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. 2008 Jun 26;29(10):1944–1949. doi: 10.1093/carcin/bgn154

Table II.

Summary table of ORs for association between six PPARA polymorphisms and breast cancer risk by menopausal status in LIBCSP

Genotype Genotypea MAFb Cases, n (%)c Controls, n (%)c P for trendd ORe 95% CI
All women
    rs135542 AA 0.224 602 (59.4) 634 (59.3) 0.90 1.00
AG 370 (36.5) 392 (36.7) 1.01 0.84, 1.21
GG 41 (4.1) 43 (4.0) 1.01 0.65, 1.57
AG + GG 411 (40.6) 435 (40.7) 1.01 0.85, 1.21
Total 1013 1069
    rs1800206 (L162V) CC (L/L) 0.054 927 (89.7) 973 (89.7) 0.72 1.00
CG (L/V) 100 (9.7) 109 (10.1) 0.97 0.73, 1.30
GG (V/V) 7 (0.7) 3 (0.3) 2.44 0.63, 9.50
L/V + V/V 107 (10.4) 112 (10.3) 1.01 0.76, 1.34
Total 1034 1085
    rs4253623 AA 0.123 811 (77.5) 849 (77.0) 0.77 1.00
AG 218 (20.8) 236 (21.4) 0.97 0.79, 1.19
GG 17 (1.6) 17 (1.5) 0.98 0.49, 1.93
AG + GG 235 (22.5) 253 (23.0) 0.97 0.79, 1.19
Total 1046 1102
    rs4253699 TT 0.220 624 (60.0) 671 (61.5) 0.52 1.00
CT 358 (34.4) 362 (33.2) 1.06 0.88, 1.27
CC 58 (5.6) 59 (5.4) 1.07 0.73, 1.57
CT + CC 416 (40.0) 421 (38.6) 1.06 0.89, 1.27
Total 1048 1092
    rs4253755 GG 0.120 803 (76.5) 845 (77.4) 0.64 1.00
AG 231 (22.0) 231 (21.2) 1.05 0.85, 1.29
AA 16 (1.5) 16 (1.5) 1.05 0.52, 2.12
AG + AA 247 (23.5) 247 (22.6) 1.05 0.86, 1.29
Total 1050 1092
    rs4253760 TT 0.186 675 (66.2) 713 (67.2) 0.41 1.00
GT 293 (28.7) 302 (28.5) 1.02 0.84, 1.24
GG 52 (5.1) 46 (4.3) 1.25 0.83, 1.87
GT + GG 345 (33.8) 348 (32.8) 1.05 0.88, 1.26
Total 1020 1061
Postmenopausal
    rs135542 AA 0.220 395 (59.0) 397 (60.0) 0.61 1.00
AG 247 (36.9) 239 (36.1) 1.07 0.85, 1.35
GG 27 (4.0) 26 (3.9) 1.04 0.59, 1.81
AG + GG 274 (41.0) 265 (40.0) 1.07 0.86, 1.33
Total 669 662
    rs1800206 (L162V) CC (L/L) 0.052 610 (89.3) 609 (89.7) 0.51 1.00
CG (L/V) 68 (10.0) 69 (10.2) 1.01 0.71, 1.44
GG (V/V) 5 (0.7) 1 (0.2) 5.07 0.59, 43.71
L/V + V/V 73 (10.7) 70 (10.3) 1.06 0.75, 1.51
Total 673 679
    rs4253623 AA 0.132 533 (77.4) 522 (75.9) 0.43 1.00
AG 145 (21.0) 150 (21.8) 0.96 0.74, 1.24
GG 11 (1.6) 16 (2.3) 0.66 0.30, 1.45
AG + GG 156 (22.6) 166 (24.1) 0.93 0.72, 1.20
Total 689 688
    rs4253699 TT 0.217 411 (59.8) 425 (62.2) 0.62 1.00
CT 243 (35.4) 220 (32.2) 1.13 0.90, 1.42
CC 33 (4.8) 38 (5.6) 0.92 0.56, 1.49
CT + CC 276 (40.2) 258 (37.8) 1.10 0.88, 1.37
Total 687 683
    rs4253755 GG 0.113 532 (76.3) 535 (78.8) 0.29 1.00
AG 153 (22.0) 135 (19.9) 1.12 0.86, 1.46
AA 12 (1.7) 9 (1.3) 1.36 0.57, 3.27
AG + AA 165 (23.7) 144 (21.2) 1.14 0.88, 1.47
Total 697 679
    rs4253760 TT 0.168 441 (65.0) 454 (69.6) 0.02 1.00
GT 199 (29.4) 177 (27.2) 1.14 0.90, 1.46
GG 38 (5.6) 21 (3.2) 1.97 1.14, 3.43
GT + GG 237 (35.0) 198 (30.4) 1.23 0.98, 1.55
Total 678 652
a

The combined heterozygotes and rare homozygotes were modeled separately and compared with common homozygotes.

b

Minor allele frequency (MAF) calculated among controls.

c

May not add up to 100.0 due to rounding.

d

P-value for trend was calculated by coding each genotype as 0, 1 or 2 based on the number of risk alleles.

e

Adjusted for age, measured in 5-year intervals.