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. Author manuscript; available in PMC: 2014 Jan 7.
Published in final edited form as: Int J Neuropsychopharmacol. 2009 Mar 17;13(1):10.1017/S1461145709000169. doi: 10.1017/S1461145709000169

Table 1.

Baseline demographic and clinical features (n = 26)

Feature
Age (yr) 48.2 ± 11.8
Sex (n, % female) 10 (39)
Ethnicity (n, % minority) 8 (31)
Body mass index (kg/m2) 29.1 ± 5.9
Received psychiatric disability (n, % yes) 12 (46)
Education (yr) 15.2 ± 2.7
IQa 114.9 ± 10.2
Number of adequate antidepressants trials (median, range)b 6.0 ± 4.1 (5, 2–18)
Past lamotrigine exposure (n, % yes) 11(42)
Age at first major depressive episode (yr) 18.5 ± 12.2
Duration of index episode (yr) 24.3 ± 16.3
Ultrachronicc (n, %) 24 (92)
Previous episodes (n) 1.9 ± 1.7
Comorbid anxiety disorder (n, % yes) 20 (77)
Family history of alcohol use disorder (n, % yes) 10 (39)
Past alcohol use disorder (n, % yes) 6 (23)
Past substance use disorder (n, % yes) 5 (19)
Family history of major depression (n, % yes) 13 (50)
Baseline IDS-C30 47.0 ± 7.7
Baseline MADRS 36.9 ± 5.4
Baseline QIDS-SR16 18.6 ± 3.9
Baseline Clinical Global Impression – Severity 5.3 ± 0.8
Expectancy rating patient outcome (1–5) 2.9 ± 1.0

IDS-C30, Inventory of Depressive Symptoms-Clinician Rated; MADRS, Montgomery–Asberg Depression Rating Scale ; QIDS-SR16, Quick Inventory of Depressive Symptomatology-Self-Report.

Values are mean ± s.d. unless otherwise indicated.

a

Weschler Abbreviated Scale of Intelligence (WASI).

b

Antidepressant Treatment History Form, minimum score of 3 (threshold for classification as medication resistant).

c

index major depressive episode ≥42 months (Gilmer et al. 2008).