Abstract

Although recent studies have shown that immunological processes play an important role in the pathophysiology of mood disorders, immune activation may only be present in specific subgroups of patients. Our study aimed to examine whether immune activation was associated with (a) the presence of manic symptoms and (b) the onset of manic symptoms during 2 years of follow-up in depressed patients. Patients with a depressive disorder at baseline (N=957) and healthy controls (N=430) were selected from the Netherlands Study of Depression and Anxiety. Assessments included lifetime manic symptoms at baseline and two-year follow up, as well as C-reactive protein (CRP), interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) at baseline. Within depressed patients, immune activation was not related to the presence or absence of lifetime manic symptoms at baseline. However, CRP levels were strongly elevated in depressed men who developed manic symptoms compared with those who did not develop manic symptoms over 2 years (P<0.001, Cohen's d=0.89). IL-6 and TNF-α were also higher in depressed men with an onset of manic symptoms, but this association was not significant. However, we found that the onset of manic symptoms was particularly high in men with multiple elevated levels of inflammatory markers. Depressed men who developed manic symptoms during follow-up had increased immunological activity (especially CRP) compared with depressed men who did not develop manic symptoms. Further research should explore whether a treatment approach focusing on inflammatory processes may be more effective in this specific subgroup of depressed patients.

Highlights

  • The underlying pathophysiology of mood disorders, such as unipolar and bipolar depression, is receiving growing interest from researchers

  • Two recent meta-analyses have reported that unipolar depressed patients showed increased levels of inflammatory markers (for example, C-reactive protein (CRP), interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-a)), compared with healthy controls.[5,6]

  • It is likely that the monocyte-T-cell theory of mood disorders does not apply to all depressed patients, and our findings add to this rapidly growing body of literature by showing that higher levels of inflammatory markers are found among depressed men who are more at risk to become bipolar

Read more

Summary

INTRODUCTION

The underlying pathophysiology of mood disorders, such as unipolar and bipolar depression, is receiving growing interest from researchers. In both men and women, significant differences were found for education level, childhood trauma, smoking status, alcohol use, number of chronic diseases and use of antidepressants. To examine whether inflammatory markers (CRP, IL-6 and TNF-a) differed for depressed patients with manic symptoms compared with healthy controls (reference group I) and depressed patients without manic patients in the highest quartile of CRP, which was significantly higher than in the three groups with lower levels of CRP (Q4 vs Q1: P 1⁄4 0.002; Q4 vs Q2: P 1⁄4 0.013; Q4 vs Q3: P 1⁄4 0.003). We investigated the additional effect of the different inflammatory markers on the association with manic symptoms by dividing our patients into four groups (with 0, 1, 2 or all 3 inflammatory markers in the highest quartile) and comparing the percentage of manic symptoms between these groups

DISCUSSION
Findings
Strengths and limitations
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