Long-term histological and immunohistochemical findings in human venous aorto-coronary bypass grafts
Clinical Science, ISSN: 0143-5221, Vol: 114, Issue: 3-4, Page: 211-220
2008
- 28Citations
- 27Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations28
- Citation Indexes28
- 28
- CrossRef25
- Captures27
- Readers27
- 27
Article Description
The aim of the present study was to analyse the long-term histology and immunohistochemistry of the plaque composition and cellular infiltration of SVGs (saphenous vein grafts) containing metallic stents. Percutaneous interventions in SVGs have a worse long-term clinical outcome compared with stenting of coronary arteries. Whether the pathological features of old degenerated SVGs condition the efficacy of drug-eluting stents is also unknown. Histology and immunohistochemistry of seven SVGs in the coronary circulation containing 12 metallic stents implanted 5 to 61 months before retrieval were analysed in patients undergoing a second aorto-coronary bypass surgery at a mean time of 11 ± 6 years. The pathology of the old SVGs showed an important thrombotic and necrotic composition of the plaque, with plaque protrusion through the stent wires and a fragile media layer that could easily be damaged by stent placement with subsequent neointimal proliferation; indeed, stents with medial fracture had significantly greater mean neointimal thickness than those without (1.37 ± 0.68 compared with 0.81 ± 0.47 mm; P < 0.02). Neointimal inflammatory cell density correlated with increased neointimal thickness in patent vessels (r = 0.43, P < 0.001). Immunostaining showed the total absence of ERs (oestrogen receptors), a poor cellular proliferative state as indicated by the presence of the Ki-67 marker, and persistent inflammation close to the stent wires as revealed by KP-1 and ACE (angiotensin-converting enzyme) immunostaining in most inflammatory cells in contact with the metal. These pathological findings may contribute to the more severe progression of disease and worse clinical outcome observed after conventional stented angioplasty of SVGs and might also interfere with the efficacy of drug-eluting stents in this specific atherosclerotic milieu. © The Authors.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=38949137886&origin=inward; http://dx.doi.org/10.1042/cs20070243; http://www.ncbi.nlm.nih.gov/pubmed/17848140; https://portlandpress.com/clinsci/article/114/3/211/68506/Long-term-histological-and-immunohistochemical; http://clinsci.org/lookup/doi/10.1042/CS20070243; https://dx.doi.org/10.1042/cs20070243; http://www.clinsci.org/cs/114/cs1140211.htm; http://www.clinsci.org/content/114/3/211; http://www.clinsci.org/content/114/3/211.abstract; http://www.clinsci.org/content/ppclinsci/114/3/211.full.pdf; http://www.clinsci.org/cgi/doi/10.1042/CS20070243; https://portlandpress.com/clinsci/article-abstract/114/3/211/68506/Long-term-histological-and-immunohistochemical?redirectedFrom=fulltext; https://portlandpress.com/clinsci/article-pdf/114/3/211/438803/cs1140211.pdf; http://www.clinsci.org/lookup/doi/10.1042/CS20070243; http://www.clinsci.org/content/114/3/211.full.pdf; http://europepmc.org/abstract/med/17848140; https://portlandpress.com/clinsci/article/114/3/211/68506/Longterm-histological-and-immunohistochemical
Portland Press Ltd.
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