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Iron Deficiency Caused by Intestinal Iron Loss—Novel Candidate Genes for Severe Anemia
The adult human body contains about 4 g of iron. About 1–2 mg of iron is absorbed every day, and in healthy individuals, the same amount is excreted. We describe a patient who presents with severe iron deficiency anemia with hemoglobin levels below 6 g/dL and ferritin levels below 30 ng/mL. Although...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8700796/ https://www.ncbi.nlm.nih.gov/pubmed/34946818 http://dx.doi.org/10.3390/genes12121869 |
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author | Huettmann, Carolina Stelljes, Matthias Sivalingam, Sugirthan Fobker, Manfred Vrachimis, Alexis Exler, Anne Wenning, Christian Wempe, Carola Penke, Matthias Buness, Andreas Ludwig, Kerstin U. Muckenthaler, Martina U. Steinbicker, Andrea U. |
author_facet | Huettmann, Carolina Stelljes, Matthias Sivalingam, Sugirthan Fobker, Manfred Vrachimis, Alexis Exler, Anne Wenning, Christian Wempe, Carola Penke, Matthias Buness, Andreas Ludwig, Kerstin U. Muckenthaler, Martina U. Steinbicker, Andrea U. |
author_sort | Huettmann, Carolina |
collection | PubMed |
description | The adult human body contains about 4 g of iron. About 1–2 mg of iron is absorbed every day, and in healthy individuals, the same amount is excreted. We describe a patient who presents with severe iron deficiency anemia with hemoglobin levels below 6 g/dL and ferritin levels below 30 ng/mL. Although red blood cell concentrates and intravenous iron have been substituted every month for years, body iron stores remain depleted. Diagnostics have included several esophago-gastro-duodenoscopies, colonoscopies, MRI of the liver, repetitive bone marrow biopsies, psychological analysis, application of radioactive iron to determine intact erythropoiesis, and measurement of iron excretion in urine and feces. Typically, gastrointestinal bleeding is a major cause of iron loss. Surprisingly, intestinal iron excretion in stool in the patient was repetitively increased, without gastrointestinal bleeding. Furthermore, whole exome sequencing was performed in the patient and additional family members to identify potential causative genetic variants that may cause intestinal iron loss. Under different inheritance models, several rare mutations were identified, two of which (in CISD1 and KRI1) are likely to be functionally relevant. Intestinal iron loss in the current form has not yet been described and is, with high probability, the cause of the severe iron deficiency anemia in this patient. |
format | Online Article Text |
id | pubmed-8700796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87007962021-12-24 Iron Deficiency Caused by Intestinal Iron Loss—Novel Candidate Genes for Severe Anemia Huettmann, Carolina Stelljes, Matthias Sivalingam, Sugirthan Fobker, Manfred Vrachimis, Alexis Exler, Anne Wenning, Christian Wempe, Carola Penke, Matthias Buness, Andreas Ludwig, Kerstin U. Muckenthaler, Martina U. Steinbicker, Andrea U. Genes (Basel) Article The adult human body contains about 4 g of iron. About 1–2 mg of iron is absorbed every day, and in healthy individuals, the same amount is excreted. We describe a patient who presents with severe iron deficiency anemia with hemoglobin levels below 6 g/dL and ferritin levels below 30 ng/mL. Although red blood cell concentrates and intravenous iron have been substituted every month for years, body iron stores remain depleted. Diagnostics have included several esophago-gastro-duodenoscopies, colonoscopies, MRI of the liver, repetitive bone marrow biopsies, psychological analysis, application of radioactive iron to determine intact erythropoiesis, and measurement of iron excretion in urine and feces. Typically, gastrointestinal bleeding is a major cause of iron loss. Surprisingly, intestinal iron excretion in stool in the patient was repetitively increased, without gastrointestinal bleeding. Furthermore, whole exome sequencing was performed in the patient and additional family members to identify potential causative genetic variants that may cause intestinal iron loss. Under different inheritance models, several rare mutations were identified, two of which (in CISD1 and KRI1) are likely to be functionally relevant. Intestinal iron loss in the current form has not yet been described and is, with high probability, the cause of the severe iron deficiency anemia in this patient. MDPI 2021-11-24 /pmc/articles/PMC8700796/ /pubmed/34946818 http://dx.doi.org/10.3390/genes12121869 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Huettmann, Carolina Stelljes, Matthias Sivalingam, Sugirthan Fobker, Manfred Vrachimis, Alexis Exler, Anne Wenning, Christian Wempe, Carola Penke, Matthias Buness, Andreas Ludwig, Kerstin U. Muckenthaler, Martina U. Steinbicker, Andrea U. Iron Deficiency Caused by Intestinal Iron Loss—Novel Candidate Genes for Severe Anemia |
title | Iron Deficiency Caused by Intestinal Iron Loss—Novel Candidate Genes for Severe Anemia |
title_full | Iron Deficiency Caused by Intestinal Iron Loss—Novel Candidate Genes for Severe Anemia |
title_fullStr | Iron Deficiency Caused by Intestinal Iron Loss—Novel Candidate Genes for Severe Anemia |
title_full_unstemmed | Iron Deficiency Caused by Intestinal Iron Loss—Novel Candidate Genes for Severe Anemia |
title_short | Iron Deficiency Caused by Intestinal Iron Loss—Novel Candidate Genes for Severe Anemia |
title_sort | iron deficiency caused by intestinal iron loss—novel candidate genes for severe anemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8700796/ https://www.ncbi.nlm.nih.gov/pubmed/34946818 http://dx.doi.org/10.3390/genes12121869 |
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