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. 2013 Jun 27;5(6):58. doi: 10.1186/gm462

Table 2.

Genetic predictions and clinical phenotypes related to metabolic and cardiovascular disorders

Sample ID Common variant prediction Clinical phenotype Clinical risk factors
CHD-1 T2D (4.5) - FMD, CD34+ cells
CHD-2 T2D (3.8); MI (1.24)a - BP, N:L ratio, SEVR, HDL-C
CHD-3 Stroke (2.18); CAD (1.21) a; obesity (1.23)b Obese Total cholesterol, TG, BP, N:L ratio, FMD, PWV, FRS (CVD)
CHD-4 T2D (1.20); CAD (1.32) a - SEVR, N:L ratio, hyperemia, CD34+ cells
CHD-5 CAD (2.09)a; T2D (2.24); stroke (2.18); MI (1.91)a - Total cholesterol, LDL-C, SEVR, hyperemia, AIX, PWV
CHD-6 Hypertriglyceridemia (3.48)b; atrial fibrillation (1.35) Hypertriglyceridemia HDL-C, SEVR, CD34+ cells
CHD-7 Stroke (2.18)b; MI (1.70); atrial fibrillation (1.35); CAD (1.40) Stroke FMD, CD34+ cells
CHD-8 Hypertriglyceridemia (1.72)b; CAD (1.38)a Hypertriglyceridemia WHR, glucose, FRS (T2D), total cholesterol, LDL-C, BP, AIX, PWV, FMD

Abbreviations: AIX: Augmentation Index; BP: blood pressure; CAD: coronary artery disease; CVD: cardiovascular disease; FMD: flow-mediated dilation; FRS: Framingham Risk Scores; HDL: high-density lipoprotein cholesterol; LDL-C: low-density lipoprotein cholesterol; MI: myocardial infarction; N:L: neutrophil:lympocyte; SEVR: sub-endocardial viability ratio; T2D: Type 2 diabetes; TG: triglycerides; PWV: pulse wave velocity;. Numbers in brackets indicate LR due to genetic variants. aconcordance with clinical risk factors, bconcordance with clinical phenotype.