Role of anti-prothrombin in antiphospholipid syndrome

We studied 99 patients with systemic autoimmune disease (5 males, 94 women; mean age 37 year, range 16-72): 28 Primary Antiphospholipid Syndrome, 67 Systemic lupus Erythematosus, 1 Mixed Connective Tissue Disease, 2 Undifferentiated Connective Tissue Disease and 1 Discoid Lupus. Based on the observa...

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Main Authors: M. Cinquini, M. Vianelli, F. Allegri, R. Cattaneo, G. Balestrieri, A. Tincani
Format: Article
Language:English
Published: PAGEPress Publications 2002-09-01
Series:Reumatismo
Online Access:https://reumatismo.org/index.php/reuma/article/view/79
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spelling doaj-bc0fd92cc89b49439fd65b49b72fbc4d2020-11-24T20:58:38ZengPAGEPress PublicationsReumatismo0048-74492240-26832002-09-0154310.4081/reumatismo.2002.243Role of anti-prothrombin in antiphospholipid syndromeM. CinquiniM. VianelliF. AllegriR. CattaneoG. BalestrieriA. TincaniWe studied 99 patients with systemic autoimmune disease (5 males, 94 women; mean age 37 year, range 16-72): 28 Primary Antiphospholipid Syndrome, 67 Systemic lupus Erythematosus, 1 Mixed Connective Tissue Disease, 2 Undifferentiated Connective Tissue Disease and 1 Discoid Lupus. Based on the observation that native PT shows conformational changes in presence of Ca++ ions and discloses new epitopes available for binding with phospholipids, we performed 3 different methods for the detection of aPT in presence and absence of Ca++, finding a different incidence of specific autoantibodies, associated with clinical features of APS (aPT in presence of Ca++) or non associated (aPT in absence of Ca++). The presence of aPT was significantly associated also with the presence of Lupus Anticoagulant (LAC). The detection of aPT (in presence of Ca++) significantly enhances diagnostic sensibility of APS allowing the identification of a subset of patients (6/99) with clinical features of APS, but with negative LAC, aCL and aβ2-GPI; in fact (limited to thrombotic episodes) the sensibility rises from 56.2% with one test (LAC) to 81.1% with the application of LAC, aCL, aβ2GPI and aPT.https://reumatismo.org/index.php/reuma/article/view/79
collection DOAJ
language English
format Article
sources DOAJ
author M. Cinquini
M. Vianelli
F. Allegri
R. Cattaneo
G. Balestrieri
A. Tincani
spellingShingle M. Cinquini
M. Vianelli
F. Allegri
R. Cattaneo
G. Balestrieri
A. Tincani
Role of anti-prothrombin in antiphospholipid syndrome
Reumatismo
author_facet M. Cinquini
M. Vianelli
F. Allegri
R. Cattaneo
G. Balestrieri
A. Tincani
author_sort M. Cinquini
title Role of anti-prothrombin in antiphospholipid syndrome
title_short Role of anti-prothrombin in antiphospholipid syndrome
title_full Role of anti-prothrombin in antiphospholipid syndrome
title_fullStr Role of anti-prothrombin in antiphospholipid syndrome
title_full_unstemmed Role of anti-prothrombin in antiphospholipid syndrome
title_sort role of anti-prothrombin in antiphospholipid syndrome
publisher PAGEPress Publications
series Reumatismo
issn 0048-7449
2240-2683
publishDate 2002-09-01
description We studied 99 patients with systemic autoimmune disease (5 males, 94 women; mean age 37 year, range 16-72): 28 Primary Antiphospholipid Syndrome, 67 Systemic lupus Erythematosus, 1 Mixed Connective Tissue Disease, 2 Undifferentiated Connective Tissue Disease and 1 Discoid Lupus. Based on the observation that native PT shows conformational changes in presence of Ca++ ions and discloses new epitopes available for binding with phospholipids, we performed 3 different methods for the detection of aPT in presence and absence of Ca++, finding a different incidence of specific autoantibodies, associated with clinical features of APS (aPT in presence of Ca++) or non associated (aPT in absence of Ca++). The presence of aPT was significantly associated also with the presence of Lupus Anticoagulant (LAC). The detection of aPT (in presence of Ca++) significantly enhances diagnostic sensibility of APS allowing the identification of a subset of patients (6/99) with clinical features of APS, but with negative LAC, aCL and aβ2-GPI; in fact (limited to thrombotic episodes) the sensibility rises from 56.2% with one test (LAC) to 81.1% with the application of LAC, aCL, aβ2GPI and aPT.
url https://reumatismo.org/index.php/reuma/article/view/79
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