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. 2021 Sep 17;11:721577. doi: 10.3389/fonc.2021.721577

Table 9.

ORs and 95% CIs for NSCLC in relation to genotypes of studied SNPs.

Genotype Cases n (%) Controls n (%) pa bCrude OR (95% CI) p cAdjusted OR (95% CI) p
Total 229 299
CD40 rs1883832 (T>C) 228 299
TT 54 (23.7) 73 (24.4) 0.003 1.414 (0.911–2.196) 0.122 1.508 (0.930–2.445) 0.096
CT 61 (26.8) 118 (39.5) 2.024 (1.348–3.039) 0.001 1.865 (1.192–2.919) 0.006
CC 113 (49.5) 108 (36.1) 1.000 - 1.000
TT+CT 115 (50.4) 191 (63.9) 0.002 1.738 (1.224–2.468) 0.002 1.701 (1.154–2.506) 0.007
vs. CC 113 (49.6) 108 (36.1)
TT 54 (23.7) 73 (24.4) 0.846 1.041 (0.695–1.558) 0.846 1.156 (0.742–1.800) 0.523
vs. CT+CC 174 (76.3) 226 (75.6)
CT 61 (26.8) 118 (39.5) 0.002 1.785 (1.228–2.594) 0.002 1.606 (1.065–2.422) 0.024
vs. TT+ CC 167 (73.2) 181 (60.5)
T allele 169 (37.1) 264 (44.1) 0.021 1.342 (1.046–1.722) 0.021 1.384 (1.052–1.821) 0.020
C allele 287 (62.9) 334 (55.9) 0.745 (0.581–0.956) 0.021 0.723 (0.549–0.951) 0.020
BAFFR rs7290134 (A>G) 229 298
AA 147 (64.2) 186 (62.4) 0.640 1.000 1.000
AG 73 (31.9) 95 (31.9) 1.029 (0.708–1.495) 0.883 1.054 (0.697–1.593)0 0.803
GG 9 (3.9) 17 (5.7) 1.493 (0.647–3.446) 0.348 1.647 (0.669–4.056) 0.278
AA vs 147 (64.2) 186 (62.4) 0.675 0.926 (0.648–1.325) 0.675 0.894 (0.603–1.326) 0.578
AG+GG 82 (35.8) 112 (37.6)
AA+AG 220 (96.1) 281 (94.3) 0.351 0.676 (0.296–1.546) 0.354 0.666 (0.271–1.637) 0.376
vs. GG 9 (3.9) 17 (5.7)
AG vs. 73 (31.9) 96 (32.1) 0.955 1.011 (0.699–1.462) 0.955 1.039 (0.691–1.561) 0.854
AA+GG 156 (68.1) 203 (67.9)
A allele 367 (80.1) 467 (78.4) 0.482 0.898 (0.664–1.213) 0.482 0.864 (0.621–1.202) 0.385
G allele 91 (19.9) 129 (21.6) 1.114 (0.492–0.929) 0.482 1.158 (0.832–1.611) 0.385
LTβR rs10849448 (A>G) 223 299
AA 24 (10.8) 55 (18.4) 0.054 1.894 (1.115–3.217) 0.018 2.051 (1.159–3.628) 0.014
AG 61 (27.4) 77 (25.8) 1.043 (0.696–1.563) 0.838 0.934 (0.593–1.473) 0.934
GG 138 (61.8) 167 (55.8) 1.000 1.000
AA vs 24 (10.8) 55 (18.4) 0.016 1.869 (1.117–3.127) 0.017 2.106 (1.210–3.667) 0.008
AG+GG 199 (89.2) 244 (81.6)
AA+AG vs 85 (38.1) 132 (44.1) 0.167 0.779 (0.547–1.110) 0.167 1.255 (0.848–1.856) 0.256
GG 138 (61.9) 167 (55.9)
AG 61 (27.4) 77 (25.8) 0.681 0.921 (0.622–1.364) 0.681 0.995 (0.978–1.013) 0.602
vs, GG+AA 162 (72.6) 222 (74.2)
A allele 109 (24.4) 187 (31.3) 0.015 1.407 (1.067–1.855) 0.016 1.436 (1.060–1.945) 0.019
G allele 337 (75.6) 411 (68.7) 0.711 (0.539–0.937) 0.016 0.696 (0.514–0.943) 0.019

ap derives from the χ2 test and refers to the overall association of genotypes with NSCLC risk. bp, OR, and 95% CI derived from logistic regression analysis using no cofactor. cp, OR, and 95% CI derived from logistic regression analysis using age and gender as cofactors.

CI, confidence interval; OR, odds ratio.

Bold text indicates a statistically significant correlation with a p-value less than 0.05.