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Changes in serum uric acid levels after allogeneic hematologic stem cell transplantation: A retrospective cohort study

BACKGROUND: Since cell turnover in the hematopoietic system constitutes a major source of uric acid (UA) production, we investigated whether hematopoietic stem cell transplantation (HSCT) is associated with significant changes in serum UA levels in patients with hematological disorders. METHODS: Pat...

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Autores principales: Joo, Sang Hyun, Park, Jin Kyun, Lee, Eunyoung Emily, Song, Yeong Wook, Yoon, Sung-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054253/
https://www.ncbi.nlm.nih.gov/pubmed/27722132
http://dx.doi.org/10.5045/br.2016.51.3.200
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author Joo, Sang Hyun
Park, Jin Kyun
Lee, Eunyoung Emily
Song, Yeong Wook
Yoon, Sung-Soo
author_facet Joo, Sang Hyun
Park, Jin Kyun
Lee, Eunyoung Emily
Song, Yeong Wook
Yoon, Sung-Soo
author_sort Joo, Sang Hyun
collection PubMed
description BACKGROUND: Since cell turnover in the hematopoietic system constitutes a major source of uric acid (UA) production, we investigated whether hematopoietic stem cell transplantation (HSCT) is associated with significant changes in serum UA levels in patients with hematological disorders. METHODS: Patients who underwent HSCT at our institution between 2001 and 2012 were retrospectively enrolled. Serum UA levels at 3 months before, 1 week before, and 3 months and 1 year after HSCT were examined. RESULTS: Complete clinical and laboratory information including data regarding UA levels was available for 93 patients. At baseline, the mean UA level was 4.9±2.1 mg/dL, with an overall prevalence of hyperuricemia of 15% (defined as serum UA>6.8 mg/dL). Mean UA levels tended to be higher in patients with acute myeloid leukemia (4.8±2.0 mg/dL) and non-Hodgkin lymphoma (5.1±2.3 mg/dL) and lower in patients with aplastic anemia (mean, 4.2±1.8 mg/dL). UA levels dropped during myeloablative conditioning, reaching a nadir on the day of HSCT (3.27±1.4 mg/dL). Over the 3 months following HSCT, UA levels rose sharply (5.0±2.1 mg/dL) and remained stable up to 1 year after HSCT (5.5±1.6 mg/dL). UA levels in HSCT recipients at 12 months correlated with those of their respective graft donors (Pearson r=0.406, P=0.001). CONCLUSION: HSCT is associated with significant changes in uric acid levels in patients with hematologic disorders.
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spelling pubmed-50542532016-10-07 Changes in serum uric acid levels after allogeneic hematologic stem cell transplantation: A retrospective cohort study Joo, Sang Hyun Park, Jin Kyun Lee, Eunyoung Emily Song, Yeong Wook Yoon, Sung-Soo Blood Res Original Article BACKGROUND: Since cell turnover in the hematopoietic system constitutes a major source of uric acid (UA) production, we investigated whether hematopoietic stem cell transplantation (HSCT) is associated with significant changes in serum UA levels in patients with hematological disorders. METHODS: Patients who underwent HSCT at our institution between 2001 and 2012 were retrospectively enrolled. Serum UA levels at 3 months before, 1 week before, and 3 months and 1 year after HSCT were examined. RESULTS: Complete clinical and laboratory information including data regarding UA levels was available for 93 patients. At baseline, the mean UA level was 4.9±2.1 mg/dL, with an overall prevalence of hyperuricemia of 15% (defined as serum UA>6.8 mg/dL). Mean UA levels tended to be higher in patients with acute myeloid leukemia (4.8±2.0 mg/dL) and non-Hodgkin lymphoma (5.1±2.3 mg/dL) and lower in patients with aplastic anemia (mean, 4.2±1.8 mg/dL). UA levels dropped during myeloablative conditioning, reaching a nadir on the day of HSCT (3.27±1.4 mg/dL). Over the 3 months following HSCT, UA levels rose sharply (5.0±2.1 mg/dL) and remained stable up to 1 year after HSCT (5.5±1.6 mg/dL). UA levels in HSCT recipients at 12 months correlated with those of their respective graft donors (Pearson r=0.406, P=0.001). CONCLUSION: HSCT is associated with significant changes in uric acid levels in patients with hematologic disorders. Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2016-09 2016-09-23 /pmc/articles/PMC5054253/ /pubmed/27722132 http://dx.doi.org/10.5045/br.2016.51.3.200 Text en © 2016 Korean Society of Hematology 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 Original Article
Joo, Sang Hyun
Park, Jin Kyun
Lee, Eunyoung Emily
Song, Yeong Wook
Yoon, Sung-Soo
Changes in serum uric acid levels after allogeneic hematologic stem cell transplantation: A retrospective cohort study
title Changes in serum uric acid levels after allogeneic hematologic stem cell transplantation: A retrospective cohort study
title_full Changes in serum uric acid levels after allogeneic hematologic stem cell transplantation: A retrospective cohort study
title_fullStr Changes in serum uric acid levels after allogeneic hematologic stem cell transplantation: A retrospective cohort study
title_full_unstemmed Changes in serum uric acid levels after allogeneic hematologic stem cell transplantation: A retrospective cohort study
title_short Changes in serum uric acid levels after allogeneic hematologic stem cell transplantation: A retrospective cohort study
title_sort changes in serum uric acid levels after allogeneic hematologic stem cell transplantation: a retrospective cohort study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054253/
https://www.ncbi.nlm.nih.gov/pubmed/27722132
http://dx.doi.org/10.5045/br.2016.51.3.200
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