Cargando…

MON-280 Plasmatic Lipocalin-2 Levels in Chronic Low-Grade Inflammation Syndromes: Comparison Between Metabolic Syndrome, Total and Partial Growth Hormone Deficiency

Lipocalin-2 (LCN2) is a secreted glycoprotein, member of the lipocalin superfamily and mediator of several chronic inflammatory processes. Metabolic syndrome (METs) and total growth hormone deficiency (GHD) are known as chronic inflammatory conditions (1,2). While discrepant results have been found...

Descripción completa

Detalles Bibliográficos
Autores principales: Vergani, Edoardo, Currò, Diego, Comi, Simone, D’Abate, Claudia, Notari, Maria Vittoria, Bruno, Carmine, Mancini, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208896/
http://dx.doi.org/10.1210/jendso/bvaa046.523
_version_ 1783530953491087360
author Vergani, Edoardo
Currò, Diego
Comi, Simone
D’Abate, Claudia
Notari, Maria Vittoria
Bruno, Carmine
Mancini, Antonio
author_facet Vergani, Edoardo
Currò, Diego
Comi, Simone
D’Abate, Claudia
Notari, Maria Vittoria
Bruno, Carmine
Mancini, Antonio
author_sort Vergani, Edoardo
collection PubMed
description Lipocalin-2 (LCN2) is a secreted glycoprotein, member of the lipocalin superfamily and mediator of several chronic inflammatory processes. Metabolic syndrome (METs) and total growth hormone deficiency (GHD) are known as chronic inflammatory conditions (1,2). While discrepant results have been found in literature on LCN2 plasmatic levels in metabolic syndrome, no studies have been performed in GHD. Partial growth hormone deficiency (pGHD) either is associated with cardiovascular risk (3). Therefore, the primary end-point of this observational cross-sectional study was to compare LCN2 in these clinical settings, trying to assess its possible role as a biomarker in these diseases, whether the secondary end-point was to evaluate the impact of BMI and indexes of insulin sensitivity/resistance on this protein plasmatic levels. 74 patients were included in the study. They were divided as follows: Group A, METs (18 patients, 13 females and 5 males, mean±SEM age 45.1±4.11 ys, BMI 31.22±1.73 kg/m(2)); Group B, GHD (18 patients, 8 F and 10 M, mean±SEM age 52.44±2.61 ys, BMI 30.49±1.87 kg/m(2)); Group C, Partial GHD (19 patients, 13 F and 6 M, mean±SEM age 48.63±2.19 ys, BMI 29.11±1.85 kg/m(2)); Group D, Controls (19 patients, 13 F and 6 M, mean±SEM age 40.26±2.87 ys, BMI 23.25±0.95 kg/m(2)). The diagnosis of metabolic syndrome was made according to NCEP ATPIII criteria (2005 revision). GHD was diagnosed with dynamic test using Growth Hormone-Releasing Hormone (GHRH 50 μg i.v. + arginine 0,5 g/Kg), with a peak GH response between 9 and 16 μg/L when BMI was < 30 kg/m(2) or 4 and 9 μg/L when BMI was > 30 kg/m(2). Partial GHD was defined with dynamic test using GHRH, with a peak GH response < 9 μg/L when BMI was < 30 kg/m(2) or < 4 μg/L when BMI was > 30 kg/m(2).They were evaluated for: serum glucose and insulin, HOMA-index, QUICKI-index, Total/LDL/HDL cholesterol, triglycerides, IGF-1 and LCN2 (measured using ELISA kit DuoSet LCN2/NGAL, R&D systems).LCN2 plasmatic levels were significantly increased in METs, while no difference with control group was found in total and partial GHD. LCN2 levels were not influenced by BMI and HOMA-index. A significant positive correlation between LCN2 and HOMA-index was found in controls, while a trend-like, yet not significant, positive correlation was evidenced in partial GHD. No correlations between these parameters were identified in METs and GHD groups. Our data support the hypothesis that LCN2 plasmatic levels increase in metabolic syndrome. As previously shown (4), different inflammatory patterns characterize the two pathological conditions. However, the correlation between HOMA index and LCN2 suggest a possible modulatory action of LCN2 on insulin resistance in normal subjects and partial GHD ones. (1): Esser et al, Diab Res Clin Prac, 105(2):141–50, 2014.(2): Caicedo et al, Int J Mol Sci, 19(1), 2018.(3): Colao et al, JCEM, 91(6):2191–200, 2006.(4): Mancini et al, Endocrine, 59(1):130–136, 2018.
format Online
Article
Text
id pubmed-7208896
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-72088962020-05-13 MON-280 Plasmatic Lipocalin-2 Levels in Chronic Low-Grade Inflammation Syndromes: Comparison Between Metabolic Syndrome, Total and Partial Growth Hormone Deficiency Vergani, Edoardo Currò, Diego Comi, Simone D’Abate, Claudia Notari, Maria Vittoria Bruno, Carmine Mancini, Antonio J Endocr Soc Neuroendocrinology and Pituitary Lipocalin-2 (LCN2) is a secreted glycoprotein, member of the lipocalin superfamily and mediator of several chronic inflammatory processes. Metabolic syndrome (METs) and total growth hormone deficiency (GHD) are known as chronic inflammatory conditions (1,2). While discrepant results have been found in literature on LCN2 plasmatic levels in metabolic syndrome, no studies have been performed in GHD. Partial growth hormone deficiency (pGHD) either is associated with cardiovascular risk (3). Therefore, the primary end-point of this observational cross-sectional study was to compare LCN2 in these clinical settings, trying to assess its possible role as a biomarker in these diseases, whether the secondary end-point was to evaluate the impact of BMI and indexes of insulin sensitivity/resistance on this protein plasmatic levels. 74 patients were included in the study. They were divided as follows: Group A, METs (18 patients, 13 females and 5 males, mean±SEM age 45.1±4.11 ys, BMI 31.22±1.73 kg/m(2)); Group B, GHD (18 patients, 8 F and 10 M, mean±SEM age 52.44±2.61 ys, BMI 30.49±1.87 kg/m(2)); Group C, Partial GHD (19 patients, 13 F and 6 M, mean±SEM age 48.63±2.19 ys, BMI 29.11±1.85 kg/m(2)); Group D, Controls (19 patients, 13 F and 6 M, mean±SEM age 40.26±2.87 ys, BMI 23.25±0.95 kg/m(2)). The diagnosis of metabolic syndrome was made according to NCEP ATPIII criteria (2005 revision). GHD was diagnosed with dynamic test using Growth Hormone-Releasing Hormone (GHRH 50 μg i.v. + arginine 0,5 g/Kg), with a peak GH response between 9 and 16 μg/L when BMI was < 30 kg/m(2) or 4 and 9 μg/L when BMI was > 30 kg/m(2). Partial GHD was defined with dynamic test using GHRH, with a peak GH response < 9 μg/L when BMI was < 30 kg/m(2) or < 4 μg/L when BMI was > 30 kg/m(2).They were evaluated for: serum glucose and insulin, HOMA-index, QUICKI-index, Total/LDL/HDL cholesterol, triglycerides, IGF-1 and LCN2 (measured using ELISA kit DuoSet LCN2/NGAL, R&D systems).LCN2 plasmatic levels were significantly increased in METs, while no difference with control group was found in total and partial GHD. LCN2 levels were not influenced by BMI and HOMA-index. A significant positive correlation between LCN2 and HOMA-index was found in controls, while a trend-like, yet not significant, positive correlation was evidenced in partial GHD. No correlations between these parameters were identified in METs and GHD groups. Our data support the hypothesis that LCN2 plasmatic levels increase in metabolic syndrome. As previously shown (4), different inflammatory patterns characterize the two pathological conditions. However, the correlation between HOMA index and LCN2 suggest a possible modulatory action of LCN2 on insulin resistance in normal subjects and partial GHD ones. (1): Esser et al, Diab Res Clin Prac, 105(2):141–50, 2014.(2): Caicedo et al, Int J Mol Sci, 19(1), 2018.(3): Colao et al, JCEM, 91(6):2191–200, 2006.(4): Mancini et al, Endocrine, 59(1):130–136, 2018. Oxford University Press 2020-05-08 /pmc/articles/PMC7208896/ http://dx.doi.org/10.1210/jendso/bvaa046.523 Text en © Endocrine Society 2020. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Neuroendocrinology and Pituitary
Vergani, Edoardo
Currò, Diego
Comi, Simone
D’Abate, Claudia
Notari, Maria Vittoria
Bruno, Carmine
Mancini, Antonio
MON-280 Plasmatic Lipocalin-2 Levels in Chronic Low-Grade Inflammation Syndromes: Comparison Between Metabolic Syndrome, Total and Partial Growth Hormone Deficiency
title MON-280 Plasmatic Lipocalin-2 Levels in Chronic Low-Grade Inflammation Syndromes: Comparison Between Metabolic Syndrome, Total and Partial Growth Hormone Deficiency
title_full MON-280 Plasmatic Lipocalin-2 Levels in Chronic Low-Grade Inflammation Syndromes: Comparison Between Metabolic Syndrome, Total and Partial Growth Hormone Deficiency
title_fullStr MON-280 Plasmatic Lipocalin-2 Levels in Chronic Low-Grade Inflammation Syndromes: Comparison Between Metabolic Syndrome, Total and Partial Growth Hormone Deficiency
title_full_unstemmed MON-280 Plasmatic Lipocalin-2 Levels in Chronic Low-Grade Inflammation Syndromes: Comparison Between Metabolic Syndrome, Total and Partial Growth Hormone Deficiency
title_short MON-280 Plasmatic Lipocalin-2 Levels in Chronic Low-Grade Inflammation Syndromes: Comparison Between Metabolic Syndrome, Total and Partial Growth Hormone Deficiency
title_sort mon-280 plasmatic lipocalin-2 levels in chronic low-grade inflammation syndromes: comparison between metabolic syndrome, total and partial growth hormone deficiency
topic Neuroendocrinology and Pituitary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208896/
http://dx.doi.org/10.1210/jendso/bvaa046.523
work_keys_str_mv AT verganiedoardo mon280plasmaticlipocalin2levelsinchroniclowgradeinflammationsyndromescomparisonbetweenmetabolicsyndrometotalandpartialgrowthhormonedeficiency
AT currodiego mon280plasmaticlipocalin2levelsinchroniclowgradeinflammationsyndromescomparisonbetweenmetabolicsyndrometotalandpartialgrowthhormonedeficiency
AT comisimone mon280plasmaticlipocalin2levelsinchroniclowgradeinflammationsyndromescomparisonbetweenmetabolicsyndrometotalandpartialgrowthhormonedeficiency
AT dabateclaudia mon280plasmaticlipocalin2levelsinchroniclowgradeinflammationsyndromescomparisonbetweenmetabolicsyndrometotalandpartialgrowthhormonedeficiency
AT notarimariavittoria mon280plasmaticlipocalin2levelsinchroniclowgradeinflammationsyndromescomparisonbetweenmetabolicsyndrometotalandpartialgrowthhormonedeficiency
AT brunocarmine mon280plasmaticlipocalin2levelsinchroniclowgradeinflammationsyndromescomparisonbetweenmetabolicsyndrometotalandpartialgrowthhormonedeficiency
AT manciniantonio mon280plasmaticlipocalin2levelsinchroniclowgradeinflammationsyndromescomparisonbetweenmetabolicsyndrometotalandpartialgrowthhormonedeficiency