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CD36 relative mean fluorescence intensity of CD105(+) nucleated erythroid cells can be used to differentiate myelodysplastic syndrome from megaloblastic anemia

This study aims to evaluate the differences in CD105(+) nucleated erythroid cell (NEC) immunophenotypes between myelodysplastic syndrome (MDS) and megaloblastic anemia (MA) using multiparameter flow cytometry and to screen potential markers. We analyzed bone marrow sample data from 37 patients with...

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Autores principales: Lu, Yan, Chen, Xuya, Zhang, Longyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235022/
https://www.ncbi.nlm.nih.gov/pubmed/37264109
http://dx.doi.org/10.1038/s41598-023-35994-9
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author Lu, Yan
Chen, Xuya
Zhang, Longyi
author_facet Lu, Yan
Chen, Xuya
Zhang, Longyi
author_sort Lu, Yan
collection PubMed
description This study aims to evaluate the differences in CD105(+) nucleated erythroid cell (NEC) immunophenotypes between myelodysplastic syndrome (MDS) and megaloblastic anemia (MA) using multiparameter flow cytometry and to screen potential markers. We analyzed bone marrow sample data from 37 patients with MDS, 35 with MA, 53 with iron-deficiency anemia (anemic controls), and 35 without anemia (normal controls). Compared with normal controls, the MDS and MA groups showed a decrease in the proportion of CD117(+)CD105(+)NEC and the relative mean fluorescence intensity (RMFI) of CD71 in CD105(+)NEC, accompanied by an increase in the coefficient of variation (CV) of CD71 and CD36. Additionally, CD36 RMFI of CD105(+)NEC increased in the MA group. Compared with anemia controls, the MDS and MA groups showed a significant increase in CD36 CV of CD105(+)NEC, and the CD36 RMFI in the MA group increased while that in the MDS group decreased. The proportions of CD117(+)CD105(+)NEC, CD36 CV, and CD36 RMFI in CD105(+)NEC differed significantly between MDS and MA groups. Among them, CD36 RMFI had good diagnostic performance (area under the curve: 0.844, 95% confidence interval: 0.753–0.935). CD36 RMFI of CD105(+)NEC may be a helpful marker in differentiating MDS and MA using multiparameter flow cytometry.
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spelling pubmed-102350222023-06-03 CD36 relative mean fluorescence intensity of CD105(+) nucleated erythroid cells can be used to differentiate myelodysplastic syndrome from megaloblastic anemia Lu, Yan Chen, Xuya Zhang, Longyi Sci Rep Article This study aims to evaluate the differences in CD105(+) nucleated erythroid cell (NEC) immunophenotypes between myelodysplastic syndrome (MDS) and megaloblastic anemia (MA) using multiparameter flow cytometry and to screen potential markers. We analyzed bone marrow sample data from 37 patients with MDS, 35 with MA, 53 with iron-deficiency anemia (anemic controls), and 35 without anemia (normal controls). Compared with normal controls, the MDS and MA groups showed a decrease in the proportion of CD117(+)CD105(+)NEC and the relative mean fluorescence intensity (RMFI) of CD71 in CD105(+)NEC, accompanied by an increase in the coefficient of variation (CV) of CD71 and CD36. Additionally, CD36 RMFI of CD105(+)NEC increased in the MA group. Compared with anemia controls, the MDS and MA groups showed a significant increase in CD36 CV of CD105(+)NEC, and the CD36 RMFI in the MA group increased while that in the MDS group decreased. The proportions of CD117(+)CD105(+)NEC, CD36 CV, and CD36 RMFI in CD105(+)NEC differed significantly between MDS and MA groups. Among them, CD36 RMFI had good diagnostic performance (area under the curve: 0.844, 95% confidence interval: 0.753–0.935). CD36 RMFI of CD105(+)NEC may be a helpful marker in differentiating MDS and MA using multiparameter flow cytometry. Nature Publishing Group UK 2023-06-01 /pmc/articles/PMC10235022/ /pubmed/37264109 http://dx.doi.org/10.1038/s41598-023-35994-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Lu, Yan
Chen, Xuya
Zhang, Longyi
CD36 relative mean fluorescence intensity of CD105(+) nucleated erythroid cells can be used to differentiate myelodysplastic syndrome from megaloblastic anemia
title CD36 relative mean fluorescence intensity of CD105(+) nucleated erythroid cells can be used to differentiate myelodysplastic syndrome from megaloblastic anemia
title_full CD36 relative mean fluorescence intensity of CD105(+) nucleated erythroid cells can be used to differentiate myelodysplastic syndrome from megaloblastic anemia
title_fullStr CD36 relative mean fluorescence intensity of CD105(+) nucleated erythroid cells can be used to differentiate myelodysplastic syndrome from megaloblastic anemia
title_full_unstemmed CD36 relative mean fluorescence intensity of CD105(+) nucleated erythroid cells can be used to differentiate myelodysplastic syndrome from megaloblastic anemia
title_short CD36 relative mean fluorescence intensity of CD105(+) nucleated erythroid cells can be used to differentiate myelodysplastic syndrome from megaloblastic anemia
title_sort cd36 relative mean fluorescence intensity of cd105(+) nucleated erythroid cells can be used to differentiate myelodysplastic syndrome from megaloblastic anemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235022/
https://www.ncbi.nlm.nih.gov/pubmed/37264109
http://dx.doi.org/10.1038/s41598-023-35994-9
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