Cited by 28Treatment of Major DepressionAnxiety, Depression, Psychometrics, Treatment, Cognitive ProcessesNeurotransmitter Receptor Influence on Behavior

The DOI matches its Crossref record.

Monoamine oxidase inhibitor-responsive depression

Abstract

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 inhibition and treatment response, and describes symptoms that distinguish markedly improved from slightly improved responders. Thirty male outpatients, ages 28-64, 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 occurred 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 showe…

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Crossref · 10.1016/0165-1781(82)90036-1

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  • Isocarboxazid (20mg) did not differ from placebo on HAMD sleep scores, but treatment responders tended to sleep better overall with isocarboxazid than with placebo.

    “(Giller et al., 1982) demonstrated that isocarboxazid (20mg) did not differ from placebo on HAMD sleep scores, but treatment responders tended to sleep better overall with isocarboxazid than with placebo.”

    From Antidepressants and their effect on sleep (2005) · cites this paper as Giller et al., 1982

  • Subjective reports of sleep were favourable with tranylcypromine and isocarboxazid.

    “Nevertheless, subjective reports of sleep were favourable with tranylcypromine (Nolen et al., 1993) and isocarboxazid (Giller et al., 1982).”

    From Antidepressants and their effect on sleep (2005) · cites this paper as Giller et al., 1982

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Research works printed but not linked: 15

  1. Bartonicek, 1970, Special application of flourescence histochemistry: Studies of eight monoamine oxidase inhibitors in brain neurons, Pharmacology, 4, 16, 10.1159/000136118 · DOI
  2. Cadoret, 1980, Somatic complaints: Harbinger of depression in primary care, Journal of Affective Disorders, 2, 61, 10.1016/0165-0327(80)90022-1 · DOI
  3. DiMascio, 1979, Differential symptom reduction by drugs and psychotherapy in acute depression, Archives of General Psychiatry, 36, 1450, 10.1001/archpsyc.1979.01780130068008 · DOI
  4. Giller, 1980, Platelet MAO and amitriptyline treatment, Psychiatry Research, 2, 259, 10.1016/0165-1781(80)90018-9 · DOI
  5. Giller, 1980, MAO inhibitors and platelet MAO inhibition, Communications in Psychopharmacology, 4, 79
  6. Glassman, 1979, Clinical characteristics of imipramine-induced orthostatic hypotension, Lancet, I, 468, 10.1016/S0140-6736(79)90824-9 · DOI
  7. Heise, 1960, Behavioral determinatio of time and dose parameters of monoamine oxidase inhibitors, Journal of Pharmacology and Experimental Therapeutics, 129, 155
  8. Pollit, 1971, Anxiety state or masked depression? A study based on the action of monoamine oxidase inhibitors, British Journal of Psychiatry, 119, 143, 10.1192/bjp.119.549.143 · DOI
  9. Quitkin, 1979, Monoamine oxidase inhibitors, Archives of General Psychiatry, 36, 749, 10.1001/archpsyc.1979.01780070027003 · DOI
  10. Ravaris, 1980, Phenelzine and amitriptyline in the treatment of depression, Archives of General Psychiatry, 37, 1075, 10.1001/archpsyc.1980.01780220113013 · DOI
  11. Robinson, 1978, Clinical pharmacology of phenelzine, Archives of General Psychiatry, 35, 629, 10.1001/archpsyc.1978.01770290111010 · DOI
  12. Robinson, 1973, The monoamine oxidase inhibitor, phenelzine, in the treatment of depressive-anxiety states, Archives of General Psychiatry, 29, 407, 10.1001/archpsyc.1973.04200030093015 · DOI
  13. Tyrer, 1976, Towards rational therapy with monoamine oxidase inhibitors, British Journal of Psychiatry, 128, 354, 10.1192/bjp.128.4.354 · DOI
  14. West, 1959, Effects of iproniazid in depressive syndromes, British Medical Journal, 1, 1491, 10.1136/bmj.1.5136.1491 · DOI
  15. Zbinden, 1960, Clinical and pharmacological considerations on mode of action of monoamine oxidase inhibitors, Diseases of the Nervous System, 21, 89

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Metadata

Authors
Giller, E., Bialos, D., Riddle, M., Sholomskas, A., & Harkness, L.
Affiliations
  • United States Department of Veterans Affairs (US)
  • Yale University (US)
Corresponding author
Giller, Earl
Venue
Psychiatry Research
Publisher
Elsevier BV
Published
1982-02
Volume
6
Issue
1
Pages
41-48
ISSN
0165-1781 (ISSN-L)
OpenAlex
W2024636395
Cited by
28
References
0
Citations by year
2025: 1
FWCI
5.23
Type
journal article
Language
en
Open access
closed
Locations
  • Psychiatry Research (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Pharmacology (medical) › Treatment of Major Depression
  • Social Sciences › Psychology › Experimental and Cognitive Psychology › Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Keywords
monoamine oxidase inhibitors, isocarboxazid, depression, antidepressant efficacy, treatment response, anxiety, psychomotor retardation, orthostatic hypotension, hypertensive crisis, adverse effects
MeSH terms
Adult, Clinical Trials as Topic, Depressive Disorder, Double-Blind Method, Humans, Isocarboxazid, Male, Middle Aged, Psychiatric Status Rating Scales

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