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. 2017 Jul 19;8(44):76357–76374. doi: 10.18632/oncotarget.19400

Table 2. Analysis of the association of the APOBEC3B deletion with ovarian cancer risk using dominant model of inheritance (A3B+/− and A3B−/− vs. A3B+/+).

Group Genotypes No of cases(%) No of controls(%) OR(95%CI) AdjustedOR(95%CI)
GDANSK: OCcases (n=343)vs. unselected controls(n=853) A3B+/+ 313 (91.25%) 759 (88.98%) 0.77(0.50-1.19)p=0.24 -
A3B+/− 28 (8.16%) 91 (10.67%)
A3B−/− 2 (0.58%) 3 (0.35%)
A3B+/− and A3B−/− 30 (8.75%) 94 (11.02%)
VILNIUS: OCcases (n=97)vs. unselected controls(n=209) A3B+/+ 90 (92.78%) 187 (89.47%) 0.66(0.27-1.61)p=0.36 -
A3B+/− 6 (6.19%) 22 (10.53%)
A3B−/− 1 (1.03%) 0 (0%)
A3B+/− and A3B−/− 7 (7.22%) 22 (10.53%)
GDANSK + VILNIUS: OCcases (n=440)vs. unselected controls(n=1062) A3B+/+ 403 (91.59%) 946 (89.08%) 0.75(0.51-1.10)p=0.14 0.75(0.51-1.11)bp=0.15
A3B+/− 34 (7.73%) 113 (10.64%)
A3B−/− 3 (0.68%) 3 (0.28%)
A3B+/− and A3B−/− 37 (8.41%) 116 (10.92%)

bAdjusted for the origin of the study.