Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a persistent and debilitating disorder marked by cognitive and sensory dysfunction and unexplained physical fatigue. Classically, cases present after a prodrome consistent with infection; however, some cases are atypical and have a different presentation and comorbidities that pose challenges for differential diagnosis. We analyzed cerebrospinal fluid (CSF) from 32 cases with classical ME/CFS and 27 cases with atypical ME/CFS using a 51-plex cytokine assay. Atypical subjects differed in cytokine profiles from classical subjects. In logistic regression models incorporating immune molecules that were identified as potential predictor variables through feature selection, we found strong associations between the atypical ME/CFS phenotype and lower CSF levels of the inflammatory mediators, interleukin 17A and CXCL9. Network analysis revealed an absence of inverse inter-cytokine relationships in CSF from atypical patients, and more sparse positive intercorrelations, than classical subjects. Interleukin 1 receptor antagonist appeared to be a negative regulator in classical ME/CFS, with patterns suggestive of disturbances in interleukin 1 signaling and autoimmunity-type patterns of immune activation. Immune signatures in the central nervous system of ME/CFS patients with atypical features may be distinct from those with more typical clinical presentations.
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a heterogeneous illness characterized by unexplained severe fatigue, sleep disturbance, pain and deficits in cognition and perception.1 Some investigators have reported evidence of immune activation or inflammation in the central nervous system (CNS) of subjects with ME/CFS. One study using ¹¹C-(R)-PK11195 PET—a ligand targeting a translocator protein that is expressed by activated microglia and astrocytes—described active inflammation in amygdala, thalamus and midbrain that correlated with patient-reported cognitive impairment.2 Other studies of the cerebrospinal fluid (CSF) proteome reported increased levels of proteins relating to the complement cascade.3, 4 In prior work defining CSF immune signatures in ME/CFS patients with classical presentations we found evidence of disrupted interleukin (IL)-1 signaling in CNS as compared with subjects with multiple sclerosis and no-disease controls.5 A proportion of patients who meet diagnostic criteria for ME/CFS at the onset of their illness have either a remote history of relatively uncommon exposures (viral encephalitis, illness after foreign travel or blood transfusion, Gulf War Illness) or develop comorbid immune-mediated6, 7 or neurological8, 9 disorders years later. Here we report discrete immunological profiles in the CSF of subjects with ME/CFS who vary in clinical presentation and comorbidity. Our findings may have utility for future work on the pathogenesis of this complex disorder and enable therapeutic interventions that target host response.
Materials and methods
The study population was comprised of 32 ME/CFS cases with classical features and presentations and 27 ME/CFS cases with atypical features or clinical presentations. CSF data for all 32 cases in the classical group were previously reported in an extended comparison with patients with multiple sclerosis (MS) and no-disease controls.5 All cases (both classical and atypical) met either the 1994 CDC criteria10 and/or the 2003 Canadian consensus criteria.11 The ‘classical’ (C-ME/CFS) group had acute onset of disease marked by a prodrome consistent with infection; ‘atypical’ (A-ME/CFS) ME/CFS patients met full diagnostic criteria for ME/CFS at onset of their illness, but had a less standard onset of ME/CFS and/or developed other disorders after illness onset of ME/CFS. Onset for the A-ME/CFS group was acute or non-acute with or without flu-like symptoms at the time of disease onset. This group tended to have more severe cognitive dysfunction and other neurological complaints. Some A-ME/CFS patients subsequently developed seizures and atypical MS or autoimmune/inflammatory disorders. Atypical MS and autoimmune/inflammatory disorders were categorized together in the ‘Immune or inflammatory’ category of atypical ME/CFS. The ‘Other’ category included patients with seizure disorder and the single subject with Gulf War Illness. Individuals who developed ME/CFS after blood transfusion or foreign travel were classified together in the ‘Probable infection’ category. The last A-ME/CFS category comprised subjects who developed malignancies after their initial diagnosis of ME/CFS (Table 1). All subjects had contributed CSF samples to biobanks at Sierra Internal Medicine (SIM), a private internal medicine clinic in Incline Village, Nevada, where they were followed over subsequent years. Based on prior work on plasma cytokines in ME/CFS showing differences according to phase of the illness,12 we categorized duration of illness as either short (⩽3 years) or long (>3 years).
Human subjects and ME/CFS biological sample collection
CSF collections followed standardized office protocol at SIM. Potential side effects or adverse events associated with specific clinically-indicated procedures such as lumbar puncture, as well as the clinical reason for these procedures, were discussed with patients in the course of their diagnostic work up and treatment planning. CSF was transferred by certified technicians from the lumbar puncture kit collection tubes into 2 ml Nalgene cryostorage tubes (Fisher Scientific, Pittsburgh, PA, USA). Excess CSF not consumed during indicated diagnostic tests was immediately stored in a −80 °C freezer located at SIM. Informed consent was obtained at the same time to allow any excess sample to be de-identified for use in any future research investigations of SIM.
Selection of case and comparator samples
CSF samples were retrieved from SIM repositories and shipped on dry ice to the Wisconsin Viral Research Group (WVRG) where they were frozen in aliquots at −80 °C. CSF samples derived from the ME/CFS subjects had previously been clinically analyzed for oligoclonal banding, total protein, glucose and amino-acid profiles, helping to rule out other known contributory diagnoses such as MS. All CSF specimens submitted to WVRG represent archived diagnostic specimens exempt from HIPAA and institutional review board consideration (46.101 (b)(4), Code of Federal Regulations). All samples were de-identified prior to shipment to the Center for Infection and Immunity at Columbia University for analysis.
The CSF concentrations of the following immune molecules were determined using a magnetic bead-based 51-plex immunoassay: interleukin (IL)-1 superfamily, IL1α, IL1β, IL1RA; type I IL/γ chain family, IL2, IL4, IL7, IL13, IL15; type I IL/β chain family, IL5, GMCSF (CSF2); IL6 (gp130) family, IL6, LIF; IL12 family, IL12p40, IL12p70; IL10 family, IL10; IL17 family, IL17A, IL17F; type I interferons (IFN), IFNα2, IFNβ; type II IFN, IFNγ; tumor necrosis factor (TNF) superfamily, TNFα (TNFSF2), TNFβ (TNFSF1), CD40 ligand (CD40L), sFasL (TNFSF6), TRAIL (TNFSF10); CC chemokines, CCL2 (MCP1), CCL3 (MIP1α), CCL4 (MIP1β), CCL5 (RANTES), CCL7 (MCP3), CCL11 (eotaxin); CXC chemokines, CXCL1 (GROα), CXCL5 (ENA78), CXCL8 (IL8), CXCL9 (MIG), CXCL10 (IP10); PDGF family/VEGF subfamily, PDGFBB, VEGFA; cell adhesion molecules, sICAM1 (CD54), VCAM1 (CD106); serine protease inhibitor, serpin E1 (PAI1); adipose-derived hormones, leptin, resistin; and neurotrophic/growth/cellular factors, TGFα, TGFβ, FGFb, βNGF, HGF, SCF, MCSF (CSF1), GCSF (CSF3) (customized Procarta immunoassay, Affymetrix, Santa Clara, CA, USA). This cytokine panel was developed as an assay for investigating acute phase (‘sickness’) responses and neuroimmune dysregulation in neuropsychiatric disorders that are postulated to be triggered by immune/infectious factors. It includes a wide range of cytokines, chemokines and cellular factors that reflect key processes relating to systemic activation of inflammatory/immune signaling pathways involved in autoimmunity and anti-inflammatory responses as well as others implicated in CNS inflammation and neurovascular disruption.
CSF samples were assayed in duplicate along with serial standards, buffer controls and in-house human control plasma samples.13 Samples from atypical and classical ME/CFS cases were run at the same time in randomized fashion on assay plates. Data from classical ME/CFS cases, with comparison to MS cases and no-disease controls, have previously been reported.5 Mean fluorescence intensities of analyte-specific immunoassay bead sets were detected by flow-based Luminex 3D suspension array system (Luminex, Austin, TX, USA).14 Cytokine concentrations were calculated by xPONENT build 4.0.846.0 (Luminex) and Milliplex Analyst software (v.184.108.40.206; VigeneTech, Boston, MA, USA) using a standard curve derived from the known reference concentrations supplied by the manufacturer. A five-parameter model was used to calculate final concentrations by interpolation. Values were expressed in pg ml−1. Concentrations obtained below the sensitivity limit of detection of the method were recoded to the mid-point between zero and the limit of detection for that analyte for statistical comparisons. Values obtained from the reading of samples that exceeded the upper limit of the sensitivity method were further diluted and re-assayed.
Categorical demographic characteristics were compared by χ2-tests (sex, short vs long duration of illness) and continuous measures were compared by t-tests (age, duration of illness in years). Due to the overall small number of subjects in the A-ME/CFS cancer group, the heterogeneity of the types of cancer, and the highly variable time between CSF collection and development of the various types of neoplasia, these subjects were only included in a limited set of analyses (Supplementary Materials). The legend in Table 1 provides further detail on the composition of individual disorders or exposures within each of the atypical categories: (1) Cancer (n=8); (2) Immune or inflammatory (n=7); (3) Probable infection (n=5); (4) Other (n=7).
For each of the 51-plex cytokine assays, we compared the mean values in CSF cytokine levels between atypical ME/CFS cases (excluding subjects later-developing cancer) and classical ME/CFS cases, as well as between cases with shorter duration of illness (⩽3 years) and cases with longer duration of illness (>3 years), using two-sample t-tests. Each cytokine served as an individual hypothesis in this portion of the analysis, and thus we did not adjust for multiple comparisons. Because distributions deviated from normality, raw cytokine levels were first transformed using Box-Cox transformation defined as:
where for each cytokine variable, optimal λ was searched for to maximize the log-likelihood function.15 After being transformed, all variables failed to reject the null hypothesis using Kolmogorov-Smirnov test at the 0.05 level, confirming at the 95% confidence level that all transformed variables followed normal distributions. Analysis of variance were applied to examine both the main effects of atypical/classical ME/CFS status and duration of illness as well as their interaction effects, adjusting for various confounding variables including sex, age and storage time in years. As a post hoc analysis for the interaction effect between atypical/classical ME/CFS status and duration of illness, we created 4 subgroups within the study population, namely atypical short-duration cases, atypical long-duration cases, classical short-duration cases and classical long-duration cases, and for each cytokine, we compared mean values of its transformed levels between every pairwise combination of these 4 subgroups. For the 6 pairwise comparisons, we controlled the family-wise error rate at the 0.05 level using the Holm-Bonferroni correction procedure16 for multiple comparisons. A logistic regression model was built for prediction of the binary atypical/classical ME/CFS status variable using the data of the 51-plex cytokine assays. To eliminate multicollinearity among these predictor variables, two feature selection methods were used to guide selection of variables for the logistic regression model. Multiple methods were used to enable capture of factors potentially missed by one individual method. Raw cytokine levels were used in these analyses to allow for computation of odds ratios (ORs).
Feature selection methods select subsets of relevant features for use in regression model construction based on the assumption that the data contain many redundant or irrelevant features. We used two of the most widely used feature selection techniques, Lasso17 and Random Forests.18 Lasso (least absolute shrinkage and selection operator) regularizes the least squares by using the constraint that the L1 norm of the parameter vector is no greater than a given value, and increasing the penalty will cause more and more of the parameters to be driven to absolute zero. To avoid over-fitting, we selected the variables with non-zero coefficients when the cross-validation deviance reached the minimum plus one standard error.
The Random Forests method examines a large ensemble of decision trees by first generating a random sample of the original data with replacement (bootstrapping), and then using a number of variables selected at random from all of the variables to determine node splitting. The out-of-bag data is used to obtain a running unbiased estimate of the classification error as trees are added to the forest. Random Forests allows for calculation of measures of importance for each variable. Here we adopted two measures of importance: the mean decrease in accuracy due to the exclusion of the variable and the Gini index.19 The variables that were ranked in the top 5 in both measures were then selected for inclusion in the logistic regression model.
For the final logistic regression model with atypical/classical ME/CFS status as the dependent variable, a cytokine was entered if it was selected by Lasso or Random Forests. The ORs, their 95% confidence intervals (CIs), and P-values of the selected cytokines were calculated accordingly. Furthermore, we included the confounding variables including sex, age, duration of illness and storage time in years into the logistic regression model, and calculated the adjusted ORs together with their 95% CIs and P-values. In order to assess the goodness-of-fit of the final logistic regression models, we calculated area under the receiver operating characteristic curve (AUROC) and Bayesian Information Criterion values. Table 3 presents the ORs of all independent variables, their 95% CIs and P-values, and the goodness-of-fit information for both the unadjusted and adjusted logistic regression models.
The NodeXL platform was used to produce a network diagram of 51-plex assays within each group.20 The platform provides a display of the relationships among the analytes, thereby facilitating discovery of different cytokine–cytokine networks across the different group populations. Bivariate Pearson’s correlations were first conducted between every pairwise combination of cytokine variables using their power-transformed (Box-Cox) values. We then used the Benjamini-Hochberg method to adjust for multiple comparisons with a 0.01 family-wise false discovery rate.21 Significantly correlated cytokine pairs were fed into the algorithm in NodeXL to produce the network diagram. Cytokines are represented by the ‘nodes’ in the diagram, and significantly correlated cytokines are connected by ‘lines’ or edges. Red lines represent negative correlations; gray lines represent positive correlations.
Statistical analyses were run in SPSS version 220.127.116.11, MATLAB version R2013a and R version 3.0.2.
Table 1 shows the demographic features of the overall study group comprising 32 C-ME/CFS subjects and 27A-ME/CFS subjects. A-ME/CFS subjects did not differ in age from the C-ME/CFS subjects (A-ME/CFS: mean±SD, 46.0±16.2 years vs C-ME/CFS: 49.9±11.2 years, P=0.283).
A-ME/CFS cases vs C-ME/CFS cases
Excluding atypical cases with later-developing malignancies, we compared cytokine levels of A-ME/CFS subjects (n=19) with those of C-ME/CFS subjects (n=32) by 2-way analysis of variance (ME/CFS presentation type [atypical, classical] and illness duration [short, long]) adjusting for sex, age and sample storage time and found significant differences between atypical and classical ME/CFS cases in a large proportion of the 51 analytes (Supplementary Table S1). Significant atypicality × illness duration interactions were identified for IL1β (P=0.021); IL6 (P=0.027); IFNβ (P=0.034); TNFα (P=0.034); TNFβ (P=0.048); CCL2 (P=0.045); CSF3 (P=0.024) and βNGF (P=0.008).
Post-hoc t-tests revealed prominent decreases in the levels of many pro- and anti-inflammatory cytokines in A-ME/CFS short-duration cases as compared with C-ME/CFS short-duration cases, including IL1β, IL5, IL7, IL13, IL17A, IFNα2, IFNγ, TNFα, TRAIL (TNFSF10), CCL2, CCL7, CXCL5, CXCL9, CSF3 (GCSF), βNGF, resistin and serpin E1 (PAI1). In contrast, only one analyte was increased in A-ME/CFS short-duration cases relative to C-ME/CFS short-duration cases: FGFb (P=0.005; Table 2; Figure 1).
Profiles of A-ME/CFS short-duration cases also differed from those of C-ME/CFS long-duration cases, with A-ME/CFS short-duration cases having lower levels of IL7 (P<0.0001), IL17 A (P=0.002), CXCL9 (P=0.004) and serpin E1 (PAI1; P=0.004).
When compared with C-ME/CFS short-duration cases, A-ME/CFS long-duration cases had significantly reduced levels of CSF IL5 (P=0.001), IL13 (P=0.0001), IL17 A (P=0.0002) and CXCL9 (MIG; P=0.007). In addition, A-ME/CFS long-duration subjects had lower levels of IL6 (P=0.001) and IL17 A (P=0.0002) than C-ME/CFS long-duration cases. In contrast, levels of SCF in CSF of A-ME/CFS long-duration subjects were higher than in C-ME/CFS subjects irrespective of duration of illness (C-ME/CFS short duration: P=0.001; C-ME/CFS long duration: P=0.002).
We next profiled CSF cytokines in the subset of A-ME/CFS subjects who developed malignancies after ME/CFS diagnosis (Supplementary Figure S1). A-ME/CFS subjects who developed malignancies (n=8) had higher levels of IL5, CSF2 and PDGFBB than other A-ME/CFS subjects (Supplementary Table S2). Routine CSF studies including glucose, protein and white blood cell counts revealed no major differences between A-ME/CFS subjects and C-ME/CFS subjects or the four C-ME/CFS exposure/comorbidity subgroups (Supplementary Table S3).
Logistic regression models
After data reduction through feature selection procedures, variables meeting LASSO and Random Forests criteria (Supplementary Table S4) were included along with clinical covariates (age, sex, duration of illness and number of storage years) to construct the final logistic regression model and calculate the associated ORs, 95% CIs and P-values. Table 3 shows results for A-ME/CFS cases (excluding those with later malignancies) vs C-ME/CFS cases. In A-ME/CFS vs C-ME/CFS cases, lower levels of IL17A (OR, 0.00; 95% CI, 0.00, 0.85; P=0.047) were strongly associated with A-ME/CFS caseness as were lower levels of CXCL9 (MIG) (OR, 0.48; 95% CI, 0.25, 0.94; P=0.032).
Network diagrams revealed unusual interrelationships among CSF cytokines in the A-ME/CFS group as compared to subjects with C-ME/CFS (Figure 2). C-ME/CFS subjects had inverse relationships between IL1ra and CSF2, and IL5 and IL17F, without correlation with IL1α or IL1β. In contrast, in A-ME/CFS subjects, IL1ra had only limited positive correlations, with IL4 and IL12p70. In addition, IL17A, which was an important predictor in our feature selection-driven logistic regression model, was richly interconnected with other cytokines in the C-ME/CFS CSF immune network, whereas in the A-ME/CFS group, IL17A was only correlated with TNFβ and sFasL.
Building on earlier work wherein we demonstrated distinct CSF immune signatures in subjects with a classical presentation of ME/CFS versus subjects with multiple sclerosis and no-disease controls,5 we compared CSF cytokine levels from the classical ME/CFS group with those from a group of ME/CFS cases who had atypical features at onset of illness or unusual comorbidities at the time of ME/CFS diagnosis. We found discrete differences in immune signatures of the CNS in ME/CFS subjects with atypical presentations that included sparse inter-cytokine networks and lower levels of two inflammatory mediators, the Th17 cytokine, IL17A, and the IFNγ- and TLR4-induced chemokine, CXCL9. Whereas network analyses showed that levels of IL1ra were inversely associated with CSF2, IL5 and IL17F in the classical ME/CFS group, there were no inverse associations among cytokines in the atypical group. These findings suggest potential differences in regulatory networks and less robust CNS immune activation in A-ME/CFS.
The strengths of this study lie in the quality of patient characterization; the large number of subjects with banked CSF samples, longitudinal surveillance for development of comorbidities and the use of a broad-based, sensitive immunoassay that captures components of the immune response relevant to neuroimmune signaling. Potential limitations, such as long storage times, were mitigated by minimization of freeze–thaw cycles and adjustments for length of storage time in the analysis. We excluded subjects in the cancer group from the main analysis due to concern that their physiology may have differed from other A-ME/CFS subjects and C-ME/CFS subjects prior to cancer diagnosis. The observation that our cohort included subjects with an A-ME/CFS profile who subsequently received a cancer diagnosis suggests that finding this profile should prompt a search for cancer, just as it does in paraneoplastic syndromes. Although few differences were apparent in cytokine levels across the different subsets within the A-ME/CFS subgroup, the atypical group as a whole had markedly lower levels of several inflammatory cytokines as compared with C-ME/CFS patients. Although some differences were noted in CSF cytokines based on duration of illness—a factor we previously found to profoundly affect plasma cytokine levels in ME/CFS in prior work12—adjustment for illness in our final logistic regression models did not eliminate findings of inhibited inflammatory cytokines in A-ME/CFS.
The importance of lower levels of IL17A and CXCL9 in the CNS in A-ME/CFS is unclear. We speculate that subjects with unusual exposures or comorbidities may have less activation of neuroimmune signaling pathways. In MS, CSF IL-17A levels are associated with disruption of the blood–brain barrier and expansion of neutrophils in CSF and directly correlated with CSF glutamate levels; IL-17A levels fall with disease duration, suggesting that glutamate toxicity may be more important in MS onset than in later stages.22 IL-17A levels tended to be lower in C-ME/CFS subjects with longer duration of illness; however, levels did not differ for atypical subjects based on disease duration. This may imply an alternate, non-Th17-dependent mechanism in atypical subjects, or a more rapid progression of neurodegeneration than in classical subjects. Recent evidence also suggests that IL-17A has minimal capacity to activate microglia.23 CXCL9 is also reported to be increased in CSF in relapsing MS, and decreases in conjunction with response to certain treatments, such as natalizumab.24
The deficits identified here in CNS interleukin 1 signaling among subjects with atypical presentations of ME/CFS, along with our finding of strong associations of very low levels of two inflammatory mediators with the atypical phenotype, suggest the potential value of vigorous pursuit of alternate, nonimmune mechanisms of pathogenesis in more complex, atypical patients with ME/CFS. Careful attention to exposure histories preceding onset of illness and longitudinal surveillance for the development of unusual medical comorbidities may help to identify novel pathways underlying dysfunction in this highly debilitated patient population.
Jason LA, Zinn ML, Zinn MA . Myalgic encephalomyelitis: symptoms and biomarkers. Curr Neuropharmacol 2015; 13: 701–734.
Nakatomi Y, Mizuno K, Ishii A, Wada Y, Tanaka M, Tazawa S et al. Neuroinflammation in patients with chronic fatigue syndrome/myalgic encephalomyelitis: An (1)(1)C-(R)-PK11195 PET Study. J Nucl Med 2014; 55: 945–950.
Schutzer SE, Angel TE, Liu T, Schepmoes AA, Clauss TR, Adkins JN et al. Distinct cerebrospinal fluid proteomes differentiate post-treatment lyme disease from chronic fatigue syndrome. PLoS ONE 2011; 6: e17287.
Baraniuk JN, Casado B, Maibach H, Clauw DJ, Pannell LK, Hess SS . A chronic fatigue syndrome - related proteome in human cerebrospinal fluid. BMC Neurol 2005; 5: 22.
Hornig M, Gottschalk G, Peterson DL, Knox KK, Schultz AF, Eddy ML et al. Cytokine network analysis of cerebrospinal fluid in myalgic encephalomyelitis/chronic fatigue syndrome. Mol Psychiatry 2016; 21: 261–269.
Chang CM, Warren JL, Engels EA . Chronic fatigue syndrome and subsequent risk of cancer among elderly US adults. Cancer 2012; 118: 5929–5936.
Calabrese LH, Davis ME, Wilke WS . Chronic fatigue syndrome and a disorder resembling Sjogren's syndrome: preliminary report. Clin Infect Dis 1994; 18: S28–S31.
Gaber TA, Oo WW, Ringrose H . Multiple sclerosis/chronic fatigue syndrome overlap: when two common disorders collide. NeuroRehabilitation 2014; 35: 529–534.
Daugherty SA, Henry BE, Peterson DL, Swarts RL, Bastien S, Thomas RS . Chronic fatigue syndrome in northern Nevada. Rev Infect Dis 1991; 13: S39–S44.
Fukuda K, Straus SE, Hickie I, Sharpe MC, Dobbins JG, Komaroff A . The chronic fatigue syndrome: a comprehensive approach to its definition and study. International Chronic Fatigue Syndrome Study Group. Ann Intern Med 1994; 121: 953–959.
Carruthers BM, Jain AK, DeMeirleir KL, Peterson DL, Klimas NG, Lerner AM et al. Myalgic Encephalomyelitis/chronic fatigue syndrome: clinical working case definition, diagnostic and treatments protocols. J Chronic Fatigue Syndr 2003; 11: 7–115.
Hornig M, Montoya JG, Klimas NG, Levine S, Felsenstein D, Bateman L et al. Distinct plasma immune signatures in ME/CFS are present early in the course of illness. Sci Adv 2015; 1: e1400121.
Martins TB . Development of internal controls for the Luminex instrument as part of a multiplex seven-analyte viral respiratory antibody profile. Clin Diagn Lab Immunol 2002; 9: 41–45.
Vignali DA . Multiplexed particle-based flow cytometric assays. J Immunol Methods 2000; 243: 243–255.
Box GEP, Cox DR . An analysis of transformations. J R Stat Soc Series B 1964; 26: 211–252.
Holm S . A simple sequentially rejective multiple test procedure. Scand J Stat 1979; 6: 65–70.
Tibshirani R . Regression shrinkage and selection via the Lasso. J R Stat Soc Series B 1996; 58: 267–288.
Breiman L . Random forests. Mach Learn 2001; 45: 5–32.
Strobl C, Boulesteix AL, Zeileis A, Hothorn T . Bias in random forest variable importance measures: illustrations, sources and a solution. BMC Bioinformatics 2007; 8: 25.
NodeXL: A Free and Open Network Overview, Discovery and Exploration Add-in for Excel 2007/2010. Available at http://nodexl.codeplex.com/ (accessed 2010).
Benjamini Y, Hochberg Y . Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc B 1995; 57: 289–300.
Kostic M, Dzopalic T, Zivanovic S, Zivkovic N, Cvetanovic A, Stojanovic I et al. IL-17 and glutamate excitotoxicity in the pathogenesis of multiple sclerosis. Scand J Immunol 2014; 79: 181–186.
Prajeeth CK, Lohr K, Floess S, Zimmermann J, Ulrich R, Gudi V et al. Effector molecules released by Th1 but not Th17 cells drive an M1 response in microglia. Brain Behav Immun 2014; 37: 248–259.
Mellergard J, Edstrom M, Vrethem M, Ernerudh J, Dahle C . Natalizumab treatment in multiple sclerosis: marked decline of chemokines and cytokines in cerebrospinal fluid. Mult Scler 2010; 16: 208–217.
We are grateful for the support of the Chronic Fatigue Initiative/Hutchins Family Foundation and the Edward P Evans Foundation (WIL and MH). We appreciate the technical support of Wai Wong, Noel Pura and Shobun Baile.
The authors declare no conflict of interest.
Supplementary Information accompanies the paper on the Translational Psychiatry website
Rights and permissions
This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
About this article
Cite this article
Hornig, M., Gottschalk, C., Eddy, M. et al. Immune network analysis of cerebrospinal fluid in myalgic encephalomyelitis/chronic fatigue syndrome with atypical and classical presentations. Transl Psychiatry 7, e1080 (2017). https://doi.org/10.1038/tp.2017.44
This article is cited by
Potential molecular mechanisms of chronic fatigue in long haul COVID and other viral diseases
Infectious Agents and Cancer (2023)
Polyphenols as possible alternative agents in chronic fatigue: a review
Phytochemistry Reviews (2022)
mapMECFS: a portal to enhance data discovery across biological disciplines and collaborative sites
Journal of Translational Medicine (2021)
Cytokine profiling of extracellular vesicles isolated from plasma in myalgic encephalomyelitis/chronic fatigue syndrome: a pilot study
Journal of Translational Medicine (2020)
Evidence of widespread metabolite abnormalities in Myalgic encephalomyelitis/chronic fatigue syndrome: assessment with whole-brain magnetic resonance spectroscopy
Brain Imaging and Behavior (2020)