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Transcoronary stem cell transfer and evolution of infarct-related artery atherosclerosis: evaluation with conventional and novel imaging techniques including Quantitative Virtual Histology (qVH)

INTRODUCTION: It has been suggested that infarct-related artery (IRA) atherosclerosis progression after stem cell transcoronary administration might represent a stem-cell mediated adverse effect. AIM: To evaluate, using conventional (quantitative coronary angiography, QCA, intravascular ultrasound –...

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Detalles Bibliográficos
Autores principales: Dabrowski, Wladyslaw, Tekieli, Lukasz, Mazurek, Adam, Lanocha, Magdalena, Banys, R. Pawel, Zmudka, Krzysztof, Majka, Marcin, Wojakowski, Wojciech, Tendera, Michal, Musialek, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031661/
https://www.ncbi.nlm.nih.gov/pubmed/36967840
http://dx.doi.org/10.5114/aic.2023.125609
Descripción
Sumario:INTRODUCTION: It has been suggested that infarct-related artery (IRA) atherosclerosis progression after stem cell transcoronary administration might represent a stem-cell mediated adverse effect. AIM: To evaluate, using conventional (quantitative coronary angiography, QCA, intravascular ultrasound – IVUS) and novel (quantitative virtual histology – qVH) tools, evolution of IRA atherosclerosis following transcoronary stem cell transfer. MATERIAL AND METHODS: QCA, IVUS, VH-IVUS and qVH were performed in 22 consecutive patients (4 women) aged 59 years (data provided as median) undergoing a distal-to-stent infusion of 2.21 × 10(6) CD34(+)CXCR4(+) autologous bone marrow cells via a cell delivery-dedicated perfusion catheter at anterior AMI day 7. Imaging was repeated at 12 months. This was a substudy of Myocardial Regeneration by Intracoronary Infusion of Selected Population of Stem Cells in Acute Myocardial Infarction (REGENT) Trial (NCT00316381). RESULTS: 18.2% subjects showed absence of distal-to-stent angiographic/IVUS atherosclerotic lesion(s) at baseline and no new lesion(s) at 12-months. In the remaining cohort, there were 28 lesions by QCA (32 by IVUS) at baseline and no new lesion(s) at follow-up. Three fibroatheromas evolved (2 to calcified fibroatheroma and 1 to a fibrocalcific lesion); other plaques maintained their stable (low-risk) phenotypes. Diameter stenosis of QCA-identified lesions was 29.5 vs. 26.5% (p = 0.012, baseline vs. 12-months). Gray-scale IVUS showed reduction in area stenosis (33.8 vs. 31.0%, p = 0.004) and plaque burden (66.27 vs. 64.56%, p = 0.009) at 12-months. Peak fibrotic plaque content increased from 70.41% to 75.0% (p = 0.004). qVH peak confluent necrotic core area and minimal fibrous cap thickness remained stable (0.64 vs. 0.59 mm(2), p = 0.290, and 0.15 vs. 0.16 mm, p = 0.646). CONCLUSIONS: This study, using a range of classic and novel imaging techniques, indicates lack of any stimulatory effect of transcoronary stem cell transfer on coronary atherosclerosis. Whether, and to what extent, a moderate reduction in plaque burden and stenosis severity at 12-months results from optimized pharmacotherapy and/or stem cell transfer requires further elucidation.