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. 2020 Jun 29;140(3):341–358. doi: 10.1007/s00401-020-02181-3

Table 2.

Canonical pathways significantly associated with PD risk through common variation in the discovery and replication phases after excluding PD known risk loci ± 1 Mb upstream and downstream

Gene set Discovery Replication
PRS R2 Beta SE P Num SNP PRS R2 Beta SE P Num SNP
Adaptive immune system (REACTOME) 0.0028 0.1560 0.0163 1.42E−21 397 0.0002 0.0438 0.0190 2.15E−02 182
Innate immune system (REACTOME) 0.0026 0.1522 0.0163 1.12E−20 621 0.0003 0.0475 0.0192 1.34E−02 332
Vesicle mediated transport (REACTOME) 0.0022 0.1398 0.0163 1.03E−17 515 0.0002 0.0439 0.0190 2.12E−02 259
Signaling by GPCR (REACTOME) 0.0019 0.1299 0.0163 1.86E−15 816 0.0002 0.0460 0.0190 1.58E−02 329
Metabolism of lipids (REACTOME) 0.0018 0.1265 0.0163 8.08E−15 538 0.0004 0.0547 0.0190 4.08E−03 275
Neutrophil degranulation (REACTOME) 0.0012 0.1026 0.0163 2.73E−10 259 0.0004 0.0593 0.0192 1.96E−03 143

PRS R2 variance explained by polygenic risk score, SE standard error, P P-value, num_SNP number of SNPs included in each pathway analysis