# Targeting low-grade inflammation in multiple sclerosis through the Wim Hof method or lifestyle intervention: a pilot comparative study

**Authors:** Darina Slezáková, Louise Mária Sabolová, Peter Marček, Pavol Kadlic, Ivan Hric, Libuša Nechalová, Viktor Bielik, Michal Páleník, Michal Pastorek, Peter Olej, Norbert Žilka, Jozef Hanes, František Jurčaga, Michal Minár

PMC · DOI: 10.1007/s10072-026-08895-8 · Neurological Sciences · 2026-02-26

## TL;DR

This study compares the Wim Hof Method and lifestyle changes in reducing inflammation in multiple sclerosis patients, finding both approaches effective in lowering certain inflammatory markers.

## Contribution

The study is the first to compare the Wim Hof Method and lifestyle interventions in MS, showing both reduce Th17-related inflammation.

## Key findings

- Both interventions significantly reduced IL-17A and IL-18, indicating anti-inflammatory effects.
- WHM decreased IFN-γ, while LIFE lowered IL-8, showing distinct cytokine modulation.
- No significant changes were observed in neurodegeneration biomarkers like NfL or GFAP.

## Abstract

Disease-modifying therapies (DMTs) in multiple sclerosis (MS) effectively reduce relapse activity but have limited impact on chronic progression and neurodegeneration. Non-pharmacological interventions such as structured exercise or the Wim Hof Method (WHM- which includes breathing exercises, cold exposure, and meditation), may offer complementary immunomodulatory and neuroprotective benefits.

To compare the effects of WHM and a lifestyle intervention (LIFE; structured physical activity and nutritional counseling) on systemic inflammation and neurodegeneration biomarkers in patients with MS.

In this randomized, prospective pilot trial, 60 MS patients (2017 McDonald criteria, EDSS 1.0–5.5) were allocated to WHM, LIFE, or control (CTRL) for 12 weeks. Serum cytokines (IFN-γ, IL-1β, IL-6, IL-8, IL-10, IL-12p70, IL-17A, IL-18), neurofilament light chain (NfL), and glial fibrillary acidic protein (GFAP) were assessed at baseline and after 12 weeks. Mixed repeated-measures ANOVA with Bonferroni correction was applied.

Complete datasets were obtained and analyzed for 43 participants (12 WHM, 17 LIFE, 14 CTRL; power= 0.81). Both interventions significantly reduced IL-17A and IL-18 (p<0.001), indicating attenuation of Th17-related inflammation. WHM further decreased IFN-γ, while LIFE lowered IL-8. No significant changes were observed for IL-1β, IL-6, IL-12p70, NfL, or GFAP. Both interventions were well tolerated, with no treatment-related adverse events.

Both WHM and lifestyle modification demonstrated comparable short-term anti-inflammatory effects in MS, supporting their safety and feasibility as adjunctive strategies to DMT. Although neurodegeneration biomarkers remained unchanged, the consistent reduction of IL-17A and IL-18 highlights their potential to modulate smoldering inflammation. Larger, longer-term trials are warranted to determine their sustained effects on disease progression.

## Linked entities

- **Proteins:** IFNG (interferon gamma), IL1B (interleukin 1 beta), IL6 (interleukin 6), CXCL8 (C-X-C motif chemokine ligand 8), IL10 (interleukin 10), IL17A (interleukin 17A), IL18 (interleukin 18), NEFL (neurofilament light chain), GFAP (glial fibrillary acidic protein)
- **Diseases:** multiple sclerosis (MONDO:0005301), MS (MONDO:0006861)

## Full-text entities

- **Genes:** CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, NEFL (neurofilament light chain) [NCBI Gene 4747] {aka CMT1F, CMT2E, CMTDIG, NF-L, NF68, NFL}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}
- **Diseases:** autoimmune and inflammatory diseases (MESH:D001327), fatigue (MESH:D005221), axonal (MESH:D012183), neurodegeneration (MESH:D019636), injury (MESH:D014947), Inflammation (MESH:D007249), axial spondylarthritis (MESH:D025241), neuroinflammation (MESH:D000090862), MS (MESH:D009103), chronic (MESH:D002908), tissue injury (MESH:D017695), hyperventilation (MESH:D006985), RRMS (MESH:D020529), weight loss (MESH:D015431)
- **Chemicals:** water (MESH:D014867), fat (MESH:D005223), cortisol (MESH:D006854), epinephrine (MESH:D004837), DMT (-), carbohydrates (MESH:D002241)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12935732/full.md

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Source: https://tomesphere.com/paper/PMC12935732