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Journal article

Iron, glucose and fat metabolism and obesity: an intertwined relationship

Abstract:
Introduction: Hereditary hemochromatosis is the most common genetic disorder in Northern Europe. It involves an overload of iron in the tissues due to a deficiency of the protein hepcidin. 85-90% of cases are associated with homozygous mutations of the C282Y gene in the HFE gene. Symptoms are nonspecific and include cardiac disorders, liver cirrhosis, hepatocellular carcinoma, diabetes, hypogonadism and sexual dysfunction, and arthritis. The diagnosis of the disease is based on demonstrating elevated serum ferritin levels and transferrin saturation, as well as identifying the mutation responsible for hereditary hemochromatosis. Early diagnosis is crucial in preventing permanent organ complications. Treatment methods include phlebotomy, therapeutic erythrocytophoresis, and the use of iron chelating drugs. Early detected and properly treated hemochromatosis allows for a lifespan comparable to the general population. Aim:  The purpose of this article is to provide a comprehensive summary of the etiology, symptoms, diagnosis and treatment of hereditary hemochromatosis with an emphasis on the importance of early detection and treatment of the disease. Review methods:  A thorough analysis of several dozen research studies from recent years on hereditary hemochromatosis and its complications was conducted. Studies available in PUBMED were reviewed, the following keywords were used to search for sources: hemochromatosis; iron; hepcidin; phlebotomy; deferoxamine; therapeutic erythrocytapheresis. Conclusion:  Hereditary hemochromatosis is a disease that in most patients runs a covert course. If unrecognized and untreated, it carries many life-threatening complications
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41366-023-01299-0

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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-7040-1932
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-4085-1083
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-8503-6103
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-2751-1770


Publisher:
Springer Nature [academic journals on nature.com]
Journal:
International Journal of Obesity More from this journal
Volume:
47
Issue:
7
Pages:
554-563
Publication date:
2023-04-07
DOI:
EISSN:
1476-5497
ISSN:
0307-0565


Language:
English
Keywords:
Pubs id:
1337553
Local pid:
pubs:1337553
Source identifiers:
W4362700288
Deposit date:
2026-05-07
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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