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. 2015 May 7;10(5):e0125876. doi: 10.1371/journal.pone.0125876

Table 1. Names and abbreviations of phenotypes and polymorphisms included in the analysis.

Variable Abr. used Indicator variable selected
1 2 3
Smoking (yes/no) smoking yes
Age age X X
Body Mass Index bmi X X X
Systolic Blood pressure sysbp X X
Diastolic Blood pressure diabp X X X
Triglycerides tg X
Total Cholesterol chol X X
Low Density Lipoprotein ldl X X
High Density Lipoprotein hdl X X
Apolipoprotein B apob X X
Apolipoprotein A apoa X X
Lipoprotein-associated phospholipase lppla2
C-reactive protein crp X X
Factor VII coagulant activity viic X X
Fibrinogen fib
ALX homeobox 4 gene rs729287 ALX4 X
Angiopoietin-like 4 gene E40K ANGPTL4 X
Apolipoprotein B gene rs585967 APOB
Apolipoprotein E gene APOE X X
Apolipoprotein-A5-A4-C3-A1 gene cluster rs6589566 ApoA5-A4-C3-A1 X
Arachidonate 5-lipoxygenase-activating protein gene rs3885907 ALOX5AP X
Calpain 10 gene rs4676411 CAPN10
Cathepsin S gene rs11576175 CTSS X
Cholesteryl ester transfer protein gene rs708272 CETP X
Coagulation factor VII gene rs6046 F7 X
Complement component 2 gene rs7746553 C2
Complement component 3 gene rs344550 C3
C-reactive protein gene rs3093077 CRP X X X
Cyclin-dependent kinase inhibitor 2A/B (Chr9p21) rs10811661 CDKN X X
Exostosin 2 gene rs3740878 EXT2 X X
Fibrinogen alpha chain gene rs4508864 FGA X X
Glucokinase (hexokinase 4) regulator gene rs780094 GCKR X X
Glutathione S-transferase mu 3 gene rs3814309 GSTM3 X X
Glutathione S-transferase mu 4 gene rs1537236 GSTM4 X X
Hepatic lipase gene rs1800588 LIPC X X X
Insulin gene rs689 INS
Insulin-like growth factor 2 gene 1252T/C AluI IGF2 X X
Interleukin 1 receptor antagonist gene rs397211 ILRN1 X X
Interleukin 18 receptor accessory protein gene rs11465699 IL18RAP X
Interleukin 6 receptor gene rs4075015 IL6R
Lipoprotein lipase gene rs301 LPL X X
Low density lipoprotein receptor gene rs6511720 LDLR
Low density lipoprotein receptor-related protein 5 gene rs11602256 LRP5 X
Nitric oxide synthase 3 gene rs3918232S3 NOS3 X
Phospholipase A2, group VII gene rs1051931 PLA2G7 X X
Platelet/endothelial cell adhesion molecule gene rs1131012 PECAM1 X X X
Proprotein convertase subtilisin/kexin type 9 gene rs11591147 PCSK9 X
Protein C receptor gene rs867186 PROCR X
Toll-like receptor 4 gene rs11536857 TLR4 X X
Transforming growth factor, beta 1 gene rs4803455 TGFB1 X X
Uncoupling protein 2 gene rs11602906 UCP2
Uncoupling protein 3 gene rs1685354 UCP3 X X

The phenotypes were selected as established risk factors or markers of CHD and their associated polymorphisms. [7]. Only the single top SNP was included for each gene considered. Before analysis each SNP was recoded as three indicator variables. To maintain the three variables per genotype coding, the continuous phenotypes were transformed to tertiles (S1 Table). The full list of phenotypic tertiles and indicator variables used can be found in S2 Table. The three last columns show the generated indicator variables selected from the TWIST procedure as predictive of CHD. Out of the original 150 variables, 75 were retained. Continuous traits in tertiles and genotypes as three genotyping classes. In the abbreviations, index numbers after the gene names refer to common homozygote (1), heterozygote (2) and rare homozygote (3). The APOE gene polymorphism was coded so that 1 were the E2 carriers, 2 were those within the E3E3 category and 3 were the E4 carriers. Smoking is a dichotomous variables of yes or no smoking.