Genetic risk analysis of coronary artery disease in Pakistani subjects using a genetic risk score of 21 variants. (March 2017)

• Record Type: Journal Article
• Authors: Shahid, Saleem Ullah; Shabana, ; Cooper, Jackie A.; Beaney, Katherine E.; Li, Kawah; Rehman, Abdul; Humphries, Steve E.
• Is Part Of: Atherosclerosis. Volume 258(2017)
• Page Start: 1
• Page End: 7
• Publication Date: 2017-03
• Subjects: Coronary artery disease -- Genetic risk score -- Conventional risk factors; Arteriosclerosis -- Periodicals; Electronic journals; 616.136
• DOI: 10.1016/j.atherosclerosis.2017.01.024
• Languages: English
• ISSNs: 0021-9150

Abstract

Abstract: Background and aims: Conventional coronary artery disease (CAD) risk factors like age, gender, blood lipids, hypertension and smoking have been the basis of CAD risk prediction algorithms, but provide only modest discrimination. Genetic risk score (GRS) may provide improved discrimination over and above conventional risk factors. Here we analyzed the genetic risk of CAD in subjects from Pakistan, using a GRS of 21 variants in 18 genes and examined whether the GRS is associated with blood lipid levels. Methods: 625 (405 cases and 220 controls) subjects were genotyped for variants, NOS3 rs1799983, SMAD3 rs17228212, APOB rs1042031, LPA rs3798220, LPA rs10455872, SORT1 rs646776, APOE rs429358, GLUL rs10911021, FTO rs9939609, MIA3 rs17465637, CDKN2A rs10757274, DAB2IP rs7025486, CXCL12 rs1746048, ACE rs4341, APOA5 rs662799, CETP rs708272, MRAS rs9818870, LPL rs328, LPL rs1801177, PCSK9 rs11591147 and APOE rs7412 by TaqMan and KASPar allele discrimination techniques. Results: Individually, the single SNPs were not associated with CAD except APOB rs1042031 and FTO rs993969 ( p = 0.01 and 0.009 respectively). However, the combined GRS of 21 SNPs was significantly higher in cases than controls (19.37 ± 2.56 vs . 18.47 ± 2.45, p = 2.9 × 10 −5 ), and compared to the bottom quintile, CAD risk in the top quintile of the GRS was 2.96 (95% CI 1.71–5.13). Atherogenic blood lipids showed significant positive association with GRS. Conclusions: The GRS was quantitatively associated with CAD risk and showed association with blood lipid levels, suggesting that the mechanism of these variants is likely to be, in part at least, through creating an atherogenic lipid profile in subjects carrying high numbers of risk alleles. Highlights: First comprehensive report on the analysis of many variants from different genes in CAD. Uses a risk score constructed from multiple variants to predict the outcome for the Pakistani population. Compares the utility of different SNPs in Pakistani vs British population.