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. 2013 Oct 29;13:107. doi: 10.1186/1475-2867-13-107

Table 2.

The association between FPGS rs1544105 genotypes and patient characteristics (N = 164)

Characteristics FPGS SNP rs1544105
p -value*
CC
CT + TT
genotype genotype
Gender
 
 
1.000
Male
9 (62.3)
95 (63.3)
Female
5 (35.7)
55 (36.7)
Age (years)
 
 
0.336
<1
0
0
1-9
13 (92.9)
123 (82.0)
≥10
1 (7.1)
27 (18.0)
Treatment group
 
 
0.797
SR
4 (28.6)
58 (38.7)
MR
8 (57.1)
73 (48.7)
HR
2 (1.3)
19 (12.6)
WBC (109/L)
 
 
0.710
<50
11 (78.6)
125 (83.3)
≥50
3 (21.4)
25 (16.7)
TEL-AML1
 
 
0.770
Positive
3 (21.4)
38 (25.3)
Negative
11 (78.6)
112 (74.7)
E2A-PBX1
 
 
1.000
Positive
1 (7.1)
15 (10.0)
Negative
13 (92.9)
135 (90.0)
BCR-ABL
 
 
0.141
Positive
2 (14.3)
6 (4.0)
Negative
12 (85.7)
144 (96.0)
MLL-AF4
 
 
1.000
Positive
0
1 (0.6)
Negative
14 (100.0)
149 (99.4)
Prednisone response
 
 
0.164
Good
1 (7.1)
1 (0.6)
Poor
13 (92.9)
149 (99.4)
CNS involvement
 
 
1.000
Absent
14 (100.0)
148 (98.7)
Present 0 2 (1.3)

*Data were calculated by χ2 test. WBC, white blood cell count; SR, standard-risk; MR, medium-risk; HR, high-risk; CNS, central nervous system.