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Serum iron and risk of nonalcoholic fatty liver disease and advanced hepatic fibrosis in US adults
Epidemiological evidence on the relationship between serum iron and liver diseases is limited. This study aims to investigate whether serum iron is associated with nonalcoholic fatty liver disease (NAFLD) and advanced hepatic fibrosis (AHF). Cross-sectional data for adults aged ≥ 18 years who partic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128903/ https://www.ncbi.nlm.nih.gov/pubmed/34002001 http://dx.doi.org/10.1038/s41598-021-89991-x |
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author | Yang, Huan-Huan Chen, Guo-Chong Li, De-Ming Lan, Lei Chen, Li-Hua Xu, Jia-Ying Qin, Li-Qiang |
author_facet | Yang, Huan-Huan Chen, Guo-Chong Li, De-Ming Lan, Lei Chen, Li-Hua Xu, Jia-Ying Qin, Li-Qiang |
author_sort | Yang, Huan-Huan |
collection | PubMed |
description | Epidemiological evidence on the relationship between serum iron and liver diseases is limited. This study aims to investigate whether serum iron is associated with nonalcoholic fatty liver disease (NAFLD) and advanced hepatic fibrosis (AHF). Cross-sectional data for adults aged ≥ 18 years who participated in the National Health and Nutrition Examination Survey (NHANES) from 1999 to 2018 were analyzed. Odds ratio (ORs) and 95% confidence intervals (CIs) of NAFLD and AHF associated with serum iron were estimated using multivariable logistic regression models. A total of 18,031 males and 18,989 females were included in the analysis. After multivariable adjustment for potential confounders, serum iron was significantly and inversely associated with NAFLD in both genders (P-trend < 0.001) and AHF in females (P-trend = 0.018). Compared to the bottom quartile, those in higher quartiles of serum iron had no significant ORs for AHF in males, but the trend across the quartiles was significant (P-trend = 0.046). In conclusion, higher serum iron level was associated with lower risk of NAFLD in males and females, and with lower risk of AHF in females but not in males. No significant racial/ethnical differences in these associations were observed. |
format | Online Article Text |
id | pubmed-8128903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81289032021-05-19 Serum iron and risk of nonalcoholic fatty liver disease and advanced hepatic fibrosis in US adults Yang, Huan-Huan Chen, Guo-Chong Li, De-Ming Lan, Lei Chen, Li-Hua Xu, Jia-Ying Qin, Li-Qiang Sci Rep Article Epidemiological evidence on the relationship between serum iron and liver diseases is limited. This study aims to investigate whether serum iron is associated with nonalcoholic fatty liver disease (NAFLD) and advanced hepatic fibrosis (AHF). Cross-sectional data for adults aged ≥ 18 years who participated in the National Health and Nutrition Examination Survey (NHANES) from 1999 to 2018 were analyzed. Odds ratio (ORs) and 95% confidence intervals (CIs) of NAFLD and AHF associated with serum iron were estimated using multivariable logistic regression models. A total of 18,031 males and 18,989 females were included in the analysis. After multivariable adjustment for potential confounders, serum iron was significantly and inversely associated with NAFLD in both genders (P-trend < 0.001) and AHF in females (P-trend = 0.018). Compared to the bottom quartile, those in higher quartiles of serum iron had no significant ORs for AHF in males, but the trend across the quartiles was significant (P-trend = 0.046). In conclusion, higher serum iron level was associated with lower risk of NAFLD in males and females, and with lower risk of AHF in females but not in males. No significant racial/ethnical differences in these associations were observed. Nature Publishing Group UK 2021-05-17 /pmc/articles/PMC8128903/ /pubmed/34002001 http://dx.doi.org/10.1038/s41598-021-89991-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yang, Huan-Huan Chen, Guo-Chong Li, De-Ming Lan, Lei Chen, Li-Hua Xu, Jia-Ying Qin, Li-Qiang Serum iron and risk of nonalcoholic fatty liver disease and advanced hepatic fibrosis in US adults |
title | Serum iron and risk of nonalcoholic fatty liver disease and advanced hepatic fibrosis in US adults |
title_full | Serum iron and risk of nonalcoholic fatty liver disease and advanced hepatic fibrosis in US adults |
title_fullStr | Serum iron and risk of nonalcoholic fatty liver disease and advanced hepatic fibrosis in US adults |
title_full_unstemmed | Serum iron and risk of nonalcoholic fatty liver disease and advanced hepatic fibrosis in US adults |
title_short | Serum iron and risk of nonalcoholic fatty liver disease and advanced hepatic fibrosis in US adults |
title_sort | serum iron and risk of nonalcoholic fatty liver disease and advanced hepatic fibrosis in us adults |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128903/ https://www.ncbi.nlm.nih.gov/pubmed/34002001 http://dx.doi.org/10.1038/s41598-021-89991-x |
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