Abstract

Previous studies demonstrate that the protein of neuropeptide Y (NPY) is abnormal in depression patients, but the changes of NPY in different types of depression are unclear. This study was aimed to examine protein and mRNA expression levels of NPY in 159 cases with four groups including post-stroke depression (PSD) group, stroke without depression (Non-PSD) group, major depressive disorder (MDD) group and normal control (NC) group. The protein and gene expression analysis were performed by enzyme-linked immunosorbent assay (ELISA) and quantitative polymerase chain reaction-based methods. One way analysis of variance (ANOVA), chi-square tests and nonparametric test were used to evaluate general characteristics, clinical and biological materials. In order to explore the role of NPY in different types of depression, the partial correlations, binary logistic regression analysis and receiver operating characteristic (ROC) curve were calculated for PSD and MDD groups. There are significant differences of NPY protein (Fdf(3) = 5.167, P = 0.002) and mRNA expression levels ( = 20.541, P < 0.001) among four groups. Bonferroni multiple comparisons found that the NPY protein was significantly decreased in PSD (FBonferroni = −7.133, P = 0.002) and Non-PSD group (FBonferroni = −5.612, P = 0.018) compared with NC group. However, contrasted with MDD group, the mRNA expression was increased in PSD and Non-PSD group by nonparametric test (all P < 0.05). In binary logistic analyses, NPY mRNA expression was independent predictors of PSD (odds ratio: 1.452, 95% CI, 1.081–1.951, P = 0.013). The ROC curve showed NPY mRNA had a general prognostic accuracy (area under the curve: 0.766, 95% CI, 0.656–0.876, P < 0.001). This is the first study to explore the distinguishing function of NPY in different types of depression. It will provide help in the identification of different subtypes of depression.

Highlights

  • Depression is one of the most frequently encountered forms of mental illness and more than 350 million people battle with it every day (Smith, 2014)

  • In the mRNA expression aspect, the statistically significant difference was found among four groups (χK2ruskal−Wallis, df(3) = 20.541, P < 0.001), multiple comparison tests showed that both the post-stroke depression (PSD) and Non-PSD groups have significantly increased expression compared to major depressive disorder (MDD) group (0.92 ± 1.27 in PSD vs. 0.11 ± 0.16 in MDD, 0.34 ± 0.34 in Non-PSD vs. 0.11 ± 0.16 in MDD, all P < 0.05, see Table 2)

  • The present study provides evidence that the protein and transcriptional changes of neuropeptide Y (NPY) occur in PSD and different depressions

Read more

Summary

Introduction

Depression is one of the most frequently encountered forms of mental illness and more than 350 million people battle with it every day (Smith, 2014). Neuropeptide Y (NPY), a 36-amino acid peptide, is widely distributed in the central and peripheral nervous systems such as most cortical areas, hippocampus, amygdala, olfactory bulb and spinal cord of the rat and human brain (Dumont et al, 1992). These brain regions are closely related to stress responses and mood disorders. The NPY mRNA which was region specific in depressive-like animal models, significantly decreased in the nucleus accumbens, medial amygdala, hippocampal dentate gyrus, CA regions and prefrontal cortex, but increased in the arcuate nucleus and anterior cingulate cortex in the FSL and chronic mild stressed rats (Caberlotto et al, 1998; Sergeyev et al, 2005; Bjørnebekk et al, 2006; Zambello et al, 2008; Melas et al, 2012)

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call