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Original articles| Volume 40, ISSUE 8, P691-696, October 15, 1996

Are neurovegetative symptoms stable in relapsing or recurrent atypical depressive episodes?

  • Andrew A. Nierenberg
    Correspondence
    Address reprint requests to Andrew A. Nierenberg, MD, Clinical Psychopharmacology Unit—ACC 815, Massachusetts General Hospital, 15 Parkman Street, Boston, MA 02114.
    Affiliations
    Depression Research Program, Clinical Psychopharmacology Unit, Massachusetts General Hospital Consolidated Department of Psychiatry, Harvard Medical School, Boston, Massachusetts, USA
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  • Joel A. Pava
    Affiliations
    Depression Research Program, Clinical Psychopharmacology Unit, Massachusetts General Hospital Consolidated Department of Psychiatry, Harvard Medical School, Boston, Massachusetts, USA
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  • Kathy Clancy
    Affiliations
    Depression Research Program, Clinical Psychopharmacology Unit, Massachusetts General Hospital Consolidated Department of Psychiatry, Harvard Medical School, Boston, Massachusetts, USA
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  • Jerrold F. Rosenbaum
    Affiliations
    Depression Research Program, Clinical Psychopharmacology Unit, Massachusetts General Hospital Consolidated Department of Psychiatry, Harvard Medical School, Boston, Massachusetts, USA
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  • Maurizio Fava
    Affiliations
    Depression Research Program, Clinical Psychopharmacology Unit, Massachusetts General Hospital Consolidated Department of Psychiatry, Harvard Medical School, Boston, Massachusetts, USA
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      This paper is only available as a PDF. To read, Please Download here.
      Few data exist that assess the presence of reversed and positive neurovegetative symptoms through successive depressive episodes. To assess the stability of depressive symptoms across episodes, we studied 74 outpatients with atypical unipolar major depression, diagnosed by the Structured Clinical Interview for DSM-III-R, before response to fluoxetine treatment and again after relapse on either fluoxetine or placebo. Patients were assessed at baseline with the Atypical Depression Diagnosis Scale and at baseline and during follow-up with the 17-item Hamilton Rating Scale for Depression. Thirty-two (43%) of responders had a relapse or recurrence, 21 (66%) of whom had a predominance of reversed of positive neurovegetative symptoms at baseline. Nine of 10 (90%) patients with reversed symptoms at baseline had the same symptoms when they relapsed; seven of 11 (64%) of those with positive symptoms at baseline had positive symptoms again (kappa 0.557). Overall, five of 21 (24%) had changes in their disturbances in sleep, appetite, or weight when they relapsed. This study supports the relative stability of neurovegetative symptoms in atypical depression across episodes.

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