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.

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