Purpose
Genome-wide association studies (GWAS) have revealed that common variants on or near
EDNRA
,
HDAC9
,
SOX17
,
RP1
,
CDKN2B-AS1
, and
RBBP8
genes are associated with intracranial aneurysm (IA) in European or Japanese populations. However, due to population heterogeneity, whether these loci are associated with IA pathogenesis in Chinese individuals is still unknown. The purpose of this study was to investigate associations among GWAS-identified loci and risk of IA in a Chinese population.
Materials and Methods
A total of 765 individuals (including 230 IA patients and 535 controls) were involved in this study. Twelve single nucleotide polymorphisms (SNPs) of candidate loci were genotyped using the Sequenom MassARRAY platform. Associations were analyzed using univariate or multivariate logistic regression analysis.
Results
SNPs in
CDKN2B-AS1
(especially rs10757272) showed significant associations with IA in dominant and additive models [odds ratio (OR), 2.99 and 1.43; 95% confidence interval (CI), 1.44–6.24 and 1.10–1.86, respectively]. A SNP near
HDAC9
(rs10230207) was associated with IA in the dominant model (OR, 1.42; 95% CI, 1.01–1.99). One SNP near
RP1
(rs1072737) showed a protective effect on IA in the dominant model (OR, 0.66; 95% CI, 0.46–0.95), while another SNP in
RP1
(rs9298506) showed a risk effect on IA in a recessive model (OR, 3.82; 95% CI, 1.84–7.91). No associations were observed among common variants near
EDNRA
,
SOX17
, or
RBBP8
and IA.
Conclusion
These data partially confirmed earlier results and showed that variants in
CDKN2B-AS1
,
RP1
, and
HDAC9
could be genetic susceptibility factors for IA in a Chinese population.