Abstract

How the presence of inflammation has repercussions for brain function is a topic of active research into depression. Signals released from immune system-related cells, including chemokines, might be indicative of active depression and can, hypothetically, serve as biomarkers of response to interventions, both pharmacological and psychological. The objective of this study is to analyze the peripheral plasma concentrations of CXCL12, CCL11, CX3CL1 and CCL2 in a cohort of depressed primary-care patients, as well as their evolution after an internet-based cognitive-behavioral intervention. The concentrations of those chemokines were measured in 66 primary-care patients with mild and moderate depression, before and after the intervention, as well as 60 controls, using multiplex immunoassays. Concentrations of CXCL12 and CCL2 were significantly higher in the clinical sample in comparison with controls. A stable multivariate discriminative model between both groups was found. Concentrations of all chemokines decreased after the internet-based psychological intervention. These findings support the implication of chemokines in depression, even in a sample of patients with mild and moderate severity. Furthermore, they demonstrate the need for further multidisciplinary research that confirms how biomarkers such as plasma chemokines can serve as a marker for depression and are sensitive to non-pharmacological interventions.

Highlights

  • Significant differences in CXCL12 and CCL2 concentrations were found between depressed patients and controls (Table 2)

  • Differences in CXCL12 and CCL2 remained, and the concentration of CX3CL1 was significantly higher in controls

  • The aim of this study was to test the relationship between depression and plasma concentrations of CCL2, CCL11, CX3CL1 and CXCL12 in mildly and moderately depressed primary-care patients, as well as the potential influence of an effective internet-based cognitive-behavioral therapy (iCBT) intervention on those molecules

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Summary

Aims of The Study

Our research group has found that some of these chemokines – CCL2, CCL11, CX3CL1, and CXCL12 – are related with depressive symptoms in patients with cocaine[24,25,26] and alcohol[27] use disorders. It is easier to find relatively naïve patients in terms of antidepressant prescription28 – in the present study, we will recruit both antidepressant-naïve and ISSR-treated patients These features are interesting for directly relating the concentrations of chemokines to depressive symptoms, without the interference of potentially confounding variables. We hypothesized that the plasma concentrations of CCL2, CCL11, CX3CL1, and CXCL12 in the sample of depressed patients would be reduced after the iCBT intervention

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