- Research article
- Open Access
Plasma nesfatin-1 level is associated with severity of depression in Chinese depressive patients
BMC Psychiatry volume 18, Article number: 88 (2018)
Nesfatin-1 plays a role in the regulation of emotional states like depression. The aim of this study was to investigate the plasma nesfatin-1levels in Chinese patients with depression and healthy subjects, and to determine the possible association between the plasma nesfatin-1 level and the severity of depression.
A total of 103 depressive patients and 32 healthy subjects were assessed. According to HAMD-17scores, 51, 18, and 34 patients were enrolled in the mild depression, moderate depression, and severe depression groups, respectively. Plasma nesfatin-1 levels were determined by the ELISA method. Differences between groups were compared and associations between plasma nesfatin-1 and other variables were analyzed.
The plasma nesfatin-1 was significantly positively correlated with HAMD-17 score (r = 0.651). Compared with healthy controls (8.11 ± 3.31 ng/mL), the plasma nesfatin-1 level significantly increased in patients with mild depression (11.17 ± 3.58 ng/mL), with moderate depression (16.33 ± 8.78 ng/mL), and with severe depression (27.65 ± 8.26 ng/mL) respectively. Plasma nesfatin-1 level (Odds ratio [OR] = 1.269) was an independent indicator for severe depression by multivariate logistic regression analysis.
The plasma nesfatin-1 level is positively correlated with the severity of depression. Plasma nesfatin-1 level may be a potential indicator for depression severity.
Depression is a state of low mood and demotivated condition that affects a person’s feelings, cognition, and behaviors. Major depressive disorder is the most common of serious psychiatric disorders and is recognized to be a high risk factor of suicide . Thus, evaluating the severity of depression is crucial for treatment . In patients diagnosed with depression, Hamilton Rating Scale for depression (HAMD) is a widely used, standardized, clinician administered questionnaire to assess and rate the severity of depression. However, there are no commonly accepted depression biomarkers to improve diagnostic accuracy or to evaluate severity ratings . Although the cellular and molecular mechanisms underlying the pathophysiology of depression are not been fully elucidated, there have been increasing interests in associations between depression and changes in various biochemical pathways, including inflammatory, neurotrophic and hypothalamic-pituitary-adrenal (HPA) axis alterations [4, 5].
Nesfatin-1, a newly discovered hormone, was derived from nucleobindin-2 (NUCB2). Some previous studies have reported that nesfatin-1 played a role in integrating feeding, glucose homeostasis, and energy expenditure [6, 7]. Furthermore, the nesfatin-1 role in the regulation of emotional states including anxiety and stress was also be found . The plasma level and mRNA expression of nesfatin-1 were increased by acute stress in rats . In fact, nesfatin-1 can activate the HPA axis, the hyperactivity of which is proposed to be among the causal factors for triggering depressive episodes . Because of the dysfunction of the HPA axes, with the important role of nesfatin-1 in the pathophysiology of depression , we hypothesized that the plasma nesfatin-1 level may be associated with depression severity. Thus, the aim of this study was to investigate the levels of plasma nesfatin-1 in Chinese patients with depression and healthy subjects, and to determine the possible association between the plasma nesfatin-1 level and the severity of depression.
All subjects in the depressive group were recruited from the outpatient department of psychological consultation and treatment center, the Second People’s Hospital of Wuhu City from January 2016 to April 2017. The inclusion criteria were the following: a) HAMD-17scores > 7; b) meeting diagnostic criteria for depression according to the Diagnostic and Statistical Manual for Psychiatric Disorders-Fourth Version. The exclusion criteria were the following: a) unstable psychiatric features; b) currently suffering from a severe medical condition; c) currently pregnant or lactating; d) presence of comorbid psychotic disorder, psychotic symptoms, psychoactive substance dependency or abuse, personality disorder, or mental retardation; e) received psychotropic medication within 2 weeks; f) had a history of bariatric surgery or any gastric disease; g) diagnosed of diabetes mellitus; h) FT3, FT4 or TSH was abnormal.
All subjects in the control group were recruited from the annual health examination of the Second People’s Hospital of Wuhu City. The inclusion criteria were the following: a) no mental disorders after being evaluated by psychiatrists; b) no family history of mental disorders and no history of taking psychiatric drugs; c) HAMD-17 scores ≤7. Exclusion criteria were the following: a) history of stroke or central nervous system disease; b) pregnant or lactating women.
The protocol was approved by the Ethical Committee of the Second People’s Hospital of Wuhu City. All subjects signed written informed consent in accordance with the Declaration of Helsinki.
The body mass index (BMI) of all participants were calculated. All blood samples from a forearm vein were collected in the morning following one night of fasting by 5-mL tubes containing EDTA. All plasma samples were obtained after centrifugation (3000×g for 5 min at 4 °C) and stored at − 80 °C until the time of assay.
The level of plasma nesfatin-1 was measured by ELISA kit from USCN Life Science Instruments (Wuhan, China) according to the manufacturer’s instructions. Thyroid Stimulating Hormone (TSH), free triiodothyronine (FT3), and free thyroxine (FT4) were assayed using an automatic electrochemistry luminescence immunoassay system (Roche Cobas E601, Mannheim, Germany). Fasting plasma glucose (FBG), triglycerides (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C) were measured by an automatic analyzer (Beckman AU5800, Tokyo, Japan) according to the standard techniques.
17-item Hamilton Depression Rating Scale(HAMD-17) was examined for all subjects . The severity of depressive symptom was classified by the following severity range for HAMD-17 score: mild depression (8–17), moderate depression (18–24), and severe depression (> 24) .
Distributions of data were tested for normality using the Shapiro-Wilk test. The continuous variables were presented as mean ± standard deviation and were analyzed with the one-way ANOVA. The Chi-squared test was employed for percentages of variables. Relationships between plasma nesfatin-1 and other variables were analyzed by Spearman correlation analysis and the independent relationships were determined by multivariate linear regression analysis. A multivariate logistic regression analysis was performed to validate the risk factors of depression severity. The receiver operating characteristic (ROC) curve analysis was used to determine the cut-off value of plasma nesfatin-1. Statistical analysis was performed using the SPSS 13.0 software package, and R version 3.3.2 (http:///www.r-project.org/). Furthermore, P-values (two-sided) < 0.05 were considered to be statistically significant.
The study population was composed of 103 depressive patients (44 male, 59 female) and 32 healthy individuals (12 male, 20 female). Demographic variables and biochemical values of depressive group and control group are shown in Table 1. Differences between the groups were not statistically significant in terms of age, gender and BMI. Compared with the healthy controls, depressive patients had higher FBG, higher TG, higher TSH, and lower HDL-C (all P < 0.05). The mean plasma nesfatin-1 level in the depressive patients was 17.52 ± 9.79 ng/mL, whereas it was 8.11 ± 3.31 ng/mL in the healthy controls. Difference of mean plasma nesfatin-1 level between groups was statistically significant (P < 0.001, Table 1). The mean HAMD-17 scores were statistically higher in patients with depression than that in the control group (19.2 ± 8.4 in depressive group vs. 4.2 ± 0.9 in control group, P < 0.001).
By Spearman correlation analysis, the plasma nesfatin-1 level was significantly correlated with age (r = − 0.287, P = 0.003), duration of depression (r = 0.302, P = 0.002), BMI (r = − 0.305, P = 0.002), FBG (r = − 0.287, P = 0.003), TC (r = 0.254, P = 0.010), HDL-C (r = 0.232, P = 0.019), TSH (r = 0.350, P < 0.001), and HAMD-17 score (r = 0.651, P < 0.001, Fig. 1) in the depressive patients. Multivariate linear regression analysis showed that plasma nesfatin-1 level was negatively associated with age, whereas that was positively associated with duration of depression, HAMD-17score, and TSH (Table 2).
The level of plasma nesfatin-1 in females (n = 59) was significantly higher than that in males (n = 44) (19.37 ± 10.05 vs. 15.04 ± 8.96, P = 0.023). Among 103 depressive patients, 51 patients (49.5%) had mild depression, 18 patients (17.5%) had moderate depression, and 34 patients (33.0%) had severe depression respectively. Figure 2 shows that a significant increased trend of the plasma nesfatin-1 level among mild depressive patients (11.17 ± 3.58 ng/mL) compared to moderate depressive patients (16.33 ± 8.78 ng/mL) (P = 0.005), and moderate depressive patients compared to severe depressive patients (27.65 ± 8.26 ng/mL) (P < 0.001).
By multivariate logistic regression analysis, BMI (OR = 0.671, P = 0.017), plasma nesfatin-1 (OR = 1.269, P = 0.001) were the independent indicators for severe depression in the depressive patients (Fig. 3). Based on the ROC curve analysis, plasma nesfatin-1 cut-off point of 20.25 ng/mL showed 82.4% sensitivity and 91.3% specificity, and with the Area Under Curve (AUC) 0.903 (95% CI 0.835–0.971) was the optimal cut-off point for identification of severe depression (Fig. 4).
Recently, nesfatin-1 has been implicated in the regulation of anxiety and depression in humans [14, 15]. In this study, the plasma nesfatin-1 levels were measured in depressive patients and healthy controls in China. According to our results, the plasma nesfatin-1 level was significantly increased in depressive patients, most notably in patients with severe depression, compared to healthy controls. Our finding is in agreement with the previous report .
There are some studies suggesting that serum nesfatin-1 levels were significantly lower in patients with type 2 diabetes mellitus compared to healthy subjects [17, 18]. Considering the effect of high blood sugar on nesfatin-1 level, we excluded patients with diabetes mellitus in our study. A positive correlation between plasma nesfatin-1and HDL-C in the depressive patients was observed in present study, and this relationship had been previously reported by Li et al.  in the diabetic patients. However, the mechanism and physiological significance of this relationship is unclear. Some studies indicate that thyroid dysfunction is associate with the mood disorders and particularly with depression [20, 21]. The symptomatic of depression could be improved through the levothyroxine replacement therapy . In addition, the relationship between nesfatin-1 and thyroid function had been reported in previous literature . Thus, the patients with abnormal TSH, FT3 and FT4 were excluded in our study. We also observed a statistically significant association between TSH and plasma nesfatin-1 by multivariate linear regression analysis.
In the present study, plasma nesfatin-1 was significantly correlated with HAMD-17 score, furthermore, we observed the level of plasma nesfatin-1 increased gradually from mild depression to moderate depression, and from moderate depression to severe depression. This increased trend suggests that plasma nesfatin-1 is associated with severity of depression. Multivariate logistic regression analysis identified that plasma nesfatin-1 was an indicator for severe depression in our study population. In addition, the patients with severe depression could be identified with a sensitivity of 82.4% at specificity of 91.3% by plasma nesfatin-1 (cut-off value = 20.25 ng/mL). Therefore, the plasma nesfatin-1 level may be considered as a biomarker to identify Chinese patients who have severe depression.
Several limitations in this study should also be acknowledged. First, all subjects were collected from a single hospital. Second, the future studies are needed to identify the role of plasma nesfatin-1 in the progression of depression. Additionally, although all drugs had been discontinued at least 2 weeks before measurement of plasma nesfatin-1, the long-term effects of previous drugs on plasma nesfatin-1 remains unknown.
The level of plasma nesfatin-1 was positively correlated with depression severity. Plasma nesfatin-1 level may be a potential indicator for depression severity. Multicentric and longitudinal studies are clearly required to validate an association between plasma nesfatin-1 level and depression severity.
Mogi T, Toda H, Yoshino A. Clinical characteristics of patients with diagnostic uncertainty of major depressive disorder. Asian J Psychiatr. 2017;30:159–62.
Setoyama D, Kato TA, Hashimoto R, Kunugi H, Hattori K, Hayakawa K, et al. Plasma metabolites predict severity of depression and suicidal ideation in psychiatric patients-a multicenter pilot analysis. PLoS One. 2016;11:e0165267.
Huang TL, Lin CC. Advances in biomarkers of major depressive disorder. Adv Clin Chem. 2015;68:177–204.
Cenik B, Cenik C, Snyder MP, Brown ES. Plasma sterols and depressive symptom severity in a population-based cohort. PLoS One. 2017;12:e0184382.
Lamers F, Milaneschi Y, de Jonge P, Giltay EJ, Penninx BWJH. Metabolic and inflammatory markers: associations with individual depressive symptoms. Psychol Med. 2017; doi: https://doi.org/10.1017/S0033291717002483.
Aydin S. Role of NUCB2/nesfatin-1 as a possible biomarker. Curr Pharm Des. 2013;19:6986–92.
Çelik F, Belviranli M, Okudan N. Circulating levels of leptin, nesfatin-1 and kisspeptin in postmenopausal obese women. Arch Physiol Biochem. 2016;122:195–9.
Emmerzaal TL, Kozicz T. Nesfatin-1; implication in stress and stress-associated anxiety and depression. Curr Pharm Des. 2013;19:6941–8.
Xu YY, Ge JF, Qin G, Peng YN, Zhang CF, Liu XR, et al. Acute, but not chronic, stress increased the plasma concentration and hypothalamic mRNA expression of NUCB2/nesfatin-1 in rats. Neuropeptides. 2015;54:47–53.
Könczöl K, Bodnár I, Zelena D, Pintér O, Papp RS, Palkovits M, et al. Nesfatin-1/NUCB2 may participate in the activation of the hypothalamic-pituitary-adrenal axis in rats. Neurochem Int. 2010;57:189–97.
Ge JF, Xu YY, Qin G, Peng YN, Zhang CF, Liu XR, et al. Depression-like behavior induced by Nesfatin-1 in rats: involvement of increased immune activation and imbalance of synaptic vesicle proteins. Front Neurosci. 2015;9:429.
Geng LY, Qian FY, Qian JF, Zhang ZJ. The combination of plasma glutamate and physical impairment after acute stroke as a potential indicator for the early-onset post-stroke depression. J Psychosom Res. 2017;96:35–41.
Liu Z, Zhu Z, Zhao J, Ren W, Cai Y, Wang Q, et al. Malondialdehyde: a novel predictive biomarker for post-stroke depression. J Affect Disord. 2017;220:95–101.
Bez Y, Ari M, Ozturk OH, Oktar S, Can Y, Sogut S. Plasma Nesfatin-1 level may be associated with disease severity in patients with panic disorder. Psychopharmacology. 2010;20:288–92.
Bez Y, Ari M, Ozturk OH, Oktar S, Can Y. Increased plasma Nesfatin-1 levels in patients with obsessive compulsive disorder. Psychopharmacology. 2012;22:5–9.
Ari M, Ozturk OH, Bez Y, Oktar S, Erduran D. High plasma nesfatin-1 level in patients with major depressive disorder. Prog Neuro-Psychopharmacol Biol Psychiatry. 2011;35:497–500.
Ding S, Qu W, Dang S, Xie X, Xu J, Wang Y, et al. Serum nesfatin-1 is reduced in type 2 diabetes mellitus patients with peripheral arterial disease. Med Sci Monit. 2015;21:987–91.
Algul S, Ozkan Y, Ozcelik O. Serum nesfatin-1 levels in patients with different glucose tolerance levels. Physiol Res. 2016;65:979–85.
Li QC, Wang HY, Chen X, Guan HZ, Jiang ZY. Fasting plasma levels of nesfatin-1 in patients with type 1 and type 2 diabetes mellitus and the nutrient-related fluctuation of nesfatin-1 level in normal humans. Regul Pept. 2010;159:72–7.
Delitala AP, Terracciano A, Fiorillo E, Orrù V, Schlessinger D, Cucca F. Depressive symptoms, thyroid hormone and autoimmunity in a population-based cohort from Sardinia. J Affect Disord. 2016;191:82–7.
Talaei A, Rafee N, Rafei F, Chehrei A. TSH cut off point based on depression in hypothyroid patients. BMC Psychiatry. 2017;17:327.
Yu J, Tian AJ, Yuan X, Cheng XX. Subclinical hypothyroidism after 131I-treatment of Graves' disease: a risk factor for depression? PLoS One. 2016;11:e0154846.
Liu F, Yang Q, Gao N, Liu F, Chen S. Decreased plasma nesfatin-1 level is related to the thyroid dysfunction in patients with type 2 diabetes mellitus. J Diabetes Res. 2014;2014:128014.
We thank the patientsand controls who participated in this study. We thank Pr. Gang Feng for technical assistance.
This research was supported by the National High Technology Research and Development Program 863 (2014AA022304). The funding bodies did not participate in the design of the study, the collection of data, analysis of data, interpretation of data or in writing the manuscript.
Availability of data and materials
The de-identified datasets used during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
All participants received an explanation of the study’s aims and provided a written indication of informed consent. Participation was voluntary. This study was approved by the Ethical Committee of the Second People’s Hospital of Wuhu City. The study was designed and is being conducted according to the latest version of the Declaration of Helsinki.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Xiao, MM., Li, JB., Jiang, LL. et al. Plasma nesfatin-1 level is associated with severity of depression in Chinese depressive patients. BMC Psychiatry 18, 88 (2018). https://doi.org/10.1186/s12888-018-1672-4
- Plasma nesfatin-1