The effect of intracoronary beta-radiation on neointimal formation and vascular remodeling in balloon-injured porcine coronary arteries: Effect of dose rate

Citation
Mn. Ali et al., The effect of intracoronary beta-radiation on neointimal formation and vascular remodeling in balloon-injured porcine coronary arteries: Effect of dose rate, J INTERV CA, 12(4), 1999, pp. 271-282
Citations number
26
Categorie Soggetti
Cardiovascular & Respiratory Systems
Journal title
JOURNAL OF INTERVENTIONAL CARDIOLOGY
ISSN journal
08964327 → ACNP
Volume
12
Issue
4
Year of publication
1999
Pages
271 - 282
Database
ISI
SICI code
0896-4327(199908)12:4<271:TEOIBO>2.0.ZU;2-3
Abstract
Background: Neointimal formation and vascular remodeling are major mechanis ms contributing to coronary restenosis after percutaneous transluminal coro nary angioplasty. Intracoronary gamma- and beta-radiation have been shown t o inhibit neointimal formation in balloon-injured porcine coronary arteries . However, the effects of intracoronary, radiation (ICR) dose and dose rate on vascular remodeling versus inhibition of neointimal formation have not been evaluated. Methods and Results: Forty-one Hanford Miniature swine were subjected to oversized balloon injury in the left anterior descending and right coronary artery. A spiral centering catheter with perfusion capabilit ies was placed in the injured segment for circumferentially uniform radiati on dose delivery to the vessel wall, Each artery was randomly afterloaded w ith a dummy wire or an active wire with the P-32 source encapsulated in eit her a short (3 mm) or long (27 mm) segment at the distal end of the wire. T he 3-mm source wire was used to deliver 650, 1,300 and 1,900 cGy while the 27-mm source wire was used to deliver 1,200 and 3,500 cGy of beta-radiation to the adventitia (approximate to 0.5 mm into the vessel wall). The dose r ate for ICR varied from 2.5 to 140 cGy/sec, depending on the mCi strength o f the P-32 source at the time of endovascular radiation. One month later re pent coronary angiography and intravascular ultrasound (NUS) to measure the external elastic lamina (EEL) area were done. The animals were sacrificed and the coronary vasculature was perfusion fired. Morphometric, quantitativ e coronary angiographic, and NUS analyses were carried out in a blinded fas hion. A significant reduction in percent area stenosis (PAS) and neointimal area (NA) was observed on morphometry in coronary arteries treated with 3, 500 cGy of beta-radiation. The PAS and NA was 44% +/- 13% and 0.96 +/- 0.25 mm(2) in the control groups versus 9% +/- 14% and 0.30 +/- 0.23 mm(2) in t he 3,500-cGy group (P < 002). There was no significant difference on morpho metry between the control and the other four beta-radiation-treated groups. There was no significant improvement in the change in minimum lumen diamet er (Delta MLD) between the control and the five radiation-treated groups. F urther analysis of angiographic data revealed that the apparent lack of ben eficial effect on angiography was due to significant reductions in lumen di ameter in the subgroups of arteries subjected to ICR at a dose rate > 50 cG y/sec with the 3-mm source wire only. The Delta MLD was -1.39 +/- 049, -1.7 9 +/- 0.64, and -1.79 +/- 0.39 mm in the 650-, 1,300-, and 1,900-cGy groups treated with a dose rate > 50 cGy/sec versus -0.56 +/- 0.95 in control (P < 0.05). This reduction in lumen diameter on angiography was associated wit h a significant reduction in vessel (EEL) area especially in the groups tre ated with the 3 mm source at a dose rate > 50 cGy/sec. The EEL area was 8.8 +/- 1.7, 9.9 +/- 1.7 and 8.9 +/- 0.6 mm(2) in the 650, 1,300 and 1,900 cGy groups treated at a dose rate > 50 cGy/sec compared to 11.7 +/- 1.6 mm(2) in control arteries (P < 0.001). Conclusions: Endovascular beta-radiation a t high doses (3,500 cGy to adventitia) and dose rare < 50 cGy/sec inhibits restenosis after balloon injury in the porcine model of coronary restenosis . This dose and nose rate is associated with a neutral effect on vascular r emodeling. While lower doses of ICR did not worsen the PAS a reduction in M LD and EEL area were observed. However, this adverse effect on angiographic restenosis mid vascular remodeling appears to be largely limited to the su bgroups treated at dose rates > 50 cGy/sec.