Studie

12‑weeks fisetin supplementation and interval resistance with aerobic training: changes in Maresin‑1 and inflammatory markers in men with obesity: a randomiserad kontrollerad studie.

Alipour M, Saeidi A, Hejazi K, Laher I, Zouhal H

FOUR-ARM PARALLEL-GROUP RANDOMISED CONTROLLED TRIAL Tier 3 2026

In 44 obese men, 200 mg/day fisetin plus 12 weeks of training produced the largest reductions in glucose, insulin and HOMA-IR.

StudiedesignFOUR-ARM PARALLEL-GROUP RANDOMISED CONTROLLED TRIAL
TierNivå 3, Blandad humana bevis, mekanism trovärdig
År2026
TidskriftTidskrift of the International Society of Sports Nutrition
Publicerad2026 dec 31
Tillagd i NO1GEVITYjun 22, 2026

Fyrtiofyra vuxna män med fetma fullföljde en 12 veckor lång randomiserad studie med fyra grupper: placebo, enbart fisetin, kombinerad intervallbaserad styrke- och konditionsträning med placebo eller samma träning med fisetin. Fisetin gavs i dosen 200 mg/dag. Training combined eight resistance exercises at 60% of one-repetition maximum with progressive aerobic work at 50% to 70% of maximum heart rate. The study measured Maresin-1, IL-6, TNF-α, fasting blood glucose, insulin, and HOMA-IR before and after treatment. Group-by-time interactions were reported for every listed marker: Maresin-1 p=0.034, and IL-6, TNF-α, glucose, insulin, and HOMA-IR each p=0.001. Maresin-1 rose in both training groups. IL-6 fell with training, training plus fisetin, and fisetin alone; TNF-α fell in all active groups. Glucose, insulin, and HOMA-IR declined in all active arms, with the largest reductions in the combined training-fisetin group. The abstract does not give the size of those reductions or direct pairwise comparisons. This is a short metabolic-biomarker study in obese men, not evidence of disease prevention or longer life.

Twelve weeks of concurrent interval resistance-aerobic training, especially when combined with fisetin, improved inflammatory and metabolic markers in obese men.
Kritikernoter

N was 44, all participants were obese adult men, and the follow-up was only 12 weeks. The endpoints were circulating markers and insulin-resistance estimates rather than clinical outcomes, and the design cannot cleanly separate fisetin from training effects.

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