Table 2.

Frequency of RBC antigens in the local donor population and RBC phenotype available on 20 Asian thalassemia patients

RBC antigenAll local donors
(n = 802)
White donors
(n = 352)
Asian donors
(n = 103)
Asian donors
(n = 435)
Asian patients (n = 20)Average antigen frequency (Asians)P
s* 93.1 91.7 90.5 99.5 100 97.86 — 
Fya* 77.1 60.2 89.5 98.2 95 96.48 — 
C* 51.7 50.5 84.4 95.7 95 93.59 — 
E* 95.5 95.4 88.5 93.7 100 92.97 — 
NA NA NA 83 75 82.65 — 
Jkb* 57.1 70.4 67 81 85 78.56 — 
NA NA NA 72 53.8 71.20 — 
Jka* 53.7 69.3 68 68 75 68.25 — 
Leb NA NA NA 64 66.6 64.11 — 
C* 80.4 77.8 43.7 53.8 35 51.26 < .0001 
E* 21.4 19 32.0 43 25 40.32 — 
P1* NA NA NA 40 33.3 39.71 — 
Lea NA NA NA 20 40 20.88 — 
Fyb* 63 78.7 16.8 18 20 17.85 < .0001 
S* 40.5 51.4 15.6 12.7 20 13.50  .001 
K*  9 1.0 0.3 < .0001 
RBC antigenAll local donors
(n = 802)
White donors
(n = 352)
Asian donors
(n = 103)
Asian donors
(n = 435)
Asian patients (n = 20)Average antigen frequency (Asians)P
s* 93.1 91.7 90.5 99.5 100 97.86 — 
Fya* 77.1 60.2 89.5 98.2 95 96.48 — 
C* 51.7 50.5 84.4 95.7 95 93.59 — 
E* 95.5 95.4 88.5 93.7 100 92.97 — 
NA NA NA 83 75 82.65 — 
Jkb* 57.1 70.4 67 81 85 78.56 — 
NA NA NA 72 53.8 71.20 — 
Jka* 53.7 69.3 68 68 75 68.25 — 
Leb NA NA NA 64 66.6 64.11 — 
C* 80.4 77.8 43.7 53.8 35 51.26 < .0001 
E* 21.4 19 32.0 43 25 40.32 — 
P1* NA NA NA 40 33.3 39.71 — 
Lea NA NA NA 20 40 20.88 — 
Fyb* 63 78.7 16.8 18 20 17.85 < .0001 
S* 40.5 51.4 15.6 12.7 20 13.50  .001 
K*  9 1.0 0.3 < .0001 

All local donors include mostly white (85%) and other ethnicities (15%). Asian donor phenotypes were collected during 2 separate time periods. Significant antigen frequency differences between white and Asian RBCs are on the rows with P values given. P was calculated for the antigens appearing in a higher frequency among the white (and total) donor population compared to the average frequency found among Asian patients. NA indicates not available.

*

Indicates clinically significant antibodies (ie, can cause a hemolytic transfusion reaction or hemolytic disease of the newborn).

Donors' phenotypes were collected in 2 separate time periods.

Frequency of Kell (K) antigen was not always examined. Therefore the known frequency among white people was used.

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