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Circulating D-dimer level correlates with disease characteristics in hepatoblastoma patients
OBJECTIVES: Hepatoblastoma (HB) is the most common pediatric liver malignancy, typically affecting children within the first 4 years of life. However, only a few validated blood biomarkers are used in clinical evaluation. The current study explored the clinical application and significance of D-dime...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708979/ https://www.ncbi.nlm.nih.gov/pubmed/29381980 http://dx.doi.org/10.1097/MD.0000000000008798 |
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author | Zhang, BinBin Liu, GongBao Liu, XiangQi Zheng, Shan Dong, Kuiran Dong, Rui |
author_facet | Zhang, BinBin Liu, GongBao Liu, XiangQi Zheng, Shan Dong, Kuiran Dong, Rui |
author_sort | Zhang, BinBin |
collection | PubMed |
description | OBJECTIVES: Hepatoblastoma (HB) is the most common pediatric liver malignancy, typically affecting children within the first 4 years of life. However, only a few validated blood biomarkers are used in clinical evaluation. The current study explored the clinical application and significance of D-dimer levels in patients with HB. METHOD: Forty-four patients with HB were included in this retrospective study. D-dimer and plasma fibrinogen levels were examined, and their correlation with other clinical features was analyzed. D-dimer and plasma fibrinogen levels were examined between HB and other benign hepatic tumors. RESULTS: D-dimer levels were significantly associated with high-risk HB features, such as advanced stage and high α-fetoprotein (AFP) levels. Higher D-dimer levels were observed in stage 4 patients compared with stage 1/2/3 patients (P = .028). Higher D-dimer levels were also observed in patients with higher AFP levels before chemotherapy compared with patients with lower AFP levels after chemotherapy (P< 0.001). In addition, higher D-dimer levels were observed in HB compared with other benign hepatic tumors such as hepatic hemangioma and hepatocellular adenoma (P = .012). No significant difference in D-dimer levels was found between sex (P = .503) and age (≥12 vs <12 months, P = .424). There was no significant difference in plasma fibrinogen levels between sex or age and high-risk HB features, such as advanced stage and high AFP levels. CONCLUSIONS: Elevated D-dimer levels could be a useful determinant biomarker for high-risk features in patients with HB. This finding also supports the clinical application of D-dimer in HB. |
format | Online Article Text |
id | pubmed-5708979 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-57089792017-12-07 Circulating D-dimer level correlates with disease characteristics in hepatoblastoma patients Zhang, BinBin Liu, GongBao Liu, XiangQi Zheng, Shan Dong, Kuiran Dong, Rui Medicine (Baltimore) 6200 OBJECTIVES: Hepatoblastoma (HB) is the most common pediatric liver malignancy, typically affecting children within the first 4 years of life. However, only a few validated blood biomarkers are used in clinical evaluation. The current study explored the clinical application and significance of D-dimer levels in patients with HB. METHOD: Forty-four patients with HB were included in this retrospective study. D-dimer and plasma fibrinogen levels were examined, and their correlation with other clinical features was analyzed. D-dimer and plasma fibrinogen levels were examined between HB and other benign hepatic tumors. RESULTS: D-dimer levels were significantly associated with high-risk HB features, such as advanced stage and high α-fetoprotein (AFP) levels. Higher D-dimer levels were observed in stage 4 patients compared with stage 1/2/3 patients (P = .028). Higher D-dimer levels were also observed in patients with higher AFP levels before chemotherapy compared with patients with lower AFP levels after chemotherapy (P< 0.001). In addition, higher D-dimer levels were observed in HB compared with other benign hepatic tumors such as hepatic hemangioma and hepatocellular adenoma (P = .012). No significant difference in D-dimer levels was found between sex (P = .503) and age (≥12 vs <12 months, P = .424). There was no significant difference in plasma fibrinogen levels between sex or age and high-risk HB features, such as advanced stage and high AFP levels. CONCLUSIONS: Elevated D-dimer levels could be a useful determinant biomarker for high-risk features in patients with HB. This finding also supports the clinical application of D-dimer in HB. Wolters Kluwer Health 2017-11-27 /pmc/articles/PMC5708979/ /pubmed/29381980 http://dx.doi.org/10.1097/MD.0000000000008798 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 6200 Zhang, BinBin Liu, GongBao Liu, XiangQi Zheng, Shan Dong, Kuiran Dong, Rui Circulating D-dimer level correlates with disease characteristics in hepatoblastoma patients |
title | Circulating D-dimer level correlates with disease characteristics in hepatoblastoma patients |
title_full | Circulating D-dimer level correlates with disease characteristics in hepatoblastoma patients |
title_fullStr | Circulating D-dimer level correlates with disease characteristics in hepatoblastoma patients |
title_full_unstemmed | Circulating D-dimer level correlates with disease characteristics in hepatoblastoma patients |
title_short | Circulating D-dimer level correlates with disease characteristics in hepatoblastoma patients |
title_sort | circulating d-dimer level correlates with disease characteristics in hepatoblastoma patients |
topic | 6200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708979/ https://www.ncbi.nlm.nih.gov/pubmed/29381980 http://dx.doi.org/10.1097/MD.0000000000008798 |
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