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. 2014 Dec 10;6(4):2573–2582. doi: 10.18632/oncotarget.2951

Table 2. Associations between NSCLC risk and individual SNPs involved in the vitamin D pathway.

Genotype Number of subject (%) P ORa(95%CIb) ORa(95%CIb)
②+③ vs. ①
ORa(95%CIb)
③ vs. ①+②
Case (n=603) Control (n=661)
CYP27B1 (rs3782130)
CC 229(38.0) 230(34.8) 0.022 1.00 1.00 1.00
CG 297(49.3) 371(56.1) 0.82(0.63-1.06) 0.90(0.70-1.15) 1.60(1.09-2.34)
GG 77(12.8) 60(9.1) 1.42(0.94-2.14)
CYP27B1 (rs10877012)
TT 235(39.0) 243(36.8) 0.331 1.00 1.00 1.00
TG 273(45.3) 326(49.4) 0.87(0.67-1.13) 0.92(0.72-1.17) 1.19(0.85-1.66)
GG 94(15.6) 91(13.8) 1.10(0.76-1.58)
CYP24A1 (rs6068816)
CC 217(36.0) 110(16.6) <0.001 1.00 1.00 1.00
CT 314(52.1) 465(70.3) 0.33(0.25-0.44) 0.34(0.26-0.45) 0.87(0.61-1.24)
TT 72(11.9) 86(13.0) 0.40(0.26-0.60)
CYP24A1 (rs4809957)
GG 234(38.8) 228(34.5) <0.001 1.00 1.00 1.00
GA 309(51.2) 406(61.4) 0.77(0.60-0.99) 0.88(0.69-1.12) 2.71(1.66-4.41)
AA 60(10.0) 27(4.1) 2.32(1.40-3.87)
VDR (rs11574129)
TT 339(56.2) 378(57.2) 0.873 1.00 1.00 1.00
TC 254(42.1) 274(41.5) 1.06(0.84-1.35) 1.07(0.84-1.36) 1.36(0.50-3.70)
CC 10(1.7) 9(1.4) 1.39(0.51-3.81)
GC (rs7041)
TT 329(54.6) 272(41.1) <0.001 1.00 1.00 1.00
TG 240(39.8) 339(51.3) 0.59(0.46-0.76) 0.59(0.46-0.75) 0.73(0.46-1.18)
GG 34(5.6) 50(7.6) 0.57(0.35-0.93)
CYP2R1 (rs10741657)
GG 252(41.9) 246(37.2) 0.216 1.00 1.00 1.00
GA 270(44.9) 326(49.3) 0.82(0.64-1.06) 0.83(0.65-1.06) 0.96(0.68-1.36)
AA 80(13.3) 89(13.5) 0.86(0.59-1.25)
Number of risk-allele
0 138(22.9) 299(45.2) 1.00
1 282(46.8) 267(40.4) 2.46(1.86-3.25)
2 147(24.4) 83(12.6) 4.25(2.96-6.12)
3 35(5.8) 12(1.8) 5.80(2.84-11.84)
a

OR: Odds Ratio adjusted by age, sex, family history of cancer and BMI.

b

CI: Confidence Interval.

① Homozygous wild genotype, ② heterozygous genotype, ③ homozygous variant genotype

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