Korean Circ J.  2001 Oct;31(10):988-995. 10.4070/kcj.2001.31.10.988.

The Relationship of Infection and Inflammation with Coronary Restenosis after Percutaneous Coronary Interventions

Affiliations
  • 1The Heart Center, Chonnam National University Hospital, The Research Institute of Medical Sciences, Kwang Ju, Korea.

Abstract

BACKGROUND AND OBJECTIVES
Possible correlations between the serologic status concerning Cytomegalovirus(CMV), Chlamydia pneumoniae (CP), Helicobacter pylori(HP), their related markers of C-reactive protein(CRP), erythrocyte sedimentation rate(ESR), and the restenosis(RS) in patients underwent percutaneous coronary intervention(PCI) were analyzed. Materials and
METHODS
The 142 patients(58.010.9 year-old, M;F=116:26) with 189 coronary lesions, who underwent follow-up angiography after PCI, were evaluated.
RESULTS
The overall RS rate was 47.1%(89/189), and the RS rate according to clinical diagnosis was 50.6% in acute myocardial infarction(MI), 41.8% in unstable angina(UA), 6.3% in stable angina(SA), and 1.3% in old MI. The values of RS rate in acute MI and UA were higher than those of old MI and SA(p=0.02). Thrombolysis In Myocardial Infarction(TIMI) flow was significantly lower in group with RS than without RS(p=0.039). Seropositivities of CMV, CP, HP were not different between groups with and without RS. Titers of CMV and HP were not different between two groups. Positivity of CRP was 56.3% in group with RS and 30.2% in group without RS(p=0.005). Titers of ESR and CRP were higher in group with RS than without RS(20.322.4 mm/hr, 2.24.5 mg/dL vs. 11.811.6 mm/hr, 0.70.8 mg/dL, p=0.007, p=0.010 respectively).
CONCLUSION
RS rate after PCI is higher in patients with acute coronary syndrome and low TIMI flow. Inflammatory markers, such as CRP and ESR, might be associated with the RS after PCI.

Keyword

Percutaneous coronary intervention; Inflammation

MeSH Terms

Acute Coronary Syndrome
Angiography
Blood Sedimentation
Chlamydophila pneumoniae
Coronary Restenosis*
Diagnosis
Follow-Up Studies
Helicobacter
Humans
Inflammation*
Percutaneous Coronary Intervention*
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