Cargando…

How to diagnose iron deficiency in chronic disease: A review of current methods and potential marker for the outcome

Iron deficiency (ID) is the most common nutritional disorder worldwide. It is often observed in patients with chronic diseases, such as heart failure (HF), chronic kidney disease (CKD), inflammatory bowel disease (IBD) and cancer. ID is associated with poor clinical outcome, including poor performan...

Descripción completa

Detalles Bibliográficos
Autores principales: Rohr, Martina, Brandenburg, Vincent, Brunner-La Rocca, Hans-Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827648/
https://www.ncbi.nlm.nih.gov/pubmed/36617559
http://dx.doi.org/10.1186/s40001-022-00922-6
_version_ 1784867093010710528
author Rohr, Martina
Brandenburg, Vincent
Brunner-La Rocca, Hans-Peter
author_facet Rohr, Martina
Brandenburg, Vincent
Brunner-La Rocca, Hans-Peter
author_sort Rohr, Martina
collection PubMed
description Iron deficiency (ID) is the most common nutritional disorder worldwide. It is often observed in patients with chronic diseases, such as heart failure (HF), chronic kidney disease (CKD), inflammatory bowel disease (IBD) and cancer. ID is associated with poor clinical outcome, including poor performance, reduced quality of life, as well as increased hospitalization and mortality. The aim of this review is to provide an overview about the role of ID in chronic diseases (HF, CKD, IBD, cancer) regarding their current definitions and clinical relevance; diagnostic accuracy of iron parameters in chronic inflammatory conditions and its potential as prognostic markers. Due to different definitions and guideline recommendations of ID, various laboratory parameters for ID diagnostic exist and there is no general consensus about the definition of ID and its treatment. Still, a general trend can be observed across all investigated indications of this review (HF, CKD, IBD, cancer) that serum ferritin and transferrin saturation (TSAT) are the two parameters mentioned most often and emphasized in all guidelines to define ID and guide treatment. The most commonly used threshold values for the diagnosis of ID are TSAT of < 20% and serum ferritin of < 100–300 µg/L. Noteworthy, both TSAT and particularly ferritin are frequently applied, but both may vary due to inflammatory conditions. Studies showed that TSAT is less affected by inflammatory processes and may therefore be more accurate and reliable than serum ferritin, particularly in conditions with elevated inflammatory state. A low iron status and particularly a low TSAT value was associated with a poor outcome in all investigated indications, with the strongest evidence in HF patients. Routine surveillance of iron status in these groups of patients with chronic conditions is advisable to detect ID early. Depending on the inflammatory state, TSAT < 20% may be the more accurate diagnostic marker of ID than ferritin. Moreover, TSAT may also be the more reliable estimate for the prognosis, particularly in HF.
format Online
Article
Text
id pubmed-9827648
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-98276482023-01-10 How to diagnose iron deficiency in chronic disease: A review of current methods and potential marker for the outcome Rohr, Martina Brandenburg, Vincent Brunner-La Rocca, Hans-Peter Eur J Med Res Review Iron deficiency (ID) is the most common nutritional disorder worldwide. It is often observed in patients with chronic diseases, such as heart failure (HF), chronic kidney disease (CKD), inflammatory bowel disease (IBD) and cancer. ID is associated with poor clinical outcome, including poor performance, reduced quality of life, as well as increased hospitalization and mortality. The aim of this review is to provide an overview about the role of ID in chronic diseases (HF, CKD, IBD, cancer) regarding their current definitions and clinical relevance; diagnostic accuracy of iron parameters in chronic inflammatory conditions and its potential as prognostic markers. Due to different definitions and guideline recommendations of ID, various laboratory parameters for ID diagnostic exist and there is no general consensus about the definition of ID and its treatment. Still, a general trend can be observed across all investigated indications of this review (HF, CKD, IBD, cancer) that serum ferritin and transferrin saturation (TSAT) are the two parameters mentioned most often and emphasized in all guidelines to define ID and guide treatment. The most commonly used threshold values for the diagnosis of ID are TSAT of < 20% and serum ferritin of < 100–300 µg/L. Noteworthy, both TSAT and particularly ferritin are frequently applied, but both may vary due to inflammatory conditions. Studies showed that TSAT is less affected by inflammatory processes and may therefore be more accurate and reliable than serum ferritin, particularly in conditions with elevated inflammatory state. A low iron status and particularly a low TSAT value was associated with a poor outcome in all investigated indications, with the strongest evidence in HF patients. Routine surveillance of iron status in these groups of patients with chronic conditions is advisable to detect ID early. Depending on the inflammatory state, TSAT < 20% may be the more accurate diagnostic marker of ID than ferritin. Moreover, TSAT may also be the more reliable estimate for the prognosis, particularly in HF. BioMed Central 2023-01-09 /pmc/articles/PMC9827648/ /pubmed/36617559 http://dx.doi.org/10.1186/s40001-022-00922-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Rohr, Martina
Brandenburg, Vincent
Brunner-La Rocca, Hans-Peter
How to diagnose iron deficiency in chronic disease: A review of current methods and potential marker for the outcome
title How to diagnose iron deficiency in chronic disease: A review of current methods and potential marker for the outcome
title_full How to diagnose iron deficiency in chronic disease: A review of current methods and potential marker for the outcome
title_fullStr How to diagnose iron deficiency in chronic disease: A review of current methods and potential marker for the outcome
title_full_unstemmed How to diagnose iron deficiency in chronic disease: A review of current methods and potential marker for the outcome
title_short How to diagnose iron deficiency in chronic disease: A review of current methods and potential marker for the outcome
title_sort how to diagnose iron deficiency in chronic disease: a review of current methods and potential marker for the outcome
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827648/
https://www.ncbi.nlm.nih.gov/pubmed/36617559
http://dx.doi.org/10.1186/s40001-022-00922-6
work_keys_str_mv AT rohrmartina howtodiagnoseirondeficiencyinchronicdiseaseareviewofcurrentmethodsandpotentialmarkerfortheoutcome
AT brandenburgvincent howtodiagnoseirondeficiencyinchronicdiseaseareviewofcurrentmethodsandpotentialmarkerfortheoutcome
AT brunnerlaroccahanspeter howtodiagnoseirondeficiencyinchronicdiseaseareviewofcurrentmethodsandpotentialmarkerfortheoutcome