Abstract
Objective. To perform replicative analysis of gene loci associated with the risk of antisocial behavior (AB) in European cohorts and the manifestation of extreme forms of AB (murder), considering ethnicity in the Russian sample. Material and methods. Two groups of individuals were examined: those with AB (n=227) and the control group (n=254), using logistic regression, in which genetic profile data as well as social and demographic parameters were used as independent variables. Results. Associations of the rs4714329*G/G variants in the LINK00951 gene (OR=2.92, p=0.006), rs7232069*G variants in the LINK00907 gene (OR=2.0, p=0.006), and rs12977121*A/A variants in the CSNK1G2 gene (OR=1.76, p=0.044) were confirmed with an increased risk of AB among Russians. A significant effect of tobacco smoking on the association of the CSNK1G2 gene locus was found: a higher risk of manifestation of AB extreme forms was observed in persons with nicotine dependence, carriers of the rs12977121*A/A genotype (OR=3.63, p=0.001). Conclusion. The data obtained indicate the potential involvement of long non-coding RNA and casein kinase genes in the development of aggressiveness.
Affiliated Institutions
Related Publications
54Mn Absorption and Excretion in Rats Fed Soy Protein and Casein Diets
Rats were fed diets containing either soy protein or casein and different levels of manganese, methionine, phytic acid, or arginine for 7 days and then fed test meals labeled wi...
Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits
The obesity epidemic is responsible for a substantial economic burden in developed countries and is a major risk factor for type 2 diabetes and cardiovascular disease. The disea...
Interpreting non-coding variation in complex disease genetics
Association studies provide genome-wide information about the genetic basis of complex disease, but medical research has primarily focused on protein-coding variants, due to the...
Identification of Functional Variants for Cleft Lip with or without Cleft Palate in or near PAX7, FGFR2, and NOG by Targeted Sequencing of GWAS Loci
Although genome-wide association studies (GWASs) for nonsyndromic orofacial clefts have identified multiple strongly associated regions, the causal variants are unknown. To addr...
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum
There is a limited understanding about the impact of rare protein-truncating variants across multiple phenotypes. We explore the impact of this class of variants on 13 quantitat...
Publication Info
- Year
- 2025
- Type
- article
- Volume
- 125
- Issue
- 11
- Pages
- 145-145
- Citations
- 0
- Access
- Closed
External Links
Social Impact
Social media, news, blog, policy document mentions
Citation Metrics
Cite This
Identifiers
- DOI
- 10.17116/jnevro2025125111145