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Published on: July 20, 2022
Increased serum HMGB1 is related to oxidative stress in patients with atrial fibrillation
Yongbo Wu1, Kai Zhang, Lin Zhao
1Department of Cardiology, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Huangshi, China.
Insights
Serum high mobility group box 1 protein (HMGB1) and oxidative stress markers are elevated in atrial fibrillation (AF) patients. HMGB1 levels correlate with oxidative stress, suggesting a potential therapeutic target for AF.
Area of Science:
- Cardiology
- Biochemistry
- Molecular Biology
Background:
- Atrial fibrillation (AF) is a common arrhythmia.
- Oxidative stress plays a role in cardiovascular diseases.
- High mobility group box 1 protein (HMGB1) is implicated in inflammation and cellular stress.
Purpose of the Study:
- To examine the association between serum HMGB1 levels and markers of oxidative stress in patients with AF.
- To determine if HMGB1 is a predictor of AF.
Main Methods:
- Serum HMGB1, malondialdehyde (MDA), and superoxide dismutase (SOD) activity were measured in patients with paroxysmal or persistent AF and in control subjects.
- Statistical analyses were performed to assess correlations and predictive values.
Main Results:
- Patients with AF exhibited significantly higher serum HMGB1 concentrations and MDA activity compared to controls.
- Serum SOD activity was significantly lower in AF patients.
- HMGB1 concentration positively correlated with MDA activity and negatively with SOD activity in AF patients.
- HMGB1, MDA, SOD, and hs-CRP were identified as independent predictors of AF.
Conclusions:
- Elevated serum HMGB1 in AF patients may be linked to increased oxidative stress.
- Targeting oxidative stress could be a potential therapeutic avenue for managing AF.
Objective:
To investigate the relationship between the serum concentration of high mobility group box 1 protein (HMGB1) and oxidative stress in patients with atrial fibrillation (AF).
Methods:
Patients with AF (paroxysmal or persistent) and matched control subjects were recruited. Serum HMGB1 concentration and malondialdehyde (MDA) and superoxide dismutase (SOD) activity were determined.
Results:
Serum hs-CRP and HMGB1 concentrations and MDA activity were significantly higher in patients with persistent AF (n = 33) or paroxysmal AF (n = 53) than in controls (n = 30). Serum SOD activity was significantly lower in both patient groups than in controls. In the patient group, HMGB1 concentration was significantly positively correlated with MDA activity (r = 0.535), and negatively correlated with SOD activity (r = -0.491). MDA, SOD, hs-CRP and HMGB1 were significant independent predictors of AF.
Conclusions:
Increased oxidative stress may contribute to increased HMGB1 concentrations in patients with AF. Inhibition of oxidative stress may provide a potential therapeutic strategy for AF.
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