Translational Psychiatry (Apr 2023)

Association of plasma cytokines and antidepressant response following mild-intensity whole-body hyperthermia in major depressive disorder

  • Michael C. Flux,
  • David G. Smith,
  • John J. B. Allen,
  • Matthias R. Mehl,
  • Andi Medrano,
  • Tommy K. Begay,
  • Brandon H. Middlemist,
  • Brandon M. Marquart,
  • Steven P. Cole,
  • Christina J. Sauder,
  • Christopher A. Lowry,
  • Charles L. Raison

DOI
https://doi.org/10.1038/s41398-023-02402-9
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 8

Abstract

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Abstract Whole-body hyperthermia (WBH) shows promise for the treatment of major depressive disorder (MDD). Because MDD is associated with increased inflammation, and anti-inflammatory agents show some promise as antidepressants, the current study sought to identify the acute and longer-term immune effects of WBH in participants with MDD and to explore whether these effects associate with the procedure’s antidepressant properties. Thirty participants who met DSM-IV-TR criteria for MDD were randomized to receive a single session of WBH (n = 16) or sham treatment (n = 14). Hamilton Depression Rating Scale (HDRS) scores were assessed at baseline and 1, 2, 4, and 6 weeks post-treatment (WBH vs. sham), and plasma cytokine concentrations were assessed at baseline, immediately post-treatment, and 1 and 4 weeks post-treatment. As previously reported, WBH produced a rapid and sustained antidepressant effect. When compared to sham, WBH increased plasma interleukin (IL)-6 immediately post-treatment (time by treatment: χ 2 (3, N=108) = 47.33, p < 0.001), while having no effect on other cytokines acutely and no impact on IL-6, or any other cytokine, at 1 or 4 weeks post treatment. In the study sample as a whole, increased IL-6 post-treatment was associated with reduced HDRS depression scores over the 6 weeks of follow-up (F (1, 102.3) = 6.74, p = 0.01). These results suggest a hitherto unrecognized relationship between hyperthermia, the immune system, and depression, and may point to WBH as a novel modality for exploring behavioral effects of IL-6 when the cytokine is activated in isolation from the inflammatory mediators with which it frequently travels.