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Methotrexate and Adalimumab Decrease the Serum Levels of Cardiovascular Disease Biomarkers (VCAM-1 and E-Selectin) in Plaque Psoriasis

Background and objectives: The shared pathogenesis of psoriasis and atherosclerosis may be determined by assaying the levels of endothelial activation molecules. This study aimed at evaluating vascular cell adhesion molecule 1 (VCAM-1) and E-selectin serum concentrations, and atherosclerosis severit...

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Autores principales: Zdanowska, Natalia, Owczarczyk-Saczonek, Agnieszka, Czerwińska, Joanna, Nowakowski, Jacek J., Kozera-Żywczyk, Anna, Owczarek, Witold, Zdanowski, Wojciech, Placek, Waldemar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7558199/
https://www.ncbi.nlm.nih.gov/pubmed/32942670
http://dx.doi.org/10.3390/medicina56090473
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author Zdanowska, Natalia
Owczarczyk-Saczonek, Agnieszka
Czerwińska, Joanna
Nowakowski, Jacek J.
Kozera-Żywczyk, Anna
Owczarek, Witold
Zdanowski, Wojciech
Placek, Waldemar
author_facet Zdanowska, Natalia
Owczarczyk-Saczonek, Agnieszka
Czerwińska, Joanna
Nowakowski, Jacek J.
Kozera-Żywczyk, Anna
Owczarek, Witold
Zdanowski, Wojciech
Placek, Waldemar
author_sort Zdanowska, Natalia
collection PubMed
description Background and objectives: The shared pathogenesis of psoriasis and atherosclerosis may be determined by assaying the levels of endothelial activation molecules. This study aimed at evaluating vascular cell adhesion molecule 1 (VCAM-1) and E-selectin serum concentrations, and atherosclerosis severity in patients with plaque psoriasis. It also aimed to determine the effects of methotrexate/adalimumab treatment for 12 weeks on the plasma levels of the aforementioned molecules. Materials and Methods: The study included 34 psoriasis patients (17 treated with methotrexate and 17 treated with adalimumab) and eight controls. The 10-year risk of a fatal cardiovascular disease, body mass index, Psoriasis Area and Severity Index, and body surface area were calculated for each subject. VCAM-1 and E-selectin levels were determined via an enzyme-linked immunosorbent assay at baseline and after 12 weeks. Results: Baseline E-selectin and VCAM-1 levels were higher in the adalimumab group than in the methotrexate and control groups. VCAM-1 levels decreased in the adalimumab (p = 0.02) and methotrexate groups (p = 0.008), while E-selectin levels decreased in the methotrexate group (p = 0.004). Conclusions: The results indicate a correlation between systemic psoriasis treatment and E-selectin and VCAM-1 plasma concentrations, which may be associated with the risk of cardiovascular disease development.
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spelling pubmed-75581992020-10-29 Methotrexate and Adalimumab Decrease the Serum Levels of Cardiovascular Disease Biomarkers (VCAM-1 and E-Selectin) in Plaque Psoriasis Zdanowska, Natalia Owczarczyk-Saczonek, Agnieszka Czerwińska, Joanna Nowakowski, Jacek J. Kozera-Żywczyk, Anna Owczarek, Witold Zdanowski, Wojciech Placek, Waldemar Medicina (Kaunas) Article Background and objectives: The shared pathogenesis of psoriasis and atherosclerosis may be determined by assaying the levels of endothelial activation molecules. This study aimed at evaluating vascular cell adhesion molecule 1 (VCAM-1) and E-selectin serum concentrations, and atherosclerosis severity in patients with plaque psoriasis. It also aimed to determine the effects of methotrexate/adalimumab treatment for 12 weeks on the plasma levels of the aforementioned molecules. Materials and Methods: The study included 34 psoriasis patients (17 treated with methotrexate and 17 treated with adalimumab) and eight controls. The 10-year risk of a fatal cardiovascular disease, body mass index, Psoriasis Area and Severity Index, and body surface area were calculated for each subject. VCAM-1 and E-selectin levels were determined via an enzyme-linked immunosorbent assay at baseline and after 12 weeks. Results: Baseline E-selectin and VCAM-1 levels were higher in the adalimumab group than in the methotrexate and control groups. VCAM-1 levels decreased in the adalimumab (p = 0.02) and methotrexate groups (p = 0.008), while E-selectin levels decreased in the methotrexate group (p = 0.004). Conclusions: The results indicate a correlation between systemic psoriasis treatment and E-selectin and VCAM-1 plasma concentrations, which may be associated with the risk of cardiovascular disease development. MDPI 2020-09-15 /pmc/articles/PMC7558199/ /pubmed/32942670 http://dx.doi.org/10.3390/medicina56090473 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zdanowska, Natalia
Owczarczyk-Saczonek, Agnieszka
Czerwińska, Joanna
Nowakowski, Jacek J.
Kozera-Żywczyk, Anna
Owczarek, Witold
Zdanowski, Wojciech
Placek, Waldemar
Methotrexate and Adalimumab Decrease the Serum Levels of Cardiovascular Disease Biomarkers (VCAM-1 and E-Selectin) in Plaque Psoriasis
title Methotrexate and Adalimumab Decrease the Serum Levels of Cardiovascular Disease Biomarkers (VCAM-1 and E-Selectin) in Plaque Psoriasis
title_full Methotrexate and Adalimumab Decrease the Serum Levels of Cardiovascular Disease Biomarkers (VCAM-1 and E-Selectin) in Plaque Psoriasis
title_fullStr Methotrexate and Adalimumab Decrease the Serum Levels of Cardiovascular Disease Biomarkers (VCAM-1 and E-Selectin) in Plaque Psoriasis
title_full_unstemmed Methotrexate and Adalimumab Decrease the Serum Levels of Cardiovascular Disease Biomarkers (VCAM-1 and E-Selectin) in Plaque Psoriasis
title_short Methotrexate and Adalimumab Decrease the Serum Levels of Cardiovascular Disease Biomarkers (VCAM-1 and E-Selectin) in Plaque Psoriasis
title_sort methotrexate and adalimumab decrease the serum levels of cardiovascular disease biomarkers (vcam-1 and e-selectin) in plaque psoriasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7558199/
https://www.ncbi.nlm.nih.gov/pubmed/32942670
http://dx.doi.org/10.3390/medicina56090473
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