Table 1.
Study (Reference) | Country, Region | Study Design | Study Length, Weeks | Medication(s) | Measure | Median Age, Years | IQR for Age, Years | Female | Na | npercentage improvement | nremit | nnonremit |
---|---|---|---|---|---|---|---|---|---|---|---|---|
European Ancestry | ||||||||||||
STAR∗D (52) | United States | Open label | 12 | Citalopram | QIDSC | 44 | 32–53 | 58% | 1163 | 1163 | 506 | 657 |
GSRD (17) | Europe | Naturalistic | >4 | Various | MADRS | 52.5 | 43–61 | 66% | 1152 | 1152 | 189 | 963 |
GENDEP (53) | Europe | Partially randomized RCT | 12 | Escitalopram, nortriptyline | MADRS | 43 | 33–51 | 63% | 783 | 783 | 291 | 365 |
DAST (see Supplement 1) | Germany | Naturalistic inpatient | 6 | Various | HAMD-21 | 50 | 37–62 | 57% | 586 | 586 | 245 | 303 |
PGRN-AMPS (54) | United States | Open label | 8 | Citalopram, escitalopram | QIDSC | 38.5 | 28–49 | 63% | 490 | 392 | 200 | 290 |
GENPOD (18) | United Kingdom | Open label | 12 | Citalopram, reboxetine | BDI | 38 | 30–48 | 69% | 474 | 474 | 169 | 305 |
PFZ (18) | United States | RCT | 6-8 | Sertraline, fluoxetine, paroxetine | HAMD-17 | 43 | 32–54 | 67% | 309 | 309 | 99 | 210 |
Mayo (16) | United States | Open label | 8 | Citalopram, escitalopram | HAMD-17 | 37 | 29–51 | 62% | 156 | 156 | 80 | 76 |
GSK (18) | United States | RCT | 8 | Escitalopram | HAMD-17 | 36 | 25.75–45 | 55% | 132 | 132 | 56 | 76 |
GODS (18) | Switzerland | Open label | 8 | Paroxetine | MADRS | 37 | 29.5–43.5 | 52% | 71 | 71 | 17 | 54 |
East Asian Ancestry | ||||||||||||
Miaoli (16) | Taiwan | Open label | 8 | Escitalopram, paroxetine | HAMD-17 | 41 | 30–52 | 82% | 233 | 233 | 103 | 130 |
Taipei (16) | Taiwan | Open label | 8 | Fluoxetine, citalopram | HAMD-17 | 46 | 34–59 | 55% | 174 | 174 | 45 | 129 |
Japan (16) | Japan | RCT | 6 | Fluvoxamine, paroxetine | HAMD-17 | 44.5 | 32–56 | 47% | 120 | 120 | 78 | 42 |
Total | 5843 | 5745 | 2078 | 3600 |
BDI, Beck Depression Inventory; DAST, Depression and Sequence of Treatment; GENDEP, Genome Based Therapeutic Drugs for Depression; GENPOD, GENetic and clinical Predictors Of treatment response in Depression; GODS, Geneva Outpatient Depression Study; GSK, Glaxo Smith Kline; GSRD, Group for the Study of Resistant Depression; HAMD-17, 17-item Hamilton Depression Rating Scale; HAMD-21, 21-item Hamilton Depression Rating Scale; IQR, interquartile range; MADRS, Montgomery–Åsberg Depression Rating Scale; PFZ, Pfizer; PGRN-AMPS, Pharmacogenomics Research Network Antidepressant Medication Pharmacogenomic Study; QIDSC, Quick Inventory of Depressive Symptomatology; RCT, randomized controlled trial; STAR∗D, Sequenced Treatment Alternatives to Relieve Depression.
Number of participants included after quality control of genetic and clinical data.