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Bone marrow macrophage iron content and sideroblast count in iron- and ESA-naïve patients with CKD-related anemia
BACKGROUND: Since in chronic kidney disease (CKD) iron deficiency anemia (IDA) can coexist with inflammation-induced immobilization of iron in macrophages (anemia of chronic disorders – ACD), we assessed the utility of ferritin, transferrin saturation (TSAT), and hepcidin for differentiation of mixe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324424/ https://www.ncbi.nlm.nih.gov/pubmed/37408484 http://dx.doi.org/10.1080/0886022X.2023.2230300 |
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author | Capusa, Cristina Mehedinti, Ana-Maria Bârsan, Liliana Stanciu, Ana Calenic, Andreea Mircescu, Gabriel |
author_facet | Capusa, Cristina Mehedinti, Ana-Maria Bârsan, Liliana Stanciu, Ana Calenic, Andreea Mircescu, Gabriel |
author_sort | Capusa, Cristina |
collection | PubMed |
description | BACKGROUND: Since in chronic kidney disease (CKD) iron deficiency anemia (IDA) can coexist with inflammation-induced immobilization of iron in macrophages (anemia of chronic disorders – ACD), we assessed the utility of ferritin, transferrin saturation (TSAT), and hepcidin for differentiation of mixed IDA-ACD from ACD, using bone marrow (BM) examination as reference. METHODS: This cross-sectional, single-center study analyzed 162 non-dialysis iron and epoietin-naïve CKD patients (52% males, median age 67 years, eGFR 14.2 mL/min 1.73 m(2), hemoglobin 9.4 g/dL). BM aspiration, serum hepcidin (ELISA), ferritin, TSAT, and C-Reactive protein (CRP) were the main studied parameters. RESULTS: ACD was seen in 51%, IDA-ACD in 40%, while “pure” IDA in only 9%. In univariate and binomial analyses, IDA-ACD differed from ACD by lower ferritin and TSAT, but not by hepcidin or CRP. Correspondingly, in receiver operating curve analysis, ferritin and TSAT differentiated IDA-ACD from ACD, at cutoffs of 165 ng/mL and 14%, but with moderate precision (sensitivity and specificity of 72%, and 61%, respectively). CONCLUSION: The mixed pattern IDA-ACD could be more prevalent than estimated in non-dialysis CKD. Ferritin and, to a lesser degree, TSAT are useful in the diagnosis of IDA superimposed on ACD, while hepcidin, although reflecting BM macrophages iron, seems to have limited utility. |
format | Online Article Text |
id | pubmed-10324424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-103244242023-07-07 Bone marrow macrophage iron content and sideroblast count in iron- and ESA-naïve patients with CKD-related anemia Capusa, Cristina Mehedinti, Ana-Maria Bârsan, Liliana Stanciu, Ana Calenic, Andreea Mircescu, Gabriel Ren Fail Clinical Study BACKGROUND: Since in chronic kidney disease (CKD) iron deficiency anemia (IDA) can coexist with inflammation-induced immobilization of iron in macrophages (anemia of chronic disorders – ACD), we assessed the utility of ferritin, transferrin saturation (TSAT), and hepcidin for differentiation of mixed IDA-ACD from ACD, using bone marrow (BM) examination as reference. METHODS: This cross-sectional, single-center study analyzed 162 non-dialysis iron and epoietin-naïve CKD patients (52% males, median age 67 years, eGFR 14.2 mL/min 1.73 m(2), hemoglobin 9.4 g/dL). BM aspiration, serum hepcidin (ELISA), ferritin, TSAT, and C-Reactive protein (CRP) were the main studied parameters. RESULTS: ACD was seen in 51%, IDA-ACD in 40%, while “pure” IDA in only 9%. In univariate and binomial analyses, IDA-ACD differed from ACD by lower ferritin and TSAT, but not by hepcidin or CRP. Correspondingly, in receiver operating curve analysis, ferritin and TSAT differentiated IDA-ACD from ACD, at cutoffs of 165 ng/mL and 14%, but with moderate precision (sensitivity and specificity of 72%, and 61%, respectively). CONCLUSION: The mixed pattern IDA-ACD could be more prevalent than estimated in non-dialysis CKD. Ferritin and, to a lesser degree, TSAT are useful in the diagnosis of IDA superimposed on ACD, while hepcidin, although reflecting BM macrophages iron, seems to have limited utility. Taylor & Francis 2023-07-05 /pmc/articles/PMC10324424/ /pubmed/37408484 http://dx.doi.org/10.1080/0886022X.2023.2230300 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Clinical Study Capusa, Cristina Mehedinti, Ana-Maria Bârsan, Liliana Stanciu, Ana Calenic, Andreea Mircescu, Gabriel Bone marrow macrophage iron content and sideroblast count in iron- and ESA-naïve patients with CKD-related anemia |
title | Bone marrow macrophage iron content and sideroblast count in iron- and ESA-naïve patients with CKD-related anemia |
title_full | Bone marrow macrophage iron content and sideroblast count in iron- and ESA-naïve patients with CKD-related anemia |
title_fullStr | Bone marrow macrophage iron content and sideroblast count in iron- and ESA-naïve patients with CKD-related anemia |
title_full_unstemmed | Bone marrow macrophage iron content and sideroblast count in iron- and ESA-naïve patients with CKD-related anemia |
title_short | Bone marrow macrophage iron content and sideroblast count in iron- and ESA-naïve patients with CKD-related anemia |
title_sort | bone marrow macrophage iron content and sideroblast count in iron- and esa-naïve patients with ckd-related anemia |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324424/ https://www.ncbi.nlm.nih.gov/pubmed/37408484 http://dx.doi.org/10.1080/0886022X.2023.2230300 |
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