Gene-drug interactions (data source: DGIdb)
Gene Name Entrez ID Drug Name Chembl ID Interaction Types Sources publications
APOE 348 BUTHIONINE SULFOXIMINE CHEMBL1609891 NCI 12615656
APOE 348 ALBUMIN HUMAN CHEMBL1201451 DrugBank 17141733, 16554356, 12860569, 12887764, 17553935
APOE 348 SIMVASTATIN CHEMBL1064 PharmGKB
APOE 348 IRBESARTAN CHEMBL1513 NCI 12827021
APOE 348 CERIVASTATIN CHEMBL1477 PharmGKB
APOE 348 RITONAVIR CHEMBL163 PharmGKB
APOE 348 PREDNISONE CHEMBL635 NCI 3185288
APOE 348 VITAMIN E CHEMBL47 NCI 12076219
APOE 348 GINKGO CHEMBL2108466 NCI 12684092
APOE 348 TRETINOIN CHEMBL38 NCI 3468509
APOE 348 SOYBEAN OIL CHEMBL1201485 NCI 3021887
APOE 348 LORAZEPAM CHEMBL580 NCI 15699298
APOE 348 STAUROSPORINE CHEMBL388978 NCI 11948667
APOE 348 TROGLITAZONE CHEMBL408 NCI 15057551
APOE 348 GONADOTROPIN, CHORIONIC CHEMBL1201509 NCI 1709885
APOE 348 LUTEIN CHEMBL173929 NCI 11413081
APOE 348 TRIAMCINOLONE CHEMBL1451 NCI 9150415
APOE 348 GANCICLOVIR CHEMBL182 NCI 16322528

Variant-drug associations (data source: PharmGKB)
Gene Name Variant Alleles Chemical Phenotype Category Significance Notes Sentence Publications Annotation ID
APOE rs7412 CT atorvastatin efficacy yes as measured by decreases in LDL-cholestrol. Genotype CT is associated with increased response to atorvastatin as compared to genotype CC. 16103896 982045529
APOE rs7412 C atorvastatin efficacy yes As measured by reduction in LDLc. Association was significant only at high doses. Allele C is associated with decreased response to atorvastatin, pravastatin or simvastatin in people with Hyperlipidemias as compared to allele T. 20031551 827807830
APOE rs405509 TT Selective serotonin reuptake inhibitors efficacy yes response measured by HDRS-17 score. Patients received SSRI or SNRI but exact drug not specified. Genotype TT is associated with increased response to Selective serotonin reuptake inhibitors in people with Depressive Disorder, Major as compared to genotypes GG + GT. 32795354 1451284760
APOE rs429358 T warfarin dosage no Allele T is not associated with decreased dose of warfarin as compared to allele C. 20072124 982037951
APOE rs429358 CC lovastatin efficacy no as measured by decreases in LDL-cholestrol. No significant association was seen between all three genotypes and response. Genotype CC is not associated with response to lovastatin as compared to genotype TT. 16103896 982045810
APOE rs7412 T warfarin dosage no Allele T is not associated with decreased dose of warfarin as compared to allele C. 20072124 982037960
APOE rs429358 CC + CT warfarin dosage yes The APOE *e4 was associated with lower warfarin dose. Doses of e4 carriers (41.5±18.5) were 21 % lower than doses of e4 non-carriers (52.5±37.5 mg). This is using Classification I. It divided the individuals into three dose ranges: <=21 mg, 21–49 mg, and >= 49 mg/week. Genotypes CC + CT is associated with decreased dose of warfarin as compared to genotype TT. 25312789 1444666244
APOE rs7412 CT + TT rosuvastatin efficacy yes The minor allele of this SNP is associated with increased fractional LDL-C reduction on rosuvastatin. Genotypes CT + TT are associated with increased response to rosuvastatin as compared to genotype CC. 22331829 1447951982
APOE rs71352238 CC + CT rosuvastatin efficacy yes The minor allele of this SNP is associated with decreased LDL-C reduction on rosuvastatin. The mean per allele effect was 4.17 mg/dL. Genotypes CC + CT are associated with decreased response to rosuvastatin as compared to genotype TT. 22331829 1447951974
APOE rs7412 CC warfarin dosage yes Genotype CC is associated with decreased dose of warfarin in people with heart valve replacement as compared to genotype CT. 28079798 1448567661
APOE rs7412 C acenocoumarol dosage no Allele C is not associated with dose of acenocoumarol or warfarin in people with venous thromboembolism as compared to allele T. 29432897 1449190764
APOE rs429358 C acenocoumarol dosage yes Allele C is associated with decreased dose of acenocoumarol in people with venous thromboembolism as compared to allele T. 29432897 1449190950
APOE rs7412 CT fluvastatin efficacy yes but only for percentage change in HDL. It was not significant for total cholesterol, LDL or TGs. Effect reported for carrier ApoE*2/*3 vs ApoE*3/*3, and vs ApoE*3/*4 or *4/*4. Genotype CT is associated with increased response to fluvastatin as compared to genotype CC. 30363031 1450972760
APOE rs7412 CC warfarin dosage yes Genotype CC is associated with increased dose of warfarin in people with Atrial Fibrillation, Pulmonary Embolism or Venous Thrombosis as compared to genotypes CT + TT. 31854268 1450942212
APOE rs7412 T acenocoumarol dosage not stated This variant was not significantly associated with acenocoumarol dose, though it did explain 1.3% of the variability in dose. Clinical variables (Age, BMI, Enzyme inducers status and Amiodarone status) explained 22% of the variability in dose. This study developed an algorithm for acenocoumarol dosing using clinical and pharmacogenetic data. Allele T is not associated with dose of acenocoumarol. 22911785 1448259332
APOE rs7412 CT + TT fenofibrate efficacy yes Subjects carrying the E2 allele had a greater relative percentage decrease in non-high density lipoprotein-cholesterol concentration between baseline and 3 months of treatment, as compared to non-E2 subjects. Genotypes CT + TT is associated with increased response to fenofibrate in people with Hypertriglyceridemia as compared to genotype CC. 12042669 1450974113
APOE rs429358 C donepezil efficacy no as measured by total ADAS-Cog score obtained at baseline with that obtained at 36 months after MCI diagnosis (diff. ADAS-Cog score) but it was not significantly different. Authors write that "APOE-ɛ4 and BCHE-K* positive subjects display an earlier age of onset of AD, an accelerated cognitive decline and a greater cognitive benefits to donepezil therapy." ADAS-Cog score difference at 36 months for ApoE4+ =–1.92, for those without E4 = –0.22. Allele C is associated with increased response to donepezil in people with Alzheimer Disease as compared to allele T. 27567841 1450973000
APOE rs429358 CC hmg coa reductase inhibitors efficacy yes Analysis of 859 subjects with AD (ROS/MAP dataset) and re-analysis of a clinical trial of simvastatin in 171 AD patients (simvastatin trial) found no significant difference in ADAS-cog scores between statin-treated patients and those treated with placebo. However, analysis of separate genotype subgroups found that E4/E4 subjects in the ROS/MAP dataset had significantly better cognitive function over a 10-year follow-up compared to those treated with placebo. Additionally, there was a non-significant trend in the simvastatin trial for subjects with the E4/E4 genotype who were treated with simvastatin to have lower ADAS-cog scores than E4/E4 patients treated with placebo. Genotype CC is associated with increased response to hmg coa reductase inhibitors in people with Alzheimer Disease as compared to genotypes CT + TT. 28212683 1450973900
APOE rs429358 C ranibizumab efficacy no Patients underwent 5 monthly injections. Good response at month 5 was defined as best-corrected visual acuity improvement of >= 8 Early Treatment Diabetic Retinopathy Study (ETDRS) letters from baseline. Bonferroni correction for multiple testing. P value was for "e4 carriers vs. others". Allele C is not associated with response to ranibizumab in people with Macular Degeneration as compared to allele T. 23842101 1450973680
APOE rs429358 CC + CT donepezil efficacy yes In patients with moderate to severe Alzheimer's disease only (baseline Mini-Mental State Examination (MMSE) score < 20); in patients with mild Alzheimer's (MMSE >=20) no significant/borderline significant results were seen (p=0.05). Adjusted for gender, age, and baseline MMSE. After 6 months of treatment with cholinesterase inhibitors, those with the E4 allele were more likely to be a non-responder to treatment, as compared to those without the E4 allele. A responder was defined as a patient who showed improvement or no deterioration in cognition comparing MMSE scores at baseline with MMSE scores after 6 months. Genotypes CC + CT is associated with decreased response to donepezil, galantamine and rivastigmine in people with Alzheimer Disease as compared to genotype TT. 24951635 1450973700
APOE rs429358 CT atorvastatin efficacy yes Effect reported for E3/E4 compared to E3/E3 (there were no E4/E4 subjects in cohort). Genotype CT is associated with decreased response to atorvastatin in people with Hypercholesterolemia as compared to genotype TT. 25860945 1450973740