Antibody profile and clinical course in primary anti phospholipid syndrome with pregnancy morbidity

被引:135
作者
Ruffatti, Amelia
Tonello, Marta
Del Ross, Teresa
Cavazzana, Anna
Grava, Chiara
Noventa, Franco
Tona, Francesco
Iliceto, Sabino
Pengo, Vittorio
机构
[1] Univ Padua, Dept Clin & Expt Med, Div Rheumatol & Clin Med 25th, I-35128 Padua, Italy
[2] Univ Padua, Dept Cardiothorac & Vasc Sci, I-35128 Padua, Italy
关键词
antiphospholipid antibodies; thrombophilia; pregnancy;
D O I
10.1160/TH06-05-0287
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In women diagnosed as having category I primary obstetric anti-phospholipid syndrome, clinical characteristics and the risk of subsequent thromboembolic events and further unsuccessful pregnancy has not been clearly documented. Women with unexplained obstetric complications and no definite autoimmune systemic diseases were tested for lupus anticoagulant (LA), IgG/IgM anticardiolipin (aCL) and IgG/IgM anti-human beta 2-Glycoprotein I (a beta 2GPI) antibodies and diagnosed as having primary anti-phospholipid syndrome (APS) in classification category I on the basis of more than one laboratory criteria present in any combination. Characteristics at the time of diagnosis and risk factors for subsequent clinical events during a mean follow-up of 6.3 years were evaluated. Fifty-three of 600 women studied were found to fulfil obstetric criteria and had more than one positive laboratory test at the time of diagnosis. All the women were aCL and a beta 2GPI positive, and 16 were also LA positive. This latter group (triple positivity) had distinct features and had more frequently experienced previous thromboembolism (OR= 122.5, 95% Cl 16-957,p < 0.001). They also had an increased rate of late pregnancy loss (OR= 16.2,95% Cl 0.9-292, p=0.01), and a higher IgG a beta 2GPI titer at diagnosis (median, 25(th) and 75(th) percentile were 118, 37-962, vs. 23, 18-32, respectively, p < 0.0001). During follow-up, the rate of thromboembolic events was significantly higher in the group of women with triple positivity and/ or previous thromboembolism (OR=57.5, 95% Cl 2.7-1160, p=0.0004) which were the only independent predictors of TE in the multivariate model. Recurrent pregnancy loss took place in seven out of 47 women who had a new pregnancy. Triple positivity and/or previous thromboembolism were again the only independent markers (OR=34.4,95% Cl 3.5-335.1, p=0.003) of an unsuccessful new pregnancy. In conclusion, in primary APS with pregnancy morbidity in classification category I, quite different groups of patients may be identified on the basis of laboratory tests. Triple positivity and/or a history of thromboembolism predict new TE events and new unsuccessful pregnancies.
引用
收藏
页码:337 / 341
页数:5
相关论文
共 32 条
[1]  
ALLISON PD, 1999, LOGISTIC REGRESSION, P39
[2]   PRELIMINARY CRITERIA FOR THE CLASSIFICATION OF SYSTEMIC-SCLEROSIS (SCLERODERMA) [J].
不详 .
ARTHRITIS AND RHEUMATISM, 1980, 23 (05) :581-590
[3]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[4]   ANTIPHOSPHOLIPID ANTIBODIES ARE NOT PRESENT IN THE MEMBRANE OF GEL-FILTERED PLATELETS OF PATIENTS WITH IGG ANTICARDIOLIPIN ANTIBODIES, LUPUS ANTICOAGULANT AND THROMBOSIS [J].
BIASIOLO, A ;
PENGO, V .
BLOOD COAGULATION & FIBRINOLYSIS, 1993, 4 (03) :425-428
[5]   POLYMYOSITIS AND DERMATOMYOSITIS .1. [J].
BOHAN, A ;
PETER, JB .
NEW ENGLAND JOURNAL OF MEDICINE, 1975, 292 (07) :344-347
[6]  
Branch DW, 2004, THROMB RES, V114, P415, DOI 10.1016/j.thromres.2004.08.005
[7]   OBSTETRIC COMPLICATIONS ASSOCIATED WITH THE LUPUS ANTICOAGULANT [J].
BRANCH, DW ;
SCOTT, JR ;
KOCHENOUR, NK ;
HERSHGOLD, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 313 (21) :1322-1326
[8]  
BRANDT JT, 1995, THROMB HAEMOSTASIS, V74, P1185
[9]   Do antibodies to β2-glycoprotein 1 contribute to the better characterization of the antiphospholipid syndrome? [J].
Detková, D ;
Gil-Aguado, A ;
Lavilla, P ;
Cuesta, MV ;
Fontán, G ;
Pascual-Salcedo, D .
LUPUS, 1999, 8 (06) :430-438
[10]  
Erkan D, 2001, ARTHRITIS RHEUM, V44, P1466, DOI 10.1002/1529-0131(200106)44:6<1466::AID-ART242>3.0.CO