Table 2 The psychiatric disorder PRS can distinguish better between groups than simulated PRS

From: Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Group

Disorder PRS

Simulated PRS min. pPRS

N simulated PRS with p ≤ p of disorder PRS

Prob. of success

95% CI

FAMBD vs. CCcontrols

BD

1 × 10−5

0

<1×10−4

0–0

SCZ

1 × 10−5

0

<1×10−4

0–0

MDD

1 × 10−5

91

0.0091

0.007–0.011

Shared

1 × 10−5

2

0.0002

0–0.001

FAMBD vs. CCBD

BD

1 × 10−7

0

<1×10−4

0–0

SCZ

1 × 10−7

2858

0.2858

0.277–0.295

MDD

1 × 10−7

744

0.0744

0.069–0.080

Shared

1 × 10−7

2229

0.2229

0.215–0.231

FAMunaffected vs. CCcontrols

BD

1 × 10−7

0

<1×10−4

0–0

SCZ

1 × 10−7

0

<1×10−4

0–0

MDD

1 × 10−7

37

0.0037

0.003–0.005

Shared

1 × 10−7

74

0.0074

0.006–0.009

FAMMDD vs. CCcontrols

BD

2 × 10−1

0

<1×10−4

0–0

SCZ

2 × 10−1

409

0.0409

0.037–0.045

MDD

2 × 10−1

2

0.0002

0–0.001

Shared

2 × 10−1

125

0.0125

0.010–0.015

  1. In binomial tests with 10,000 trials, the number of successes was the number of simulated PRS that showed the same or a stronger association than the disorder PRS (one-sided p-values). The 10,000 simulated PRS with ten p-value thresholds each were calculated by drawing random variants from across the genome, using the same number of variants as for the BD PRS at each threshold and random effect sizes from the pool of all available BD, SCZ, and MDD effects. For the present test, the pPRS of the simulated PRS showing the lowest mean association p-value was chosen. Prob. = binomial test probability estimate of success; CI = confidence interval of the probability estimate, both calculated using the R package binom (method: exact). Significance threshold: 0.05/16 = 0.003125, comparisons surpassing this threshold are shown in bold font