TY - JOUR
T1 - Monoamine oxidase inhibitor-responsive depression
AU - Giller, Earl
AU - Bialos, Donald
AU - Riddle, Mark
AU - Sholomskas, Alan
AU - Harkness, Laurie
N1 - Funding Information:
Acknowledgments. The research reported was supported by VA research funds, NIMH Grant MH-30939, and Hoffman-LaRoche. We thank Emanuel Lerner for statistical help, Helen Hall and Janet Wojciechowski for technical assistance,M argo Cinquanta for data coding, and Mary Murray and Deborah Beauvais for manuscript preparation.
PY - 1982/2
Y1 - 1982/2
N2 - Double-blind, placebo-controlled trials have documented the efficacy of some monoamine oxidase (MAO) inhibitors in treating certain depressed patients. This preliminary report of a 6-week, double-blind, placebo-controlled study of the MAO inhibitor isocarboxazid (Marplan) examines the time course of platelet MAO inhibitor isocarboxazid (Marplan) examines the time course of platelet MAO inhibition and treatment response, and describes symptoms that distinguish markedly improved from slightly improved responders. Thirty male outpatients, ages28-64, randomly divided into placebo (n=15) and active medication (n=15) groups, were followed weekly. Medication was started at 20 mg daily and increased to achieve 90% platelet MAO inhibition. Data were analyzed for 24 patients who completed at least 3 weeks of the study. A clinician's global change rating at the study's conclusion showed that 12 of 13 patients (92%) in the active medication group improved, while 3 of 11 (27%) patients in the placebo group improved. Significant symptomatic improvement occured in the active treatment group by week 3. Trends suggest that anxiety improved first (week 2), followed by depression (week 3), and finally cognitive outlook (week 6). Only minimal difficulties were observed with orthostatic hypotension, hypertensive crises, or other side effects. At baseline, the only significant difference between the markedly improved and slightly improved groups was greater psychomotor retardation in the markedly improved group. Trends suggest that the markedly improved group showed less depression, anxiety, sleep disturbance, and weight loss, fewer gastrointestinal complaints, and more helplessness and worthlessness.
AB - Double-blind, placebo-controlled trials have documented the efficacy of some monoamine oxidase (MAO) inhibitors in treating certain depressed patients. This preliminary report of a 6-week, double-blind, placebo-controlled study of the MAO inhibitor isocarboxazid (Marplan) examines the time course of platelet MAO inhibitor isocarboxazid (Marplan) examines the time course of platelet MAO inhibition and treatment response, and describes symptoms that distinguish markedly improved from slightly improved responders. Thirty male outpatients, ages28-64, randomly divided into placebo (n=15) and active medication (n=15) groups, were followed weekly. Medication was started at 20 mg daily and increased to achieve 90% platelet MAO inhibition. Data were analyzed for 24 patients who completed at least 3 weeks of the study. A clinician's global change rating at the study's conclusion showed that 12 of 13 patients (92%) in the active medication group improved, while 3 of 11 (27%) patients in the placebo group improved. Significant symptomatic improvement occured in the active treatment group by week 3. Trends suggest that anxiety improved first (week 2), followed by depression (week 3), and finally cognitive outlook (week 6). Only minimal difficulties were observed with orthostatic hypotension, hypertensive crises, or other side effects. At baseline, the only significant difference between the markedly improved and slightly improved groups was greater psychomotor retardation in the markedly improved group. Trends suggest that the markedly improved group showed less depression, anxiety, sleep disturbance, and weight loss, fewer gastrointestinal complaints, and more helplessness and worthlessness.
KW - Depression
KW - isocarboxazid
KW - monoamine oxidase inhibitor
KW - recovery time course
KW - response predictors
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U2 - 10.1016/0165-1781(82)90036-1
DO - 10.1016/0165-1781(82)90036-1
M3 - Article
C2 - 7036196
AN - SCOPUS:0020046033
SN - 0165-1781
VL - 6
SP - 41
EP - 48
JO - Psychiatry research
JF - Psychiatry research
IS - 1
ER -