Serum brain-derived neurotrophic factor,vascular endothelial growth factor and leptin levels in patients with a diagnosis of severe major depressive disorder with melancholic features

Abstract

Objective: Brain-derived neurotrophic factor (BDNF), vascular endothelial growth factor (VEGF) and leptin have been hypothesized to be involved in the neurobiology of depression. The aim of this study was to investigate BDNF, VEGF and leptin levels in patients with severe melancholic depression.

Methods: A total of 40 drug-free patients with major depressive disorder (MDD) with melancholic features and 40 healthy controls were included in the study. Demographic information, psychiatric evaluation and physical examination were documented for both groups. Serum BDNF, VEGF levels were determined by enzyme-linked immunosorbent assay and leptin with radioimmunoassay methods. The Hamilton Depression Rating Scale and Hamilton Anxiety Rating Scale were applied to the patients.

Results: There were no significant differences in serum BDNF, VEGF and leptin levels between the patient and control groups. There was a negative correlation between BDNF levels and the number of depressive episodes. It was noted that VEGF levels decreased with increasing severity of depression.

Conclusions: These findings suggest that BDNF levels might be associated with the recurrence of depression and VEGF levels might be a determinant of the severity of depression.

Keywords

brain-derived neurotrophic factor depression leptin vascular endothelial growth factor

Introduction

Major depressive disorder (MDD) is a devastating disease that afflicts approximately 8% of men and 15% of women [Kessler et al. 1994]. Approximately 25–30% of depressed patients are classified as ‘melancholic type’ [Rush and Weissenburger, 1994]. Clinical research has demonstrated that melancholic type-depressed patients are less likely to respond to placebo therapy, supporting the hypothesis of a biological foundation and the need for suitable pharmacotherapy [Peselow et al. 1992].

The word ‘neuroplasticity’ denotes the capacity of the brain to adapt continually to the demands placed on it by experience and major depression may be related to impairments of structural plasticity [Fuchs et al. 2004]. Neurotrophic factors are critical regulators of the formation and plasticity of neuronal networks. Recently, the involvement of neurotrophic factors, particularly brain-derived neurotrophic factor (BDNF), have been under intense investigation regarding their possible role in the pathophysiology of mood disorders and its antidepressant effects [Castren et al. 2007]. BDNF is a small dimeric neuroprotective protein and a member of the neurotrophin family, which is widely expressed in the mammalian adult brain [Hofer et al. 1990]. Its normal physiological role is to encourage the outgrowth of dendrites from nerve endings, and to help stabilize connections between neurons [Hartmann et al. 2001]. According to the neurotrophin hypothesis of depression, BDNF is of major importance because it modulates the plasticity, inhibits cell death cascades and increases cell survival proteins that are responsible for the proliferation and maintenance of central nervous system neurons [Yulug et al. 2009].

Some animal models of depression showed that both acute and chronic stress decreased expression of BDNF [Angelucci et al. 2000; Roceri et al. 2002], and direct administration of BDNF into specific brain regions has been shown to mimic antidepressant effects [Siuciak et al. 1997; Hoshaw et al. 2005; Shirayama et al. 2002]. However, some authors reported that mutant mouse lines with low or no detectable BDNF expression did not exhibit depressive-like behaviour [Chan et al. 2006; Chourbaji et al. 2004; MacQueen et al. 2001; Saarelainen et al. 2003]. Pan and colleagues demonstrated that BDNF crosses the blood–brain barrier (BBB), which suggests that serum BDNF levels may reflect BDNF levels of the brain [Pan et al. 1998]. It was found that brain and serum BDNF levels undergo similar changes during maturation and ageing, and there is a positive correlation between serum and cortical BDNF levels [Karege et al. 2002]. Data about serum BDNF concentrations in major depression are conflicting, some authors reported levels as decreased [Karege et al. 2002, 2005; Shimizu et al. 2003; Aydemir et al. 2006; Monteleone et al. 2008], and others as unchanged [Ziegenhorn et al. 2007], compared with the healthy controls. Serum levels of BDNF have been found to be 200-fold higher than plasma levels [Rosenfeld et al. 1995]. This difference could reflect the amount of BDNF stored in platelets. Accordingly, it was suggested that BDNF levels of the plasma may reflect circulating levels since platelets are not seriously damaged during the separation of plasma [Lee et al. 2007]. However, studies that investigated plasma BDNF levels of depressed patients also yielded conflicting results as decreased, unchanged or increased levels [Grassi-Oliveira et al. 2008; Karege et al. 2005; Lee et al. 2007; Piccinni et al. 2008; Lee and Kim, 2009; Bocchio-Chiavetto et al. 2010; Serra-Millàs et al. 2011].

The vascular endothelial growth factor (VEGF) is an angiogenic cytokine able to induce vasopermeability in many types of tissues, including the BBB, and to facilitate the neurogenesis and proliferation of neurons in the adult hippocampus. Recent evidence indicates that VEGF can act as a neuroprotective factor in the adult brain, inhibiting apoptosis and inducing growth of the associated vascular–neuronal networks. VEGF influences synaptic plasticity in hippocampus-dependent processes, such as learning and memory, and modulates synaptic transmission [Ventriglia et al. 2009]. Exposure to unpredictable stress decreases the expression of VEGF in the hippocampus [Heine et al. 2005].

The hormone leptin encoded by the obese (ob) gene is predominantly synthesized by adipocytes and circulates in the plasma in amounts proportional to the body fat content [Zhang et al. 1994; Maffei et al. 1995]. It was first identified by its ability to regulate food intake and body weight through its actions in the hypothalamus. However, recent studies have shown that the neuronal actions of leptin are not confined to the hypothalamus. There is accumulating evidence that leptin plays an important part in regulating neuroendocrine function, in addition to conveying the status of energy stores to the central nervous system. In the hippocampus, under conditions where N-methyl-D-aspartate (NMDA) receptors are activated, leptin acts as a potential cognitive enhancer as it facilitates synaptic plasticity by selective enhancement of NMDA responses. Regarding its functions, leptin emerges to play a novel role in the regulation of mood and emotion. On the basis of the finding of low circulating leptin levels in animal models of depression, it was hypothesized that leptin insufficiency may underlie depression-like behavioural deficits [Lu et al. 2006]. Furthermore, systemic leptin administration was found to reverse the depressive state [Lu et al. 2006; Kim et al. 2006; Hirano et al. 2007]. Available information about the role of leptin signalling in human depression is limited and controversial. Leptin levels were reported as decreased [Kraus et al. 2001; Jow et al. 2006, Yang et al. 2007], and as unchanged [Deuschle et al. 1996; Moosa et al. 2003; Kauffman et al. 2005], in patients with depression. There are also studies reporting that leptin levels were increased only in women with depression [Antonijevic et al. 1998; Rubin et al. 2002; Esel et al. 2005; Pasco et al. 2008].

The relationship between stress and depression is complex, and subjects who receive a depression diagnosis are likely to represent heterogeneous populations of phenocopies with a varying contribution from stress exposure [Kendler et al. 2001]. Depression type is not indicated in the studies investigating BDNF, VEGF and leptin in MDD. However, there is growing evidence that depressive disorders encompass a group of disorders represented by differences in pathophysiological mechanisms and the identification of distinct endophenotypes for MDD will improve understanding of the disease [Antonijevic, 2006]. In this study we created a homogeneous group with patients diagnosed as severe melancholic depression in which biological factors are of major importance. In these patients, we aimed to determine serum BDNF, VEGF and leptin levels, which are all related to a neurotrophic hypothesis of depression and compare them with healthy controls.

Methods

Subjects

The study included 40 MDD patients with melancholic features (18–65 years of age) evaluated by a semi-structured psychiatric examination. The patients were diagnosed according to the Diagnostic and Statistical Manual of Mental Disorders [American Psychiatric Association, 1994]. Patients with an Axis I disorder other than MDD, alcohol/substance users, patients with any systemic or endocrinological disorder, pregnant women, women using oral contraceptives and patients with severe abnormalities in blood tests were excluded from the study. The patients had been drug-free for at least 3 months. Healthy controls (n = 40) were recruited from the hospital–university staff and were also assessed by a semi-structured psychiatric interview. Informed consent was obtained from all of the participants. The study had local ethic committee approval.

Complete blood count, serum electrolyte assay, liver and thyroid function tests, several hormone assays and electrocardiography were performed on all participants after an overnight fast between 8:00 and 10:00 a.m. following a general physical examination.

The Hamilton Depression Rating Scale (HDRS) and Hamilton Anxiety Rating Scale were applied to patients to evaluate the severity of depression and anxiety.

Sample preparation and analysis

Blood was withdrawn from the antecubital vein in the fasting state. Blood samples were drawn into heparin-coated, ethylenediaminetetraacetic acid-containing and nonadditive tubes and were processed in the laboratory immediately after collection. Complete blood count, serum electrolyte assay, liver function tests, thyroid function tests, cortisol, adrenocorticotropic hormone, growth hormone, sex hormones, prolactin, insulin and serum lipid profile were determined on the same day that the blood was collected. Serum samples obtained for determination of BDNF, VEGF and leptin were kept at −80^oC until the analyses. The time range for collecting the samples was about 6 months. BDNF (Phoenix Pharmaceuticals, Inc., Burlingame, CA, USA) and VEGF (Invitrogen, Camarillo, CA, USA) levels were determined by enzyme-linked immunosorbent assay kits. Leptin levels were determined by a radioimmunoassay method (Linco Research, St. Charles, MO, USA). BDNF and VEGF levels were given as pg/ml and leptin levels were given as ng/ml.

Statistical analysis

All statistical analyses were performed with SPSS version 13.0. Continuous variables were expressed as mean ± standard deviation. Categorical variables were expressed as frequency. The Shapiro-Wilk test was used as normality test. Continuous variables were compared using the Student’s t-test and Mann–Whitney test when the data were not normally distributed. Categorical variables were compared using Pearson’s chi-square test and Fisher’s exact test. Correlations between variables were tested using Pearson and Spearman correlation coefficients. A p-value < 0.05 was considered as significant. Bonferroni correction was used for multiple comparisons.

Results

Demographic findings and laboratory results of study groups are given in Table 1. Clinical characteristics of MDD patients are given in Table 2. There were no significant differences in age, sex distribution and body mass indices (BMI) between the study groups. In the MDD group 14 patients (35%) had their first depressive episode and never used antidepressants; whereas 20 patients (50%) had their second and 6 patients (15%) had their third depressive episodes.

Table 1.

Demographic findings and laboratory results of patients with major depressive disorder and the control group.

	Major depressive disorder group (n = 40)	Control group (n = 40)		p-value
Age (years)	35 ± 8	34 ± 8	t = 0.614	0.541
Body mass index (kg/m2)	23.5 ± 4.2	25.2 ± 5.3	t = -1.626	0.108*
Sex (female/male)	32/8	32/8		NS^$
Smokers/nonsmokers	12/28	15/25		NS^$
Total cholesterol (mmol/l)	4.7 ± 1.1	4.9 ± 1.1	U = 676.50	NS*
LDL-cholesterol (mmol/l)	2.9 ± 0.8	3.0 ± 0.8	U = 712.50	NS*
VLDL-cholesterol (mg/dl)	20.1 ± 12.2	23.0 ± 10.9	U = 628.00	NS*
HDL-cholesterol (mmol/l)	1.3 ± 0.3	1.3 ± 0.3	U = 771.00	NS*
Triglyceride (mmol/l)	1.14 ± 0.7	1.3 ± 0.6	U = 628.00	NS*
Cortisol (nmol/l)	328.3 ± 212.8	338.3 ± 115.8	U = 718.00	NS*
Insulin (ng/ml)	7.8 ± 4.3	8.3 ± 7.1	U = 766.00	NS*
BDNF (pg/ml)	1577 ± 510	1624 ± 329	U = 729.00	NS*
VEGF (pg/ml)	300 ± 158	358 ± 217	U = 678.00	NS*
Leptin (µg/l)	12.9 ± 11.2	11.6 ± 9.0	U = 679.50	NS*

Student’s t-test for independent groups. ^$Chi-square test. Data are expressed as mean ± standard deviation. A p-value < 0.05 was considered significant. BDNF, brain-derived neurotrophic factor; HDL, high density lipoprotein; LDL, low density lipoprotein; NS, not significant; VEGF, vascular endothelial growth factor; VLDL, very low density lipoprotein.

Table 2.

Clinical characteristics of major depressive disorder patients.

Duration of episode (months)	5.2 ± 4.6
Beginning age of depression (years)	28.2 ± 7.2
Number of depressive episodes	1.8 ± 0.7
Hamilton Depression Rating Scale	31.1 ± 3.2
Hamilton Anxiety Rating Scale	26.2 ± 5.9
Suicidal/nonsuicidal	6/34
Family history (+)/family history (-)	15/25

There was no significant difference between patient and control groups in terms of serum levels of BDNF, VEGF and leptin. There was also no difference between these parameters when compared according to sex. There was no correlation between BDNF and VEGF levels in terms of age and BMI in both groups. There was no statistical difference between BDNF levels of suicidal depressive patients, nonsuicidal depressive patients and controls. The number of depressive episodes and BDNF levels were found to be negatively correlated (r = -0.390, p = 0.017) (Figure 1). VEGF levels were negatively correlated with HDRS scores (r = -0.326, p = 0.043) in the patient group.

Figure 1.

Comparison of serum BDNF levels in first episode and recurrent depressive patients.

Serum leptin levels correlated positively with BMI in both groups (r = 0.416, p = 0.009). Leptin levels were significantly higher in women in the control group (p = 0.030), but no such difference was observed in the patient group. Leptin levels correlated positively with triglyceride, very low density lipoprotein and insulin levels in the patient group (p < 0.01); no such relation was present in control group. There was no difference between cortisol levels in patient and control groups and leptin was not found to be correlated with cortisol. There was no correlation between leptin levels and HDRS scores, number of depressive episodes or suicidality in the patient group.

Discussion

In the present study, there were no significant differences between melancholic depressive patient and control groups in terms of serum BDNF, VEGF and leptin levels. However, BDNF levels were found to be negatively correlated with the number of depressive episodes. In addition, VEGF levels were found to be negatively correlated with increased severity of depression.

To our knowledge this study is the first to have investigated serum BDNF, VEGF and leptin levels in purely melancholic depressive patients. In parallel with our findings, Basterzi and colleagues and Ziegenhorn and colleagues reported that serum BDNF levels were not significantly different between depressive patients and controls [Basterzi et al. 2009; Ziegenhorn et al. 2007]. Furthermore, Kim and colleagues and Lee and Kim investigated BDNF levels in the plasma of depressive patients and also found unchanged levels [Kim et al. 2007; Lee and Kim, 2008]. We had difficulties in comparing our results with those of the other studies since subtypes of depression were not defined or evaluated as separate groups in almost all of the studies.

We found that patients with recurrent depressive episodes have lower BDNF serum levels compared with patients with a single episode and healthy controls. This finding is in line with the study of Dell’Osso and colleagues who stated that patients who were suffering from a recurrent episode had significantly lower levels of plasma BDNF [Dell’Osso et al. 2010]. Kauer-Sant’Anna and colleagues have shown that bipolar patients later in the course of their illness have greater decrements in BDNF compared with those earlier in the illness, suggesting a possible cumulative deficit in BDNF after multiple episodes [Kauer-Sant’Anna et al. 2009]. Furthermore, there are several studies indicating that BDNF levels correlate negatively with increased severity of depression [Karege et al. 2002; Shimizu et al. 2003; Gonul et al. 2005; Dell’Osso et al. 2010; Bus et al. 2011]. However, we also assessed the severity of depression with the use of HDRS and did not find any relation between the severity of depression and BDNF levels. This finding was in line with the study of Lee and colleagues [Lee et al. 2007].

The number of studies investigating the association of VEGF with depression is limited. Kahl and colleagues found increased concentrations of VEGF in nonmedicated depressive patients with borderline personality disorder in comparison with healthy controls [Kahl et al. 2009]. Iga and colleagues had previously suggested that a higher expression of VEGF mRNA in the peripheral leucocytes might be associated with the depressive state [Iga et al. 2007]. Takebayashi and colleagues reported that plasma VEGF levels were increased significantly in MDD patients compared with matched controls [Takebayashi et al. 2010]. However, patients were taking psychotrophic agents in the last two studies. In parallel with our findings Dome and colleagues and Ventriglia and colleagues did not find any significant differences in serum VEGF levels between the MDD patients and healthy controls [Dome et al. 2008; Ventriglia et al. 2009]. In a recent animal study, Elfving and colleagues reported that VEGF levels were significantly decreased in the hippocampus and frontal cortex of a genetic depression rat model [Elfving et al. 2010]; however, no such difference was observed in serum levels of VEGF. Although these results suggest that VEGF is not a peripheral marker of depression, we observed that VEGF levels were negatively correlated with HDRS scores. To our knowledge, this is the first study suggesting a relation between serum levels of VEGF and severity of depression.

In the present study, in line with several studies [Deuschle et al. 1996; Moosa et al. 2003; Kauffman et al. 2005], there was no significant difference in serum leptin levels between the MDD patients and controls. No relation was found between leptin levels and severity of depression, suicidality and recurrence of depressive episodes. We think that our data about leptin levels are noteworthy considering that the study had a very homogeneous subgroup of depression with a predominantly biological etiology.

It is surprising that there was no significant difference between serum cortisol levels of patients and controls as approximately 50% of depressed patients exhibit dysregulation of the hypothalamic–pituitary–adrenal (HPA) axis, which results in sustained elevations in cortisol levels [Gold and Chrousos, 2002; Swaab et al. 2005]. Elevation of basal cortisol levels [Belanoff et al. 2001], and nonsuppression on the dexamethasone suppression test [Nelson and Davis, 1997], were most clearly evident in psychotic depression. None of our patients had any psychotic symptoms. Moreover, hypercortisolaemia has not been a stable finding in all studies and a dysfunction of the HPA axis has been proposed as an alternative hypothesis [Peeters et al. 2004]. Peeters and colleagues suggested that erratic cortisol secretion may be a more characteristic feature of HPA-axis dysregulation than hypercortisolism, especially in outpatient populations [Peeters et al. 2004]. Assies and colleagues found no difference between the cortisol levels of depressed patients and controls and indicated that dehydroepiandrosterone-sulphate may be a more important indicator of depression [Assies et al. 2004]. Michopoulos and colleagues found that depressive patients had normal cortisol blood levels and there was no significant difference between melancholic and nonmelancholic depressive patients [Michopoulos et al. 2008]. Glucocorticoids play a critical role in mediating stress-induced downregulation of BDNF in the hippocampus [Schmidt and Duman, 2007]. Thus, our finding that there is no significant difference between serum BDNF levels of patients and controls is concordant with the finding that there is also no significant difference between the cortisol levels of the two groups.

One of the limitations of the study was the absence of a control group composed of other types of MDDs. One might consider the selection of serum instead of plasma as the specimen for BDNF as a limitation, however, as mentioned above, data about BDNF levels in serum or plasma of depressive patients are conflicting. Furthermore, it was reported that plasma BDNF has shown high interindividual variability [Piccinni et al. 2009]. Lommatzsch and colleagues found that plasma BDNF levels decreased significantly with increasing age, weight or cholesterol, whereas platelet levels (an important source of serum BDNF) did not [Lommatzsch et al. 2005]. Furthermore, there is evidence for the stability of BDNF levels in platelets or serum [Trajkovska et al. 2007], whereas in plasma, it circulates for less than 1 h [Kishino et al. 2001; Poduslo and Curran, 1996]. Another limitation of the study is that we did not consider the phases of menstrual cycle in female subjects. We know that leptin and BDNF levels especially differ according to hormonal changes. Another limitation is that we measured leptin only once so that we could not observe changes in its diurnal rhythm and pulsatility in depressive patients. Further studies with larger samples are required to investigate biological markers in homogeneous MDD groups.

This study showed that there are no significant differences in BDNF, VEGF and leptin levels in MDD patients with melancholic features compared with those of healthy controls. We think that this finding is significant as we studied with a diagnostically homogeneous group of patients. BDNF may be related to the recurrence of depressive episodes as its level decreased with remitting depression. VEGF may be a determinant of the severity of depression as its levels decreased with the increasing HDRS. Further investigations aiming to identify the role and putative function of neurotrophins in the pathogenesis of depressive disorders and their peripheral indicators in the blood are necessary for new diagnostic and therapeutic options. Neurotrophic factor levels may be a guide in the assessment of suicidality, severity and recurrence of depression and, accordingly, in the development of therapeutic interventions. Furthermore, treatment regimens with the direct or adjunctive addition of these neurotrophins may be indicated in the future.

Footnotes

The study was supported by the foundation of Uludag University (2008/37). This research received no specific grant from any funding agency in the public, commercial, or not- for-profit sectors.

The authors declare no conflicts of interest in preparing this article.

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