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The Comparison of Predictive Value Among Chemerin, IL-18 and Hormonal Parameters in Assessing the Risk of Metabolic Syndrome in Men

Chemerin (CHEM) is a new proinflammatory adipokine involved in the immune, metabolic and reproductive processes. Low–grade state inflammation (LGSI) is a key element in the pathogenesis of metabolic syndrome (MS). Low SHBG is a good marker of male hypogonadism in MS. This study evaluated the prognos...

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Autores principales: Jarecki, Piotr, Herman, Waldemar A, Losy, Jacek, Lacka, Katarzyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326632/
https://www.ncbi.nlm.nih.gov/pubmed/34330167
http://dx.doi.org/10.1177/15579883211034984
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author Jarecki, Piotr
Herman, Waldemar A
Losy, Jacek
Lacka, Katarzyna
author_facet Jarecki, Piotr
Herman, Waldemar A
Losy, Jacek
Lacka, Katarzyna
author_sort Jarecki, Piotr
collection PubMed
description Chemerin (CHEM) is a new proinflammatory adipokine involved in the immune, metabolic and reproductive processes. Low–grade state inflammation (LGSI) is a key element in the pathogenesis of metabolic syndrome (MS). Low SHBG is a good marker of male hypogonadism in MS. This study evaluated the prognostic value of selected adipokine, LGSI, and androgenic parameters in predicting the risk of MS among men. One hundred thirty-two random men aged 40 to 70 years old were enrolled. Measurements of anthropometric indices, blood pressure, and laboratory tests were carried out. A total of 62 men (47%) were diagnosed with MS. Chemerin concentrations were higher in men diagnosed with MS compared to healthy: 89.48 (78.12–112.10) vs. 77.9 (65.12–98.64) ng/mL; p = .002. Men diagnosed with MS presented with lower levels of total testosterone: 5.75 (4.00–6.57) vs. 6.40 (5.50–8.40) ng/mL; p = .0014 and SHBG: 46.58 (35.13–66.28) vs. 71.97 (56.1–92.7) nM/L; p < 0.000001. Elevated LGSI indices were demonstrated in men with MS as opposed to healthy [IL–18: 530.64 (409.12–640.56) vs. 418.85 (348.14–496.44) pg/mL; p = .000033 and hs–CRP: 2.15 (0.97–4.26) vs. 1.01 (0.41–2.68) ng/mL; p = .0057)]. In multivariate regression analysis, the highest negative predictive value in assessing the risk of MS was SHBG serum concentration, while the highest positive predictive values were: IL-18, hypertriglyceridemia, and waist circumference. Decreased SHBG levels, combined with elevated IL-18 concentrations in men showing hypertriglyceridemic waist phenotype, significantly increase the risk of MS.
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spelling pubmed-83266322021-08-09 The Comparison of Predictive Value Among Chemerin, IL-18 and Hormonal Parameters in Assessing the Risk of Metabolic Syndrome in Men Jarecki, Piotr Herman, Waldemar A Losy, Jacek Lacka, Katarzyna Am J Mens Health Original Article Chemerin (CHEM) is a new proinflammatory adipokine involved in the immune, metabolic and reproductive processes. Low–grade state inflammation (LGSI) is a key element in the pathogenesis of metabolic syndrome (MS). Low SHBG is a good marker of male hypogonadism in MS. This study evaluated the prognostic value of selected adipokine, LGSI, and androgenic parameters in predicting the risk of MS among men. One hundred thirty-two random men aged 40 to 70 years old were enrolled. Measurements of anthropometric indices, blood pressure, and laboratory tests were carried out. A total of 62 men (47%) were diagnosed with MS. Chemerin concentrations were higher in men diagnosed with MS compared to healthy: 89.48 (78.12–112.10) vs. 77.9 (65.12–98.64) ng/mL; p = .002. Men diagnosed with MS presented with lower levels of total testosterone: 5.75 (4.00–6.57) vs. 6.40 (5.50–8.40) ng/mL; p = .0014 and SHBG: 46.58 (35.13–66.28) vs. 71.97 (56.1–92.7) nM/L; p < 0.000001. Elevated LGSI indices were demonstrated in men with MS as opposed to healthy [IL–18: 530.64 (409.12–640.56) vs. 418.85 (348.14–496.44) pg/mL; p = .000033 and hs–CRP: 2.15 (0.97–4.26) vs. 1.01 (0.41–2.68) ng/mL; p = .0057)]. In multivariate regression analysis, the highest negative predictive value in assessing the risk of MS was SHBG serum concentration, while the highest positive predictive values were: IL-18, hypertriglyceridemia, and waist circumference. Decreased SHBG levels, combined with elevated IL-18 concentrations in men showing hypertriglyceridemic waist phenotype, significantly increase the risk of MS. SAGE Publications 2021-07-30 /pmc/articles/PMC8326632/ /pubmed/34330167 http://dx.doi.org/10.1177/15579883211034984 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Jarecki, Piotr
Herman, Waldemar A
Losy, Jacek
Lacka, Katarzyna
The Comparison of Predictive Value Among Chemerin, IL-18 and Hormonal Parameters in Assessing the Risk of Metabolic Syndrome in Men
title The Comparison of Predictive Value Among Chemerin, IL-18 and Hormonal Parameters in Assessing the Risk of Metabolic Syndrome in Men
title_full The Comparison of Predictive Value Among Chemerin, IL-18 and Hormonal Parameters in Assessing the Risk of Metabolic Syndrome in Men
title_fullStr The Comparison of Predictive Value Among Chemerin, IL-18 and Hormonal Parameters in Assessing the Risk of Metabolic Syndrome in Men
title_full_unstemmed The Comparison of Predictive Value Among Chemerin, IL-18 and Hormonal Parameters in Assessing the Risk of Metabolic Syndrome in Men
title_short The Comparison of Predictive Value Among Chemerin, IL-18 and Hormonal Parameters in Assessing the Risk of Metabolic Syndrome in Men
title_sort comparison of predictive value among chemerin, il-18 and hormonal parameters in assessing the risk of metabolic syndrome in men
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326632/
https://www.ncbi.nlm.nih.gov/pubmed/34330167
http://dx.doi.org/10.1177/15579883211034984
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