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. 2015 Jan 6;16(1):1143–1159. doi: 10.3390/ijms16011143

Table 5.

The effect of FXIII-B subunit polymorphisms on FXIII activity and antigen concentration.

Subjects Wild Type for the Mutation Carriers of the Mutation
n FXIII Activity (%) FXIII Antigen (mg/L) n FXIII Activity (%) FXIII Antigen (mg/L)
p.His95Arg Polymorphism
All 594 103 ± 21 22.9 ± 5.0 93 109 ± 23 24.0 ± 5.1 *
CAS−MI− 202 103 ± 20 22.9 ± 4.7 35 112 ± 23 * 24.3 ± 5.3
CAS+MI− 189 101 ± 22 22.6 ± 5.1 25 107 ± 25 23.7 ± 5.5
CAS+MI+ 180 106 ± 22 23.4 ± 5.3 30 107 ± 20 23.7 ± 4.3
CAS+ 369 103 ± 22 22.9 ± 5.2 55 107 ± 22 23.7 ± 4.9
MI+ 203 105 ± 23 23.4 ± 5.3 33 109 ± 21 24.0 ± 4.6
Intron K nt29756 C>G Polymorphism
All 486 106 ± 21 23.8 ± 5.0 201 97 ± 21 21.3 ± 4.7
CAS−MI− 158 106 ± 21 23.9 ± 5.0 79 100 ± 20 * 21.8 ± 4.1
CAS+MI− 155 106 ± 22 23.7 ± 5.1 59 94 ± 21 20.7 ± 4.9
CAS+MI+ 151 109 ± 20 24.2 ± 4.9 59 98 ± 24 21.6 ± 5.5
CAS+ 306 107 ± 21 23.9 ± 5.0 118 96 ± 22 21.1 ± 5.2
MI+ 173 108 ± 21 24.1 ± 5.0 63 99 ± 24 21.7 ± 5.3

FXIII levels are expressed as mean ± SD. FXIII levels were adjusted to gender, smoking, serum total cholesterol and plasma fibrinogen levels. The levels of significance were calculated for the difference between wild type individuals and carriers of the respective mutation. CAS+ and CAS−, patients with and without coronary atherosclerosis, respectively; MI+ and MI−, patients with and without a history of myocardial infarction, respectively; n, number of individuals in each subgroup; * p < 0.05, p < 0.01, p < 0.001.