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Rapid diagnostics for point-of-care quantification of soluble transferrin receptor
BACKGROUND: Iron deficiency (ID) and anaemia are major health concerns, particularly in young children. Screening for ID based on haemoglobin (Hb) concentration alone has been shown to lack sensitivity and specificity. The American Academy of Pediatrics (AAP) recommends soluble transferrin receptor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491390/ https://www.ncbi.nlm.nih.gov/pubmed/30885726 http://dx.doi.org/10.1016/j.ebiom.2019.03.017 |
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author | Srinivasan, Balaji Finkelstein, Julia L. O’Dell, Dakota Erickson, David Mehta, Saurabh |
author_facet | Srinivasan, Balaji Finkelstein, Julia L. O’Dell, Dakota Erickson, David Mehta, Saurabh |
author_sort | Srinivasan, Balaji |
collection | PubMed |
description | BACKGROUND: Iron deficiency (ID) and anaemia are major health concerns, particularly in young children. Screening for ID based on haemoglobin (Hb) concentration alone has been shown to lack sensitivity and specificity. The American Academy of Pediatrics (AAP) recommends soluble transferrin receptor (sTfR) as a promising approach to screen for iron deficiency. However, in most settings, assessment of iron status requires access to centralized laboratories. There is an urgent need for rapid, sensitive, and affordable diagnostics for sTfR at the point-of-care. METHODS: An immunochromatographic assay-based point-of-care screening device was developed for rapid quantification of sTfR from a drop of serum within a few minutes. Performance optimization of the assay was done in sTfR-spiked buffer and commercially available sTfR calibrator, followed by a small-scale proof-of-concept validation with archived serum samples. FINDINGS: On preliminary testing with archived serum samples and comparison with Ramco ELISA, a correlation of 0.93 (P < 0.0001) was observed, demonstrating its potential for point-of-care assessment of iron status. INTERPRETATION: The analytical performance of the point-of-care sTfR screening device indicates the potential for application in home-use test kits and field settings, especially in low- and middle-income settings. An added advantage of sTfR quantification in combination with our previously reported serum ferritin diagnostics is in integration of Cook's equation as a quantitative and minimally-invasive indicator of total body iron stores. FUND: Thrasher Research Fund (Early Career Award #13379), NIH R03 EB 023190, NSF grant #1343058, and Nutrition International (project #10-8007-CORNE-01). |
format | Online Article Text |
id | pubmed-6491390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-64913902019-05-06 Rapid diagnostics for point-of-care quantification of soluble transferrin receptor Srinivasan, Balaji Finkelstein, Julia L. O’Dell, Dakota Erickson, David Mehta, Saurabh EBioMedicine Research paper BACKGROUND: Iron deficiency (ID) and anaemia are major health concerns, particularly in young children. Screening for ID based on haemoglobin (Hb) concentration alone has been shown to lack sensitivity and specificity. The American Academy of Pediatrics (AAP) recommends soluble transferrin receptor (sTfR) as a promising approach to screen for iron deficiency. However, in most settings, assessment of iron status requires access to centralized laboratories. There is an urgent need for rapid, sensitive, and affordable diagnostics for sTfR at the point-of-care. METHODS: An immunochromatographic assay-based point-of-care screening device was developed for rapid quantification of sTfR from a drop of serum within a few minutes. Performance optimization of the assay was done in sTfR-spiked buffer and commercially available sTfR calibrator, followed by a small-scale proof-of-concept validation with archived serum samples. FINDINGS: On preliminary testing with archived serum samples and comparison with Ramco ELISA, a correlation of 0.93 (P < 0.0001) was observed, demonstrating its potential for point-of-care assessment of iron status. INTERPRETATION: The analytical performance of the point-of-care sTfR screening device indicates the potential for application in home-use test kits and field settings, especially in low- and middle-income settings. An added advantage of sTfR quantification in combination with our previously reported serum ferritin diagnostics is in integration of Cook's equation as a quantitative and minimally-invasive indicator of total body iron stores. FUND: Thrasher Research Fund (Early Career Award #13379), NIH R03 EB 023190, NSF grant #1343058, and Nutrition International (project #10-8007-CORNE-01). Elsevier 2019-03-16 /pmc/articles/PMC6491390/ /pubmed/30885726 http://dx.doi.org/10.1016/j.ebiom.2019.03.017 Text en © 2019 The Authors. Published by Elsevier B.V. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research paper Srinivasan, Balaji Finkelstein, Julia L. O’Dell, Dakota Erickson, David Mehta, Saurabh Rapid diagnostics for point-of-care quantification of soluble transferrin receptor |
title | Rapid diagnostics for point-of-care quantification of soluble transferrin receptor |
title_full | Rapid diagnostics for point-of-care quantification of soluble transferrin receptor |
title_fullStr | Rapid diagnostics for point-of-care quantification of soluble transferrin receptor |
title_full_unstemmed | Rapid diagnostics for point-of-care quantification of soluble transferrin receptor |
title_short | Rapid diagnostics for point-of-care quantification of soluble transferrin receptor |
title_sort | rapid diagnostics for point-of-care quantification of soluble transferrin receptor |
topic | Research paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491390/ https://www.ncbi.nlm.nih.gov/pubmed/30885726 http://dx.doi.org/10.1016/j.ebiom.2019.03.017 |
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