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. Author manuscript; available in PMC: 2014 May 20.
Published in final edited form as: Eur Neuropsychopharmacol. 2012 Oct 22;23(8):931–940. doi: 10.1016/j.euroneuro.2012.09.008

Table 1.

Demographic and treatment data at baseline.

Study Group Open-label Glycine (n=10) Placebo-controlled
Glycine (n=4) Placebo (n=4)
Characteristic Mean(SD) Mean(SD) Mean(SD)
Age (yr) 17.3 (3.3) 15.3 (0.5) 16.5 (2.4)
Current GAF 44.3 (4.7) 40.5 (4.0) 39.0 (9.0)
No. (%) No. (%) No. (%)
Male 7 (70) 3 (75) 3 (75)
White nonHispanic 6 (60) 3 (75) 2 (50)
Single 10 (100) 4 (100) 4 (100)
Prodromal syndrome
    APS 10 (100) 4 (100) 4 (100)
    BIPS 1 (10) 0 (0) 0 (0)
    GRD 0 (0) 0 (0) 0 (0)
First degree family history
    Psychosis 0 (0) 0 (0) 0 (0)
    Nonpsychotic major depression 1 (10) 1 (25) 2 (50)
    Nonpsychotic bipolar disorder 2 (20) 0 (0) 0 (0)
Medication use at baseline*
    Antidepressants 3 (30) 1 (25) 1 (25)
    Antipsychotics 0 (0) 0 (0) 0 (0)
    Benzodiazepines/hypnotics 0 (0) 0 (0) 0 (0)
    Mood stabilizers 0 (0) 0 (0) 0 (0)
    Stimulants 0 (0) 0 (0) 0 (0)
Lifetime substance abuse/dependence
    Marijuana 1 (10) 0 (0) 0 (0)
    Other (except nicotine)** 1 (10) 0 (0) 0 (0)

All comparisons n.s. GAF, Global Assessment of Functioning.

*

Patients taking antidepressants, anxiolytics, mood stabilizers, or stimulants were permitted to continue these medications but not to change dose. Doses were required to be stable ≥8 weeks at baseline.

**

Other in substance abuse/dependence includes: alcohol, sedatives, opioid, cocaine, hallucinogen and other.