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Role of Soluble Transferrin Receptor – An Iron Marker in Hemodialysis Patients
BACKGROUND: Iron status assessment is crucial in end-stage renal disease hemodialysis (ESRD-HD) patients because iron deficiency may cause unresponsiveness to erythropoiesis-stimulating agent. Soluble transferrin receptor (sTfR) is a potential iron marker that is not influenced by inflammation, and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9872933/ https://www.ncbi.nlm.nih.gov/pubmed/36704598 http://dx.doi.org/10.4103/ijn.IJN_486_20 |
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author | Yusra, Lismawati, Effendy, Devi A. Kurniawan, Linny L. Lydia, Aida |
author_facet | Yusra, Lismawati, Effendy, Devi A. Kurniawan, Linny L. Lydia, Aida |
author_sort | Yusra, |
collection | PubMed |
description | BACKGROUND: Iron status assessment is crucial in end-stage renal disease hemodialysis (ESRD-HD) patients because iron deficiency may cause unresponsiveness to erythropoiesis-stimulating agent. Soluble transferrin receptor (sTfR) is a potential iron marker that is not influenced by inflammation, and the results among studies are still conflicting. This study evaluated the role of sTfR in determining iron deficiency in ESRD-HD patients. METHODS: This cross-sectional study was conducted at the Hemodialysis Unit in Cipto Mangunkusumo Hospital, Indonesia, from August to September 2018 and included 127 ESRD-HD patients. The sTfR level, sTfR index (sTfR/log ferritin), iron status, ferritin level, and complete blood count were assessed. Transferrin saturation (TSAT) was used as a reference. The role of sTfR was analyzed using the Chi-square test and receiver operating characteristic curve analysis. RESULTS: The median sTfR was 3.0 (range, 1.0–8.5) mg/l, and the median TSAT was 23% (4.0%–100%). The sTfR level in ESRD-HD patients with absolute iron deficiency was 3.9 (1.9–8.5) mg/l, in those with functional iron deficiency was 3.5 (1.9–5.4) mg/l, and in those with no iron deficiency was 2.6 (1.0–6.4) mg/l. The previous sTfR cut-off value of 2.5 mg/l had a sensitivity of 83.3%, specificity of 48.2%, positive predictive value (PPV) of 44.3%, and negative predictive value (NPV) of 85.4%, whereas the new sTfR cut-off value of 2.71 mg/l had a sensitivity of 83.3%, specificity of 56.5%, PPV of 48.6%, and NPV of 87.3%. TSAT and index TSAT were not influenced by inflammation. CONCLUSION: The cut-off sTfR value of 2.71 mg/l is better than 2.5 mg/l to determine the iron status in ESRD-HD patients. |
format | Online Article Text |
id | pubmed-9872933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-98729332023-01-25 Role of Soluble Transferrin Receptor – An Iron Marker in Hemodialysis Patients Yusra, Lismawati, Effendy, Devi A. Kurniawan, Linny L. Lydia, Aida Indian J Nephrol Original Article BACKGROUND: Iron status assessment is crucial in end-stage renal disease hemodialysis (ESRD-HD) patients because iron deficiency may cause unresponsiveness to erythropoiesis-stimulating agent. Soluble transferrin receptor (sTfR) is a potential iron marker that is not influenced by inflammation, and the results among studies are still conflicting. This study evaluated the role of sTfR in determining iron deficiency in ESRD-HD patients. METHODS: This cross-sectional study was conducted at the Hemodialysis Unit in Cipto Mangunkusumo Hospital, Indonesia, from August to September 2018 and included 127 ESRD-HD patients. The sTfR level, sTfR index (sTfR/log ferritin), iron status, ferritin level, and complete blood count were assessed. Transferrin saturation (TSAT) was used as a reference. The role of sTfR was analyzed using the Chi-square test and receiver operating characteristic curve analysis. RESULTS: The median sTfR was 3.0 (range, 1.0–8.5) mg/l, and the median TSAT was 23% (4.0%–100%). The sTfR level in ESRD-HD patients with absolute iron deficiency was 3.9 (1.9–8.5) mg/l, in those with functional iron deficiency was 3.5 (1.9–5.4) mg/l, and in those with no iron deficiency was 2.6 (1.0–6.4) mg/l. The previous sTfR cut-off value of 2.5 mg/l had a sensitivity of 83.3%, specificity of 48.2%, positive predictive value (PPV) of 44.3%, and negative predictive value (NPV) of 85.4%, whereas the new sTfR cut-off value of 2.71 mg/l had a sensitivity of 83.3%, specificity of 56.5%, PPV of 48.6%, and NPV of 87.3%. TSAT and index TSAT were not influenced by inflammation. CONCLUSION: The cut-off sTfR value of 2.71 mg/l is better than 2.5 mg/l to determine the iron status in ESRD-HD patients. Wolters Kluwer - Medknow 2022 2022-11-21 /pmc/articles/PMC9872933/ /pubmed/36704598 http://dx.doi.org/10.4103/ijn.IJN_486_20 Text en Copyright: © 2022 Indian Journal of Nephrology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Yusra, Lismawati, Effendy, Devi A. Kurniawan, Linny L. Lydia, Aida Role of Soluble Transferrin Receptor – An Iron Marker in Hemodialysis Patients |
title | Role of Soluble Transferrin Receptor – An Iron Marker in Hemodialysis Patients |
title_full | Role of Soluble Transferrin Receptor – An Iron Marker in Hemodialysis Patients |
title_fullStr | Role of Soluble Transferrin Receptor – An Iron Marker in Hemodialysis Patients |
title_full_unstemmed | Role of Soluble Transferrin Receptor – An Iron Marker in Hemodialysis Patients |
title_short | Role of Soluble Transferrin Receptor – An Iron Marker in Hemodialysis Patients |
title_sort | role of soluble transferrin receptor – an iron marker in hemodialysis patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9872933/ https://www.ncbi.nlm.nih.gov/pubmed/36704598 http://dx.doi.org/10.4103/ijn.IJN_486_20 |
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