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Association between Serum Zinc and Calcification Propensity (T(50)) in Patients with Type 2 Diabetes Mellitus and In Vitro Effect of Exogenous Zinc on T(50)

Zinc inhibits vascular calcification in vivo and in vitro. Patients with type 2 diabetes mellitus show hypozincemia and are at an elevated risk of cardiovascular events. Recently, an in vitro test (T(50)-test) was developed for determination of serum calcification propensity and a shorter T(50) mean...

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Autores principales: Nakatani, Shinya, Mori, Katsuhito, Sonoda, Mika, Nishide, Kozo, Uedono, Hideki, Tsuda, Akihiro, Emoto, Masanori, Shoji, Tetsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555216/
https://www.ncbi.nlm.nih.gov/pubmed/32916995
http://dx.doi.org/10.3390/biomedicines8090337
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author Nakatani, Shinya
Mori, Katsuhito
Sonoda, Mika
Nishide, Kozo
Uedono, Hideki
Tsuda, Akihiro
Emoto, Masanori
Shoji, Tetsuo
author_facet Nakatani, Shinya
Mori, Katsuhito
Sonoda, Mika
Nishide, Kozo
Uedono, Hideki
Tsuda, Akihiro
Emoto, Masanori
Shoji, Tetsuo
author_sort Nakatani, Shinya
collection PubMed
description Zinc inhibits vascular calcification in vivo and in vitro. Patients with type 2 diabetes mellitus show hypozincemia and are at an elevated risk of cardiovascular events. Recently, an in vitro test (T(50)-test) was developed for determination of serum calcification propensity and a shorter T(50) means a higher calcification propensity. This cross-sectional study investigated the association between serum zinc and T(50) in 132 type 2 diabetes mellitus patients with various kidney functions. Furthermore, the effect of exogenous zinc on T(50) was also investigated in vitro using separately pooled serum samples obtained from healthy volunteers and patients with hemodialysis. We measured T(50) levels using the established nephelometric method. The median (interquartile range) levels of T(50) and serum zinc were 306 (269 to 332) min, and 80.0 (70.1 to 89.8) µg/dL, respectively. Serum zinc level showed a weak, but positive correlation with T(50) (r(s) = 0.219, p = 0.012). This association remained significant in multivariable-adjusted analysis, and was independent of known factors including phosphate, calcium, and magnesium. Kidney function and glycemic control were not significantly associated with T(50). Finally, in vitro experiments showed that addition of a physiological concentration of exogenous zinc chloride significantly increased serum T(50). Our results indicate that serum zinc is an independent factor with a potential role in suppressing calcification propensity in serum.
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spelling pubmed-75552162020-10-19 Association between Serum Zinc and Calcification Propensity (T(50)) in Patients with Type 2 Diabetes Mellitus and In Vitro Effect of Exogenous Zinc on T(50) Nakatani, Shinya Mori, Katsuhito Sonoda, Mika Nishide, Kozo Uedono, Hideki Tsuda, Akihiro Emoto, Masanori Shoji, Tetsuo Biomedicines Article Zinc inhibits vascular calcification in vivo and in vitro. Patients with type 2 diabetes mellitus show hypozincemia and are at an elevated risk of cardiovascular events. Recently, an in vitro test (T(50)-test) was developed for determination of serum calcification propensity and a shorter T(50) means a higher calcification propensity. This cross-sectional study investigated the association between serum zinc and T(50) in 132 type 2 diabetes mellitus patients with various kidney functions. Furthermore, the effect of exogenous zinc on T(50) was also investigated in vitro using separately pooled serum samples obtained from healthy volunteers and patients with hemodialysis. We measured T(50) levels using the established nephelometric method. The median (interquartile range) levels of T(50) and serum zinc were 306 (269 to 332) min, and 80.0 (70.1 to 89.8) µg/dL, respectively. Serum zinc level showed a weak, but positive correlation with T(50) (r(s) = 0.219, p = 0.012). This association remained significant in multivariable-adjusted analysis, and was independent of known factors including phosphate, calcium, and magnesium. Kidney function and glycemic control were not significantly associated with T(50). Finally, in vitro experiments showed that addition of a physiological concentration of exogenous zinc chloride significantly increased serum T(50). Our results indicate that serum zinc is an independent factor with a potential role in suppressing calcification propensity in serum. MDPI 2020-09-09 /pmc/articles/PMC7555216/ /pubmed/32916995 http://dx.doi.org/10.3390/biomedicines8090337 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nakatani, Shinya
Mori, Katsuhito
Sonoda, Mika
Nishide, Kozo
Uedono, Hideki
Tsuda, Akihiro
Emoto, Masanori
Shoji, Tetsuo
Association between Serum Zinc and Calcification Propensity (T(50)) in Patients with Type 2 Diabetes Mellitus and In Vitro Effect of Exogenous Zinc on T(50)
title Association between Serum Zinc and Calcification Propensity (T(50)) in Patients with Type 2 Diabetes Mellitus and In Vitro Effect of Exogenous Zinc on T(50)
title_full Association between Serum Zinc and Calcification Propensity (T(50)) in Patients with Type 2 Diabetes Mellitus and In Vitro Effect of Exogenous Zinc on T(50)
title_fullStr Association between Serum Zinc and Calcification Propensity (T(50)) in Patients with Type 2 Diabetes Mellitus and In Vitro Effect of Exogenous Zinc on T(50)
title_full_unstemmed Association between Serum Zinc and Calcification Propensity (T(50)) in Patients with Type 2 Diabetes Mellitus and In Vitro Effect of Exogenous Zinc on T(50)
title_short Association between Serum Zinc and Calcification Propensity (T(50)) in Patients with Type 2 Diabetes Mellitus and In Vitro Effect of Exogenous Zinc on T(50)
title_sort association between serum zinc and calcification propensity (t(50)) in patients with type 2 diabetes mellitus and in vitro effect of exogenous zinc on t(50)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555216/
https://www.ncbi.nlm.nih.gov/pubmed/32916995
http://dx.doi.org/10.3390/biomedicines8090337
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