International Centre for Research in Human Development, Tomsk State University, Russia;
Goldsmiths, University of London, United Kingdom
Background. Recent research has suggested a unifactorial structure of spatial ability (SA). However, further studies are needed to replicate this finding in different populations.
Objective. is study aims to explore the factorial structure of SA in samples of 921 Russian and 229 Chinese university students.
Design. A gamified spatial abilities battery was administered to all participants. e battery consists of 10 different domains of SA, including 2D and 3D visualization, mental rotation, spatial pattern assembly, spatial relations, spatial planning, mechanical reasoning, spatial orientation, and spatial decision-making speed and flexibility.
Results. The results of the factor analysis showed a somewhat different pattern for different samples. In the Russian sample, the unifactorial structure, shown previously in a large UK sample (Rimfeld et al., 2017), was replicated. A single factor explained 40% of the variance. In the Chinese sample two factors emerged: the first factor explained 26% of the variance and the second factor, including only mechanical reasoning and cross-sections tests, explained 14%. e results also showed that the Chinese sample significantly outperformed the Russian sample in five out of the 10 tests. Russian students showed better performance in only two of the tests. The effects of all group comparisons were small.
Conclusion. Overall, a similar amount of variance in the 10 tests was explained in the two samples, replicating results from the UK sample. Future research is needed to explain the observed differences in the structure of SA.
Keywords: spatial ability (SA), factorial structure, Russian and Chinese students
Background. Behavioral genetic findings suggest that complex traits, such as mathematical ability, general cognitive ability (intelligence; g), and spatial ability, are influenced by many common genetic variants of very small effects that operate across the ability continuum. Common genetic variants may also be responsible for cognitive deficits associated with rare genetic syndromes, in which whole genomic regions may be affected. To date, relatively few common genetic variants involved in cognitive traits have been identified, and these only explain a small proportion of variance in these traits.
Objective. The aim of the study was to find associations between mathematics-related traits and single-nucleotide polymorphisms (SNPs) within chromosomal regions involved in Williams and Prader-Willi disorders. Both disorders are characterized by patterns of weaknesses and strengths in cognitive abilities. Two types of analyses were performed (SNP-based and gene-based), using genotypic and phenotypic data available for 3000 participants from the UK.
Results. SNP-based tests indicated that none of the SNPs passed the demanding multiple testing correction level for any of the phenotypes. Gene-based analysis suggested that 2 pseudo-genes (i.e., GOLGA8I and WHAMMP3) were significantly associated with intelligence, and 1 gene (i.e., TUBGCP5) was significantly associated with mathematics at 16 years of age.
Conclusion. The results are consistent with other findings demonstrating that cognitive traits are influenced by many common genetic variants with very small effects. The results also suggest that a small number of these variants may be located in the chromosomal regions affected in Prader-Willi and Williams syndrome regions.
Keywords: mathematical ability, spatial ability, intelligence, genetic variation, single-nucleotide polymorphism (SNP)