| Literature DB >> 31186284 |
Yibin Liu1,2, Hongkun Ma1,2, Qian Zhu2, Bin Zhang2, Hong Yan1,2, Hanping Li1,2, Jinxiu Meng1,2, Weihua Lai3, Liwen Li4, Danqing Yu4, Shilong Zhong5,2,3.
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.Entities:
Keywords: SYNTAX score; genetics; lipid and lipoprotein metabolism; metabolic disease; single nucleotide polymorphism
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Year: 2019 PMID: 31186284 PMCID: PMC6672037 DOI: 10.1194/jlr.P091009
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922