Effect of statins on atherogenic serum amyloid A and α1-antitrypsin low-density lipoprotein complexes

Int J Cardiol. 2016 Dec 15:225:332-336. doi: 10.1016/j.ijcard.2016.09.116. Epub 2016 Oct 3.

Abstract

Purpose: HMG-CoA reductase inhibitors, also termed statins, are used to reduce the risk of coronary artery disease. Two oxidatively modified low-density lipoprotein (LDL) complexes, serum amyloid A-LDL (SAA-LDL) and α1-antitrypsin-LDL (AT-LDL), serve as atherosclerotic, inflammatory, and cardiovascular risk markers. In this study, we examined the effects of hydrophilic rosuvastatin (RSV) and lipophilic pitavastatin (PTV) on these markers in patients with hypercholesterolemia.

Methods: The present study was a sub-analysis of our previous STAT-LVDF study. The subjects were treated with RSV or PTV for 24weeks. Changes in glucose-lipid metabolism, serum levels of SAA-LDL and AT-LDL, and C-reactive protein (CRP) level were assessed.

Results: In total, 53 patients were analyzed in the present study. RSV and PTV significantly decreased SAA-LDL (RSV: p=0.003, PTV: p=0.012) and AT-LDL levels (RSV: p=0.013, PTV: p=0.037). Changes in SAA-LDL level were significantly and positively correlated with those in CRP in both the RSV (r=0.549, p=0.003) and PTV (r=0.576, p=0.004) groups. Moreover, a positive correlation between changes of SAA-LDL levels and those of HbA1c levels was observed in the PTV group (r=0.442, p=0.030) but not in the RSV group (r=-0.100, p=0.611).

Conclusions: Both hydrophilic rosuvastatin and lipophilic pitavastatin reduce serum levels of atherosclerotic and inflammatory markers. These findings also indicate differential effects of RSV and PTV on glucose tolerance.

Keywords: AT-LDL; Dyslipidemia; Pitavastatin; Rosuvastatin; SAA-LDL; Statins.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Atherosclerosis / blood*
  • Atherosclerosis / drug therapy*
  • Biomarkers / blood
  • Dyslipidemias / blood
  • Dyslipidemias / drug therapy
  • Female
  • Follow-Up Studies
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use*
  • Lipoproteins, LDL / antagonists & inhibitors
  • Lipoproteins, LDL / blood*
  • Male
  • Middle Aged
  • Quinolines / pharmacology
  • Quinolines / therapeutic use
  • Rosuvastatin Calcium / pharmacology
  • Rosuvastatin Calcium / therapeutic use
  • Serum Amyloid A Protein / antagonists & inhibitors
  • Serum Amyloid A Protein / metabolism*
  • Treatment Outcome
  • Ventricular Dysfunction, Left / blood
  • Ventricular Dysfunction, Left / drug therapy
  • alpha 1-Antitrypsin / blood*

Substances

  • Biomarkers
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Lipoproteins, LDL
  • Quinolines
  • Serum Amyloid A Protein
  • alpha 1-Antitrypsin
  • Rosuvastatin Calcium
  • pitavastatin