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Iron metabolism and type 2 diabetes mellitus: A meta‐analysis and systematic review
AIMS/INTRODUCTION: Iron metabolism can directly or indirectly affect the occurrence and development of type 2 diabetes. This meta‐analysis and systematic review aimed to analyze the association between serum iron metabolism indicators and type 2 diabetes. MATERIALS AND METHODS: The databases PubMed...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378429/ https://www.ncbi.nlm.nih.gov/pubmed/31975563 http://dx.doi.org/10.1111/jdi.13216 |
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author | Liu, Jingfang Li, Qingxiu Yang, Yaxian Ma, Lihua |
author_facet | Liu, Jingfang Li, Qingxiu Yang, Yaxian Ma, Lihua |
author_sort | Liu, Jingfang |
collection | PubMed |
description | AIMS/INTRODUCTION: Iron metabolism can directly or indirectly affect the occurrence and development of type 2 diabetes. This meta‐analysis and systematic review aimed to analyze the association between serum iron metabolism indicators and type 2 diabetes. MATERIALS AND METHODS: The databases PubMed and Embase were searched for studies on the correlations between serum iron metabolism indicators (iron, ferritin, transferrin, hepcidin and soluble transferrin receptor) and type 2 diabetes since January 2006. Relevant data were extracted from the included studies, and meta‐analysis was carried out. RESULTS: A total of 12 case–control and cohort studies were analyzed. Of the 12 studies, 11 described the correlation between serum ferritin levels and type 2 diabetes. The median and high serum ferritin concentrations were significantly associated with the risks of type 2 diabetes (odds ratio [OR] 1.20, 95% confidence interval [CI] 1.08–1.33 and OR 1.43, 95% CI 1.29–1.59, respectively). However, the low concentration was not correlated with the risk of type 2 diabetes (OR 0.99, 95% CI 0.89–1.11). No significant association was observed between serum soluble transferrin receptor and type 2 diabetes, whereas the soluble transferrin receptor‐to‐ferritin ratio was significantly inversely related to the risk of type 2 diabetes in the median and high ratio subgroups (OR 0.71, 95% CI 0.51, 0.99 and OR 0.65, 95% CI 0.45–0.95). CONCLUSIONS: The elevated serum ferritin was one of the risk factors for type 2 diabetes, and soluble transferrin receptor‐to‐ferritin ratio was inversely related to the risk of type 2 diabetes. A systematic review showed that serum transferrin and hepcidin might be directly or indirectly related to the development of diabetes. |
format | Online Article Text |
id | pubmed-7378429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73784292020-07-27 Iron metabolism and type 2 diabetes mellitus: A meta‐analysis and systematic review Liu, Jingfang Li, Qingxiu Yang, Yaxian Ma, Lihua J Diabetes Investig Articles AIMS/INTRODUCTION: Iron metabolism can directly or indirectly affect the occurrence and development of type 2 diabetes. This meta‐analysis and systematic review aimed to analyze the association between serum iron metabolism indicators and type 2 diabetes. MATERIALS AND METHODS: The databases PubMed and Embase were searched for studies on the correlations between serum iron metabolism indicators (iron, ferritin, transferrin, hepcidin and soluble transferrin receptor) and type 2 diabetes since January 2006. Relevant data were extracted from the included studies, and meta‐analysis was carried out. RESULTS: A total of 12 case–control and cohort studies were analyzed. Of the 12 studies, 11 described the correlation between serum ferritin levels and type 2 diabetes. The median and high serum ferritin concentrations were significantly associated with the risks of type 2 diabetes (odds ratio [OR] 1.20, 95% confidence interval [CI] 1.08–1.33 and OR 1.43, 95% CI 1.29–1.59, respectively). However, the low concentration was not correlated with the risk of type 2 diabetes (OR 0.99, 95% CI 0.89–1.11). No significant association was observed between serum soluble transferrin receptor and type 2 diabetes, whereas the soluble transferrin receptor‐to‐ferritin ratio was significantly inversely related to the risk of type 2 diabetes in the median and high ratio subgroups (OR 0.71, 95% CI 0.51, 0.99 and OR 0.65, 95% CI 0.45–0.95). CONCLUSIONS: The elevated serum ferritin was one of the risk factors for type 2 diabetes, and soluble transferrin receptor‐to‐ferritin ratio was inversely related to the risk of type 2 diabetes. A systematic review showed that serum transferrin and hepcidin might be directly or indirectly related to the development of diabetes. John Wiley and Sons Inc. 2020-02-23 2020-07 /pmc/articles/PMC7378429/ /pubmed/31975563 http://dx.doi.org/10.1111/jdi.13216 Text en © 2020 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Articles Liu, Jingfang Li, Qingxiu Yang, Yaxian Ma, Lihua Iron metabolism and type 2 diabetes mellitus: A meta‐analysis and systematic review |
title | Iron metabolism and type 2 diabetes mellitus: A meta‐analysis and systematic review |
title_full | Iron metabolism and type 2 diabetes mellitus: A meta‐analysis and systematic review |
title_fullStr | Iron metabolism and type 2 diabetes mellitus: A meta‐analysis and systematic review |
title_full_unstemmed | Iron metabolism and type 2 diabetes mellitus: A meta‐analysis and systematic review |
title_short | Iron metabolism and type 2 diabetes mellitus: A meta‐analysis and systematic review |
title_sort | iron metabolism and type 2 diabetes mellitus: a meta‐analysis and systematic review |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378429/ https://www.ncbi.nlm.nih.gov/pubmed/31975563 http://dx.doi.org/10.1111/jdi.13216 |
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