Factor V:Q(506) mutation and anticardiolipin antibodies in systemic lupus erythematosus

被引:17
作者
Bengtsson, A [1 ]
Zoller, B [1 ]
de Frutos, PG [1 ]
Dahlback, B [1 ]
Sturfelt, G [1 ]
机构
[1] MALMO GEN HOSP, DEPT CLIN CHEM, S-20502 MALMO, SWEDEN
关键词
factor V; SLE; APC-resistance; thrombosis; aCL;
D O I
10.1177/096120339600500607
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Inherited resistance to activated protein C (APC resistance) is an important risk factor of venous thrombosis. It is caused by a point mutation in the gene coding for coagulation factor V, called FV:Q(506). Arterio-venous thrombosis is a common and serious medical problem in patients with systemic lupus erythematosus (SLE). We studied the prevalence of the factor V mutation associated with APC resistance and IgG anticardiolipin antibodies (aCLs) in an epidemiological cohort of 78 Swedish SLE patients, to determine their roles as risk factors for thrombosis. In addition, a detailed evaluation of the clinical manifestations in these patients was performed. Totally, 19 (24%) of the 78 SLE patients had thrombosis, 11 (14%) had venous thrombosis and 8 (10%) had a cerebral infarction caused by occlusion of cerebral vessels. Twenty-six (33%) SLE patients were aCL positive and 8 (10%) were heterozygous for the factor V mutation. Only one of the patients with venous thrombosis and one of the patients with cerebral thrombosis had the FV:Q(506) mutation, whereas 3 patients with venous thrombosis and 5 patients with cerebral infarction were aCL positive. Eleven of 19 patients with heart valve disease were aCL positive, a statistically significant association (P=0.01). In conclusion, we found no statistically significant association between venous thrombosis and FV:Q(506) mutation or venous thrombosis and aCL positivity. There was, however, an association between heart valve disease and aCL positivity.
引用
收藏
页码:598 / 601
页数:4
相关论文
共 47 条
[1]  
ASHERSON RA, 1992, J RHEUMATOL, V11, P370
[2]   MUTATION IN BLOOD-COAGULATION FACTOR-V ASSOCIATED WITH RESISTANCE TO ACTIVATED PROTEIN-C [J].
BERTINA, RM ;
KOELEMAN, BPC ;
KOSTER, T ;
ROSENDAAL, FR ;
DIRVEN, RJ ;
DERONDE, H ;
VANDERVELDEN, PA ;
REITSMA, PH .
NATURE, 1994, 369 (6475) :64-67
[3]  
BEUCHAMP NJ, 1994, BRIT J HAEMATOL, V88, P219
[4]   SYSTEMIC LUPUS-ERYTHEMATOSUS - EMERGING CONCEPTS .2. DERMATOLOGICAL AND JOINT DISEASE, THE ANTIPHOSPHOLIPID ANTIBODY SYNDROME, PREGNANCY AND HORMONAL-THERAPY, MORBIDITY AND MORTALITY, AND PATHOGENESIS [J].
BOUMPAS, DT ;
FESSLER, BJ ;
AUSTIN, HA ;
BALOW, JE ;
KLIPPEL, JH ;
LOCKSHIN, MD .
ANNALS OF INTERNAL MEDICINE, 1995, 123 (01) :42-53
[5]   FAMILIAL THROMBOPHILIA DUE TO A PREVIOUSLY UNRECOGNIZED MECHANISM CHARACTERIZED BY POOR ANTICOAGULANT RESPONSE TO ACTIVATED PROTEIN-C - PREDICTION OF A COFACTOR TO ACTIVATED PROTEIN-C [J].
DAHLBACK, B ;
CARLSSON, M ;
SVENSSON, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (03) :1004-1008
[6]   THE PROTEIN-C ANTICOAGULANT SYSTEM - INHERITED DEFECTS AS BASIS FOR VENOUS THROMBOSIS [J].
DAHLBACK, B .
THROMBOSIS RESEARCH, 1995, 77 (01) :1-43
[7]  
DAHLBACK B, 1983, BLOOD, V62, P218
[8]   FACTOR-V LEIDEN MUTATION AND VENOUS THROMBOSIS [J].
DAVIES, KA ;
IRELAND, H ;
ATHANASSIOU, P ;
LOIZOU, S ;
LANE, D ;
WALPORT, MJ .
LANCET, 1995, 345 (8942) :132-133
[9]  
FAIONI EM, 1993, THROMB HAEMOSTASIS, V70, P1067
[10]  
FAUNO P, 1995, THROMB HAEMOSTASIS, V73, P1371