Effect of aspirin plus clopidogrel on inflammatory markers in patients with non-ST-segment elevation acute coronary

Yu-guo Chen1, Feng Xu, Yun Zhang

  • 1Department of Emergency and Center of Chest Pain, Qilu Hospital of Shandong University, Ji'nan 250012, China.

Chinese Medical Journal
|February 4, 2006
PubMed

Insights

Aspirin plus clopidogrel significantly reduced inflammatory markers, high sensitivity C-reactive protein (hs-CRP) and tumor necrosis factor-alpha (TNF-alpha), in non-ST-segment elevation acute coronary syndrome (NSTEACS) patients more than aspirin alone. This combination therapy may offer greater clinical benefits.

Area of Science:

  • Cardiology
  • Pharmacology
  • Immunology

Background:

  • Aspirin is known to inhibit inflammation and platelet aggregation.
  • The combined anti-inflammatory and antiplatelet effects of aspirin plus clopidogrel are not well understood.
  • Investigating the impact of dual antiplatelet therapy on inflammation in acute coronary syndromes is crucial.

Purpose of the Study:

  • To evaluate the efficacy of aspirin plus clopidogrel in suppressing inflammation in patients with non-ST-segment elevation acute coronary syndrome (NSTEACS).
  • To compare the anti-inflammatory effects of aspirin alone versus aspirin plus clopidogrel in NSTEACS patients.

Main Methods:

  • 115 NSTEACS patients were randomized into two groups: aspirin alone (n=58) or aspirin plus clopidogrel (n=57).
  • Dosing regimens included a loading dose followed by daily maintenance doses of aspirin and/or clopidogrel.
  • Serum levels of high sensitivity C-reactive protein (hs-CRP) and tumor necrosis factor-alpha (TNF-alpha) were measured at baseline, 7 days, and 30 days. A control group of 30 healthy volunteers was included.

Main Results:

  • Both treatment groups showed significant reductions in hs-CRP and TNF-alpha levels from baseline at 7 and 30 days (P <0.01).
  • Patients receiving aspirin plus clopidogrel demonstrated significantly lower levels of hs-CRP and TNF-alpha compared to those on aspirin alone at 30 days (P <0.05).
  • Baseline inflammatory markers were significantly higher in NSTEACS patients compared to healthy controls.

Conclusions:

  • Aspirin plus clopidogrel significantly reduced serum hs-CRP and TNF-alpha levels more effectively than aspirin monotherapy in NSTEACS patients.
  • The findings suggest that the combination of aspirin and clopidogrel possesses potent anti-inflammatory properties.
  • Long-term dual antiplatelet therapy may confer greater clinical advantages over aspirin alone in managing NSTEACS.
Abstract

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