Do prothrombotic factors influence clinical phenotype of severe haemophilia? - A review of the literature

被引:60
作者
van Dijk, K
van der Bom, JG
Fischer, K
Grobbee, DE
van den Berg, HM
机构
[1] UMCU, Van Creveldklin, Dutch Natl Hemophilia Treatment Ctr, NL-3508 GA Utrecht, Netherlands
[2] UMC, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[3] UMC, Dept Clin Epidemiol, Leiden, Netherlands
[4] UMC, Wilhelmina Childrens Hosp, Utrecht, Netherlands
关键词
severe haemophilia; phenotype; prothrombotic factors;
D O I
10.1160/TH04-02-0112
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There is considerable variability in bleeding patterns of severe haemophilia (< 1% factor VIII). Knowledge of the contribution of thrombophilic factors in these patterns may improve individually tailored treatment strategies. We reviewed the literature regarding the relation between prothrombotic factors and clinical phenotype of severe haemophilia. Medline and EMBASE were searched for relevant articles. 9369 articles published between 1963 and September 2003 were screened and seven relevant papers were retrieved. Each of these reported on a different combination of thrombophilic factors. Presence of the factor V Leiden mutation appears to decrease the severity of severe haemophilia most consistently. Findings on other thrombophilic factors were inconclusive. There is a clear need for additional research on potential determinants of phenotypes of severe haemophilia before such knowledge can be translated into individual care for severe haemophilia patients with confidence.
引用
收藏
页码:305 / 310
页数:6
相关论文
共 46 条
[31]  
Nowak-Gottl U, 2003, Hamostaseologie, V23, P36
[32]  
PETKOVA R, 2001, BALK J MED GENET, V4, P37
[33]  
PETTERSSON H, 1980, CLIN ORTHOP RELAT R, P153
[34]   When are children diagnosed as having severe haemophilia and when do they start to bleed?: A 10-year single-centre PUP study [J].
Pollmann, H ;
Richter, H ;
Ringkamp, H ;
Jürgens, H .
EUROPEAN JOURNAL OF PEDIATRICS, 1999, 158 (Suppl 3) :S166-S170
[35]   A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis [J].
Poort, SR ;
Rosendaal, FR ;
Reitsma, PH ;
Bertina, RM .
BLOOD, 1996, 88 (10) :3698-3703
[36]   3-YEAR STUDY OF ADOLESCENT BOYS SUFFERING FROM HEMOPHILIA AND ALLIED DISORDERS [J].
RAINSFORD, SG ;
HALL, A .
BRITISH JOURNAL OF HAEMATOLOGY, 1973, 24 (05) :539-551
[37]  
RAMGREN O, 1962, ACTA MED SCAND, V171, P237
[38]   MUTATION IN THE GENE CODING FOR COAGULATION-FACTOR-V AND THE RISK OF MYOCARDIAL-INFARCTION, STROKE, AND VENOUS THROMBOSIS IN APPARENTLY HEALTHY-MEN [J].
RIDKER, PM ;
HENNEKENS, CH ;
LINDPAINTER, K ;
STAMPFER, MJ ;
EISENBERG, PR ;
MILETICH, JP .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (14) :912-917
[39]   Thrombin generation in severe haemophilia A and B: the endogenous thrombin potential in platelet-rich plasma [J].
Siegemund, T ;
Petros, S ;
Siegemund, A ;
Scholz, U ;
Engelmann, L .
THROMBOSIS AND HAEMOSTASIS, 2003, 90 (05) :781-786
[40]  
Souto JC, 1998, THROMB HAEMOSTASIS, V80, P366