Abstract

Lipoprotein (a) [Lp(a)] is a genetically determined risk factor of coronary artery disease (CAD). Previous genome-wide association studies (GWASs), which were mostly carried out in Caucasians, have identified many Lp(a)-associated SNPs. Here, we performed a GWAS on Lp(a) levels and further explored the relationships between Lp(a)-associated SNPs and CAD severity in 1,403 Han Chinese subjects. We observed that elevated Lp(a) levels were significantly associated with the increased synergy between percutaneous coronary intervention with TAXUS and cardiac surgery (SYNTAX) score and the counts of heavily calcified lesions and long-range lesions (LRLs; P < 0.05), which are defined as lesions spanning >20 mm. Moreover, we identified four independent SNPs, namely, rs7770628, rs73596816, and rs6926458 in LPA, and rs144217738 in SLC22A2, that were significantly associated with Lp(a) levels. We also found that rs7770628 was associated with high SYNTAX scores [odds ratio (OR) (95% CI): 1.37 (1.05-1.80), P = 0.0213, false discovery rate (FDR) = 0.0852], and that rs7770628 and rs73596816 were associated with high risk of harboring LRLs [OR (95% CI): 1.53 (1.17-2.01), P = 0.0018, FDR = 0.0072 and 1.72 (1.19-2.49), P = 0.0040, FDR = 0.0080, respectively]. Our study was a large-scale GWAS to identify Lp(a)-associated variants in the Han Chinese population. Our findings highlight the importance and potential of Lp(a) intervention and expand our understanding of CAD prevention and treatment.

Highlights

  • Lipoprotein (a) [Lp(a)] is a genetically determined risk factor of coronary artery disease (CAD)

  • We confirmed the association between increased Lp(a) levels and the CAD severity, which was evaluated through coronary angiography (CAG)

  • We observed that high Lp(a) levels were significantly associated with increased CAD severity, which is represented by a high SYNTAX score and the presence of long-range lesion (LRL) and heavily calcified lesion (HCL)

Read more

Summary

Introduction

Lipoprotein (a) [Lp(a)] is a genetically determined risk factor of coronary artery disease (CAD). Previous genome-wide association studies (GWASs), which were mostly carried out in Caucasians, have identified many Lp(a)-associated SNPs. Here, we performed a GWAS on Lp(a) levels and further explored the relationships between Lp(a)-associated SNPs and CAD severity in 1,403 Han Chinese subjects. Our study was a large-scale GWAS to identify Lp(a)-associated variants in the Han Chinese population. A genome-wide association study on lipoprotein (a) levels and coronary artery disease severity in a Chinese population. Racial differences should not Abbreviations: AST, aspartate aminotransferase; CAD, coronary artery disease; CAG, coronary angiography; CNV, copy number variation; CREA, creatinine; FDR, false discovery rate; GWAS, genome-wide association study; HCL, heavily calcified lesion; LD, linkage disequilibrium; LDLC, LDL cholesterol; LDLCc, corrected LDL cholesterol; Lp(a), lipoprotein (a); LRL, long-range lesion; MAF, minor allele frequency; OR, odds ratio; PCI, percutaneous coronary intervention; QC, quality control. This association indicates that rs7770628 and rs73596816 have potential roles in CAD progression

Methods
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call