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Clinical Usefulness of Measuring Red Blood Cell Distribution Width in Patients with Hepatitis B

BACKGROUND: Red blood cell distribution width (RDW), an automated measure of red blood cell size heterogeneity (e.g., anisocytosis) that is largely overlooked, is a newly recognized risk marker in patients with cardiovascular diseases, but its role in persistent viral infection has not been well-def...

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Autores principales: Lou, YuFeng, Wang, ManYi, Mao, WeiLin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359289/
https://www.ncbi.nlm.nih.gov/pubmed/22649548
http://dx.doi.org/10.1371/journal.pone.0037644
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author Lou, YuFeng
Wang, ManYi
Mao, WeiLin
author_facet Lou, YuFeng
Wang, ManYi
Mao, WeiLin
author_sort Lou, YuFeng
collection PubMed
description BACKGROUND: Red blood cell distribution width (RDW), an automated measure of red blood cell size heterogeneity (e.g., anisocytosis) that is largely overlooked, is a newly recognized risk marker in patients with cardiovascular diseases, but its role in persistent viral infection has not been well-defined. The present study was designed to investigate the association between RDW values and different disease states in hepatitis B virus (HBV)-infected patients. In addition, we analyzed whether RDW is associated with mortality in the HBV-infected patients. METHODOLOGY/PRINCIPAL FINDINGS: One hundred and twenty-three patients, including 16 with acute hepatitis B (AHB), 61 with chronic hepatitis B (CHB), and 46 with chronic severe hepatitis B (CSHB), and 48 healthy controls were enrolled. In all subjects, a blood sample was collected at admission to examine liver function, renal function, international normalized ratio and routine hematological testing. All patients were followed up for at least 4 months. A total of 10 clinical chemistry, hematology, and biochemical variables were analyzed for possible association with outcomes by using Cox proportional hazards and multiple regression models. RDW values at admission in patients with CSHB (18.30±3.11%, P<0.001), CHB (16.37±2.43%, P<0.001) and AHB (14.38±1.72%, P<0.05) were significantly higher than those in healthy controls (13.03±1.33%). Increased RDW values were clinically associated with severe liver disease and increased 3-month mortality rate. Multivariate analysis demonstrated that RDW values and the model for end-stage liver disease score were independent predictors for mortality (both P<0.001). CONCLUSION: RDW values are significantly increased in patients with hepatitis B and associated with its severity. Moreover, RDW values are an independent predicting factor for the 3-month mortality rate in patients with hepatitis B.
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spelling pubmed-33592892012-05-30 Clinical Usefulness of Measuring Red Blood Cell Distribution Width in Patients with Hepatitis B Lou, YuFeng Wang, ManYi Mao, WeiLin PLoS One Research Article BACKGROUND: Red blood cell distribution width (RDW), an automated measure of red blood cell size heterogeneity (e.g., anisocytosis) that is largely overlooked, is a newly recognized risk marker in patients with cardiovascular diseases, but its role in persistent viral infection has not been well-defined. The present study was designed to investigate the association between RDW values and different disease states in hepatitis B virus (HBV)-infected patients. In addition, we analyzed whether RDW is associated with mortality in the HBV-infected patients. METHODOLOGY/PRINCIPAL FINDINGS: One hundred and twenty-three patients, including 16 with acute hepatitis B (AHB), 61 with chronic hepatitis B (CHB), and 46 with chronic severe hepatitis B (CSHB), and 48 healthy controls were enrolled. In all subjects, a blood sample was collected at admission to examine liver function, renal function, international normalized ratio and routine hematological testing. All patients were followed up for at least 4 months. A total of 10 clinical chemistry, hematology, and biochemical variables were analyzed for possible association with outcomes by using Cox proportional hazards and multiple regression models. RDW values at admission in patients with CSHB (18.30±3.11%, P<0.001), CHB (16.37±2.43%, P<0.001) and AHB (14.38±1.72%, P<0.05) were significantly higher than those in healthy controls (13.03±1.33%). Increased RDW values were clinically associated with severe liver disease and increased 3-month mortality rate. Multivariate analysis demonstrated that RDW values and the model for end-stage liver disease score were independent predictors for mortality (both P<0.001). CONCLUSION: RDW values are significantly increased in patients with hepatitis B and associated with its severity. Moreover, RDW values are an independent predicting factor for the 3-month mortality rate in patients with hepatitis B. Public Library of Science 2012-05-23 /pmc/articles/PMC3359289/ /pubmed/22649548 http://dx.doi.org/10.1371/journal.pone.0037644 Text en Lou et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lou, YuFeng
Wang, ManYi
Mao, WeiLin
Clinical Usefulness of Measuring Red Blood Cell Distribution Width in Patients with Hepatitis B
title Clinical Usefulness of Measuring Red Blood Cell Distribution Width in Patients with Hepatitis B
title_full Clinical Usefulness of Measuring Red Blood Cell Distribution Width in Patients with Hepatitis B
title_fullStr Clinical Usefulness of Measuring Red Blood Cell Distribution Width in Patients with Hepatitis B
title_full_unstemmed Clinical Usefulness of Measuring Red Blood Cell Distribution Width in Patients with Hepatitis B
title_short Clinical Usefulness of Measuring Red Blood Cell Distribution Width in Patients with Hepatitis B
title_sort clinical usefulness of measuring red blood cell distribution width in patients with hepatitis b
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359289/
https://www.ncbi.nlm.nih.gov/pubmed/22649548
http://dx.doi.org/10.1371/journal.pone.0037644
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