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Table 2 Comparison of clinical manifestations and laboratory features between SLC22A3 hypomethylated and hypermethylated MDS patients

From: SLC22A3 methylation-mediated gene silencing predicts adverse prognosis in acute myeloid leukemia

Patient’s parameter

Hypomethylated

(n = 38)

Hypermethylated

(n = 10)

P value

Sex (male/female)

20/18

8/2

0.304

Age (years)

57 (27–83)

67 (28–84)

0.454

WBC (× 109/L)

4.0 (1.2–82.4)

4.4 (1.2–19)

0.493

HB (g/L)

61 (35–140)

62 (46–107)

0.493

PLT (× 109/L)

61 (0–1176)

56 (12–323)

0.919

BM blasts (%)

5 (0–19)

6 (0–17)

0.648

WHO classification

  

0.268

 MDS-SLD/MLD

13

3

 

 MDS-RS

7

0

 

 MDS with isolated del(5q)

1

0

 

 MDS-EB1

5

4

 

 MDS-EB2

12

3

 

Cytogenetic classification

  

1.000

 Favorable

23 (60%)

7 (70%)

 

 Intermediate

6 (16%)

1 (10%)

 

 Adverse

6 (16%)

1 (10%)

 

 No data

3 (8%)

1 (10%)

 

IPSS

  

0.476

 Low

6 (16%)

0 (0%)

 

 Int-1

15 (39%)

7 (70%)

 

 Int-2

9 (24%)

1 (10%)

 

 High

5 (13%)

1 (10%)

 

 No data

3 (8%)

1 (10%)

 

Gene mutations

   

 CEBPA ( ±)

0/31

0/10

 

 IDH1/2 ( ±)

1/30

0/10

1.000

 DNMT3A ( ±)

0/31

0/10

 

 U2AF1 ( ±)

1/30

1/9

0.433

 SF3B1 ( ±)

4/27

0/10

0.556

 SRSF2 ( ±)

0/31

2/8

0.055

 SETBP1 ( ±)

1/30

0/10

1.000

  1. WBC white blood cells, HB hemoglobin, PLT platelet count, BM bone marrow, IPSS International Prognostic Scoring System, WHO World Health Organization, MDS-SLD/MLD MDS with signal lineage dysplasia/multilineage dysplasia, MDS-RS MDS with ringed sideroblasts, MDS-EB MDS with excess blasts, IPSS International Prognostic Scoring System