Genotype/phenotype correlations for coagulation factor XIII: Specific normal polymorphisms are associated with high or low factor XIII specific activity

被引:121
作者
Anwar, R [1 ]
Gallivan, L [1 ]
Edmonds, SD [1 ]
Markham, AF [1 ]
机构
[1] Univ Leeds, St Jamess Univ Hosp, Mol Med Unit, Leeds LS9 7TF, W Yorkshire, England
关键词
D O I
10.1182/blood.V93.3.897.403k02_897_905
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Factor XIII is a transglutaminase essential for normal hemostasis. We have studied the plasma FXIII levels and FXIII activity in 71 individuals and found these to be normally distributed. FXIII specific activity is also normally distributed. However, we show that FXIII activity is not directly dependent on FXIII revels, and individuals with low FXIII levels may have high FXIII activity and vice versa. We have determined the FXIIIA genotype in these individuals to assess whether the variation observed in FXIII specific activity is dependent on specific polymorphisms in the FXIIIA gene. Our data show that the Leu34 and Leu564 variants give rise to increased FXIII specific activity, while the Phe204 variant results in lower FXIII specific activity. We also report preliminary evidence that the Phe204 polymorphism may be associated with recurrent miscarriage. Overall, we have identified 23 unique FXIIIA genotypes. Certain specific FXIIIA genotypes consistently give rise to high, low, or median FXIII specific activity levels, while others appear to have little or no consistent influence on the FXIII phenotype. These genotype to phenotype relationships are discussed in light of the growing interest in the role of FXIII in clinical problems involving an increased thrombotic tendency. (C) 1999 by The American Society of Hematology.
引用
收藏
页码:897 / 905
页数:9
相关论文
共 36 条
  • [1] AESHLIMANN D, 1994, THROMB HAEMOSTASIS, V71, P402
  • [2] Anwar R, 1998, THROMB HAEMOSTASIS, V79, P1151
  • [3] MOLECULAR-BASIS OF INHERITED FACTOR-XIII DEFICIENCY - IDENTIFICATION OF MULTIPLE MUTATIONS PROVIDES INSIGHTS INTO PROTEIN FUNCTION
    ANWAR, R
    STEWART, AD
    MILOSZEWSKI, KJA
    LOSOWSKY, MS
    MARKHAM, AF
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1995, 91 (03) : 728 - 735
  • [4] Identification of a large deletion, spanning exons 4 to 11 of the human factor XIIIA gene, in a factor XIII-deficient family
    Anwar, R
    Miloszewski, KJA
    Markham, AF
    [J]. BLOOD, 1998, 91 (01) : 149 - 153
  • [5] BARRY ELR, 1989, J BIOL CHEM, V264, P4179
  • [6] Bernardi F, 1996, ARTERIOSCL THROM VAS, V16, P72
  • [7] BORTH W, 1991, J BIOL CHEM, V266, P18149
  • [8] GENETIC-VARIATION AT THE PLASMINOGEN-ACTIVATOR INHIBITOR-1 LOCUS IS ASSOCIATED WITH ALTERED LEVELS OF PLASMA PLASMINOGEN-ACTIVATOR INHIBITOR-1 ACTIVITY
    DAWSON, S
    HAMSTEN, A
    WIMAN, B
    HENNEY, A
    HUMPHRIES, S
    [J]. ARTERIOSCLEROSIS AND THROMBOSIS, 1991, 11 (01): : 183 - 190
  • [9] Identification of tissue transglutaminase as the autoantigen of celiac disease
    Dieterich, W
    Ehnis, T
    Bauer, M
    Donner, P
    Volta, U
    Riecken, EO
    Schuppan, D
    [J]. NATURE MEDICINE, 1997, 3 (07) : 797 - 801
  • [10] A HITHERTO UNDESCRIBED CONGENITAL HAEMORRHAGIC DIATHESIS PROBABLY DUE TO FIBRIN STABILIZING FACTOR DEFICIENCY
    DUCKERT, F
    JUNG, E
    SHMERLING, DH
    [J]. THROMBOSIS ET DIATHESIS HAEMORRHAGICA, 1960, 5 (02): : 179 - 186