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Serum sphingolipid level in psoriatic patients with obesity

INTRODUCTION: Psoriasis is a chronic inflammatory disease associated with metabolic syndrome, including obesity. Ceramides (CER) and sphingosine-1-phosphate (S1P), which belongs to sphingolipids, have both biological and structural functions in the human epidermis. AIM: To evaluate serum concentrati...

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Autores principales: Kozłowska, Dorota, Harasim-Symbor, Ewa, Myśliwiec, Hanna, Milewska, Anna J., Chabowski, Adrian, Flisiak, Iwona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986291/
https://www.ncbi.nlm.nih.gov/pubmed/31998000
http://dx.doi.org/10.5114/ada.2019.91422
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author Kozłowska, Dorota
Harasim-Symbor, Ewa
Myśliwiec, Hanna
Milewska, Anna J.
Chabowski, Adrian
Flisiak, Iwona
author_facet Kozłowska, Dorota
Harasim-Symbor, Ewa
Myśliwiec, Hanna
Milewska, Anna J.
Chabowski, Adrian
Flisiak, Iwona
author_sort Kozłowska, Dorota
collection PubMed
description INTRODUCTION: Psoriasis is a chronic inflammatory disease associated with metabolic syndrome, including obesity. Ceramides (CER) and sphingosine-1-phosphate (S1P), which belongs to sphingolipids, have both biological and structural functions in the human epidermis. AIM: To evaluate serum concentrations of selected CER in psoriatic patients in different weight ranges, the impact of obesity on the concentration of circulating CERs, their association with the course of psoriasis and selected inflammatory markers. MATERIAL AND METHODS: Eigthy-five patients with active plaque-type psoriasis and 32 healthy controls were enrolled in the study. Patients were divided into 3 groups: normal weight, overweight and obese. Serum concentrations of 14 ceramides were measured by gas-liquid chromatography. The results were correlated with the Psoriasis Area and Severity Index (PASI), serum lipid profile and inflammatory markers. RESULTS: There were no significant differences in total serum CER concentration between psoriatic groups of patients. The S1P concentration was higher in psoriatic patients with normal body weight and overweight than in the control group (p = 0.002 and p = 0.04, respectively). In psoriatic patients with normal body weight, nervonic ceramide (C24:1) correlated with PASI (r = 0.38; p = 0.042) and CRP (C-reactive protein) (r = 0.42; p = 0.023). In overweight patients, the concentration of lignoceric ceramide (C24:0) correlated inversely with the severity of the disease (r = –0.41; p = 0.022) and CRP (r = –0.6; p = 0.0004). CONCLUSIONS: We have demonstrated an abnormal sphingolipid profile in psoriatic patients in different weight groups. Selected CER might be the biomarkers of psoriasis severity and inflammation, may reflect lipid disturbances and contribute to the development of metabolic syndrome.
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spelling pubmed-69862912020-01-29 Serum sphingolipid level in psoriatic patients with obesity Kozłowska, Dorota Harasim-Symbor, Ewa Myśliwiec, Hanna Milewska, Anna J. Chabowski, Adrian Flisiak, Iwona Postepy Dermatol Alergol Original Paper INTRODUCTION: Psoriasis is a chronic inflammatory disease associated with metabolic syndrome, including obesity. Ceramides (CER) and sphingosine-1-phosphate (S1P), which belongs to sphingolipids, have both biological and structural functions in the human epidermis. AIM: To evaluate serum concentrations of selected CER in psoriatic patients in different weight ranges, the impact of obesity on the concentration of circulating CERs, their association with the course of psoriasis and selected inflammatory markers. MATERIAL AND METHODS: Eigthy-five patients with active plaque-type psoriasis and 32 healthy controls were enrolled in the study. Patients were divided into 3 groups: normal weight, overweight and obese. Serum concentrations of 14 ceramides were measured by gas-liquid chromatography. The results were correlated with the Psoriasis Area and Severity Index (PASI), serum lipid profile and inflammatory markers. RESULTS: There were no significant differences in total serum CER concentration between psoriatic groups of patients. The S1P concentration was higher in psoriatic patients with normal body weight and overweight than in the control group (p = 0.002 and p = 0.04, respectively). In psoriatic patients with normal body weight, nervonic ceramide (C24:1) correlated with PASI (r = 0.38; p = 0.042) and CRP (C-reactive protein) (r = 0.42; p = 0.023). In overweight patients, the concentration of lignoceric ceramide (C24:0) correlated inversely with the severity of the disease (r = –0.41; p = 0.022) and CRP (r = –0.6; p = 0.0004). CONCLUSIONS: We have demonstrated an abnormal sphingolipid profile in psoriatic patients in different weight groups. Selected CER might be the biomarkers of psoriasis severity and inflammation, may reflect lipid disturbances and contribute to the development of metabolic syndrome. Termedia Publishing House 2019-12-30 2019-12 /pmc/articles/PMC6986291/ /pubmed/31998000 http://dx.doi.org/10.5114/ada.2019.91422 Text en Copyright © 2019 Termedia 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 (http://creativecommons.org/licenses/by-nc-sa/4.0/)
spellingShingle Original Paper
Kozłowska, Dorota
Harasim-Symbor, Ewa
Myśliwiec, Hanna
Milewska, Anna J.
Chabowski, Adrian
Flisiak, Iwona
Serum sphingolipid level in psoriatic patients with obesity
title Serum sphingolipid level in psoriatic patients with obesity
title_full Serum sphingolipid level in psoriatic patients with obesity
title_fullStr Serum sphingolipid level in psoriatic patients with obesity
title_full_unstemmed Serum sphingolipid level in psoriatic patients with obesity
title_short Serum sphingolipid level in psoriatic patients with obesity
title_sort serum sphingolipid level in psoriatic patients with obesity
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986291/
https://www.ncbi.nlm.nih.gov/pubmed/31998000
http://dx.doi.org/10.5114/ada.2019.91422
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