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Impact of premature coronary artery disease on adverse event risk following first percutaneous coronary intervention
OBJECTIVES: We assessed differences in risk profile and 3-year outcome between patients undergoing percutaneous coronary intervention (PCI) for premature and non-premature coronary artery disease (CAD). BACKGROUND: The prevalence of CAD increases with age, yet some individuals develop obstructive CA...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512829/ https://www.ncbi.nlm.nih.gov/pubmed/37745109 http://dx.doi.org/10.3389/fcvm.2023.1160201 |
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author | Pinxterhuis, Tineke H. Ploumen, Eline H. Zocca, Paolo Doggen, Carine J. M. Schotborgh, Carl E. Anthonio, Rutger L. Roguin, Ariel Danse, Peter W. Benit, Edouard Aminian, Adel Hartmann, Marc Linssen, Gerard C. M. von Birgelen, Clemens |
author_facet | Pinxterhuis, Tineke H. Ploumen, Eline H. Zocca, Paolo Doggen, Carine J. M. Schotborgh, Carl E. Anthonio, Rutger L. Roguin, Ariel Danse, Peter W. Benit, Edouard Aminian, Adel Hartmann, Marc Linssen, Gerard C. M. von Birgelen, Clemens |
author_sort | Pinxterhuis, Tineke H. |
collection | PubMed |
description | OBJECTIVES: We assessed differences in risk profile and 3-year outcome between patients undergoing percutaneous coronary intervention (PCI) for premature and non-premature coronary artery disease (CAD). BACKGROUND: The prevalence of CAD increases with age, yet some individuals develop obstructive CAD at younger age. METHODS: Among participants in four randomized all-comers PCI trials, without previous coronary revascularization or myocardial infarction (MI), we compared patients with premature (men <50 years; women <55 years) and non-premature CAD. Various clinical endpoints were assessed, including multivariate analyses. RESULTS: Of 6,171 patients, 887 (14.4%) suffered from premature CAD. These patients had fewer risk factors than patients with non-premature CAD, but were more often smokers (60.7% vs. 26.4%) and overweight (76.2% vs. 69.8%). In addition, premature CAD patients presented more often with ST-segment elevation MI and underwent less often treatment of multiple vessels, and calcified or bifurcated lesions. Furthermore, premature CAD patients had a lower all-cause mortality risk (adj.HR: 0.23, 95%-CI: 0.10–0.52; p < 0.001), but target vessel revascularization (adj.HR: 1.63, 95%-CI: 1.18–2.26; p = 0.003) and definite stent thrombosis risks (adj.HR: 2.24, 95%-CI: 1.06–4.72; p = 0.034) were higher. MACE rates showed no statistically significant difference (6.6% vs. 9.4%; adj.HR: 0.86, 95%-CI: 0.65–1.16; p = 0.33) CONCLUSIONS: About one out of seven PCI patients was treated for premature CAD. These patients had less complex risk profiles than patients with non-premature CAD; yet, their risk of repeated revascularization and stent thrombosis was higher. As lifetime event risk of patients with premature CAD is known to be particularly high, further efforts should be made to improve modifiable risk factors such as smoking and overweight. TWENTE TRIALS: (TWENTE I, clinicaltrials.gov: NCT01066650), DUTCH PEERS (TWENTE II, NCT01331707), BIO-RESORT (TWENTE III, NCT01674803), and BIONYX (TWENTE IV, NCT02508714). |
format | Online Article Text |
id | pubmed-10512829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105128292023-09-22 Impact of premature coronary artery disease on adverse event risk following first percutaneous coronary intervention Pinxterhuis, Tineke H. Ploumen, Eline H. Zocca, Paolo Doggen, Carine J. M. Schotborgh, Carl E. Anthonio, Rutger L. Roguin, Ariel Danse, Peter W. Benit, Edouard Aminian, Adel Hartmann, Marc Linssen, Gerard C. M. von Birgelen, Clemens Front Cardiovasc Med Cardiovascular Medicine OBJECTIVES: We assessed differences in risk profile and 3-year outcome between patients undergoing percutaneous coronary intervention (PCI) for premature and non-premature coronary artery disease (CAD). BACKGROUND: The prevalence of CAD increases with age, yet some individuals develop obstructive CAD at younger age. METHODS: Among participants in four randomized all-comers PCI trials, without previous coronary revascularization or myocardial infarction (MI), we compared patients with premature (men <50 years; women <55 years) and non-premature CAD. Various clinical endpoints were assessed, including multivariate analyses. RESULTS: Of 6,171 patients, 887 (14.4%) suffered from premature CAD. These patients had fewer risk factors than patients with non-premature CAD, but were more often smokers (60.7% vs. 26.4%) and overweight (76.2% vs. 69.8%). In addition, premature CAD patients presented more often with ST-segment elevation MI and underwent less often treatment of multiple vessels, and calcified or bifurcated lesions. Furthermore, premature CAD patients had a lower all-cause mortality risk (adj.HR: 0.23, 95%-CI: 0.10–0.52; p < 0.001), but target vessel revascularization (adj.HR: 1.63, 95%-CI: 1.18–2.26; p = 0.003) and definite stent thrombosis risks (adj.HR: 2.24, 95%-CI: 1.06–4.72; p = 0.034) were higher. MACE rates showed no statistically significant difference (6.6% vs. 9.4%; adj.HR: 0.86, 95%-CI: 0.65–1.16; p = 0.33) CONCLUSIONS: About one out of seven PCI patients was treated for premature CAD. These patients had less complex risk profiles than patients with non-premature CAD; yet, their risk of repeated revascularization and stent thrombosis was higher. As lifetime event risk of patients with premature CAD is known to be particularly high, further efforts should be made to improve modifiable risk factors such as smoking and overweight. TWENTE TRIALS: (TWENTE I, clinicaltrials.gov: NCT01066650), DUTCH PEERS (TWENTE II, NCT01331707), BIO-RESORT (TWENTE III, NCT01674803), and BIONYX (TWENTE IV, NCT02508714). Frontiers Media S.A. 2023-09-07 /pmc/articles/PMC10512829/ /pubmed/37745109 http://dx.doi.org/10.3389/fcvm.2023.1160201 Text en © 2023 Pinxterhuis, Ploumen, Zocca, Doggen, Schotborgh, Anthonio, Roguin, Danse, Benit, Aminian, Hartmann, Linssen and von Birgelen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Pinxterhuis, Tineke H. Ploumen, Eline H. Zocca, Paolo Doggen, Carine J. M. Schotborgh, Carl E. Anthonio, Rutger L. Roguin, Ariel Danse, Peter W. Benit, Edouard Aminian, Adel Hartmann, Marc Linssen, Gerard C. M. von Birgelen, Clemens Impact of premature coronary artery disease on adverse event risk following first percutaneous coronary intervention |
title | Impact of premature coronary artery disease on adverse event risk following first percutaneous coronary intervention |
title_full | Impact of premature coronary artery disease on adverse event risk following first percutaneous coronary intervention |
title_fullStr | Impact of premature coronary artery disease on adverse event risk following first percutaneous coronary intervention |
title_full_unstemmed | Impact of premature coronary artery disease on adverse event risk following first percutaneous coronary intervention |
title_short | Impact of premature coronary artery disease on adverse event risk following first percutaneous coronary intervention |
title_sort | impact of premature coronary artery disease on adverse event risk following first percutaneous coronary intervention |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512829/ https://www.ncbi.nlm.nih.gov/pubmed/37745109 http://dx.doi.org/10.3389/fcvm.2023.1160201 |
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