# Impact of creatine supplementation on inflammation: evidence from a systematic review and meta-analysis of randomized double-blind placebo trials

**Authors:** Kell Mazzini Ribeiro de Camargo, Alejandro Bruna-Mejías, Juan José Valenzuela-Fuenzalida, Luana A. Gonzaga, Sandra Maria Barbalho, Alexandre L. Barroca, Andrey A. Porto, Rodrigo D. Raimundo, Luiz Carlos de Abreu, Vitor E. Valenti

PMC · DOI: 10.3389/fimmu.2026.1743603 · 2026-02-19

## TL;DR

This study reviews and analyzes the effects of creatine supplementation on inflammation in humans, finding no significant reduction in inflammatory biomarkers.

## Contribution

The study provides a systematic review and meta-analysis of creatine's anti-inflammatory effects using randomized trials.

## Key findings

- Creatine supplementation does not significantly reduce inflammatory biomarkers like CRP and IL-6.
- Results remain inconsistent across populations, with no strong evidence for anti-inflammatory benefits.
- Moderate certainty of evidence was rated for all outcomes, with missing data being a common limitation.

## Abstract

Creatine supplementation is widely recognized for its ergogenic effects on strength and body composition. Recent studies have explored its potential anti-inflammatory properties, particularly in exercise-induced stress and aging-related chronic inflammation. However, results across randomized trials remain inconsistent. This systematic review and meta-analysis aimed to assess the effects of creatine supplementation on inflammatory biomarkers in human populations.

A systematic review and meta-analysis were conducted following PRISMA 2020 guidelines and registered in PROSPERO (CRD420251027784). Eight randomized controlled trials were included, evaluating creatine supplementation (various dosages and durations) versus placebo in healthy individuals, athletes, and clinical populations. The primary outcomes were inflammatory markers, including C-reactive protein (CRP), interleukin-6 (IL-6), IL-1β, TNF-α, and prostaglandin E2. Data extraction and risk of bias assessments were performed by two independent reviewers. The certainty of evidence was rated using the GRADE framework.

Pooled analysis showed no significant acute effects of creatine on CRP (SMD = 0.32; 95% CI: -0.29 to 0.94; p = 0.30; I² = 28%). Chronic effects of creatine on CRP (SMD = -0.11; 95% CI: -0.69 to 0.48; p = 0.73; I² = 0%) and IL-6 (SMD = -0.06; 95% CI: -0.64 to 0.53; p = 0.84; I² = 0%) were also no significant. The certainty of evidence was rated as moderate for all outcomes. Risk of bias varied, with missing outcome data being the most frequent limitation.

Creatine supplementation does not significantly reduce inflammatory biomarkers in humans based on current evidence. Although certain benefits were observed under intense endurance conditions, results remain inconsistent across populations. Future well-powered trials with standardized protocols are needed to clarify creatine’s role in modulating inflammation.

https://www.crd.york.ac.uk/prospero/, identifier CRD420251027784.

## Linked entities

- **Proteins:** IL6 (interleukin 6), IL6 (interleukin 6), IL1B (interleukin 1 beta), TNF (tumor necrosis factor)
- **Chemicals:** creatine (PubChem CID 586)

## Full-text entities

- **Genes:** SLC2A4 (solute carrier family 2 member 4) [NCBI Gene 6517] {aka GLUT4}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNFRSF8 (TNF receptor superfamily member 8) [NCBI Gene 943] {aka CD30, D1S166E, Ki-1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, IFNA1 (interferon alpha 1) [NCBI Gene 3439] {aka IFL, IFN, IFN-ALPHA, IFN-alphaD, IFNA13, IFNA@}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, ADORA2A (adenosine A2a receptor) [NCBI Gene 135] {aka A2aR, ADORA2, RDC8}, 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}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, COMP (cartilage oligomeric matrix protein) [NCBI Gene 1311] {aka CTS2, EDM1, EPD1, MED, PSACH, THBS5}
- **Diseases:** knee osteoarthritis (MESH:D020370), dehydration (MESH:D003681), LDH (MESH:C538133), fires (MESH:D000092422), insulin resistance (MESH:D007333), cardiovascular diseases (MESH:D002318), gastrointestinal discomfort (MESH:D005767), Malnutrition (MESH:D044342), cramping (MESH:D009120), tissue injury (MESH:D017695), chronic (MESH:D002908), necrotic (MESH:D009336), muscle dysfunction (MESH:D009135), DOMS (MESH:D063806), Type 2 Diabetes Mellitus (MESH:D003924), gastrointestinal, musculoskeletal, or inflammatory complications (MESH:D009140), renal dysfunction (MESH:D007674), swelling (MESH:D004487), pain (MESH:D010146), muscle trauma (MESH:D019042), trauma (MESH:D014947), sarcopenia (MESH:D055948), Inflammation (MESH:D007249), muscle damage (MESH:D009133), cardiometabolic disease (MESH:D024821), reduction in muscle mass (MESH:C536030), cartilage degradation (MESH:D002357), OA (MESH:D010003), metabolic disease (MESH:D008659), diarrhea (MESH:D003967), knee pain (MESH:D046788), hypoxic (MESH:D002534), microbial infections (MESH:D015163)
- **Chemicals:** Creatine (MESH:D003401), PCr (MESH:D010725), Homocysteine (MESH:D006710), CreaPure (-), glucose (MESH:D005947), creatinine (MESH:D003404), ATP (MESH:D000255), Maltodextrin (MESH:C008315), cholesterol (MESH:D002784), Blood glucose (MESH:D001786), CLA (MESH:D044243), PGE2 (MESH:D015232), water (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606], Citrus x limon (lemon, species) [taxon 2708]
- **Mutations:** A2A

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12961398/full.md

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Source: https://tomesphere.com/paper/PMC12961398