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Myelodysplastic syndrome: the other cause of anemia in end-stage renal disease patients undergoing dialysis
In end-stage renal disease (ESRD) patients receiving dialysis, anemia is common and related to a higher mortality rate. Erythropoietin (EPO) resistance and iron refractory anemia require red blood cell transfusions. Myelodysplastic syndrome (MDS) is a disease with hematopoietic dysplasia. There are...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511931/ https://www.ncbi.nlm.nih.gov/pubmed/32968161 http://dx.doi.org/10.1038/s41598-020-72568-5 |
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author | Chang, Min-Yu Lin, Sheng-Fung Wu, Shih-Chi Yang, Wen-Chi |
author_facet | Chang, Min-Yu Lin, Sheng-Fung Wu, Shih-Chi Yang, Wen-Chi |
author_sort | Chang, Min-Yu |
collection | PubMed |
description | In end-stage renal disease (ESRD) patients receiving dialysis, anemia is common and related to a higher mortality rate. Erythropoietin (EPO) resistance and iron refractory anemia require red blood cell transfusions. Myelodysplastic syndrome (MDS) is a disease with hematopoietic dysplasia. There are limited reports regarding ESRD patients with MDS. We aim to assess whether, for ESRD patients, undergoing dialysis is a predictive factor of MDS by analyzing data from the Taiwan National Health Insurance Research Database. We enrolled 74,712 patients with chronic renal failure (ESRD) who underwent dialysis and matched 74,712 control patients. In our study, we noticed that compared with the non-ESRD controls, in ESRD patients, undergoing dialysis (subdistribution hazard ratio [sHR] = 1.60, 1.16–2.19) and age (sHR = 1.03, 1.02–1.04) had positive predictive value for MDS occurrence. Moreover, more units of red blood cell transfusion (higher than 4 units per month) was also associated with a higher incidence of MDS. The MDS cumulative incidence increased with the duration of dialysis in ESRD patients. These effects may be related to exposure to certain cytokines, including interleukin-1, tumor necrosis factor-α, and tumor growth factor-β. In conclusion, we report the novel finding that ESRD patients undergoing dialysis have an increased risk of MDS. |
format | Online Article Text |
id | pubmed-7511931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75119312020-09-29 Myelodysplastic syndrome: the other cause of anemia in end-stage renal disease patients undergoing dialysis Chang, Min-Yu Lin, Sheng-Fung Wu, Shih-Chi Yang, Wen-Chi Sci Rep Article In end-stage renal disease (ESRD) patients receiving dialysis, anemia is common and related to a higher mortality rate. Erythropoietin (EPO) resistance and iron refractory anemia require red blood cell transfusions. Myelodysplastic syndrome (MDS) is a disease with hematopoietic dysplasia. There are limited reports regarding ESRD patients with MDS. We aim to assess whether, for ESRD patients, undergoing dialysis is a predictive factor of MDS by analyzing data from the Taiwan National Health Insurance Research Database. We enrolled 74,712 patients with chronic renal failure (ESRD) who underwent dialysis and matched 74,712 control patients. In our study, we noticed that compared with the non-ESRD controls, in ESRD patients, undergoing dialysis (subdistribution hazard ratio [sHR] = 1.60, 1.16–2.19) and age (sHR = 1.03, 1.02–1.04) had positive predictive value for MDS occurrence. Moreover, more units of red blood cell transfusion (higher than 4 units per month) was also associated with a higher incidence of MDS. The MDS cumulative incidence increased with the duration of dialysis in ESRD patients. These effects may be related to exposure to certain cytokines, including interleukin-1, tumor necrosis factor-α, and tumor growth factor-β. In conclusion, we report the novel finding that ESRD patients undergoing dialysis have an increased risk of MDS. Nature Publishing Group UK 2020-09-23 /pmc/articles/PMC7511931/ /pubmed/32968161 http://dx.doi.org/10.1038/s41598-020-72568-5 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Chang, Min-Yu Lin, Sheng-Fung Wu, Shih-Chi Yang, Wen-Chi Myelodysplastic syndrome: the other cause of anemia in end-stage renal disease patients undergoing dialysis |
title | Myelodysplastic syndrome: the other cause of anemia in end-stage renal disease patients undergoing dialysis |
title_full | Myelodysplastic syndrome: the other cause of anemia in end-stage renal disease patients undergoing dialysis |
title_fullStr | Myelodysplastic syndrome: the other cause of anemia in end-stage renal disease patients undergoing dialysis |
title_full_unstemmed | Myelodysplastic syndrome: the other cause of anemia in end-stage renal disease patients undergoing dialysis |
title_short | Myelodysplastic syndrome: the other cause of anemia in end-stage renal disease patients undergoing dialysis |
title_sort | myelodysplastic syndrome: the other cause of anemia in end-stage renal disease patients undergoing dialysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511931/ https://www.ncbi.nlm.nih.gov/pubmed/32968161 http://dx.doi.org/10.1038/s41598-020-72568-5 |
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