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Correlation of Paraoxonase-1 with the Severity of Crohn’s Disease

Diagnostics of Crohn’s disease (CD) requires noninvasive biomarkers facilitating early detection and differentiation of the disease. Therefore, in this study, we aimed to determine the relationship between paraoxonase-1 (PON-1), the severity of CD, oxidative stress, and inflammation in CD. The CD ac...

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Autores principales: Szczeklik, Katarzyna, Mach, Tomasz, Cibor, Dorota, Owczarek, Danuta, Sapa, Jacek, Papież, Monika, Pytko-Polończyk, Jolanta, Krzyściak, Wirginia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222603/
https://www.ncbi.nlm.nih.gov/pubmed/30314292
http://dx.doi.org/10.3390/molecules23102603
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author Szczeklik, Katarzyna
Mach, Tomasz
Cibor, Dorota
Owczarek, Danuta
Sapa, Jacek
Papież, Monika
Pytko-Polończyk, Jolanta
Krzyściak, Wirginia
author_facet Szczeklik, Katarzyna
Mach, Tomasz
Cibor, Dorota
Owczarek, Danuta
Sapa, Jacek
Papież, Monika
Pytko-Polończyk, Jolanta
Krzyściak, Wirginia
author_sort Szczeklik, Katarzyna
collection PubMed
description Diagnostics of Crohn’s disease (CD) requires noninvasive biomarkers facilitating early detection and differentiation of the disease. Therefore, in this study, we aimed to determine the relationship between paraoxonase-1 (PON-1), the severity of CD, oxidative stress, and inflammation in CD. The CD activity index was based on the current classification. Plasma PON-1 was measured in 47 patients with CD, and in 23 control volunteers. Using quantitative variables such as receiver operating characteristics (ROC) (area under the curve (AUC)), the diagnostic utility of PON-1 in differentiating the severity of CD was assessed. Circulating PON-1 was found to be decreased in the CD group compared to the control group (269.89 vs. 402.56 U/L, respectively), and it correlated well with the disease activity. PON-1 correlated positively with hemoglobin (Hb) (r = 0.539, p < 0.001), hematocrit (Ht) (r = 0.48, p < 0.001), total cholesterol (TC) (r = 0.343, p < 0.001), high density lipoprotein (HDL) (r = 0.536, p < 0.001), low density lipoprotein (LDL) (r = 0.54, p < 0.001), and triglyceride (TG) (r = 0.561, p < 0.001) and correlated negatively with white blood cell count (WBC) (r = −0.262, p = 0.029), platelet count (PLT) (r = −0.326, p = 0.006), C-reactive protein (CRP) (r = −0.61, p < 0.001), and malondialdehyde (MDA) (r = −0.924, p < 0.001). PON-1 as a marker for CD differentiation possessed a sensitivity and specificity of 93.62% and 91.30%, respectively. CD was found to be associated with the decrease in the levels of PON-1, which correlates well with activity of the disease and reflects the intensification of inflammation, as well as intensified lipid peroxidation. High sensitivity and specificity of PON-1 determines its selection as a good screening test for CD severity.
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spelling pubmed-62226032018-11-13 Correlation of Paraoxonase-1 with the Severity of Crohn’s Disease Szczeklik, Katarzyna Mach, Tomasz Cibor, Dorota Owczarek, Danuta Sapa, Jacek Papież, Monika Pytko-Polończyk, Jolanta Krzyściak, Wirginia Molecules Article Diagnostics of Crohn’s disease (CD) requires noninvasive biomarkers facilitating early detection and differentiation of the disease. Therefore, in this study, we aimed to determine the relationship between paraoxonase-1 (PON-1), the severity of CD, oxidative stress, and inflammation in CD. The CD activity index was based on the current classification. Plasma PON-1 was measured in 47 patients with CD, and in 23 control volunteers. Using quantitative variables such as receiver operating characteristics (ROC) (area under the curve (AUC)), the diagnostic utility of PON-1 in differentiating the severity of CD was assessed. Circulating PON-1 was found to be decreased in the CD group compared to the control group (269.89 vs. 402.56 U/L, respectively), and it correlated well with the disease activity. PON-1 correlated positively with hemoglobin (Hb) (r = 0.539, p < 0.001), hematocrit (Ht) (r = 0.48, p < 0.001), total cholesterol (TC) (r = 0.343, p < 0.001), high density lipoprotein (HDL) (r = 0.536, p < 0.001), low density lipoprotein (LDL) (r = 0.54, p < 0.001), and triglyceride (TG) (r = 0.561, p < 0.001) and correlated negatively with white blood cell count (WBC) (r = −0.262, p = 0.029), platelet count (PLT) (r = −0.326, p = 0.006), C-reactive protein (CRP) (r = −0.61, p < 0.001), and malondialdehyde (MDA) (r = −0.924, p < 0.001). PON-1 as a marker for CD differentiation possessed a sensitivity and specificity of 93.62% and 91.30%, respectively. CD was found to be associated with the decrease in the levels of PON-1, which correlates well with activity of the disease and reflects the intensification of inflammation, as well as intensified lipid peroxidation. High sensitivity and specificity of PON-1 determines its selection as a good screening test for CD severity. MDPI 2018-10-11 /pmc/articles/PMC6222603/ /pubmed/30314292 http://dx.doi.org/10.3390/molecules23102603 Text en © 2018 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
Szczeklik, Katarzyna
Mach, Tomasz
Cibor, Dorota
Owczarek, Danuta
Sapa, Jacek
Papież, Monika
Pytko-Polończyk, Jolanta
Krzyściak, Wirginia
Correlation of Paraoxonase-1 with the Severity of Crohn’s Disease
title Correlation of Paraoxonase-1 with the Severity of Crohn’s Disease
title_full Correlation of Paraoxonase-1 with the Severity of Crohn’s Disease
title_fullStr Correlation of Paraoxonase-1 with the Severity of Crohn’s Disease
title_full_unstemmed Correlation of Paraoxonase-1 with the Severity of Crohn’s Disease
title_short Correlation of Paraoxonase-1 with the Severity of Crohn’s Disease
title_sort correlation of paraoxonase-1 with the severity of crohn’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222603/
https://www.ncbi.nlm.nih.gov/pubmed/30314292
http://dx.doi.org/10.3390/molecules23102603
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