Journal of Translational Medicine (Dec 2017)

Cytokine signatures in chronic fatigue syndrome patients: a Case Control Study and the effect of anakinra treatment

  • Megan E. Roerink,
  • Hans Knoop,
  • Ewald M. Bronkhorst,
  • Henk A. Mouthaan,
  • Luuk J. A. C. Hawinkels,
  • Leo A. B. Joosten,
  • Jos W. M. van der Meer

DOI
https://doi.org/10.1186/s12967-017-1371-9
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 10

Abstract

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Abstract Background Cytokine disturbances have been suggested to be associated with the Chronic Fatigue Syndrome/Myalgic encephalomyelitis (CFS/ME) for decades. Methods Fifty female CFS patients were included in a study on the effect of the interleukin-1-receptor antagonist anakinra or placebo during 4 weeks. EDTA plasma was collected from patients before and directly after treatment. At baseline, plasma samples were collected at the same time from 48 healthy, age-matched female neighborhood controls. A panel of 92 inflammatory markers was determined in parallel in 1 μL samples using a ‘proximity extension assay’ (PEA) based immunoassay. Since Transforming growth factor beta (TGF-β) and interleukin-1 receptor antagonist (IL-1Ra) were not included in this platform, these cytokines were measured with ELISA. Results In CFS/ME patients, the ‘normalized protein expression’ value of IL-12p40 and CSF-1 was significantly higher (p value 0.0042 and 0.049, respectively). Furthermore, using LASSO regression, a combination of 47 markers yielded a prediction model with a corrected AUC of 0.73. After correction for multiple testing, anakinra had no effect on circulating cytokines. TGF-β did not differ between patients and controls. Conclusions In conclusion, this study demonstrated increased IL-12p40 and CSF-1 concentrations in CFS/ME patients in addition to a set of predictive biomarkers. There was no effect of anakinra on circulating cytokines other than IL-1Ra. Trial Registration: ClinicalTrials.gov Identifier: NCT02108210 , Registered April 2014

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