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Atorvastatin reduces serum HMGB1 levels in patients with hyperlipidemia
Daoqun Jin1, Yongbo Wu, Lin Zhao
1Department of Cardiology, Central Hospital of Huangshi, Huangshi, P.R. China.
Insights
High mobility group box 1 protein (HMGB1) is elevated in hyperlipidemia and linked to inflammation. Atorvastatin treatment significantly reduced HMGB1 and cholesterol levels in hyperlipidemic patients, suggesting a therapeutic benefit.
Area of Science:
- Cardiovascular Medicine
- Biochemistry
- Pharmacology
Background:
- High mobility group box 1 protein (HMGB1) is recognized as a pro-inflammatory cytokine implicated in coronary artery disease.
- Hyperlipidemia is associated with increased inflammatory markers and cardiovascular risk.
Purpose of the Study:
- To investigate the impact of atorvastatin on serum HMGB1 levels in patients diagnosed with hyperlipidemia.
- To assess changes in lipid profiles and high-sensitivity C-reactive protein (hs-CRP) following atorvastatin treatment.
Main Methods:
- A cohort of 72 hyperlipidemic patients and 32 controls were analyzed for serum HMGB1, total cholesterol (TC), triglycerides (TG), HDL-C, LDL-C, and hs-CRP.
- Hyperlipidemic patients received atorvastatin (20 mg/day) for three months, with pre- and post-treatment measurements of serum HMGB1 and other biomarkers.
Main Results:
- Hyperlipidemic patients exhibited significantly higher TC, LDL-C, hs-CRP, and HMGB1 levels compared to controls (P<0.05).
- Atorvastatin treatment for three months led to significant reductions in TC, LDL-C, hs-CRP, and HMGB1 levels in hyperlipidemic patients (P<0.05).
Conclusions:
- Serum HMGB1 levels are elevated in individuals with hyperlipidemia, indicating its potential role in the inflammatory processes of this condition.
- Atorvastatin therapy effectively reduces serum HMGB1 levels alongside improvements in lipid profiles and hs-CRP, highlighting its anti-inflammatory and lipid-lowering effects.
Abstract:
High mobility group box 1 protein (HMGB1) has been identified as a novel pro-inflammatory cytokine in coronary artery disease. This study investigated the effect of atorvastatin on serum HMGB1 levels in patients with hyperlipidemia. In 72 patients with hyperlipidemia, serum total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C) and high-sensitivity C-reactive protein (hs-CRP) were compared with the levels in 32 control patients. In hyperlipidemic patients, serum HMGB1 levels were also determined by ELISA before and after a 3-month treatment of atorvastatin (20 mg/day). TC and LDL-C levels in the hyperlipidemic group (6.37±0.94 and 4.99±0.75 mmol/l, respectively) were significantly higher compared to those in the control group (4.34±0.89 and 2.57±0.82 mmol/l, respectively) (both P<0.05). Hs-CRP and HMGB1 levels in the hyperlipidemic group (3.91±1.06 mg/l and 5.42±1.56 ng/ml, respectively) were also significantly higher compared to those in the control group (1.53±0.45 mg/l and 2.11±0.95 ng/ml, respectively) (both P<0.05). After treatment with atorvasatin for three months, TC and LDL-C levels in the hyperlipidemic group were significantly decreased compared to those prior to treatment (TC, 4.67±0.89 vs. 6.37±0.94 mmol/l and LDL-C, 2.75±0.92 vs. 4.99±0.75 mmol/l, respectively) (both P<0.05). HMGB1 and hs-CRP levels in the hyperlipidemic group (3.07±1.24 ng/ml and 1.87±0.79 mg/l, respectively) were also significantly decreased compared to levels prior to treatment (5.42±1.56 ng/ml and 3.91±1.06 mg/l, respectively) (both P<0.05). Serum HMGB1 levels are increased in patients with hyperlipidemia which could be reduced by atorvastatin.
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