Anderson et al.
[18]
|
USA |
200 (101/99) |
Warfarin |
CYP2C9 VKORC1 |
% out-of-range INRs |
Relative % reduction = 7.3, P = 0.47 |
53% |
61 years |
94% Caucasian |
Borgman et al.
[35]
|
USA |
26 (13/13) |
Warfarin |
CYP2C9 VKORC1 |
% time within therapeutic range |
Experimental = 70.3 ± 17.9 |
54% |
Control = 77.7 ± 11.3 |
52 years |
P = 0.441 |
92% Caucasian |
Burmester et al.
[36]
|
USA |
225 (112/113) |
Warfarin |
CYP2C9 VKORC1 CYP4F2 |
1. Absolute prediction error relative to therapeutic dose |
1. Median difference = 0.39 mg day−1 (95% CI 0.26, 0.57), favours genotype model |
59% |
68 years (median) |
2. Time in therapeutic target range for 1st 14 days |
2. Median for both arms = 28.6%, P = 0.564 |
100% Caucasian/Hispanic |
Caraco et al.
[21]
|
Israel |
191 (95/96) |
Warfarin |
CYP2C9 |
1. Time to reach therapeutic INR range |
1. Adjusted HR 3.95 (95% CI 2.77, 5.65), favours genotype model |
52% |
59 years (median) |
2. Time to reach stable anticoagulation |
2. HR 4.23 (95% CI 2.95, 6.07), favours genotype model |
Not stated |
Hillman et al.
[19]
|
USA |
38 (18/20) |
Warfarin |
CYP2C9 VKORC1 |
Feasibility |
Application of a CYP2C9 gene-based multivariate warfarin dosage calculator is feasible |
45% |
70 years |
100% Caucasian |
Huang et al.
[37]
|
China |
121 (61/60) |
Warfarin |
CYP2C9 VKORC1 |
Time to reach stable warfarin dose |
HR 1.93 (95% CI 1.26, 2.97), favours genotype model |
31% |
42 years |
100% Chinese |
Kimmel et al.
[23]
|
USA |
955 (514/501) |
Warfarin |
CYP2C9 VKORC1 |
% time within therapeutic range |
Adjusted mean difference: −8.3%, P = 0.01, favours control |
51% |
58 years (median) |
27% Black, 73% Non-Black |
Mallal et al.
[29]
|
19 Countries |
1650 (803/847) |
Abacavir |
HLA-B*5701 |
Reduced incidence of hypersensitivity reaction |
OR 0.03 (95% CI 0.00, 0.62), favours genotype model |
73% |
42 years |
83% Caucasian |
Meynard et al.
[30]
|
France |
525 (187/186/152) |
Antiretroviral agents (12) |
HIV anti-retroviral resistance mutations |
Proportion with plasma HIV-1 RNA |
Phenotyping = 35% |
81% |
<200 copies ml−1 at week 12 |
Genotyping = 44% |
41 years |
unknown |
Controls = 36%. No significant difference between arms. |
Newman et al.
[31]
|
UK |
322 (163/159) |
Azathioprine |
TMPT |
Stopping azathioprine due to adverse drug reaction |
OR 1.1 (95% CI 0.66, 1.8) |
83% |
42 years |
91% Caucasian |
Pirmohamed et al.
[6]
|
UK |
427 (211/216) |
Warfarin |
CYP2C9 VKORC1 |
% time within therapeutic range |
Adjusted mean difference: |
Sweden |
62% |
7% (95% CI 3.3, 10.6), favours genotype model. |
|
68 years |
|
99% Caucasian |
Roberts et al.
[32]
|
Canada |
187 (91/96) |
Clopidogrel/prasugrel |
CYP2C19 |
Proportion with P2Y12 reactivity unit >234 after 1 week dual therapy treatment. |
Experimental = 9 (10%) |
78% |
Control = 16 (17%) |
60 years |
Adjusted P = 0.07 |
95% Caucasian |
Thervet et al.
[33]
|
France |
236 (116/120) |
Tacrolimus |
CYP3A5 |
Proportion within targeted therapeutic trough concentration after six doses. |
Experimental = 43.2% (95% CI 36, 51.2) |
67% |
47 years |
Control = 29.1% (95% CI 22.8, 35.5) |
90% Caucasian |
P = 0.03 |
Verhoef et al.
[34]
|
Greece |
484 (239/245) |
Acenocoumarol/phenprocoumon |
CYP2C9 VKORC1 |
% time within therapeutic range. |
Experimental = 61.6 ± 23.3 |
Netherlands |
60% |
Control = 60.2 ± 23.2 |
68 years |
Difference: 1.4 (95% CI −2.8, 5.5) |
97% Caucasian |
P = 0.52 |
Wang et al.
[38]
|
China |
101 (50/51) |
Warfarin |
CYP2C9 VKORC1 |
Time to reach stable warfarin dose |
HR 1.57 (95% CI 1.10, 3.28), favours genotype model. |
31% |
42 years |
100% Chinese |