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Decreased Levels of Histidine-Rich Glycoprotein in Advanced Lung Cancer: Association with Prothrombotic Alterations

BACKGROUND: Histidine-rich glycoprotein (HRG) displays anticoagulant and antifibrinolytic properties in animal models, but its effects in humans are unclear. We investigated serum HRG levels and their associations with the disease stage and prothrombotic alterations in lung cancer (LC) patients. MET...

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Autores principales: Winiarska, Aleksandra, Zareba, Lech, Krolczyk, Grzegorz, Czyzewicz, Grzegorz, Zabczyk, Michal, Undas, Anetta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421726/
https://www.ncbi.nlm.nih.gov/pubmed/30944671
http://dx.doi.org/10.1155/2019/8170759
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author Winiarska, Aleksandra
Zareba, Lech
Krolczyk, Grzegorz
Czyzewicz, Grzegorz
Zabczyk, Michal
Undas, Anetta
author_facet Winiarska, Aleksandra
Zareba, Lech
Krolczyk, Grzegorz
Czyzewicz, Grzegorz
Zabczyk, Michal
Undas, Anetta
author_sort Winiarska, Aleksandra
collection PubMed
description BACKGROUND: Histidine-rich glycoprotein (HRG) displays anticoagulant and antifibrinolytic properties in animal models, but its effects in humans are unclear. We investigated serum HRG levels and their associations with the disease stage and prothrombotic alterations in lung cancer (LC) patients. METHODS: In 148 patients with advanced LC prior to anticancer therapy (87 non-small-cell LC and 61 small-cell LC) versus 100 well-matched controls, we measured HRG levels in association with clot permeability (K(s)), clot turbidimetry (lag phase and maximum absorbance), and clot lysis time (CLT). RESULTS: Compared to controls, LC patients had 45.9% lower HRG levels with no associations with demographics and comorbidities. Decreased HRG, defined as the 90(th) percentile of control values (<52.7 μg/ml), was 16 times more common in subjects with than without LC (OR = 16.4, 95% CI 9.2-23.5, p < 0.01). HRG < 38 μg/ml discriminated stage IIIAB/limited disease from IV/extensive disease (ED) LC. In LC patients, HRG correlated inversely with CLT (r = −0.41, p < 0.001), but not with other fibrin variables. Among stage IV/ED LC, HRG correlated significantly with K(s) and lag phase (r = 0.28 and r = 0.33, respectively, both p < 0.001). LC patients with low K(s) (10(th) percentile of control values) combined with prolonged CLT (90(th) percentile of control values) had reduced HRG levels compared to the remainder (p = 0.003). No such observations were noted in controls. CONCLUSIONS: Our study is the first to show that decreased HRG levels occur in advanced LC and are associated with the disease stage and hypofibrinolysis.
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spelling pubmed-64217262019-04-03 Decreased Levels of Histidine-Rich Glycoprotein in Advanced Lung Cancer: Association with Prothrombotic Alterations Winiarska, Aleksandra Zareba, Lech Krolczyk, Grzegorz Czyzewicz, Grzegorz Zabczyk, Michal Undas, Anetta Dis Markers Research Article BACKGROUND: Histidine-rich glycoprotein (HRG) displays anticoagulant and antifibrinolytic properties in animal models, but its effects in humans are unclear. We investigated serum HRG levels and their associations with the disease stage and prothrombotic alterations in lung cancer (LC) patients. METHODS: In 148 patients with advanced LC prior to anticancer therapy (87 non-small-cell LC and 61 small-cell LC) versus 100 well-matched controls, we measured HRG levels in association with clot permeability (K(s)), clot turbidimetry (lag phase and maximum absorbance), and clot lysis time (CLT). RESULTS: Compared to controls, LC patients had 45.9% lower HRG levels with no associations with demographics and comorbidities. Decreased HRG, defined as the 90(th) percentile of control values (<52.7 μg/ml), was 16 times more common in subjects with than without LC (OR = 16.4, 95% CI 9.2-23.5, p < 0.01). HRG < 38 μg/ml discriminated stage IIIAB/limited disease from IV/extensive disease (ED) LC. In LC patients, HRG correlated inversely with CLT (r = −0.41, p < 0.001), but not with other fibrin variables. Among stage IV/ED LC, HRG correlated significantly with K(s) and lag phase (r = 0.28 and r = 0.33, respectively, both p < 0.001). LC patients with low K(s) (10(th) percentile of control values) combined with prolonged CLT (90(th) percentile of control values) had reduced HRG levels compared to the remainder (p = 0.003). No such observations were noted in controls. CONCLUSIONS: Our study is the first to show that decreased HRG levels occur in advanced LC and are associated with the disease stage and hypofibrinolysis. Hindawi 2019-03-03 /pmc/articles/PMC6421726/ /pubmed/30944671 http://dx.doi.org/10.1155/2019/8170759 Text en Copyright © 2019 Aleksandra Winiarska et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Winiarska, Aleksandra
Zareba, Lech
Krolczyk, Grzegorz
Czyzewicz, Grzegorz
Zabczyk, Michal
Undas, Anetta
Decreased Levels of Histidine-Rich Glycoprotein in Advanced Lung Cancer: Association with Prothrombotic Alterations
title Decreased Levels of Histidine-Rich Glycoprotein in Advanced Lung Cancer: Association with Prothrombotic Alterations
title_full Decreased Levels of Histidine-Rich Glycoprotein in Advanced Lung Cancer: Association with Prothrombotic Alterations
title_fullStr Decreased Levels of Histidine-Rich Glycoprotein in Advanced Lung Cancer: Association with Prothrombotic Alterations
title_full_unstemmed Decreased Levels of Histidine-Rich Glycoprotein in Advanced Lung Cancer: Association with Prothrombotic Alterations
title_short Decreased Levels of Histidine-Rich Glycoprotein in Advanced Lung Cancer: Association with Prothrombotic Alterations
title_sort decreased levels of histidine-rich glycoprotein in advanced lung cancer: association with prothrombotic alterations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421726/
https://www.ncbi.nlm.nih.gov/pubmed/30944671
http://dx.doi.org/10.1155/2019/8170759
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