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. 2021 May 14;48(1):20–26. doi: 10.1093/schbul/sbab052

Table 2.

Associations Between PRS and Case-Control Status Stratified by the Presence of OCs

P T < 5 × 10−8 P T < 10−6
Sample N exp(B) R 2 P exp(B) R 2 P
Sweden All 547 1.48 0.030 2.2E-04 1.59 0.053 1.9E-06
OCs− 368 1.49 0.040 7.8E-04 1.57 0.050 1.1E-04
OCs+ 179 1.18 0.006 .34 1.62 0.046 .01
Verona Alla 298 1.03 0.000 .85 1.12 0.003 .45
OCs− 154 0.97 0.000 .86 1.03 0.000 .87
OCs+ 76 1.17 0.004 .57 1.23 0.007 .45
MFS Alla 170 1.13 0.002 .71 1.22 0.006 .6
OCs− 48 0.82 0.005 .65 0.86 0.003 .73
OCs+ 28 1.95 0.061 .26 3.08 0.112 .15
UKB All 220 908 1.26 0.003 2.8E-04 1.33 0.005 8.0E-06
OCs− 198 739 1.27 0.003 3.6E-04 1.33 0.004 2.2E-05
OCs+ 22 169 1.16 0.001 .39 1.30 0.004 .154

Note: MFS, Maudsley Family Study; OC, obstetric complication; PRS, polygenic risk score; UKB, UK Biobank. Association between PRS and case-control status in the total sample (All), the subsample without OCs history (OCs−), and the subsample with OCs history (OCs+). R2, the Nagelkerke R2. Significant results in bold.

aIn Verona and MFS, the total sample (All) is higher than the sum of the OCs− and OCs+ as individuals with missing OC data were included.