Identification of hub genes involved in early-onset schizophrenia: from genetic susceptibility to predicted regulated gene expression.

Despite high heritability, much of the genetic architecture of schizophrenia (SZ) remains unexplained, and early-onset SZ may represent a more genetically homogeneous subtype. We examined genetically regulated expression risk scores (GeRS) to identify gene networks associated with early-onset SZ and characterize their biological functions. Using genotype data from patients in multiplex families (223 early-onset and 372 late-onset) and simplex families (matched for sex and onset age), SZ-GeRS were estimated based on single-nucleotide polymorphism (SNP)-expression prediction models derived from two transcriptomic reference panels (dorsolateral prefrontal cortex tissue from individuals with psychiatric disorders and brain cortex tissue from the general population). Panel-specific GeRS were constructed using transcriptome-wide association studies (TWAS)-derived effect sizes and integrated using a fixed-effects meta-analytic framework. Module-based SZ-GeRS were constructed by aggregating genes within empirically derived co-expression clusters, followed by network analysis to identify hub genes and functional mapping to infer biological context. Among 13 co-expression modules, meta-analysis identified a significant association between early-onset SZ and Module 10 GeRS (M10