Stachteas · Experimental physiology 2025 · systematic review and meta-analysis · n=103 studies (1418 participants)

Optimal timing to assess exercise-induced oxidative stress: A systematic review and meta-analysis.

Cited 2 times in the scientific literature.

Level 1 - systematic review of randomized trials

Systematic review and meta-analysis of randomized and non-randomized studies

PubMed 41318971 · doi:10.1113/EP092963 · record verified 2026-08-29

What was done

Systematic review and meta-analysis (PROSPERO CRD42024508049) of 103 studies (n = 1418) to determine optimal post-exercise assessment timing for three redox biomarkers: glutathione, F2-isoprostanes, and protein carbonyls. Standardised mean differences (SMD) were calculated using random-effects models with 95% confidence and prediction intervals. Study quality was evaluated using RoB2, ROBINS-I, Egger's test, funnel plots, and GRADE certainty rating.

What was found

Glutathione decreased immediately (Hedges' g = -0.70; 95% CI: -0.96, -0.44; P < 0.001), at 30 min to 2 h (g = -0.81; 95% CI: -1.19, -0.43; P < 0.001), and at 48 h (g = -0.98; 95% CI: -1.50, -0.46; P < 0.01). F2-isoprostanes increased immediately (g = 1.01; 95% CI: 0.70, 1.33; P < 0.001) and at 30 min to 2 h (g = 0.46; 95% CI: 0.23, 0.69; P < 0.001). Protein carbonyls were elevated at all time points, especially at 48 h (g = 1.17; 95% CI: 0.73, 1.60; P < 0.001) and peaked at 72 h (g = 1.33; 95% CI: 0.52, 2.14; P = 0.0048). Non-muscle-damaging exercise elicited responses within 2 h, whereas muscle-damaging exercise produced delayed peaks at 48 to 72 h.

Why it matters

This review establishes empirical time windows for redox biomarker sampling after exercise, showing that timing must be tailored specifically to whether the exercise protocol induces muscle damage.

Limits

Egger's test indicated significant publication bias for F2-isoprostanes (P = 0.017) and protein carbonyls (P = 0.031). Risk of bias was moderate in randomized controlled trials and serious in non-randomized studies. The analysis was limited to only three specific redox biomarkers.

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