A novel genetic marker for coronary spasm in women from a genome-wide single nucleotide polymorphism analysis

Objective: Coronary spasm plays an important role in pathogenesis of variant angina and also ischernic heart diseases in general, and it is more likely to occur in angiographically normal coronary arteries than in coronary arteries. We previously found a - 786T/C polymorphism in the 5'-flanking region of the nitric oxide synthase (eNOS) gene and reported that polymorphism is associated with coronary spasm. We report on an investigation of the genetic factor(s) associated with coronary spasm utilizing a case-control study. Methods and results: We recruited 411 consecutive Japanese women (201 with coronary spasm; 210 who were all underwent an acetylcholine provocation For single nucleotide polymorphism analysis (SNP), 116 204 SNPs were genotyped for 100 women (50 with coronary spasm; 50 controls) utilizing the Affymetrix GeneChip 100 K Set. Case-control studies were with 311 women (151 with coronary spasm; 160 using the 10 lowest permutation P value SNPs from the initial SNP analysis. Finally, we discovered SNP rs10498345, a genetic marker for coronary spasm in Japanese women (Odds ratio= 0.43, P= 9.48 x 10-7). Haplotype analysis showed that haplotype H2, the only haplotype containing the protective A allele at SNP rs10498345, was most strongly associated with coronary spasm (permutation P value < 1 X 10(-4)). SNP rs10498345 was strongly associated with the vasoconstrictor response to acetylcholine. Northern blot analysis revealed a novel 4.7 kb RNA transcript, which lacked poly (A), nearby SN P rs10498345. Conclusions: SNP rs10498345 was strongly associated with coronary spasm in Japanese women utilizing genome-wide SNP analysis.