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Table 2 The association between FPGS rs1544105 genotypes and patient characteristics (N = 164)

From: FPGS rs1544105 polymorphism is associated with treatment outcome in pediatric B-cell precursor acute lymphoblastic leukemia

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)

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