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Factors associated with erythropoiesis-stimulating agent hyporesponsiveness anemia in chronic kidney disease patients

Anemia is one of the most common problems in chronic kidney disease (CKD). Despite comprehensive investigations in several cases, definite causes of anemia frequently remain unknown. Our study aimed to analyze the factors that possibly affect anemia in CKD patients who were referred for hematology c...

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Autores principales: Amnuay, Kamalas, Srisawat, Nattachai, Wudhikarn, Kitsada, Assanasen, Thamathorn, Polprasert, Chantana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761458/
https://www.ncbi.nlm.nih.gov/pubmed/31579107
http://dx.doi.org/10.4081/hr.2019.8183
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author Amnuay, Kamalas
Srisawat, Nattachai
Wudhikarn, Kitsada
Assanasen, Thamathorn
Polprasert, Chantana
author_facet Amnuay, Kamalas
Srisawat, Nattachai
Wudhikarn, Kitsada
Assanasen, Thamathorn
Polprasert, Chantana
author_sort Amnuay, Kamalas
collection PubMed
description Anemia is one of the most common problems in chronic kidney disease (CKD). Despite comprehensive investigations in several cases, definite causes of anemia frequently remain unknown. Our study aimed to analyze the factors that possibly affect anemia in CKD patients who were referred for hematology consultation. A total of 87 patients were retrospectively included in the cohort. Forty-four cases were excluded, including 30 cases with unavailable intact parathyroid hormone (iPTH) data, 11 cases with bone marrow diseases (8 Pure red cell aplasia, 3 Myelodysplastic syndrome) and 3 cases with thalassemia. In total, 43 patients were analyzed. Patients with high iPTH had a significantly lower Hemoglobin (Hb) level and required a higher dose of erythropoiesis stimulating agents (ESAs) compared with the normal iPTH group (Hb 8.29 vs 9.24 mg/dL, P=0.032 and ESAs dose of 16,352.94 vs. 12,444.44 U/week, P=0.024). Univariate, followed by stepwise multivariate analysis was performed and determined that serum phosphate (PO4) was significantly associated with lower Hb level (P=0.01 and P=0.013, respectively). In addition, Hb level was inversely correlated with iPTH and serum phosphate (PO4) level (r=-0.54, P<0.001 and r=-0.47, P=0.005; respectively). Mineral disequilibrium is an important factor associated with anemia in ESA hyporesponsive CKD. Also, hyperphosphatemia and secondary hyperparathyroidism are significantly correlated with low Hb. As a result, we strongly suggest correction of mineral disequilibrium factors prior to performing bone marrow study.
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spelling pubmed-67614582019-10-02 Factors associated with erythropoiesis-stimulating agent hyporesponsiveness anemia in chronic kidney disease patients Amnuay, Kamalas Srisawat, Nattachai Wudhikarn, Kitsada Assanasen, Thamathorn Polprasert, Chantana Hematol Rep Article Anemia is one of the most common problems in chronic kidney disease (CKD). Despite comprehensive investigations in several cases, definite causes of anemia frequently remain unknown. Our study aimed to analyze the factors that possibly affect anemia in CKD patients who were referred for hematology consultation. A total of 87 patients were retrospectively included in the cohort. Forty-four cases were excluded, including 30 cases with unavailable intact parathyroid hormone (iPTH) data, 11 cases with bone marrow diseases (8 Pure red cell aplasia, 3 Myelodysplastic syndrome) and 3 cases with thalassemia. In total, 43 patients were analyzed. Patients with high iPTH had a significantly lower Hemoglobin (Hb) level and required a higher dose of erythropoiesis stimulating agents (ESAs) compared with the normal iPTH group (Hb 8.29 vs 9.24 mg/dL, P=0.032 and ESAs dose of 16,352.94 vs. 12,444.44 U/week, P=0.024). Univariate, followed by stepwise multivariate analysis was performed and determined that serum phosphate (PO4) was significantly associated with lower Hb level (P=0.01 and P=0.013, respectively). In addition, Hb level was inversely correlated with iPTH and serum phosphate (PO4) level (r=-0.54, P<0.001 and r=-0.47, P=0.005; respectively). Mineral disequilibrium is an important factor associated with anemia in ESA hyporesponsive CKD. Also, hyperphosphatemia and secondary hyperparathyroidism are significantly correlated with low Hb. As a result, we strongly suggest correction of mineral disequilibrium factors prior to performing bone marrow study. PAGEPress Publications, Pavia, Italy 2019-09-18 /pmc/articles/PMC6761458/ /pubmed/31579107 http://dx.doi.org/10.4081/hr.2019.8183 Text en ©Copyright: the Author(s), 2019 http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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.
spellingShingle Article
Amnuay, Kamalas
Srisawat, Nattachai
Wudhikarn, Kitsada
Assanasen, Thamathorn
Polprasert, Chantana
Factors associated with erythropoiesis-stimulating agent hyporesponsiveness anemia in chronic kidney disease patients
title Factors associated with erythropoiesis-stimulating agent hyporesponsiveness anemia in chronic kidney disease patients
title_full Factors associated with erythropoiesis-stimulating agent hyporesponsiveness anemia in chronic kidney disease patients
title_fullStr Factors associated with erythropoiesis-stimulating agent hyporesponsiveness anemia in chronic kidney disease patients
title_full_unstemmed Factors associated with erythropoiesis-stimulating agent hyporesponsiveness anemia in chronic kidney disease patients
title_short Factors associated with erythropoiesis-stimulating agent hyporesponsiveness anemia in chronic kidney disease patients
title_sort factors associated with erythropoiesis-stimulating agent hyporesponsiveness anemia in chronic kidney disease patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761458/
https://www.ncbi.nlm.nih.gov/pubmed/31579107
http://dx.doi.org/10.4081/hr.2019.8183
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