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Table 2 Univariate Cox regression of 13 genes and available clinical variables

From: DNA methylation gene-based models indicating independent poor outcome in prostate cancer

 

HRa(95% CI)

LRbχ2

Adjustedc P -value

Harrell’s c-index

Total Nod

Event Noe

Gleason score

2.33 (1.99, 2.73)

105.3

2.2*10-16

0.79

367

99

Extent of disease

1.27 (1.21, 1.34)

80.1

2.2*10-16

0.76

367

99

PSA

1.36 (1.28, 1.45)

68.9

6.3*10-16

0.76

367

99

Age

1.04 (1.00, 1.09)

3.2

0.08

0.52

367

99

MAL

1.28 (1.17, 1.40)

25.4

2.0*10-6

0.64

352

95

DPYS

1.20 (1.12, 1.29)

24.2

2.9*10-6

0.65

344

95

TIG1

1.25 (1.14, 1.36)

20.9

1.4*10-5

0.65

350

90

GSTP1

1.17 (1.08, 1.26)

16.4

1.2*10-4

0.62

357

98

APC

1.18 (1.08, 1.29)

10.9

0.002

0.61

365

99

PDLIM4

1.16 (1.06, 1.26)

10.9

0.002

0.60

365

98

RARB

1.13 (1.04, 1.24)

7.7

0.01

0.60

351

98

SLIT2

1.17 (1.05, 1.31)

6.6

0.016

0.58

350

94

SFN

1.13 (1.02, 1.25)

5.8

0.023

0.57

363

99

CCND2

1.12 (1.02, 1.23)

5.2

0.029

0.56

364

99

HIN1

1.09 (1.01, 1.18)

5.1

0.029

0.59

350

97

HSPB1

1.12 (1.02, 1.22)

5.0

0.029

0.52

349

91

SERPINB5

0.95 (0.83, 1.08)

0.7

0.408

0.53

357

95

  1. aThe hazard ratios were calculated per 10 units increase in age, PSA, extent of disease and gene methylation while it is per unit increase in Gleason score, i.e. 4 through 10.
  2. bLR = likelihood ratio test.
  3. cThe Benjamin and Hochberg step-up procedure for controlling false discovery rate (FDR) was applied with FDR of 5%.
  4. dThe total number of patients for which DNAme was successfully measured. The clinical variables were available for all men included in the study.
  5. eThe number of patients for which a DNAme result was obtained and who died of prostate cancer.