Risk for Early Pregnancy Loss by Factor XIII Val34Leu: The Impact of Fibrinogen Concentration

被引:11
作者
Dossenbach-Glaninger, Astrid [1 ]
van Trotsenburg, Mick [2 ]
Oberkanins, Christian [3 ]
Atamaniuk, Johanna [4 ]
机构
[1] Rudolfstiftung Hosp, Dept Lab Med, Vienna, Austria
[2] Free Univ Amsterdam, Med Ctr, Dept Obstet & Gynecol, Amsterdam, Netherlands
[3] ViennaLab Diagnost GmbH, A-1120 Vienna, Austria
[4] Kaiser Franz Josef Hosp, Inst Lab Diagnost, A-1100 Vienna, Austria
关键词
recurrent pregnancy loss; factor XIII; fibrinogen; factor XIII Val34Leu polymorphism; coagulation; COAGULATION-FACTOR-XIII; THROMBOPHILIC GENE-MUTATIONS; ACE I/D POLYMORPHISM; RECURRENT MISCARRIAGE; FETAL LOSS; WOMEN; COMPLICATIONS; POPULATION; THROMBOSIS; INTRAUTERINE;
D O I
10.1002/jcla.21626
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BackgroundWe have already described a significantly elevated overall risk for recurrent pregnancy loss (RPL) in women carrying the coagulation factor XIII (FXIII) Val34Leu and/or the plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism assuming that these polymorphisms contribute synergistically to RPL because of impaired hypofibrinolysis. Recent studies on FXIII indicate that the impact of the FXIII 34Leu genotype on fibrin structure and fibrinolysis is affected by fibrinogen concentration. Therefore, we reinvestigated the association between fibrinogen concentrations and FXIII Val34Leu with early RPL. Materials and MethodsIn this case-control study, we enrolled 49 women with a history of two consecutive or three to six nonconsecutive pregnancy losses between the 8th and 12th week of gestation and 48 healthy controls. The risk for RPL in carriers of FXIII 34Leu at fibrinogen levels above or below the median and first tertile of controls was evaluated. ResultsIn carriers of the 34Leu allele, fibrinogen levels below the median (i.e., 300 mg/dl) and the first tertile (i.e., 284 mg/dl) of controls were associated with an increased risk for RPL [(2.9 (1.1-7.7), 3.9(1.0-15.0)]. ConclusionsThe FXIII Val34Leu polymorphism may be associated with the development of early RPL in association with fibrinogen concentrations. At fibrinogen levels in the low normal range, FXIII 34Leu may modify fibrin structure toward an increased resistance to fibrinolysis.
引用
收藏
页码:444 / 449
页数:6
相关论文
共 39 条
  • [1] The factor XIII V34L polymorphism accelerates thrombin activation of factor XIII and affects cross-linked fibrin structure
    Ariens, RAS
    Philippou, H
    Nagaswami, C
    Weisel, JW
    Lane, DA
    Grant, PJ
    [J]. BLOOD, 2000, 96 (03) : 988 - 995
  • [2] Ethnic heterogeneity of the factor XIII Val34Leu polymorphism
    Attié-Castro, FA
    Zago, MA
    Lavinha, J
    Elion, J
    Rodriguez-Delfin, L
    Guerreiro, JF
    Franco, RF
    [J]. THROMBOSIS AND HAEMOSTASIS, 2000, 84 (04) : 601 - 603
  • [3] Tyr204Phe and Val34Leu polymorphisms in two Brazilian ethnic groups and in patients with recurrent miscarriages
    Barbosa, HCL
    Carvalho, ECC
    Barini, R
    Siqueira, LH
    Costa, DSP
    Annichino-Bizzacchi, JM
    [J]. FERTILITY AND STERILITY, 2004, 82 (05) : 1455 - 1457
  • [4] Modulation of the risk of coronary sclerosis/myocardial infarction by the interaction between factor XIII subunit A Val34Leu polymorphism and fibrinogen concentration in the high risk Hungarian population
    Bereczky, Zsuzsanna
    Balogh, Emilia
    Katona, Eva
    Pocsai, Zsuzsa
    Czuriga, Istvan
    Szeles, Gyoergy
    Karpati, Levente
    Adany, Roza
    Edes, Istvan
    Muszbek, Laszlo
    [J]. THROMBOSIS RESEARCH, 2007, 120 (04) : 567 - 573
  • [5] Thrombophilia-associated pregnancy wastage
    Blumenfeld, Z
    Brenner, B
    [J]. FERTILITY AND STERILITY, 1999, 72 (05) : 765 - 774
  • [6] Fibrinogen plasma levels modify the association between the factor XIII Val34Leu variant and risk of coronary artery disease: the EPIC-Norfolk prospective population study
    Boekholdt, S. M.
    Sandhu, M. S.
    Wareham, N. J.
    Luben, R.
    Reitsma, P. H.
    Khaw, K-T
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2006, 4 (10) : 2204 - 2209
  • [7] Brenner B, 1999, THROMB HAEMOSTASIS, V82, P634
  • [8] Brenner B, 1999, THROMB HAEMOSTASIS, V82, P6
  • [9] Polymorphisms in the ACE and PAI-1 genes are associated with recurrent spontaneous miscarriages
    Buchholz, T
    Lohse, P
    Rogenhofer, N
    Kosian, E
    Pihusch, R
    Thaler, CJ
    [J]. HUMAN REPRODUCTION, 2003, 18 (11) : 2473 - 2477
  • [10] Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage
    Coulam, CB
    Jeyendran, RS
    Fishel, LA
    Roussev, R
    [J]. AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2006, 55 (05) : 360 - 368