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Ferritin modifies the relationship between inflammation and arterial stiffness in hypertensive patients with different glucose tolerance

BACKGROUND: Ferritin, a crucial element for iron homeostasis, is associated with chronic diseases characterized by subclinical inflammation such as essential arterial hypertension and type 2 diabetes mellitus (T2DM), showing a prognostic value in different clinical settings. We investigated whether...

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Autores principales: Sciacqua, Angela, Ventura, Ettore, Tripepi, Giovanni, Cassano, Velia, D’Arrigo, Graziella, Roumeliotis, Stefanos, Maio, Raffale, Miceli, Sofia, Perticone, Maria, Andreozzi, Francesco, Sesti, Giorgio, Perticone, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409693/
https://www.ncbi.nlm.nih.gov/pubmed/32758229
http://dx.doi.org/10.1186/s12933-020-01102-8
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author Sciacqua, Angela
Ventura, Ettore
Tripepi, Giovanni
Cassano, Velia
D’Arrigo, Graziella
Roumeliotis, Stefanos
Maio, Raffale
Miceli, Sofia
Perticone, Maria
Andreozzi, Francesco
Sesti, Giorgio
Perticone, Francesco
author_facet Sciacqua, Angela
Ventura, Ettore
Tripepi, Giovanni
Cassano, Velia
D’Arrigo, Graziella
Roumeliotis, Stefanos
Maio, Raffale
Miceli, Sofia
Perticone, Maria
Andreozzi, Francesco
Sesti, Giorgio
Perticone, Francesco
author_sort Sciacqua, Angela
collection PubMed
description BACKGROUND: Ferritin, a crucial element for iron homeostasis, is associated with chronic diseases characterized by subclinical inflammation such as essential arterial hypertension and type 2 diabetes mellitus (T2DM), showing a prognostic value in different clinical settings. We investigated whether ferritin is associated with arterial stiffness (AS), an early indicator of atherosclerosis, and if it could act as effect modifier on the relationship between inflammation and AS in hypertensive patients with different glucose tolerance. METHODS: We enrolled 462 newly diagnosed untreated hypertensive (HT) patients. All subjects underwent an oral glucose tolerance test. Insulin sensitivity was assessed by MATSUDA index and ferritin levels were estimated by immunoradiometric assay. AS was defined by carotid-femoral pulse wave velocity (PWV). RESULTS: Out of 462 patients, 271 showed normal glucose tolerance (HT/NGT), 146 impaired glucose tolerance (HT/IGT) and 45 were diabetic (HT/T2DM). Iron levels significantly decreased and transferrin and ferritin significantly increased from the first to the third group. PWV values were significantly higher in HT/IGT and HT/T2DM patients. PWV was related directly with ferritin, high sensitivity C reactive protein (hs-CRP), transferrin, and inversely with MATSUDA index. Ferritin resulted the strongest determinant of PWV explaining a 14.9% of its variation; moreover it was a strong modifier of the relationship between hs-CRP and PWV. The estimated augmentation in PWV portended by a fixed increase in hs-CRP, was higher across increasing values of ferritin. CONCLUSION: Ferritin represents an independent risk factor of arterial stiffness in our study population and a strong effect modifier on the relationship between inflammation and PWV. However, further studies are needed to fully elucidate the potential role of this biomarker in human atherosclerosis.
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spelling pubmed-74096932020-08-10 Ferritin modifies the relationship between inflammation and arterial stiffness in hypertensive patients with different glucose tolerance Sciacqua, Angela Ventura, Ettore Tripepi, Giovanni Cassano, Velia D’Arrigo, Graziella Roumeliotis, Stefanos Maio, Raffale Miceli, Sofia Perticone, Maria Andreozzi, Francesco Sesti, Giorgio Perticone, Francesco Cardiovasc Diabetol Original Investigation BACKGROUND: Ferritin, a crucial element for iron homeostasis, is associated with chronic diseases characterized by subclinical inflammation such as essential arterial hypertension and type 2 diabetes mellitus (T2DM), showing a prognostic value in different clinical settings. We investigated whether ferritin is associated with arterial stiffness (AS), an early indicator of atherosclerosis, and if it could act as effect modifier on the relationship between inflammation and AS in hypertensive patients with different glucose tolerance. METHODS: We enrolled 462 newly diagnosed untreated hypertensive (HT) patients. All subjects underwent an oral glucose tolerance test. Insulin sensitivity was assessed by MATSUDA index and ferritin levels were estimated by immunoradiometric assay. AS was defined by carotid-femoral pulse wave velocity (PWV). RESULTS: Out of 462 patients, 271 showed normal glucose tolerance (HT/NGT), 146 impaired glucose tolerance (HT/IGT) and 45 were diabetic (HT/T2DM). Iron levels significantly decreased and transferrin and ferritin significantly increased from the first to the third group. PWV values were significantly higher in HT/IGT and HT/T2DM patients. PWV was related directly with ferritin, high sensitivity C reactive protein (hs-CRP), transferrin, and inversely with MATSUDA index. Ferritin resulted the strongest determinant of PWV explaining a 14.9% of its variation; moreover it was a strong modifier of the relationship between hs-CRP and PWV. The estimated augmentation in PWV portended by a fixed increase in hs-CRP, was higher across increasing values of ferritin. CONCLUSION: Ferritin represents an independent risk factor of arterial stiffness in our study population and a strong effect modifier on the relationship between inflammation and PWV. However, further studies are needed to fully elucidate the potential role of this biomarker in human atherosclerosis. BioMed Central 2020-08-05 /pmc/articles/PMC7409693/ /pubmed/32758229 http://dx.doi.org/10.1186/s12933-020-01102-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Original Investigation
Sciacqua, Angela
Ventura, Ettore
Tripepi, Giovanni
Cassano, Velia
D’Arrigo, Graziella
Roumeliotis, Stefanos
Maio, Raffale
Miceli, Sofia
Perticone, Maria
Andreozzi, Francesco
Sesti, Giorgio
Perticone, Francesco
Ferritin modifies the relationship between inflammation and arterial stiffness in hypertensive patients with different glucose tolerance
title Ferritin modifies the relationship between inflammation and arterial stiffness in hypertensive patients with different glucose tolerance
title_full Ferritin modifies the relationship between inflammation and arterial stiffness in hypertensive patients with different glucose tolerance
title_fullStr Ferritin modifies the relationship between inflammation and arterial stiffness in hypertensive patients with different glucose tolerance
title_full_unstemmed Ferritin modifies the relationship between inflammation and arterial stiffness in hypertensive patients with different glucose tolerance
title_short Ferritin modifies the relationship between inflammation and arterial stiffness in hypertensive patients with different glucose tolerance
title_sort ferritin modifies the relationship between inflammation and arterial stiffness in hypertensive patients with different glucose tolerance
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409693/
https://www.ncbi.nlm.nih.gov/pubmed/32758229
http://dx.doi.org/10.1186/s12933-020-01102-8
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