4.5 Article

Association between iron metabolism and non-alcoholic fatty liver disease: results from the National Health and Nutrition Examination Survey (NHANES 2017-2018) and a controlled animal study

期刊

NUTRITION & METABOLISM
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12986-022-00715-y

关键词

National Health and Nutrition Examination Survey; Non-alcoholic fatty liver disease; Serum iron; Serum ferritin; Transferrin saturation; Soluble transferrin receptor; Hepcidin

资金

  1. `Double First-Class' University Project [CPU2018GF10, CPU2018GY31]

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This study explores the relationship between biomarkers of iron metabolism and non-alcoholic fatty liver disease (NAFLD) through statistical analysis and animal experiments. The results show that patients with NAFLD have decreased levels of serum iron, serum ferritin, and transferrin saturation, while soluble transferrin receptor levels are increased. The study also finds a significant correlation between lower transferrin saturation levels and a higher risk of NAFLD. Additionally, the expression of hepatic hepcidin is decreased, while ferroportin gene expression is increased in the livers of NAFLD patients and mice.
Background: Iron metabolism may be involved in the pathogenesis of the non-alcoholic fatty liver disease (NAFLD). The relationship between iron metabolism and NAFLD has not been clearly established. This study aimed to clarify the relationship between biomarkers of iron metabolism and NAFLD. Methods: Based on the National Health and Nutrition Examination Survey (NHANES), restricted cubic spline models and multivariable logistic regression were used to examine the association between iron metabolism [serum iron (SI), serum ferritin (SF), transferrin saturation (TSAT), and soluble transferrin receptor (sTfR)] and the risk for NAFLD. In addition, stratified subgroup analysis was performed for the association between TSAT and NAFLD. Moreover, serum TSAT levels were determined in male mice with NAFLD. The expression of hepcidin and ferroportin, vital regulators of iron metabolism, were analyzed in the livers of mice by quantitative real-time PCR (qRT-PCR) and patients with NAFLD by microarray collected from the GEO data repository. Results: Patients with NAFLD showed decreased SI, SF, and TSAT levels and increased STfR levels based on the NHANES. After adjusting for confounding factors, TSAT was significantly negatively correlated with NAFLD. Of note, the relationship between TSAT and NAFLD differed in the four subgroups of age, sex, race, and BMI (P for interaction < 0.05). Consistently, mice with NAFLD exhibited decreased serum TSAT levels. Decreased hepcidin and increased ferroportin gene expression were observed in the livers of patients and mice with NAFLD. Conclusion: Serum TSAT levels and hepatic hepcidin expression were decreased in both patients and mice with NAFLD. Among multiple biomarkers of iron metabolism, lower TSAT levels were significantly associated with a higher risk of NAFLD in the U.S. general population. These findings might provide new ideas for the prediction, diagnosis, and mechanistic exploration of NAFLD.

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