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Mean Corpuscular Volume Predicts In-Stent Restenosis Risk for Stable Coronary Artery Disease Patients Receiving Elective Percutaneous Coronary Intervention
BACKGROUND: The purpose of this study was to analyze predictive performance of MCV in midterm ischemic events among SCAD patients undergoing elective PCI. MATERIAL/METHODS: We retrospectively included 226 consecutive patients with SCAD who received elective PCI. The patients were grouped based on MC...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6559005/ https://www.ncbi.nlm.nih.gov/pubmed/31136565 http://dx.doi.org/10.12659/MSM.914654 |
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author | Sun, Lin Zhang, Chunyan Ju, Yinghui Tang, Bin Gu, Meixiu Pan, Baishen Guo, Wei Wang, Beili |
author_facet | Sun, Lin Zhang, Chunyan Ju, Yinghui Tang, Bin Gu, Meixiu Pan, Baishen Guo, Wei Wang, Beili |
author_sort | Sun, Lin |
collection | PubMed |
description | BACKGROUND: The purpose of this study was to analyze predictive performance of MCV in midterm ischemic events among SCAD patients undergoing elective PCI. MATERIAL/METHODS: We retrospectively included 226 consecutive patients with SCAD who received elective PCI. The patients were grouped based on MCV quartile values. The prognostic significance of MCV was assessed using univariate and multivariate Cox proportional hazard regression analyses. RESULTS: According to MCV quartile points (87.5 fL, 89.7 fL, and 92.4 fL, respectively), the included patients were divided into 4 groups, with an average follow-up of 34.2 months. There were 28 (48.3%) patients with stent thrombosis in the 1(st) quartile, 24 (29.1%) in the 2(nd) quartile, 18 (31.6%) in the 3(rd) quartile, and 15 (27.8%) in the 4(th) quartile (log-rank test, P=0.027). Multivariate analysis confirmed that MCV 1(st) quartile (HRadj=2.047, 95% CI 1.041–4.026; P=0.038), ALT (HRadj=1.013, 95% CI 1.004–1.023; P=0.004) and number of PCI vessels (HRadj=1.198 95% CI 1.013–1.415; P=0.034) were risk factors for ischemic events. The restenosis rate in patients belonging to the MCV 1(st) quartile was 2 times higher than that in MCV 2(nd), 3(rd), and 4(th) quartile groups (P=0.007). CONCLUSIONS: MCV value may be independently correlated with restenosis in SCAD patients undergoing PCI. Low MCV predicts high risk of in-stent restenosis. |
format | Online Article Text |
id | pubmed-6559005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65590052019-06-26 Mean Corpuscular Volume Predicts In-Stent Restenosis Risk for Stable Coronary Artery Disease Patients Receiving Elective Percutaneous Coronary Intervention Sun, Lin Zhang, Chunyan Ju, Yinghui Tang, Bin Gu, Meixiu Pan, Baishen Guo, Wei Wang, Beili Med Sci Monit Lab/In Vitro Research BACKGROUND: The purpose of this study was to analyze predictive performance of MCV in midterm ischemic events among SCAD patients undergoing elective PCI. MATERIAL/METHODS: We retrospectively included 226 consecutive patients with SCAD who received elective PCI. The patients were grouped based on MCV quartile values. The prognostic significance of MCV was assessed using univariate and multivariate Cox proportional hazard regression analyses. RESULTS: According to MCV quartile points (87.5 fL, 89.7 fL, and 92.4 fL, respectively), the included patients were divided into 4 groups, with an average follow-up of 34.2 months. There were 28 (48.3%) patients with stent thrombosis in the 1(st) quartile, 24 (29.1%) in the 2(nd) quartile, 18 (31.6%) in the 3(rd) quartile, and 15 (27.8%) in the 4(th) quartile (log-rank test, P=0.027). Multivariate analysis confirmed that MCV 1(st) quartile (HRadj=2.047, 95% CI 1.041–4.026; P=0.038), ALT (HRadj=1.013, 95% CI 1.004–1.023; P=0.004) and number of PCI vessels (HRadj=1.198 95% CI 1.013–1.415; P=0.034) were risk factors for ischemic events. The restenosis rate in patients belonging to the MCV 1(st) quartile was 2 times higher than that in MCV 2(nd), 3(rd), and 4(th) quartile groups (P=0.007). CONCLUSIONS: MCV value may be independently correlated with restenosis in SCAD patients undergoing PCI. Low MCV predicts high risk of in-stent restenosis. International Scientific Literature, Inc. 2019-05-28 /pmc/articles/PMC6559005/ /pubmed/31136565 http://dx.doi.org/10.12659/MSM.914654 Text en © Med Sci Monit, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Lab/In Vitro Research Sun, Lin Zhang, Chunyan Ju, Yinghui Tang, Bin Gu, Meixiu Pan, Baishen Guo, Wei Wang, Beili Mean Corpuscular Volume Predicts In-Stent Restenosis Risk for Stable Coronary Artery Disease Patients Receiving Elective Percutaneous Coronary Intervention |
title | Mean Corpuscular Volume Predicts In-Stent Restenosis Risk for Stable Coronary Artery Disease Patients Receiving Elective Percutaneous Coronary Intervention |
title_full | Mean Corpuscular Volume Predicts In-Stent Restenosis Risk for Stable Coronary Artery Disease Patients Receiving Elective Percutaneous Coronary Intervention |
title_fullStr | Mean Corpuscular Volume Predicts In-Stent Restenosis Risk for Stable Coronary Artery Disease Patients Receiving Elective Percutaneous Coronary Intervention |
title_full_unstemmed | Mean Corpuscular Volume Predicts In-Stent Restenosis Risk for Stable Coronary Artery Disease Patients Receiving Elective Percutaneous Coronary Intervention |
title_short | Mean Corpuscular Volume Predicts In-Stent Restenosis Risk for Stable Coronary Artery Disease Patients Receiving Elective Percutaneous Coronary Intervention |
title_sort | mean corpuscular volume predicts in-stent restenosis risk for stable coronary artery disease patients receiving elective percutaneous coronary intervention |
topic | Lab/In Vitro Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6559005/ https://www.ncbi.nlm.nih.gov/pubmed/31136565 http://dx.doi.org/10.12659/MSM.914654 |
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