Table 1:
Major depressive disorder patients |
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---|---|---|---|---|---|---|---|---|
Characteristic | Non-remitters (N=29) | Partial-remitters (N=26) | Full-remitters (N=37) | Healthy control subjects (N=58) | ||||
Age (years) | Mean | SD | Mean | SD | Mean | SD | Mean | SD |
51.0 | 16.0 | 46.1 | 15.5 | 42.6 | 12.4 | 43.8 | 16.4 | |
Female | N | % | N | % | N | % | N | % |
19 | 66 | 16 | 62 | 23 | 62 | 24 | 41 | |
Racea | N | % | N | % | N | % | N | % |
Caucasian | 25 | 86 | 19 | 76 | 30 | 86 | 50 | 86 |
African American | 1 | 3 | 1 | 4 | 0 | 0 | 2 | 3 |
Hispanic | 3 | 10 | 3 | 12 | 5 | 14 | 2 | 3 |
Other | 0 | 0 | 2 | 8 | 0 | 0 | 4 | 7 |
MRI exam indicationb | N | % | N | % | N | % | N | % |
1. Assess for transient aphasia, ataxia, vertigo, altered mental state, one-sided transient sensation loss or numbness | 10 | 35 | 7 | 27 | 9 | 24 | 18 | 31 |
2. Routine imaging | 8 | 28 | 6 | 23 | 12 | 32 | 18 | 31 |
3. Chronic headaches and/or migraines | 7 | 24 | 8 | 31 | 13 | 35 | 11 | 19 |
4. Rule out brain metastasis | 1 | 3 | 3 | 12 | 0 | 0 | 10 | 17 |
5. Assess for transient syncope, dizziness, fainting | 3 | 10 | 2 | 8 | 3 | 8 | 1 | 2 |
Medicationsc | Median | IQR | Median | IQR | Median | IQR | Median | IQR |
Unique antidepressants | 2 | 2-3 | 3 | 1-4 | 2 | 1-2 | n/a | n/a |
Total prescriptions | 3 | 2-4 | 4 | 1-6 | 2 | 1-3 | n/a | n/a |
SSRI prescriptions | 1 | 1-1 | 1 | 1-2 | 1 | 1-1 | n/a | n/a |
Non-SSRI prescriptions | 2 | 1-3 | 2 | 1-2 | 1 | 1-1 | n/a | n/a |
Abbreviations: MDD, major depressive disorder; N, number of subjects; SD, standard deviation; IQR, interquartile range; n/a, not applicable.
Caucasians were overrepresented in each group (p<0.001).
Exam reasons did not differ by group (X2=15.43, df=12, p=0.22), and all exams were concluded unremarkable.
Antidepressant medications prescribed within 12 months prior to MRI. See supplemental Table S1 for more details on antidepressant prescriptions among MDD patients. Refractory patients were free of any ECT and TMS therapy in the 12 months prior to MRI exam.