative symptoms, and positive symptoms. Kolmogorov-Smirnov one sample test was performed to test non-parametric variables. Spearman's correlation was performed to examine the correlations between the cytokines of interest and psychopathology. Benjamini-Hochberg procedure was applied for multiple corrections.

Results

Serum GDNF levels correlated negatively with the BPRS-total (r = -0.533, corrected p = 0.002) and BPRS-manic (r = -0.456, corrected p = 0.011) subtests. BDNF levels showed a positive correlation with BPRS-total (r = 0.480, corrected p = 0.007). In addition, NGF-beta did not associate with psychopathology measured by BPRS scores.

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