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Iron-Induced Liver Injury: A Critical Reappraisal
Steven A Bloomer1, Kyle E Brown2,3,4
1Division of Science and Engineering, Penn State University, Abington College, Abington, PA 19001, USA. sab320@psu.edu.
Insights
Iron overload is less harmful to the liver than commonly believed, rarely causing severe damage or significant fibrosis in humans. Its role in liver disease progression may be overstated and often requires inflammation to cause injury.
Area of Science:
- Hepatology
- Toxicology
- Biochemistry
Background:
- Iron plays a role in various human liver diseases, including hereditary hemochromatosis.
- Iron is suspected to contribute to the progression of chronic liver conditions like hepatitis C and nonalcoholic fatty liver disease.
Purpose of the Study:
- To review and evaluate the evidence regarding iron's hepatotoxicity.
- To critically assess the role of iron overload in the pathogenesis of liver diseases.
Main Methods:
- Analysis of data from cell culture experiments.
- Review of findings from animal models.
- Examination of results from clinical studies.
Main Results:
- Iron overload demonstrates weak fibrogenic potential in animal models.
- Serious liver damage in humans due to iron overload is uncommon.
- Hepatocyte necrosis, driven by inflammation, is a key factor in iron-induced liver fibrogenesis.
Conclusions:
- The concept of iron overload as a major cause of hepatotoxicity is questionable.
- Iron's direct causal role in liver injury, in both animal models and human disease, warrants careful evaluation.
- Inflammation may potentiate iron's pathogenicity in liver damage.
Abstract:
Iron is implicated in the pathogenesis of a number of human liver diseases. Hereditary hemochromatosis is the classical example of a liver disease caused by iron, but iron is commonly believed to contribute to the progression of other forms of chronic liver disease such as hepatitis C infection and nonalcoholic fatty liver disease. In this review, we present data from cell culture experiments, animal models, and clinical studies that address the hepatotoxicity of iron. These data demonstrate that iron overload is only weakly fibrogenic in animal models and rarely causes serious liver damage in humans, calling into question the concept that iron overload is an important cause of hepatotoxicity. In situations where iron is pathogenic, iron-induced liver damage may be potentiated by coexisting inflammation, with the resulting hepatocyte necrosis an important factor driving the fibrogenic response. Based on the foregoing evidence that iron is less hepatotoxic than is generally assumed, claims that assign a causal role to iron in liver injury in either animal models or human liver disease should be carefully evaluated.
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