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Table 1 Logistic regression analysis of associations between genotypes of H19 promoter SNPs and advanced CRC susceptibility

From: Functional polymorphisms of the lncRNA H19 promoter region contribute to the cancer risk and clinical outcomes in advanced colorectal cancer

Genotypes

Controls number (%)a

Cases number (%)

P b

Adjusted OR (95% CI)b

rs4930101 (G/T)

 TT

56 (10.09)

30 (5.24)

 

1.00

 GT

222 (40.00)

228 (39.86)

0.007

1.92 (1.19–3.10)

 GG

277 (49.91)

314 (54.90)

0.001

2.12 (1.32–3.39)

 GT/GG

499 (89.91)

542 (94.76)

0.002

2.03 (1.28–3.21)

 T allele

334 (30.09)

288 (25.17)

 

1.00

 G allele

776 (69.91)

856 (74.83)

0.009

1.28 (1.06–1.54)

rs2735970 (G/A)

 AA

228 (41.08)

174 (30.42)

 

1.00

 GA

242 (43.60)

302 (52.80)

0.001

1.64 (1.26–2.12)

 GG

85 (15.32)

96 (16.78)

0.029

1.48 (1.04–2.11)

 GA/GG

327 (58.92)

398 (69.58)

0.001

1.60 (1.25–2.04)

 A allele

698 (62.88)

650 (56.82)

  

 G allele

412 (37.12)

494 (43.18)

0.003

1.29 (1.09–1.52)

rs11042170 (G/A)

 AA

60 (10.81)

35 (6.12)

 

1.00

 GA

226 (40.72)

223 (38.99)

0.023

1.69 (1.07–2.67)

 GG

269 (48.47)

314 (54.90)

0.002

2.00 (1.28–3.13)

 GA/GG

495 (89.19)

537 (93.88)

0.005

1.86 (1.20–2.87)

 A allele

346 (31.17)

293 (25.61)

 

1.00

 G allele

764 (68.83)

851 (74.39)

0.003

1.32 (1.09–1.58)

Combined effect of risk genotypesc

 0

36 (6.49)

8 (1.40)

 

1.00

 1

162 (29.19)

127 (22.20)

0.0012

3.53 (1.58–7.86)

 2

133 (23.96)

298 (52.10)

< 0.0001

10.08 (4.56–22.28)

 3

224 (40.36)

139 (24.30)

0.0087

2.79 (1.26–6.18)

 ≤ 1

36 (6.49)

8 (1.40)

 

1.00

 > 1

519 (93.61)

564 (98.60)

< 0.0001

6.48 (2.97–14.15)

  1. The significance levels are P < 0.05 for all the italics values
  2. aThe observed genotype frequency among individuals in the control group was in agreement with Hardy–Weinberg equilibrium
  3. bP values, adjusted OR and 95% CI values were calculated by logistic regression adjusted for age, gender, body weight, smoking status, first-degree family history of cancer status
  4. cRisk genotypes used for the calculation were H19 rs4930101GT/GG + rs2735970GA/GG + rs11042170GA/GG