4.7 Article

Vitamin D and inflammation in major depressive disorder

期刊

JOURNAL OF AFFECTIVE DISORDERS
卷 267, 期 -, 页码 33-41

出版社

ELSEVIER
DOI: 10.1016/j.jad.2020.01.168

关键词

Vitamin D; 25(OH)D; Inflammation; Major depressive disorder; Suicidal ideation

资金

  1. National Institute of Mental Health (NIMH) [R01-MH083784]
  2. O'Shaughnessy Foundation
  3. Tinberg family
  4. UCSF Academic Senate
  5. UCSF Research Evaluation and Allocation Committee (REAC)
  6. National Institutes of Health/National Center for Research Resources (NIH/NCRR)
  7. National Center for Advancing Translational Sciences, National Institutes of Health, through UCSF-CTSI Grant [UL1 RR024131]
  8. National Science Foundation Graduate Research Fellowship Program (NSF Grant) [DGE-1650604]
  9. Swedish Research Council [2015-00387]
  10. Marie Sklodowska Curie Actions, Cofund [INCA 600398]
  11. Swedish Society of Medicine
  12. Soderstrom-Konigska Foundation
  13. Sjobring Foundation
  14. OM Persson Foundation
  15. province of Scania (Sweden) state grants (ALF)

向作者/读者索取更多资源

Background: Increased inflammation is reported in Major Depressive Disorder (MDD), which may be more pronounced in suicidal subjects. Vitamin D deficiency may drive this pro-inflammatory state due to vitamin D's anti-inflammatory effects. Methods: We quantified plasma 25-hydroxyvitamin D (25(OH)D) and inflammatory markers interleukin (IL)-6 and tumor necrosis factor (TNF)-alpha, and other inflammatory indices, neutrophil-to-lymphocyte ratio (NLR) and white blood cell count (WBC) in 48 un-medicated MDD subjects (n = 17 with mild-to-moderate suicidal ideation [SI]) and 54 controls. IL-6 and TNF-alpha were combined into a composite inflammation score. Results: There were no significant differences in 25(OH)D levels between MDD and controls (p = 0.24) or between MDD with and without SI (p = 0.61). However, 25(OH)D was negatively correlated with all measured inflammatory markers; these correlations were stronger in MDD subjects, and particularly in those with SI. MDD status significantly moderated the relationships between 25(OH)D and NLR (p = 0.03), and 25(OH)D and WBC (p < 0.05), and SI significantly moderated the relationship between 25(OH)D and NLR (p = 0.03). Limitations: The study was cross-sectional, thereby limiting causal inference, and had a small sample size. Only seventeen of the MDD subjects had SI. Conclusion: While 25(OH)D levels did not significantly differ in MDD vs. controls, or in MDD with or without SI, lower 25(OH)D was associated with indices of immune activation in MDD, especially in cases with SI. Although our findings do not address causality, they are consistent with findings that relatively low 25(OH)D levels in MDD are associated with a pro-inflammatory state.

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