# Using polygenic scores to assess liability to antisocial behavior

**Authors:** A.V. Kazantseva, D.V. Yakovleva, Yu.D. Davydova, E.K. Khusnutdinova

PMC · DOI: 10.18699/vjgb-25-91 · Vavilov Journal of Genetics and Breeding · 2025-10-01

## TL;DR

This study uses genetic and social factors to assess liability to antisocial behavior in a Russian population, finding that social factors have a stronger influence than genetic scores.

## Contribution

The study evaluates polygenic scores and social factors for antisocial behavior in a Russian cohort, a population not previously studied in this context.

## Key findings

- Social factors like traumatic brain injury and tobacco smoking significantly increased liability to antisocial behavior.
- Polygenic scores alone explained only 1.1–1.5% of the variance in antisocial behavior liability.
- The best model combined genetic and social factors, explaining 16.2–21.2% of the variance.

## Abstract

To date, several genome-wide association studies (GWAS) of antisocial behavior (ASB) have been conducted in Europeans, which promoted research aimed at evaluating liability to ASB-related phenotypes in independent samples. Such studies implemented a polygenic score (PGS) approach, which represents a composite score considering a number of “risky” alleles. Since no GWAS of ASB has been conducted in Russians, the present study aimed to perform a replication study of liability to severe criminal behavior (homicide) in individuals from Russia using PGS. Moreover, we sought to obtain the best model considering PGS and potential social factors as predictors. Genotyping of the “top” ten SNPs previously identified in GWAS meta-analysis of ASB (CADM2, REV3L, FOXP1, FOXP2, BDNF, FURIN, XKR6, TMEM18, SORCS3, and ZIC4 genes) was conducted via real-time PCR in 227 homicide offenders and 254 healthy donors from the Volga-Ural region of Russia. Multiple regression models included “weighted” and “unweighted” PGS and potential social factors as predictors. The best regression model of liability to severe ASB was based on genetic effects of examined SNPs and social predictors, including traumatic brain injury, severe chronic disease, and tobacco smoking, which was more pronounced among subjects with a family history of mental illness (p = 2 × 10–13). PGS alone explained a small proportion of variance in liability to ASB (1.1–1.5 %), while the inclusion of social parameters increased variance explained (16.2–21.2 %). Revealed findings evidence a higher impact of social factors than a composite effect of selected “top” SNPs in predicting liability to ASB in the examined cohort. A higher probability of ASB was linked to comorbid substance abuse, traumatic brain injury, and family history of mental illness, which may also represent a result of a “risky” genetic profile.

## Linked entities

- **Genes:** CADM2 (cell adhesion molecule 2) [NCBI Gene 253559], REV3L (REV3 like, DNA directed polymerase zeta catalytic subunit) [NCBI Gene 5980], FOXP1 (forkhead box P1) [NCBI Gene 27086], FOXP2 (forkhead box P2) [NCBI Gene 93986], BDNF (brain derived neurotrophic factor) [NCBI Gene 627], FURIN (furin, paired basic amino acid cleaving enzyme) [NCBI Gene 5045], XKR6 (XK related 6) [NCBI Gene 286046], TMEM18 (transmembrane protein 18) [NCBI Gene 129787], SORCS3 (sortilin related VPS10 domain containing receptor 3) [NCBI Gene 22986], ZIC4 (Zic family zinc finger 4) [NCBI Gene 84107]
- **Diseases:** mental illness (MONDO:0002025), substance abuse (MONDO:0002491)

## Full-text entities

- **Diseases:** chronic disease (MESH:D002908), substance abuse (MESH:D019966), ASB (MESH:D000987), traumatic brain injury (MESH:D000070642), mental illness (MESH:D001523)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12559687/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12559687/full.md

---
Source: https://tomesphere.com/paper/PMC12559687