Risk factors for clinical manifestations in carriers of Factor V Leiden and prothrombin gene mutations

被引:6
|
作者
DeSancho, Maria Teresa [1 ]
Berlus, Nickisha [2 ]
Christos, Paul J. [3 ]
Rand, Jacob [4 ]
机构
[1] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, New Brunswick, NJ USA
[3] Cornell Univ, Div Biostat & Epidemiol, Weill Med Coll, Dept Publ Hlth, Bronx, NY USA
[4] Albert Einstein Coll Med, Bronx, NY 10467 USA
关键词
aPLAs; arterial thrombosis; case-control study; FVL; hereditary thrombophilia; PGM; recurrent pregnancy loss; risk factors; venous thrombosis; RECURRENT PREGNANCY LOSS; VENOUS THROMBOSIS; ORAL-CONTRACEPTIVES; PULMONARY-EMBOLISM; G20210A MUTATION; BLOOD-GROUP; THROMBOPHILIA; THROMBOEMBOLISM; WOMEN; POPULATION;
D O I
10.1097/MBC.0b013e32832d6ce7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Carriers of Factor V Leiden and prothrombin G20210A gene mutations have an increased risk of developing thromboembolic events and adverse outcomes of pregnancy. The objective of the present study was to identify risk factors which may predispose carriers of Factor V Leiden and/or prothrombin G20210A gene mutations to develop thromboembolic events and adverse outcomes of pregnancy. A retrospective case-control study of 217 carriers of Factor V Leiden and/or prothrombin G20210A gene mutations at two tertiary centers between January 2000 and December 2006. Symptomatic carriers (cases) were compared with asymptomatic carriers (controls) for the following risk factors: environmental, cardiovascular, family history of thrombosis, and presence of other thrombophilias. For female carriers, we included the use of female hormones, pregnancy, and the postpartum period. Of the 217 carriers, there were 155 (71%) cases and 62 (29%) controls. Of the 155 cases, 90 (58%) had venous thrombosis and 26 (17%) arterial thrombosis. Among the 123 symptomatic female carriers, 55 (45%) had recurrent pregnancy losses and nine (7%) other adverse outcomes of pregnancy. The postoperative state and the presence of antiphospholipid antibodies were risk factors for thromboembolic events and adverse outcomes of pregnancy in 10 (6%) and 22 (13%) cases, respectively. The presence of antiphospholipid antibodies in symptomatic carriers increased the risk of developing thromboembolic events 4.4-fold. The postoperative state and the presence of anti phospholipid antibodies were significant risk factors for thromboembolic events and adverse outcomes of pregnancy among Factor V Leiden and/or prothrombin G20210A gene mutation carriers. Testing for the presence of antiphospholipid antibodies may be warranted in Factor V Leiden and/or prothrombin G20210A gene mutation carriers who develop these adverse clinical manifestations. Blood Coagul Fibrinolysis 21:11-15 (C) 2010 Wolters Kluwer Health | Lippincott Williams & Wilkins.
引用
收藏
页码:11 / 15
页数:5
相关论文
共 50 条
  • [31] Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives
    Aznar, J
    Vaya, A
    Estellés, A
    Mira, Y
    Seguí, R
    Villa, P
    Ferrando, F
    Falco, C
    Corella, D
    Espana, F
    HAEMATOLOGICA, 2000, 85 (12) : 1271 - 1276
  • [32] PHENOTYPIC PRESENTATION OF THROMBOPHILIA IN DOUBLE HETEROZYGOTE FOR FACTOR V LEIDEN AND PROTHROMBIN 20210 G>A MUTATIONS - CASE REPORT
    Nagorni-Obradovic, Ljudmila
    Maksimovic, Nela
    Miljic, Predrag
    Cvetkovic, Dragana
    Stevic, Ruza
    Pesut, Dragica
    GENETIKA-BELGRADE, 2014, 46 (02): : 621 - 629
  • [33] Clinical significance of factor V Leiden and prothrombin G20210A-mutations in cerebral venous thrombosis - comparison with arterial ischemic stroke
    Beye, Aida
    Pindur, Gerhard
    CLINICAL HEMORHEOLOGY AND MICROCIRCULATION, 2017, 67 (3-4) : 261 - 266
  • [34] Risk of cardiovascular disease in double heterozygous carriers and homozygous carriers of F5 R506Q (factor V Leiden) and F2 (prothrombin) G20210A: a retrospective family cohort study
    Roach, Rachel E. J.
    Roshani, Sara
    Meijer, Karina
    Hamulyak, Karly
    Lijfering, Willem M.
    Prins, Martin H.
    Buller, Harry R.
    Middeldorp, Saskia
    BRITISH JOURNAL OF HAEMATOLOGY, 2011, 153 (01) : 134 - 136
  • [35] The association of factor V Leiden with various clinical patterns of venous thromboembolism-the factor V Leiden paradox
    Hirmerova, J.
    Seidlerova, J.
    Subrt, I.
    QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 2014, 107 (09) : 715 - 720
  • [36] Mesenteric vein thrombosis in a patient heterozygous for factor V Leiden and G20210A prothrombin genotypes
    Karmacharya, Paras
    Aryal, Madan Raj
    Donato, Anthony
    WORLD JOURNAL OF GASTROENTEROLOGY, 2013, 19 (43) : 7813 - 7815
  • [37] Factor V Leiden, prothrombin 20210A and the risk of venous thrombosis among cancer patients
    Kennedy, M
    Andreescu, ACM
    Greenblatt, MS
    Jiang, HY
    Thomas, CA
    Chassereau, L
    Wong, C
    Durda, P
    Cushman, M
    BRITISH JOURNAL OF HAEMATOLOGY, 2005, 128 (03) : 386 - 388
  • [38] Prenatal thrombosis of renal veins and the inferior vena cava in a newborn with double heterozygosity for the factor V Leiden and prothrombin gene G20210A mutations: a case report
    Bulut, Ozgul
    Ince, Zeynep
    Uzunhan, Ozan
    Coban, Asuman
    BLOOD COAGULATION & FIBRINOLYSIS, 2018, 29 (02) : 220 - 222
  • [39] Outcome of Patients with Venous Thromboembolism and Factor V Leiden or Prothrombin 20210 Carrier Mutations During the Course of Anticoagulation
    Tzoran, Inna
    Papadakis, Manolis
    Brenner, Benjamin
    Fidalgo, Angeles
    Rivas, Agustina
    Wells, Philip S.
    Gavin, Olga
    Dolores Adarraga, Maria
    Moustafa, Fares
    Monreal, Manuel
    AMERICAN JOURNAL OF MEDICINE, 2017, 130 (04): : 482.e1 - 482.e9
  • [40] Prevalence and association of the factor V Leiden and prothrombin G20210A in healthy subjects and patients with venous thromboembolism
    Coen, D
    Zadro, R
    Honovic, L
    Banfic, L
    Rukavina, AS
    CROATIAN MEDICAL JOURNAL, 2001, 42 (04) : 488 - 492