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Association of Circulating Heme Oxygenase-1, Lipid Profile and Coronary Disease Phenotype in Patients with Chronic Coronary Syndrome

Background. The NF-E2–related factor 2 (Nrf2)/Heme Oxygenase-1 (HO-1) pathway has an emerging role in atherosclerosis. Activated by oxidative stress, it is deemed to exert athero-protective effects. We aimed at evaluating the relationships between plasma HO-1, clinical/molecular profiles and coronar...

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Autores principales: Caselli, Chiara, De Caterina, Raffaele, Ragusa, Rosetta, Liga, Riccardo, Gimelli, Alessia, Scholte, Arthur J. H. A., Clerico, Aldo, Knuuti, Juhani, Neglia, Danilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698632/
https://www.ncbi.nlm.nih.gov/pubmed/34943105
http://dx.doi.org/10.3390/antiox10122002
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author Caselli, Chiara
De Caterina, Raffaele
Ragusa, Rosetta
Liga, Riccardo
Gimelli, Alessia
Scholte, Arthur J. H. A.
Clerico, Aldo
Knuuti, Juhani
Neglia, Danilo
author_facet Caselli, Chiara
De Caterina, Raffaele
Ragusa, Rosetta
Liga, Riccardo
Gimelli, Alessia
Scholte, Arthur J. H. A.
Clerico, Aldo
Knuuti, Juhani
Neglia, Danilo
author_sort Caselli, Chiara
collection PubMed
description Background. The NF-E2–related factor 2 (Nrf2)/Heme Oxygenase-1 (HO-1) pathway has an emerging role in atherosclerosis. Activated by oxidative stress, it is deemed to exert athero-protective effects. We aimed at evaluating the relationships between plasma HO-1, clinical/molecular profiles and coronary disease patterns in patients with chronic coronary syndromes (CCS). Methods. HO-1 was measured in 526 patients (60 ± 9 years, 318 males) with CCS. Coronary computed tomography angiography (CTA) and stress imaging were used to assess the disease phenotype (coronary atherosclerosis and myocardial ischemia) in a subgroup of 347 patients. Results. In the overall population, HO-1 median value (25–75 percentile) was 5.195 (1.75–8.25) ng/mL. Patients with higher HO-1 were more frequently male, had a higher BMI and lower LVEF%, but otherwise similar risk factors than the other patients. Their bio-humoral profile was characterized by higher markers of endothelial/myocardial dysfunction, but lower levels of cholesterol lipoproteins. Coronary artery disease was characterized by more diffuse atherosclerosis, with mainly non-obstructive and calcified plaques, and a higher prevalence of functional ischemia. Conclusion: In patients with CCS, higher plasma HO-1 levels are associated with lower cholesterol and a more diffuse but mainly non-obstructive coronary atherosclerosis, confirming a potential role for the Nrf2/HO-1 pathway as a protective feedback.
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spelling pubmed-86986322021-12-24 Association of Circulating Heme Oxygenase-1, Lipid Profile and Coronary Disease Phenotype in Patients with Chronic Coronary Syndrome Caselli, Chiara De Caterina, Raffaele Ragusa, Rosetta Liga, Riccardo Gimelli, Alessia Scholte, Arthur J. H. A. Clerico, Aldo Knuuti, Juhani Neglia, Danilo Antioxidants (Basel) Article Background. The NF-E2–related factor 2 (Nrf2)/Heme Oxygenase-1 (HO-1) pathway has an emerging role in atherosclerosis. Activated by oxidative stress, it is deemed to exert athero-protective effects. We aimed at evaluating the relationships between plasma HO-1, clinical/molecular profiles and coronary disease patterns in patients with chronic coronary syndromes (CCS). Methods. HO-1 was measured in 526 patients (60 ± 9 years, 318 males) with CCS. Coronary computed tomography angiography (CTA) and stress imaging were used to assess the disease phenotype (coronary atherosclerosis and myocardial ischemia) in a subgroup of 347 patients. Results. In the overall population, HO-1 median value (25–75 percentile) was 5.195 (1.75–8.25) ng/mL. Patients with higher HO-1 were more frequently male, had a higher BMI and lower LVEF%, but otherwise similar risk factors than the other patients. Their bio-humoral profile was characterized by higher markers of endothelial/myocardial dysfunction, but lower levels of cholesterol lipoproteins. Coronary artery disease was characterized by more diffuse atherosclerosis, with mainly non-obstructive and calcified plaques, and a higher prevalence of functional ischemia. Conclusion: In patients with CCS, higher plasma HO-1 levels are associated with lower cholesterol and a more diffuse but mainly non-obstructive coronary atherosclerosis, confirming a potential role for the Nrf2/HO-1 pathway as a protective feedback. MDPI 2021-12-15 /pmc/articles/PMC8698632/ /pubmed/34943105 http://dx.doi.org/10.3390/antiox10122002 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Caselli, Chiara
De Caterina, Raffaele
Ragusa, Rosetta
Liga, Riccardo
Gimelli, Alessia
Scholte, Arthur J. H. A.
Clerico, Aldo
Knuuti, Juhani
Neglia, Danilo
Association of Circulating Heme Oxygenase-1, Lipid Profile and Coronary Disease Phenotype in Patients with Chronic Coronary Syndrome
title Association of Circulating Heme Oxygenase-1, Lipid Profile and Coronary Disease Phenotype in Patients with Chronic Coronary Syndrome
title_full Association of Circulating Heme Oxygenase-1, Lipid Profile and Coronary Disease Phenotype in Patients with Chronic Coronary Syndrome
title_fullStr Association of Circulating Heme Oxygenase-1, Lipid Profile and Coronary Disease Phenotype in Patients with Chronic Coronary Syndrome
title_full_unstemmed Association of Circulating Heme Oxygenase-1, Lipid Profile and Coronary Disease Phenotype in Patients with Chronic Coronary Syndrome
title_short Association of Circulating Heme Oxygenase-1, Lipid Profile and Coronary Disease Phenotype in Patients with Chronic Coronary Syndrome
title_sort association of circulating heme oxygenase-1, lipid profile and coronary disease phenotype in patients with chronic coronary syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698632/
https://www.ncbi.nlm.nih.gov/pubmed/34943105
http://dx.doi.org/10.3390/antiox10122002
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