51. Inflammatory Cell Infiltrates in Vessels With Different Susceptibility to Atherosclerosis in Rheumatic and Non-Rheumatic Patients A Controlled Study of Biopsy Specimens Obtained at Coronary Artery Surgery
- Author
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Geir Aamodt, Matthew H. Liang, Øystein Førre, Ingjerd Lien Kvelstad, Richard A. Prayson, Sven M. Almdahl, Hans C. Nossent, Ivana Hollan, Knut Mikkelsen, and Kjell Saatvedt
- Subjects
Pathology ,medicine.medical_specialty ,Aorta ,medicine.diagnostic_test ,business.industry ,Inflammation ,General Medicine ,Odds ratio ,Peripheral blood mononuclear cell ,medicine.anatomical_structure ,medicine.artery ,Internal medicine ,Adventitia ,Biopsy ,cardiovascular system ,medicine ,Cardiology ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business ,Vein ,Artery - Abstract
Background The main aim of the present study was to compare the occurrence of inflammatory cell infiltrates in the aorta, a vessel with a high occurrence of atherosclerosis, with that in the saphenous vein (SV) and internal mammary artery (IMA), which are protected from atherosclerosis. Methods and Results Samples from the aorta, SV, and IMA of 65 patients with inflammatory rheumatic diseases (IRD) and from 51 control patients undergoing coronary artery bypass graft surgery were examined for the presence and location of inflammatory cell infiltrates and atherosclerotic lesions. Mononuclear cell infiltrates (MCIs) in the media or adventitia were observed in 2% IMAs, 17% SVs, and 35% aortic specimens (SV vs IMA: p=0.006; SV vs aorta: p=0.001). Atherosclerotic lesions were present in none IMA, 3% SVs and 18% aortic specimens. IRD and smoking increased the odds of MCI in the aorta (odds ratio (OR)=3.6, 95% confidence interval (CI): 1.6-8.5 and OR=4.0, 95% CI: 1.5-10.9), but not in the SV or IMA. Conclusions The occurrence of medial and adventitial MCI in the aorta, SV, and IMA paralleled each vessel's susceptibility to atherosclerosis: it was highest in the aorta and lowest in IMA. Local vascular inflammation may be involved in atherogenesis, and influence the patency of vascular grafts. (Circ J 2008; 72: 1986 - 1992)
- Published
- 2008