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Relationship between the IL-1β serum concentration, mRNA levels and rs16944 genotype in the hyperglycemic normalization of T2D patients

To evaluate Interleukin 1-beta (IL-1β) serum and mononuclear leucocyte mRNA levels, also rs16944 (−511C/T) genotype, in relation to hyperglycemic normalization in Type 2 diabetes (T2D) patients, we recruited 30 individuals recently T2D diagnosed with hyperglycemia studied at basal time and after 6 a...

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Autores principales: Iglesias Molli, Andrea Elena, Bergonzi, María Fernanda, Spalvieri, Mónica Paula, Linari, María Amelia, Frechtel, Gustavo Daniel, Cerrone, Gloria Edith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7305205/
https://www.ncbi.nlm.nih.gov/pubmed/32561825
http://dx.doi.org/10.1038/s41598-020-66751-x
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author Iglesias Molli, Andrea Elena
Bergonzi, María Fernanda
Spalvieri, Mónica Paula
Linari, María Amelia
Frechtel, Gustavo Daniel
Cerrone, Gloria Edith
author_facet Iglesias Molli, Andrea Elena
Bergonzi, María Fernanda
Spalvieri, Mónica Paula
Linari, María Amelia
Frechtel, Gustavo Daniel
Cerrone, Gloria Edith
author_sort Iglesias Molli, Andrea Elena
collection PubMed
description To evaluate Interleukin 1-beta (IL-1β) serum and mononuclear leucocyte mRNA levels, also rs16944 (−511C/T) genotype, in relation to hyperglycemic normalization in Type 2 diabetes (T2D) patients, we recruited 30 individuals recently T2D diagnosed with hyperglycemia studied at basal time and after 6 and 12 months of the normalization treatment. At basal time, the T polymorphic allele of the rs16944 was associated with lower IL-1β mRNA expression (p = 0.006); and higher glucose level was positive correlated to IL-1β protein levels (p = 0.015). After treatment, the individuals showed a significant decrease in glucose level (p = 0.003), but they did not express significant changes in the IL-1β serum levels. Surprisingly, we observed that the greater decreases in glucose level were associated to increased IL-1β serum levels (p = 0.040). This is the first follow-up study evaluating IL-1β mRNA expression and serum levels in hyperglycemic T2D individuals and after glycemic normalization treatment. The current results contribute to the knowledge of the relationship between inflammation and glucose metabolism in T2D.
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spelling pubmed-73052052020-06-23 Relationship between the IL-1β serum concentration, mRNA levels and rs16944 genotype in the hyperglycemic normalization of T2D patients Iglesias Molli, Andrea Elena Bergonzi, María Fernanda Spalvieri, Mónica Paula Linari, María Amelia Frechtel, Gustavo Daniel Cerrone, Gloria Edith Sci Rep Article To evaluate Interleukin 1-beta (IL-1β) serum and mononuclear leucocyte mRNA levels, also rs16944 (−511C/T) genotype, in relation to hyperglycemic normalization in Type 2 diabetes (T2D) patients, we recruited 30 individuals recently T2D diagnosed with hyperglycemia studied at basal time and after 6 and 12 months of the normalization treatment. At basal time, the T polymorphic allele of the rs16944 was associated with lower IL-1β mRNA expression (p = 0.006); and higher glucose level was positive correlated to IL-1β protein levels (p = 0.015). After treatment, the individuals showed a significant decrease in glucose level (p = 0.003), but they did not express significant changes in the IL-1β serum levels. Surprisingly, we observed that the greater decreases in glucose level were associated to increased IL-1β serum levels (p = 0.040). This is the first follow-up study evaluating IL-1β mRNA expression and serum levels in hyperglycemic T2D individuals and after glycemic normalization treatment. The current results contribute to the knowledge of the relationship between inflammation and glucose metabolism in T2D. Nature Publishing Group UK 2020-06-19 /pmc/articles/PMC7305205/ /pubmed/32561825 http://dx.doi.org/10.1038/s41598-020-66751-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Iglesias Molli, Andrea Elena
Bergonzi, María Fernanda
Spalvieri, Mónica Paula
Linari, María Amelia
Frechtel, Gustavo Daniel
Cerrone, Gloria Edith
Relationship between the IL-1β serum concentration, mRNA levels and rs16944 genotype in the hyperglycemic normalization of T2D patients
title Relationship between the IL-1β serum concentration, mRNA levels and rs16944 genotype in the hyperglycemic normalization of T2D patients
title_full Relationship between the IL-1β serum concentration, mRNA levels and rs16944 genotype in the hyperglycemic normalization of T2D patients
title_fullStr Relationship between the IL-1β serum concentration, mRNA levels and rs16944 genotype in the hyperglycemic normalization of T2D patients
title_full_unstemmed Relationship between the IL-1β serum concentration, mRNA levels and rs16944 genotype in the hyperglycemic normalization of T2D patients
title_short Relationship between the IL-1β serum concentration, mRNA levels and rs16944 genotype in the hyperglycemic normalization of T2D patients
title_sort relationship between the il-1β serum concentration, mrna levels and rs16944 genotype in the hyperglycemic normalization of t2d patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7305205/
https://www.ncbi.nlm.nih.gov/pubmed/32561825
http://dx.doi.org/10.1038/s41598-020-66751-x
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