Skip to main content
. 2019 Jul 10;7(8):e846. doi: 10.1002/mgg3.846

Table 5.

Relative risk of cardiovascular outcomes by the VKORC1 and Chr.9p21.3 interactions during a longitudinal follow‐up of stroke patients

VKORC1 rs2359612 Chr.9p21.3 rs10757274 Person‐years Outcomes, n (%) Adjusted Hazards ratio (95% CI)* p value*
Stroke recurrence
TT AA 1,293.48 49 (16.4%) 1.00  
TT AG+GG 3,272.89 169 (21.7%) 1.45 (1.05–2.00) .02
CT AA 256.46 12 (19.7%) 1.41 (0.75–2.66) .29
CT+CC AG+GG 789.97 50 (25.9%) 1.84 (1.24–2.73) .003
CVD events
TT AA 1,231.65 61 (20.5%) 1.00  
TT AG+GG 3,089.48 194 (24.9%) 1.32 (0.99–1.76) .06
CT AA 253.16 13 (21.3%) 1.18 (0.65–2.16) .59
CT+CC AG+GG 751.52 57 (29.5%) 1.65 (1.15–2.38) .007
CVD mortality
TT AA 1,290.37 23 (7.7%) 1.00  
TT AG+GG 3,269.28 93 (11.9%) 1.64 (1.04–2.59) .04
CT AA 271.70 3 (4.9%) 0.74 (0.22–2.48) .63
CT+CC AG+GG 814.07 27 (14.0%) 2.16 (1.24–3.79) .007

Abbreviations: Chr.9p21.3, Chromosome 9p21.3; CVD, cardiovascular diseases; VKORC1, vitamin K epoxide reductase complex subunit 1.

*

Adjusted Hazards ratio (95% CI) and p values were obtained by the Cox regression analysis after adjustment for age, gender, BMI, fasting glucose, triglycerides, total cholesterol, HDL‐cholesterol, LDL‐cholesterol, family history of stroke, systolic and diastolic blood pressure, smoking, and drinking status.