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Are Circulating Mg(2+) Levels Associated with Glucose Tolerance Profiles and Incident Type 2 Diabetes?
Magnesium (Mg(2+)) is an enzyme co-factor that plays a key role in many biochemical reactions, as well as in glucose metabolism. Clinical evidences have demonstrated that depletion of serum Mg(2+) increases exponentially with the duration of type 2 diabetes mellitus (T2DM). Diabetes is associated wi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835462/ https://www.ncbi.nlm.nih.gov/pubmed/31615167 http://dx.doi.org/10.3390/nu11102460 |
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author | Spiga, Rosangela Mannino, Gaia Chiara Mancuso, Elettra Averta, Carolina Paone, Claudia Rubino, Mariangela Sciacqua, Angela Succurro, Elena Perticone, Francesco Andreozzi, Francesco Sesti, Giorgio |
author_facet | Spiga, Rosangela Mannino, Gaia Chiara Mancuso, Elettra Averta, Carolina Paone, Claudia Rubino, Mariangela Sciacqua, Angela Succurro, Elena Perticone, Francesco Andreozzi, Francesco Sesti, Giorgio |
author_sort | Spiga, Rosangela |
collection | PubMed |
description | Magnesium (Mg(2+)) is an enzyme co-factor that plays a key role in many biochemical reactions, as well as in glucose metabolism. Clinical evidences have demonstrated that depletion of serum Mg(2+) increases exponentially with the duration of type 2 diabetes mellitus (T2DM). Diabetes is associated with low Mg(2+), and hypomagnesemia is associated with insulin resistance, inflammation, and increased risk for cardiovascular disease. In subjects at high risk of inflammation and insulin resistance, supplementation of Mg(2+) alone ameliorates both phenotypes, slowing the development and progression of hepatic steatosis. We analyze the relationship between serum Mg(2+) levels and the onset of T2DM in a large cohort of well-characterized adult white individuals participating in the CATAMERI study, who were reexamined after a mean follow-up of 5.6 ± 0.9 years. In our analysis we acquired a significant negative correlation between Mg(2+) levels, fasting glucose, and 2h-post load glucose in subjects who underwent an OGTT. Moreover, Mg(2+) levels correlated negatively with fasting insulin levels, and positively with the lipid profile. As for the detrimental effect of lower circulating Mg(2+) levels, our data revealed a significant reduction of T2DM risk of about 20% for each 1 mg/dL increase of circulating Mg(2+). The present results are consistent with the theory that Mg(2+) supplementation could ameliorate insulin sensitivity reducing the risk to develop T2DM. |
format | Online Article Text |
id | pubmed-6835462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68354622019-11-25 Are Circulating Mg(2+) Levels Associated with Glucose Tolerance Profiles and Incident Type 2 Diabetes? Spiga, Rosangela Mannino, Gaia Chiara Mancuso, Elettra Averta, Carolina Paone, Claudia Rubino, Mariangela Sciacqua, Angela Succurro, Elena Perticone, Francesco Andreozzi, Francesco Sesti, Giorgio Nutrients Article Magnesium (Mg(2+)) is an enzyme co-factor that plays a key role in many biochemical reactions, as well as in glucose metabolism. Clinical evidences have demonstrated that depletion of serum Mg(2+) increases exponentially with the duration of type 2 diabetes mellitus (T2DM). Diabetes is associated with low Mg(2+), and hypomagnesemia is associated with insulin resistance, inflammation, and increased risk for cardiovascular disease. In subjects at high risk of inflammation and insulin resistance, supplementation of Mg(2+) alone ameliorates both phenotypes, slowing the development and progression of hepatic steatosis. We analyze the relationship between serum Mg(2+) levels and the onset of T2DM in a large cohort of well-characterized adult white individuals participating in the CATAMERI study, who were reexamined after a mean follow-up of 5.6 ± 0.9 years. In our analysis we acquired a significant negative correlation between Mg(2+) levels, fasting glucose, and 2h-post load glucose in subjects who underwent an OGTT. Moreover, Mg(2+) levels correlated negatively with fasting insulin levels, and positively with the lipid profile. As for the detrimental effect of lower circulating Mg(2+) levels, our data revealed a significant reduction of T2DM risk of about 20% for each 1 mg/dL increase of circulating Mg(2+). The present results are consistent with the theory that Mg(2+) supplementation could ameliorate insulin sensitivity reducing the risk to develop T2DM. MDPI 2019-10-14 /pmc/articles/PMC6835462/ /pubmed/31615167 http://dx.doi.org/10.3390/nu11102460 Text en © 2019 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 Spiga, Rosangela Mannino, Gaia Chiara Mancuso, Elettra Averta, Carolina Paone, Claudia Rubino, Mariangela Sciacqua, Angela Succurro, Elena Perticone, Francesco Andreozzi, Francesco Sesti, Giorgio Are Circulating Mg(2+) Levels Associated with Glucose Tolerance Profiles and Incident Type 2 Diabetes? |
title | Are Circulating Mg(2+) Levels Associated with Glucose Tolerance Profiles and Incident Type 2 Diabetes? |
title_full | Are Circulating Mg(2+) Levels Associated with Glucose Tolerance Profiles and Incident Type 2 Diabetes? |
title_fullStr | Are Circulating Mg(2+) Levels Associated with Glucose Tolerance Profiles and Incident Type 2 Diabetes? |
title_full_unstemmed | Are Circulating Mg(2+) Levels Associated with Glucose Tolerance Profiles and Incident Type 2 Diabetes? |
title_short | Are Circulating Mg(2+) Levels Associated with Glucose Tolerance Profiles and Incident Type 2 Diabetes? |
title_sort | are circulating mg(2+) levels associated with glucose tolerance profiles and incident type 2 diabetes? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835462/ https://www.ncbi.nlm.nih.gov/pubmed/31615167 http://dx.doi.org/10.3390/nu11102460 |
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