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J Clin Pathol 2006;59:196-201 doi:10.1136/jcp.2005.027235
  • Original article

Colocalisation of intraplaque C reactive protein, complement, oxidised low density lipoprotein, and macrophages in stable and unstable angina and acute myocardial infarction

  1. M Meuwissen1,
  2. A C van der Wal2,
  3. H W M Niessen3,
  4. K T Koch1,
  5. R J de Winter1,
  6. C M van der Loos2,
  7. S Z H Rittersma1,
  8. S A J Chamuleau1,
  9. J G P Tijssen1,
  10. A E Becker2,
  11. J J Piek1
  1. 1Department of Cardiology, Academic Medical Centre, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands
  2. 2Department of Cardiovascular Pathology, Academic Medical Centre, University of Amsterdam
  3. 3Department of Pathology, Vrije Universiteit Medical Centre, Amsterdam, 1081 HV, The Netherlands
  1. Correspondence to:
 Dr J J Piek
 Academic Medical Centre, Department of Cardiology, University of Amsterdam, Room B2-250, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands; m.meuwissen{at}amc.uva.nl
  • Accepted 18 April 2005

Abstract

Background: C reactive protein (CRP), an important serum marker of atherosclerotic vascular disease, has recently been reported to be active inside human atherosclerotic plaques.

Aims: To investigate the simultaneous presence of macrophages, CRP, membrane attack complex C5b–9 (MAC), and oxidised low density lipoprotein (oxLDL) in atherectomy specimens from patients with different coronary syndromes.

Methods: In total, 54 patients with stable angina (SA; n = 21), unstable angina (UA; n = 15), and myocardial infarction (MI; n = 18) underwent directional coronary atherectomy for coronary lesions. Cryostat sections of atherosclerotic plaques were immunohistochemically stained with monoclonal antibodies: anti-CD68 (macrophages), anti-5G4 (CRP), aE11 (MAC), and 12E7 (oxLDL). Immunopositive areas were evaluated in relation to fibrous and neointima tissues, atheroma, and media. Quantitative analysis was performed using image cytometry with systematic random sampling (percentage immunopositive/total tissue area).

Results: Macrophages, CRP, MAC, and oxLDL were simultaneously present in a higher proportion of fibrous tissue and atheroma of atherectomy specimens from patients with UA and MI compared with SA (p<0.05). Quantitative analysis showed significantly higher mean percentages of macrophages in plaques from patients with MI (44%) than UA (30%; p<0.01) and SA (20%; p<0.001). Significantly higher mean percentages of CRP were also seen in MI (25%) and UA (25%) compared with SA (12%; p<0.05).

Conclusions: The presence of CRP, complement, and oxLDL in a high proportion of plaque tissue from patients with unstable coronary artery disease implies that these surrogate markers have important proinflammatory effects inside atherosclerotic plaques. This may increase vulnerability to plaque rupture and thrombosis, with subsequent clinical sequelae.

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