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Paraoxonase-1 and other factors related to oxidative stress in psoriasis

INTRODUCTION: Psoriasis is considered as a risk factor for atherosclerosis and contributes to myocardial infarction, ischemic heart disease and brain stroke. AIM: To estimate the atherogenic potential of psoriasis by analysing antioxidative and prooxidative factors (paraoxonase-1, α-tocopherol, uric...

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Autores principales: Oszukowska, Magdalena, Kozłowska, Magdalena, Kaszuba, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247073/
https://www.ncbi.nlm.nih.gov/pubmed/32467691
http://dx.doi.org/10.5114/ada.2020.93386
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author Oszukowska, Magdalena
Kozłowska, Magdalena
Kaszuba, Andrzej
author_facet Oszukowska, Magdalena
Kozłowska, Magdalena
Kaszuba, Andrzej
author_sort Oszukowska, Magdalena
collection PubMed
description INTRODUCTION: Psoriasis is considered as a risk factor for atherosclerosis and contributes to myocardial infarction, ischemic heart disease and brain stroke. AIM: To estimate the atherogenic potential of psoriasis by analysing antioxidative and prooxidative factors (paraoxonase-1, α-tocopherol, uric acid, homocysteine), compare levels of these parameters between groups of psoriatic patients and healthy individuals as well as to analyse the impact of psoriasis severity and duration on the factors under the study and to define correlation between the marked factors and patients’ lifestyles, body mass index (BMI) and abdominal circumference. MATERIAL AND METHODS: The investigated group consisted of 66 patients with psoriasis vulgaris, while the control group comprised 30 persons. Both groups were comparable as regards their age, sex and BMI as well as abdominal circumference. RESULTS: A significantly lower activity of paraoxonase-1 (p < 0.001), level of tocopherol (p < 0.05) and significantly higher concentration of homocysteine (p < 0.01), uric acid (p < 0.05) were found in patients with psoriasis as compared to the reference group. A higher homocysteine level occurs in patients with a negative family history of psoriasis (p < 0.05). In the group of patients with psoriasis and metabolic syndrome, the uric acid level was significantly higher (p < 0.05). Concentration of uric acid correlated negatively with the abdominal circumference value (p < 0.001). CONCLUSIONS: Psoriasis promotes arteriosclerosis development by decreasing the levels of antiatherogenic and increasing the levels of proatherogenic agents. Adverse changes in psoriatic patients involve activity of paraoxonase-1, levels of α-tocopherol, uric acid, homocysteine as compared to healthy individuals selected by their age, BMI and abdominal circumference value.
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spelling pubmed-72470732020-05-27 Paraoxonase-1 and other factors related to oxidative stress in psoriasis Oszukowska, Magdalena Kozłowska, Magdalena Kaszuba, Andrzej Postepy Dermatol Alergol Original Paper INTRODUCTION: Psoriasis is considered as a risk factor for atherosclerosis and contributes to myocardial infarction, ischemic heart disease and brain stroke. AIM: To estimate the atherogenic potential of psoriasis by analysing antioxidative and prooxidative factors (paraoxonase-1, α-tocopherol, uric acid, homocysteine), compare levels of these parameters between groups of psoriatic patients and healthy individuals as well as to analyse the impact of psoriasis severity and duration on the factors under the study and to define correlation between the marked factors and patients’ lifestyles, body mass index (BMI) and abdominal circumference. MATERIAL AND METHODS: The investigated group consisted of 66 patients with psoriasis vulgaris, while the control group comprised 30 persons. Both groups were comparable as regards their age, sex and BMI as well as abdominal circumference. RESULTS: A significantly lower activity of paraoxonase-1 (p < 0.001), level of tocopherol (p < 0.05) and significantly higher concentration of homocysteine (p < 0.01), uric acid (p < 0.05) were found in patients with psoriasis as compared to the reference group. A higher homocysteine level occurs in patients with a negative family history of psoriasis (p < 0.05). In the group of patients with psoriasis and metabolic syndrome, the uric acid level was significantly higher (p < 0.05). Concentration of uric acid correlated negatively with the abdominal circumference value (p < 0.001). CONCLUSIONS: Psoriasis promotes arteriosclerosis development by decreasing the levels of antiatherogenic and increasing the levels of proatherogenic agents. Adverse changes in psoriatic patients involve activity of paraoxonase-1, levels of α-tocopherol, uric acid, homocysteine as compared to healthy individuals selected by their age, BMI and abdominal circumference value. Termedia Publishing House 2020-03-09 2020-02 /pmc/articles/PMC7247073/ /pubmed/32467691 http://dx.doi.org/10.5114/ada.2020.93386 Text en Copyright: © 2020 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Oszukowska, Magdalena
Kozłowska, Magdalena
Kaszuba, Andrzej
Paraoxonase-1 and other factors related to oxidative stress in psoriasis
title Paraoxonase-1 and other factors related to oxidative stress in psoriasis
title_full Paraoxonase-1 and other factors related to oxidative stress in psoriasis
title_fullStr Paraoxonase-1 and other factors related to oxidative stress in psoriasis
title_full_unstemmed Paraoxonase-1 and other factors related to oxidative stress in psoriasis
title_short Paraoxonase-1 and other factors related to oxidative stress in psoriasis
title_sort paraoxonase-1 and other factors related to oxidative stress in psoriasis
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247073/
https://www.ncbi.nlm.nih.gov/pubmed/32467691
http://dx.doi.org/10.5114/ada.2020.93386
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