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. Author manuscript; available in PMC: 2010 Oct 1.
Published in final edited form as: Int J Cancer. 2009 Oct 1;125(7):1685–1691. doi: 10.1002/ijc.24477

Table 4.

Association between +331G/A PR polymorphism and risk of postmenopausal breast cancer by duration of PMH used

PMH use status GG AG+AA 2P - int
Cases, n (%) Controls, n (%) OR (95%CI)1 Cases, n (%) Controls, n (%) OR (95%CI)
Never 258 (83%) 607 (92%) 1.00 (ref) 53 (17%) 50 (8%) 2.57 (1.64-4.02)
Past
 < 5 years 178 (87%) 370 (91%) 1.00 (ref) 26 (13%) 37 (9%) 1.62 (0.89-2.94)
 ≥ 5 years 158 (92%) 204 (92%) 1.00 (ref) 13 (8%) 17 (8%) 0.93 (0.41-2.11)
Current
 < 5 years 174 (89%) 209 (92%) 1.00 (ref) 21 (11%) 18 (8%) 1.60 (0.79-3.24)
 ≥ 5 years 630 (89%) 682 (90%) 1.00 (ref) 76 (11%) 79 (10%) 1.06 (0.75-1.51)
0.04
1

Unconditional logistic regression adjusted for age, date blood draw, age at menarche, age at menopause, age at first birth/parity, BMI at age 18, weight gain since age 18, history of benign breast disease, first-degree family history of breast cancer, and alcohol consumption.

2

P - int = P for interaction based on likelihood ratio test comparing unconditional logistic regression models with and without interaction terms between PMH use status (past or current, <5 or ≥5 years) and genotype (GG, AG+GG)(degrees of freedom = 4).