Table 1

VWF laboratory test results and bleeding scores for type 1 VWD subjects with and without D1472H

Type 1 VWD subjectsD1472H (n = 36)
No D1472H (n = 241)
Mean ± 1 SDMedianInterquartile rangeMean ± 1 SDMedianInterquartile rangeP value
FVIII activity, IU/dL 56 ± 20 56 48-72 55 ± 22 54 42-73 NS 
VWF:Ag, IU/dL 32 ± 13 34 24-41 36 ± 15 39 26-48 P < .036 
VWF:RCo, IU/dL* 29 ± 10 30 23-37 37 ± 15 39 27-47 P < .001 
VWF:RCo/VWF:Ag ratio* 0.94 ± 0.24 0.92 0.79-1.07 1.04 ± 0.20 1.02 0.90-1.13 P < .012 
VWF:CB, IU/dL 34 ± 13 37 22-42 41 ± 18 46 29-55 P < .01 
Bleeding score 6.72 ± 6.5 2-11 5.44 ± 4.6 2-7 NS 
Type 1 VWD subjectsD1472H (n = 36)
No D1472H (n = 241)
Mean ± 1 SDMedianInterquartile rangeMean ± 1 SDMedianInterquartile rangeP value
FVIII activity, IU/dL 56 ± 20 56 48-72 55 ± 22 54 42-73 NS 
VWF:Ag, IU/dL 32 ± 13 34 24-41 36 ± 15 39 26-48 P < .036 
VWF:RCo, IU/dL* 29 ± 10 30 23-37 37 ± 15 39 27-47 P < .001 
VWF:RCo/VWF:Ag ratio* 0.94 ± 0.24 0.92 0.79-1.07 1.04 ± 0.20 1.02 0.90-1.13 P < .012 
VWF:CB, IU/dL 34 ± 13 37 22-42 41 ± 18 46 29-55 P < .01 
Bleeding score 6.72 ± 6.5 2-11 5.44 ± 4.6 2-7 NS 
*

22 type 1 subjects (2 with D1472H and 20 without D1472H) had a VWF:RCo <10 IU/dL (the lower limit of detection in our laboratory); therefore, a ratio was unable to be calculated and those subjects were excluded from analysis. Inclusion of these subjects using a VWF:RCo value of 5 IU/dL did not change the statistical significance of the results.

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