Effects of aerobic, resistance, and combined exercise on inflammatory markers in patients with metabolic syndrome: A
Shih-Ming Chuang1,2,3,4, Kuo-Liong Chien1
1Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Background:
The comparative effectiveness of different exercise modalities on systemic inflammation in patients with metabolic syndrome (MetS) remains poorly defined.
Objective:
To systematically evaluate and rank the effects of aerobic exercise (AE), resistance training (RT), and combined training (COM) on inflammatory markers (C-reactive protein (CRP), tumor necrosis factor-alpha (TNF-α), and interleukin-6 (IL-6) in MetS.
Methods:
A network meta-analysis of 28 randomized controlled trials (RCTs) was conducted. Data were synthesized using frequentist random-effects models. Treatment efficacy was ranked using the Surface Under the Cumulative Ranking Curve (SUCRA).
Results:
Compared to the control group, all exercise modalities were associated with reductions in TNF-α levels, though the strength of this evidence is limited by high heterogeneity and potential publication bias. Among the interventions, COM showed the greatest effect (SMD = -1.74; 95% CI: -3.06 to -0.43; SUCRA = 75.7%), followed by RT and AE. For CRP, significant reductions were observed in COM (SMD = -0.79; 95% CI: -1.36 to -0.21; SUCRA = 86.8%) and AE (SMD = -0.64; 95% CI: -0.95 to -0.32), while RT demonstrated a smaller effect. No modalities reached statistical significance for IL-6, although RT ranked highest in SUCRA (75.8%). Notably, CRP findings were robust with moderate certainty and no publication bias (p = 0.86), whereas TNF-α and IL-6 exhibited significant publication bias (p < 0.05) and extreme heterogeneity (I2 > 90%).
Conclusion:
Exercise, particularly COM, appears to be a promising intervention for reducing CRP and TNF-α in MetS. While the findings for CRP are robust, results for TNF-α should be interpreted with caution due to observed heterogeneity and potential publication bias.
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