Circulating endothelial progenitor cells and depression: a possible novel link between heart and soul
1Fifth Department of Psychiatry, National Institute of Psychiatry and Neurology, Budapest, Hungary.
Insights
Major depression is linked to fewer circulating endothelial progenitor cells (EPCs), which are crucial for blood vessel repair. This study found lower EPC counts in depressed patients, correlating with symptom severity and elevated TNF-alpha.
Area of Science:
- Cardiovascular Research
- Neuroscience
- Immunology
Background:
- Depression is a known cardiovascular risk factor, but underlying mechanisms remain unclear.
- Reduced endothelial progenitor cells (EPCs) are observed in patients with cardiovascular risk factors.
- This study investigates the potential link between depression and EPC numbers.
Purpose of the Study:
- To determine if major depression is associated with altered numbers of circulating endothelial progenitor cells (EPCs).
- To explore the relationship between EPC levels, depressive symptom severity, and inflammatory markers.
Main Methods:
- Flow cytometry was used to quantify mature (CD34+/VEGFR2+) and immature (CD133+/VEGFR2+) EPCs in 33 depressed patients and 16 controls.
- Plasma levels of VEGF, C-reactive protein (CRP), and tumor necrosis factor-alpha (TNF-alpha) were measured.
- Quantitative RT-PCR assessed mRNA levels of EPC markers (CD34, CD133, VEGFR2).
Main Results:
- EPC counts were significantly lower in depressed patients compared to controls (P<0.01).
- EPC levels showed a significant inverse correlation with depression severity.
- Elevated TNF-alpha levels were observed in patients, inversely correlating with EPC counts (P<0.05).
- A trend towards decreased EPC-specific mRNA was noted, with significant reductions in VEGFR2 and CD133 mRNA.
Conclusions:
- This study provides the first evidence of decreased circulating EPC numbers in patients with major depression.
- Depression may negatively impact EPC levels, potentially contributing to cardiovascular risks.
- Inflammatory processes, indicated by elevated TNF-alpha, may play a role in mediating this relationship.
Abstract:
Although depression is known to be an independent risk factor for cardiovascular disorders, the mechanisms behind this connection are not well understood. However, the reduction in the number of endothelial progenitor cells (EPCs) in patients with cardiovascular risk factors has led us to hypothesize that depression influences the number of EPCs. EPCs labeled with CD34, CD133 and vascular endothelial growth factor receptor-2 (VEGFR2) antibodies were counted by flow cytometry in the peripheral blood (PB) of 33 patients with a current episode of major depression and of 16 control subjects. Mature (CD34+/VEGFR2+) and immature (CD133+/VEGFR2+) EPC counts were decreased in patients (vs controls; P<0.01 for both comparisons), and there was a significant inverse relationship between EPC levels and the severity of depressive symptoms (P<0.01 for both EPC phenotypes). Additionally, we assayed the plasma levels of VEGF, C-reactive protein (CRP) and tumor necrosis factor (TNF)-alpha and observed significantly elevated TNF-alpha concentrations in patients (vs controls; P<0.05) and, moreover, a significant inverse correlation between TNF-alpha and EPC levels (P<0.05). Moreover, by means of a quantitative RT-PCR approach, we measured CD34, CD133 and VEGFR2 mRNA levels of PB samples and found a net trend toward a decrease in all the investigated EPC-specific mRNA levels in patients as compared with controls. However, statistical significance was reached only for VEGFR2 and CD133 levels (P<0.01 for both markers). This is the first paper that demonstrates evidence of decreased numbers of circulating EPCs in patients with a current episode of major depression.
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