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Association between Circulating Levels of 25-Hydroxyvitamin D(3) and Matrix Metalloproteinase-10 (MMP-10) in Patients with Type 2 Diabetes

Background: Matrix metalloproteinase-10 (MMP-10) levels increase progressively starting from early diabetic kidney disease (DKD) stages. Vitamin D(3) (vitD(3)) deficit is associated with a higher risk of diabetic microangiopathy. Reduced MMP-10 expression has been observed after exposure to vitD(3)....

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Autores principales: Abasheva, Daria, Dolcet-Negre, Marta M., Fernández-Seara, María A., Mora-Gutiérrez, José María, Orbe, Josune, Escalada, Francisco Javier, Garcia-Fernandez, Nuria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458174/
https://www.ncbi.nlm.nih.gov/pubmed/36079742
http://dx.doi.org/10.3390/nu14173484
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author Abasheva, Daria
Dolcet-Negre, Marta M.
Fernández-Seara, María A.
Mora-Gutiérrez, José María
Orbe, Josune
Escalada, Francisco Javier
Garcia-Fernandez, Nuria
author_facet Abasheva, Daria
Dolcet-Negre, Marta M.
Fernández-Seara, María A.
Mora-Gutiérrez, José María
Orbe, Josune
Escalada, Francisco Javier
Garcia-Fernandez, Nuria
author_sort Abasheva, Daria
collection PubMed
description Background: Matrix metalloproteinase-10 (MMP-10) levels increase progressively starting from early diabetic kidney disease (DKD) stages. Vitamin D(3) (vitD(3)) deficit is associated with a higher risk of diabetic microangiopathy. Reduced MMP-10 expression has been observed after exposure to vitD(3). Aim: to assess how vitD(3) status is related to MMP-10 levels in patients with Type 2 diabetes (T2D). Methods: 256 patients with T2D were included in this cross-sectional study. Demographic, clinical and serum MMP-10 and 25-hydroxyvitamin D(3) (25(OH)D(3)) levels were collected from each patient. The association between MMP-10 and (25(OH)D(3)) levels was assessed using a correlation analysis and fitting a multivariate linear regression model. Results: Serum MMP-10 levels were inversely correlated with circulating 25(OH)D(3) (rho = −0.25; p < 0.001). In the subgroup analysis this correlation was significant in patients with DKD (rho = −0.28; p = 0.001) and in subjects with vitD(3) deficit (rho = −0.24; p = 0.005). In the regression model adjusted for kidney function, body adiposity, smoking and vitD supplementation MMP-10 levels were 68.7 pg/mL lower in patients with 25(OH)D(3) > 20 ng/mL, with respect to ≤20 ng/mL (p = 0.006). Conclusions: vitD(3) repletion status is an independent predictor of MMP-10 levels in T2D patients. Perhaps, high 25(OH)D(3) values should be targeted in these patients in order to prevent vascular complications.
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spelling pubmed-94581742022-09-09 Association between Circulating Levels of 25-Hydroxyvitamin D(3) and Matrix Metalloproteinase-10 (MMP-10) in Patients with Type 2 Diabetes Abasheva, Daria Dolcet-Negre, Marta M. Fernández-Seara, María A. Mora-Gutiérrez, José María Orbe, Josune Escalada, Francisco Javier Garcia-Fernandez, Nuria Nutrients Article Background: Matrix metalloproteinase-10 (MMP-10) levels increase progressively starting from early diabetic kidney disease (DKD) stages. Vitamin D(3) (vitD(3)) deficit is associated with a higher risk of diabetic microangiopathy. Reduced MMP-10 expression has been observed after exposure to vitD(3). Aim: to assess how vitD(3) status is related to MMP-10 levels in patients with Type 2 diabetes (T2D). Methods: 256 patients with T2D were included in this cross-sectional study. Demographic, clinical and serum MMP-10 and 25-hydroxyvitamin D(3) (25(OH)D(3)) levels were collected from each patient. The association between MMP-10 and (25(OH)D(3)) levels was assessed using a correlation analysis and fitting a multivariate linear regression model. Results: Serum MMP-10 levels were inversely correlated with circulating 25(OH)D(3) (rho = −0.25; p < 0.001). In the subgroup analysis this correlation was significant in patients with DKD (rho = −0.28; p = 0.001) and in subjects with vitD(3) deficit (rho = −0.24; p = 0.005). In the regression model adjusted for kidney function, body adiposity, smoking and vitD supplementation MMP-10 levels were 68.7 pg/mL lower in patients with 25(OH)D(3) > 20 ng/mL, with respect to ≤20 ng/mL (p = 0.006). Conclusions: vitD(3) repletion status is an independent predictor of MMP-10 levels in T2D patients. Perhaps, high 25(OH)D(3) values should be targeted in these patients in order to prevent vascular complications. MDPI 2022-08-24 /pmc/articles/PMC9458174/ /pubmed/36079742 http://dx.doi.org/10.3390/nu14173484 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Abasheva, Daria
Dolcet-Negre, Marta M.
Fernández-Seara, María A.
Mora-Gutiérrez, José María
Orbe, Josune
Escalada, Francisco Javier
Garcia-Fernandez, Nuria
Association between Circulating Levels of 25-Hydroxyvitamin D(3) and Matrix Metalloproteinase-10 (MMP-10) in Patients with Type 2 Diabetes
title Association between Circulating Levels of 25-Hydroxyvitamin D(3) and Matrix Metalloproteinase-10 (MMP-10) in Patients with Type 2 Diabetes
title_full Association between Circulating Levels of 25-Hydroxyvitamin D(3) and Matrix Metalloproteinase-10 (MMP-10) in Patients with Type 2 Diabetes
title_fullStr Association between Circulating Levels of 25-Hydroxyvitamin D(3) and Matrix Metalloproteinase-10 (MMP-10) in Patients with Type 2 Diabetes
title_full_unstemmed Association between Circulating Levels of 25-Hydroxyvitamin D(3) and Matrix Metalloproteinase-10 (MMP-10) in Patients with Type 2 Diabetes
title_short Association between Circulating Levels of 25-Hydroxyvitamin D(3) and Matrix Metalloproteinase-10 (MMP-10) in Patients with Type 2 Diabetes
title_sort association between circulating levels of 25-hydroxyvitamin d(3) and matrix metalloproteinase-10 (mmp-10) in patients with type 2 diabetes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458174/
https://www.ncbi.nlm.nih.gov/pubmed/36079742
http://dx.doi.org/10.3390/nu14173484
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