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. Author manuscript; available in PMC: 2010 Feb 1.
Published in final edited form as: Breast Cancer Res Treat. 2008 Mar 14;113(3):585–594. doi: 10.1007/s10549-008-9962-z

Table 2.

The main effect of COMT Val158Met polymorphism and its interaction with MPO T-764C polymorphism on breast cancer risk.

Cases (%) Controls (%) OR (95%CI)a
COMT Genotype* 1212(100) 1683(100)
Val/Val 271(22.4) 400(23.8) 1.00(Ref)
Val/Met 607(50.1) 837(49.7) 1.02(0.83, 1.24)
Met/Met 334(27.6) 446(26.5) 1.02(0.82, 1.28)
Val/Val 271(22.4) 400(23.8) 1.00(Ref)
Val/Met + Met/Met 941(77.6) 1283(76.2) 1.02(0.84, 1.23)

COMT | MPO Genotype* 1175(100) 1631(100)
Met158 Met | MPO T-764T 204 (17.4) 280 (17.2) 1.00 (Ref)
Met158 Met | MPO T-764C 105 (8.9) 141 (8.7) 0.98 (0.71, 1.37)
Met158 Met | MPO C-764C 11 (0.9) 13 (0.8) 1.21 (0.51, 2.86)
Met158 Val | MPO T-764T 369 (31.4) 500 (30.7) 1.03 (0.81, 1.31)
Met158 Val | MPO T-764C 202 (17.2) 266 (16.3) 1.11 (0.84, 1.46)
Met158 Val | MPO C-764C 25 (2.1) 39 (2.4) 0.88 (0.51, 1.53)
Val158 Val | MPO T-764T 169 (14.4) 252 (15.5) 0.99 (0.74, 1.31)
Val158 Val | MPO T-764C 86 (7.3) 123 (7.5) 1.08 (0.76, 1.54)
Val158 Val | MPO C-764C 4 (0.3) 17 (1.0) 0.28 (0.08, 1.00)
a

Unconditional logistic regression adjusted for the matching factors and BMI at age 18, weight gain since age 18, age at menarche, personal history of benign breast disease, first-degree family history of breast cancer, age at first birth/parity, age at menopause, and duration of postmenopausal hormone use.

*

Numbers do not add to the total number of women due to missing values in genotyping or covariates.

The sum of percentage does not add up to 100 due to rounding.

P-interaction = 0.57