Table 3.
Association of breast cancer risk with the c.-2265C>T SNP in the BRCA1 gene, on subjects recruited in the Hong Kong Chinese and in the Shanghai Breast Cancer Study.
| Hong Kong | Shanghai | Test of heterogeneity | Combined analysis†† | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| c.-2265C>T | Cases (%) | Controls (%) | p-value* | OR (95% CI)* | Cases (%) | Controls (%) | p-value** | OR (95% CI)** | p-value | p-value | OR (95% CI) |
| All subjectsa | |||||||||||
| (368 cases, 375 controls) | (1109 cases, 1185 controls) | ||||||||||
| CC | 143 (38.9%) | 109 (29.1%) | 1.00 (reference) | 469 (42.3%) | 457 (38.6%) | 1.00 (reference) | 1.00 (reference) | ||||
| CT/TT | 225 (61.1%) | 266 (70.9%) | 0.005 | 0.64 (0.47–0.88) | 640 (57.7%) | 728 (61.4%) | 0.054 | 0.85 (0.71–1.00) | 0.11 | 0.003 | 0.80 (0.69–0.93) |
| HWE† | p=0.23 | p=0.22 | p=0.07 | p=0.55 | |||||||
| Subjects without family history of breast cancer | |||||||||||
| (333 cases, 363controls) | (1070 cases, 1156 controls) | ||||||||||
| CC | 129 (38.7%) | 107 (29.5%) | 1.00 (reference) | 459 (42.9%) | 442 (38.2%) | 1.00 (reference) | 1.00 (reference) | ||||
| CT/TT | 204 (61.3%) | 256 (70.5%) | 0.01 | 0.66 (0.48–0.91) | 611 (57.1%) | 714 (61.8%) | 0.019 | 0.81 (0.69–0.97) | 0.23 | 0.001 | 0.78 (0.68–0.91) |
| Subjects ≥ 45 yrs at first diagnosis and without family history of breast cancer | |||||||||||
| (166 cases, 166 controls) | (637 cases, 678 controls) | ||||||||||
| CC | 71 (42.8%) | 46 (27.7%) | 1.00 (reference) | 281 (44.1%) | 265 (39.1%) | 1.00 (reference) | 1.00 (reference) | ||||
| CT/TT | 95 (57.2%) | 120 (72.3%) | 0.006 | 0.51 (0.32–0.81) | 356 (55.9%) | 413 (60.9%) | 0.039 | 0.79 (0.63–0.99) | 0.08 | 0.004 | 0.75 (0.61–0.91) |
p-values were obtained by Chi-square test, df=1.
Logistic regression analysis adjusted for age, education, body mass index, waist-to-hip ratio, physical activity, menopausal status, age at menarche, and age at first live birth.
p-values for HWE were calculated by Chi-square test, df=1.
Combined analysis was performed using Mentel-Hanzel test.
Overall cases and control subjects successfully genotyped.