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. Author manuscript; available in PMC: 2009 Sep 1.
Published in final edited form as: Clin Pharmacol Ther. 2008 Jul 2;84(3):332–339. doi: 10.1038/clpt.2008.101

Table 4.

Dosing algorithm for African Americans and Caucasians in the multivariate linear regression model (outcome variable is log warfarin maintenance dose per day).*

Variable N Regression coefficient
(95% CI)
Intercept 259 2.81 (2.45 to 3.17)
Race (African Americans=1) 112 −0.08 (−0.22 to 0.06)
Age 259 −0.01 (−0.01 to −0.01)
VKORC1 1173 (CT=1) 90 −0.39 (−0.50 to −0.27)
VKORC1 1173 (TT=1) 14 −0.82 (−1.04 to −0.59)
Factor 7 −401 (GT=1) 81 −0.11 (−0.22 to 0.00)
Factor 7 −401 (TT=1) 14 −0.19 (−0.42 to 0.03)
CYP2C9 (any*2=1) 52 −0.16 (−0.29 to −0.03)
CYP2C9 (any*3=1) 18 −0.30 (−0.50 to −0.10)
BMI (less than 25=1) 82 −0.18 (−0.30 to −0.06)
BMI (25 to 30=1) 89 −0.23 (−0.35 to −0.10)
Number of medications that potentiate warfarin 259 −0.08 (−0.12 to −0.04)
Most drinks on one occasion 259 0.06 (0.01 to 0.11)
History of deep vein thrombosis (yes=1) 38 0.58 (0.12 to 1.03)
Gender (female=1) 89 −0.10 (−0.20 to 0.01)
Race x history of deep vein thrombosis (yes and African American=1) 237 −0.33 (−0.61 to −0.05)
Race x most drinks on one occasion 147 −0.03 (−0.06 to 0.00)
*

Dose (mg/day) = exp[2.81 −(0.08 X African American) −(0.01 X age) −(0.39 X VKORC1 1173CT) −(0.82 X VKORC1 1173TT) −(0.11X Factor 7 −401GT) −(0.19X Factor 7 −401TT) −(0.16 X CYP2C9 any*2) −(0.30 X CYP2C9 any*3) −(0.18 X BMI <25) −(0.23 X BMI 25 to 30) –(0.08 X number of medications that potentiate warfarin) −(0.10 X female) +(0.06 X most alcoholic drinks on one occasion) −(0.03 X African American x most drinks on one occasion) +(0.58 X history of deep vein thrombosis) −(0.33 X African American x history of deep vein thrombosis)]

Age, number of medications that potentiate warfarin, and most drinks on one occasion were entered as linear terms in the model and dummy variables (0=absent, 1=present) for the other variables.