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. Author manuscript; available in PMC: 2012 Mar 1.
Published in final edited form as: Pharmacogenet Genomics. 2011 Mar;21(3):130–135. doi: 10.1097/FPC.0b013e3283436b86

Table 3.

Association of genetic polymorphism with warfarin dose requirements in Egyptians

Gene Variant Genotype Frequency (n = 207) Mean ± SD warfarin dose (mg/week) P valuea
CYP2C9 *2*3*4*5*8 *1/*1 122 (62.56%) 40.3 ± 19.5 0.0028
*1/*2 34 (17.44%) 35.0 ± 16.9
*1/*3 23 (11.79%) 26.6 ± 10.4
*1/*4 1 (0.51%) 35
*1/*5 2 (1.03%) 28.0 ± 10
*1/*8 3 (1.45%) 39.7 ± 10.7
*2/*2 2 (1.03%) 29.8 ± 2.5
*2/*3 8 (4.10%) 32.4 ± 17.2
*3/*3 2 (1.03%) 33.3 ± 17.3
*5/*5 1 (0.51%) 31.5
VKORC1 3673G > A GG 50 (25.51%) 43.4 ± 21.6 < 0.0001
GA 111 (56.63%) 38.1 ± 16.4
AA 35 (17.86%) 25.6 ± 12.3
CYP4F2 V433M CC 68 (35.42%) 35.2 ± 16.1 0.31
CT 87 (45.31%) 37.3 ± 18.7
TT 37 (19.27%) 41.1 ± 20.9
APOE ε2/ε2 3 (1.54%) 21.0 ± 3.5 ε2 haplotype 0, 1, 2: P = 0.08
ε2/ε3 20 (10.26%) 31.0 ± 15.1
ε2/ε4 3 (1.54%) 49.0 ± 18.2
ε3/ε3 146 (74.87%) 38.2 ± 17.9
ε3/ε4 23 (11.79%) 35.6 ± 22.0
CALU rs339097 TT 186 (95.38%) 36.5 ± 17.9 0.04
CT 9 (4.62%) 50.6 ± 21.3

SD, standard deviation.

a

These P values were generated using nonparametric methods (Kruskal–Wallis or Wilcoxon Rank-sum test as appropriate).