Background-Venous coronary artery bypass grafts (CABGs) are prone to accelerated atherosclerosis. In atherosclerotic diseases, serum C-reactive protein (CRP) levels have become an important diagnostic and prognostic marker. The origin of CRP in this setting remains to be elucidated. Methods and Results-Monoclonal anti-CRP identified CRP expression in medial and intimal ␣-actin-positive smooth muscle cells (SMCs) of diseased CABGs with type V and VI lesions and also of native saphenous veins of atherosclerotic individuals. In addition, patent coronary arteries with type IV and V but not with type I through III lesions exhibited intense SMC staining for CRP. Calcified desobliterates of occluded coronary arteries with end-stage disease did not show SMC staining for CRP and were consistently negative for CRP mRNA, as detected by means of real-time polymerase chain reaction. However, CRP mRNA was expressed in 11 of 15 diseased CABGs and also in 10 of 15 native veins. By contrast, only 3 of 18 internal mammary and 4 of 12 radial arteries with virtually no atherosclerosis were positive for CRP mRNA. Conclusions-CRP is produced by SMCs of atherosclerotic lesions with active disease but not in end-stage plaques. The role of CRP constitutively expressed by normal vascular tissue in vein graft disease has yet to be elucidated. Key Words: atherosclerosis Ⅲ inflammation Ⅲ restenosis I n recent years, serum C-reactive protein (CRP) has become a powerful marker of future cardiovascular events. 1,2 CRP is linked to vascular inflammation because it attracts monocytes and mediates LDL uptake by macrophages. 3,4 Furthermore, CRP induces adhesion molecule expression but attenuates NO production of human endothelial cells. 5,6 Histological investigations have described an association between intimal CRP deposition and the development of atherosclerotic plaques. 7,8 None of these studies supposed that CRP immunoreactivity resulted from local expression of CRP. We speculated that elevated serum CRP levels do not reflect continuous hepatic CRP synthesis but rather represent local production. This hypothesis has recently been corroborated by findings of detectable CRP mRNA and protein in postmortem cases of aortosclerotic plaques. 9 Yasojima et al 9 described smooth muscle cells (SMCs) and macrophages as sites of CRP production. These data-together with our observation of CRP production by renal epithelial cells 10 -argue against the liver as the only site of CRP formation. The aim of the present study was to examine local generation of CRP in human atherosclerotic lesions. Because we have been interested for years in the increased reocclusion rate of coronary artery venous bypass grafts (CABGs), 11 we investigated samples of diseased CABGs for CRP mRNA and protein expression. The results were compared with patent atherosclerotic coronary arteries and calcified coronary desobliterates as well as with native saphenous veins, internal mammary arteries (IMAs), and radial arteries (RAs). Methods Sample CollectionFor CRP mRNA detection, 10 d...
The Perceval sutureless valve resulted in low 1-year event rates in intermediate-risk patients undergoing AVR. New York Heart Association class improved in more than three-quarters of patients and remained stable. These data support the safety and efficacy to 1 year of the Perceval sutureless valve in this intermediate-risk population.
on behalf of the German-Dutch Ross Registry Background-Autograft reinforcement interventions (R) during the Ross procedure are intended to preserve autograft function and improve durability. The aim of this study is to evaluate this hypothesis. Methods and Results-1335 adult patients (mean age:43.5Ϯ12.0 years) underwent a Ross procedure (subcoronary, SC, nϭ637; root replacement, Root, nϭ698). 592 patients received R of the annulus, sinotubular junction, or both. Regular clinical and echocardiographic follow-up was performed (mean:6.09Ϯ3.97, range:0.01 to 19.2 years). Longitudinal assessment of autograft function with time was performed using multilevel modeling techniques. The Root without R (RootϪR) group was associated with a 6ϫ increased reoperation rate compared to Root with R (RootϩR), SC with R (SCϩR), and without R (SC-R; 12.9% versus 2.3% versus 2.5%.versus 2.6%, respectively; PϽ0.001). SC and Root groups had similar rate of aortic regurgitation (AR) development over time. RootϩR patients had no progression of AR, whereas RootϪR had 6 times higher AR development compared to RootϩR. In SC, R had no remarkable effect on the annual AR progression. The SC technique was associated with lower rates of autograft dilatation at all levels of the aortic root compared to the Root techniques. R did not influence autograft dilatation rates in the Root group. Conclusions-For the time period of the study surgical autograft stabilization techniques preserve autograft function and result in significantly lower reoperation rates. The nonreinforced Root was associated with significant adverse outcome. Therefore, surgical stabilization of the autograft is advisable to preserve long-term autograft function, especially in the Root Ross procedure. (Circulation. 2009;120[suppl 1]:S146-S154.)
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