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Kempfer, Ana Catalina  
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Paiva, J.  
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Woods, Adriana Inés  
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Nuñez, M.  
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Ponteville, C.  
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Casinelli, Maria Marta  
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Lazzari, María Ángela  
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Sánchez Luceros, Analía Gabriela  
dc.date.available
2024-12-02T10:04:32Z  
dc.date.issued
2019  
dc.identifier.citation
ADAMTS13 Antigen together to collagen binding to von Willebrand Factor (VWF:CB) and VWF Antigen (VWF:Ag) were potential markers of acute disease severity in acquired thrombotic thrombocytopenic purpura (aTTP); XXVII Congress of the International Society on Thrombosis and Haemostasis; Melbourne; Australia; 2019; 1-2  
dc.identifier.issn
2451-9456  
dc.identifier.uri
http://hdl.handle.net/11336/249076  
dc.description.abstract
Background : The reduced levels of circulating ADAMTS13 antigen (Ag), at first presentation in patients (P) with non- inhibitory antibodies (ab), appear to be a major determinant of disease severity in aTTP (Thomas, 2015). Lack of larger VWF multimers was strongly correlated with low VWF:CB/VWF:Ag and the ratio could be a marker of crisis severity aTTP (Lotta, 2011).Aims : To evaluate the relationship between ADAMTS13 parameters and other laboratory markers to the severity of aTTP crisis in 57P.Methods : ADAMTS13 activity, Ag, free IgG, IgM, IgA anti-ADAMTS13 ab, VWF:CB collagen type I, VWF:Ag were evaluated (ELISA). Detection of circulating immune complexes (CIC) was done by A) ELISA with mouse monoclonal ab anti- ADAMTS13 (ABCAM) and anti- human IgG- HRP and B) ADAMTS13Ag kit and anti- humanIgG- HRP. Assessment of von Willebrand multimers by normalized multimer ratio. Interquartile Range (IQR) was obtained using normal plasma. Other variables were reported: platelet count, hematocrit, hemoglobin, white blood cells, and blood group. Informed consent and ethical approval were obtained.Results : Some of our results were reported in Table I. In addition, P usually had their first aTTP episode between their 19 and 74 years. Prevalence of women was 82%. CIC median of positive P (n=10) was 0.52 (IQR, 0.51- 0.65)We verified normal distribution of CIC, VWF:CB, VWF:Ag, Hematocrit, VWF:CB/VWF:Ag, and normalized multimers, whereas ADAMTS13 Ag needed to be Ln- transformed. Correlations were showed in Table II.A multiple linear regression model was applied to generate a more precise estimate of parameters. The result was Ln (ADAMTS13Ag)=- 2.343+0.017VWF:CB- 0.012VWF:Ag.Conclusions : In our cohort, 25% of P tested positive CIC, therefore during aTTP crisis do not seem to be a biomarker of disease severity.We can predict a value of Ln ADAMTS13 Ag from the values of VWF:CB and VWF:Ag. These variables can be candidate markers of disease severity in aTTP as ADAMTS13 Ag is.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Wiley  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
VWD adquirido  
dc.subject
anticuerpos  
dc.subject.classification
Hematología  
dc.subject.classification
Medicina Clínica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
ADAMTS13 Antigen together to collagen binding to von Willebrand Factor (VWF:CB) and VWF Antigen (VWF:Ag) were potential markers of acute disease severity in acquired thrombotic thrombocytopenic purpura (aTTP)  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.type
info:eu-repo/semantics/conferenceObject  
dc.type
info:ar-repo/semantics/documento de conferencia  
dc.date.updated
2022-11-01T23:11:23Z  
dc.journal.pagination
1-2  
dc.journal.pais
Australia  
dc.journal.ciudad
Melbourne  
dc.description.fil
Fil: Kempfer, Ana Catalina. Academia Nacional de Medicina de Buenos Aires. Instituto de Investigaciones Hematológicas "Mariano R. Castex". Departamento de Hemostasia y Trombosis; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
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Fil: Paiva, J.. Academia Nacional de Medicina de Buenos Aires. Instituto de Investigaciones Hematológicas "Mariano R. Castex". Departamento de Hemostasia y Trombosis; Argentina  
dc.description.fil
Fil: Woods, Adriana Inés. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Medicina Experimental. Academia Nacional de Medicina de Buenos Aires. Instituto de Medicina Experimental; Argentina  
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Fil: Nuñez, M.. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; Argentina  
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Fil: Ponteville, C.. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; Argentina  
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Fil: Casinelli, Maria Marta. Academia Nacional de Medicina de Buenos Aires. Instituto de Investigaciones Hematológicas "Mariano R. Castex". Departamento de Hemostasia y Trombosis; Argentina  
dc.description.fil
Fil: Lazzari, María Ángela. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Medicina Experimental. Academia Nacional de Medicina de Buenos Aires. Instituto de Medicina Experimental; Argentina  
dc.description.fil
Fil: Sánchez Luceros, Analía Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Medicina Experimental. Academia Nacional de Medicina de Buenos Aires. Instituto de Medicina Experimental; Argentina  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/toc/24750379/2019/3/S1  
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dc.coverage
Internacional  
dc.type.subtype
Congreso  
dc.description.nombreEvento
XXVII Congress of the International Society on Thrombosis and Haemostasis  
dc.date.evento
2019-07-06  
dc.description.ciudadEvento
Melbourne  
dc.description.paisEvento
Australia  
dc.type.publicacion
Journal  
dc.description.institucionOrganizadora
International Society on Thrombosis and Haemostasis  
dc.source.revista
Research Practice on Thrombosis and Haemostasis  
dc.date.eventoHasta
2019-07-10  
dc.type
Congreso