Skip to main content
. 2026 Jul 7;6(1):182. doi: 10.1007/s44192-026-00540-2

Table 2.

Pathway enrichment comparison (Early Dx / childhood vs. late Dx)

Gene Set Early Dx Enrich. (MW-P) Late Dx Enrich. (MW-P) Δ (Late stronger) Notes
KEGG_Long_Term_Potentiation 1.10 × (0.035) 1.34 × (1.4e-8) + 0.24× Synaptic plasticity
REACTOME_Complement_Cascade 1.09× (NS) 1.22 × (5.1e-5) + 0.13× Immune/inflammation
GOBP_Synaptic_Transmission_Glutamatergic 0.80× (NS) 1.01× (NS) + 0.21× Glutamate signaling
Adult_Microglia_Markers 1.13 × (0.052) 0.73× (NS) –0.40× Neurodev./autism-like
HGNC_Histocompatibility_Complex 1.12 × (0.096) 0.65× (NS) –0.47× MHC/immune
Housekeeping / Monoamines / others ~ 1.0× (NS) ~ 1.0× (NS) — No difference

Bold values indicate statistical significance or near-significance driving the interpretation. NS = Not significant. P-values in Tables 2, 3 and 4are nominal unless otherwise stated. Across 26 gene-set tests, a simple Bonferroni threshold is approximately 0.0019; the late-diagnosed long-term potentiation and complement cascade signals exceed this threshold, whereas the childhood microglia and MHC signals are suggestive only