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Hemostatic Dysfunction Is Increased in Patients with Hepatosplenic Schistosomiasis Mansoni and Advanced Periportal Fibrosis

BACKGROUND: Schistosomiasis mansoni is an endemic parasitic disease and a public health problem in Northeast Brazil. In some patients, hepatic abnormalities lead to periportal fibrosis and result in the most severe clinical form, hepatosplenic schistosomiasis. This study aimed to evaluate whether ab...

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Autores principales: Leite, Luiz Arthur Calheiros, Pimenta Filho, Adenor Almeida, da Fonseca, Caíque Silveira Martins, dos Santos, Bianka Santana, Ferreira, Rita de Cássia dos Santos, Montenegro, Silvia Maria Lucena, Lopes, Edmundo Pessoa, Domingues, Ana Lúcia Coutinho, Owen, James Stuart, Lima, Vera Lúcia de Menezes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715409/
https://www.ncbi.nlm.nih.gov/pubmed/23875049
http://dx.doi.org/10.1371/journal.pntd.0002314
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author Leite, Luiz Arthur Calheiros
Pimenta Filho, Adenor Almeida
da Fonseca, Caíque Silveira Martins
dos Santos, Bianka Santana
Ferreira, Rita de Cássia dos Santos
Montenegro, Silvia Maria Lucena
Lopes, Edmundo Pessoa
Domingues, Ana Lúcia Coutinho
Owen, James Stuart
Lima, Vera Lúcia de Menezes
author_facet Leite, Luiz Arthur Calheiros
Pimenta Filho, Adenor Almeida
da Fonseca, Caíque Silveira Martins
dos Santos, Bianka Santana
Ferreira, Rita de Cássia dos Santos
Montenegro, Silvia Maria Lucena
Lopes, Edmundo Pessoa
Domingues, Ana Lúcia Coutinho
Owen, James Stuart
Lima, Vera Lúcia de Menezes
author_sort Leite, Luiz Arthur Calheiros
collection PubMed
description BACKGROUND: Schistosomiasis mansoni is an endemic parasitic disease and a public health problem in Northeast Brazil. In some patients, hepatic abnormalities lead to periportal fibrosis and result in the most severe clinical form, hepatosplenic schistosomiasis. This study aimed to evaluate whether abnormal blood coagulation and liver function tests in patients with hepatosplenic schistosomiasis (n = 55) correlate with the severity of their periportal fibrosis. METHODOLOGY/PRINCIPAL FINDINGS: Blood samples were used for liver function tests, hemogram and prothrombin time (International Normalized Ratio, INR). The blood coagulation factors (II, VII, VIII, IX and X), protein C and antithrombin IIa (ATIIa), plasminogen activator inhibitor 1 (PAI-1) and D-dimer were measured by photometry or enzyme linked immunosorbent assay. Hyperfibrinolysis was defined on the basis of PAI-1 levels and a D-dimer concentration greater than a standard cut-off of 483 ng/mL. Standard liver function tests were all abnormal in the patient group compared to healthy controls (n = 29), including raised serum transaminases (p<0.001) and lower levels of albumin (p = 0.0156). Platelet counts were 50% lower in patients, while for coagulation factors there was a 40% increase in the INR (p<0.001) and reduced levels of Factor VII and protein C in patients compared to the controls (both p<0.001). Additionally, patients with more advanced fibrosis (n = 38) had lower levels of protein C compared to those with only central fibrosis (p = 0.0124). The concentration of plasma PAI-1 in patients was one-third that of the control group (p<0.001), and D-dimer levels 2.2 times higher (p<0.001) with 13 of the 55 patients having levels above the cut-off. CONCLUSION/SIGNIFICANCE: This study confirms that hemostatic abnormalities are associated with reduced liver function and increased liver fibrosis. Of note was the finding that a quarter of patients with hepatosplenic schistosomiasis and advanced periportal fibrosis have hyperfibrinolysis, as judged by excessive levels of D-dimer, which may predispose them to gastrointestinal bleeding.
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spelling pubmed-37154092013-07-19 Hemostatic Dysfunction Is Increased in Patients with Hepatosplenic Schistosomiasis Mansoni and Advanced Periportal Fibrosis Leite, Luiz Arthur Calheiros Pimenta Filho, Adenor Almeida da Fonseca, Caíque Silveira Martins dos Santos, Bianka Santana Ferreira, Rita de Cássia dos Santos Montenegro, Silvia Maria Lucena Lopes, Edmundo Pessoa Domingues, Ana Lúcia Coutinho Owen, James Stuart Lima, Vera Lúcia de Menezes PLoS Negl Trop Dis Research Article BACKGROUND: Schistosomiasis mansoni is an endemic parasitic disease and a public health problem in Northeast Brazil. In some patients, hepatic abnormalities lead to periportal fibrosis and result in the most severe clinical form, hepatosplenic schistosomiasis. This study aimed to evaluate whether abnormal blood coagulation and liver function tests in patients with hepatosplenic schistosomiasis (n = 55) correlate with the severity of their periportal fibrosis. METHODOLOGY/PRINCIPAL FINDINGS: Blood samples were used for liver function tests, hemogram and prothrombin time (International Normalized Ratio, INR). The blood coagulation factors (II, VII, VIII, IX and X), protein C and antithrombin IIa (ATIIa), plasminogen activator inhibitor 1 (PAI-1) and D-dimer were measured by photometry or enzyme linked immunosorbent assay. Hyperfibrinolysis was defined on the basis of PAI-1 levels and a D-dimer concentration greater than a standard cut-off of 483 ng/mL. Standard liver function tests were all abnormal in the patient group compared to healthy controls (n = 29), including raised serum transaminases (p<0.001) and lower levels of albumin (p = 0.0156). Platelet counts were 50% lower in patients, while for coagulation factors there was a 40% increase in the INR (p<0.001) and reduced levels of Factor VII and protein C in patients compared to the controls (both p<0.001). Additionally, patients with more advanced fibrosis (n = 38) had lower levels of protein C compared to those with only central fibrosis (p = 0.0124). The concentration of plasma PAI-1 in patients was one-third that of the control group (p<0.001), and D-dimer levels 2.2 times higher (p<0.001) with 13 of the 55 patients having levels above the cut-off. CONCLUSION/SIGNIFICANCE: This study confirms that hemostatic abnormalities are associated with reduced liver function and increased liver fibrosis. Of note was the finding that a quarter of patients with hepatosplenic schistosomiasis and advanced periportal fibrosis have hyperfibrinolysis, as judged by excessive levels of D-dimer, which may predispose them to gastrointestinal bleeding. Public Library of Science 2013-07-18 /pmc/articles/PMC3715409/ /pubmed/23875049 http://dx.doi.org/10.1371/journal.pntd.0002314 Text en © 2013 Leite 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
Leite, Luiz Arthur Calheiros
Pimenta Filho, Adenor Almeida
da Fonseca, Caíque Silveira Martins
dos Santos, Bianka Santana
Ferreira, Rita de Cássia dos Santos
Montenegro, Silvia Maria Lucena
Lopes, Edmundo Pessoa
Domingues, Ana Lúcia Coutinho
Owen, James Stuart
Lima, Vera Lúcia de Menezes
Hemostatic Dysfunction Is Increased in Patients with Hepatosplenic Schistosomiasis Mansoni and Advanced Periportal Fibrosis
title Hemostatic Dysfunction Is Increased in Patients with Hepatosplenic Schistosomiasis Mansoni and Advanced Periportal Fibrosis
title_full Hemostatic Dysfunction Is Increased in Patients with Hepatosplenic Schistosomiasis Mansoni and Advanced Periportal Fibrosis
title_fullStr Hemostatic Dysfunction Is Increased in Patients with Hepatosplenic Schistosomiasis Mansoni and Advanced Periportal Fibrosis
title_full_unstemmed Hemostatic Dysfunction Is Increased in Patients with Hepatosplenic Schistosomiasis Mansoni and Advanced Periportal Fibrosis
title_short Hemostatic Dysfunction Is Increased in Patients with Hepatosplenic Schistosomiasis Mansoni and Advanced Periportal Fibrosis
title_sort hemostatic dysfunction is increased in patients with hepatosplenic schistosomiasis mansoni and advanced periportal fibrosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715409/
https://www.ncbi.nlm.nih.gov/pubmed/23875049
http://dx.doi.org/10.1371/journal.pntd.0002314
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