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Am J Psychiatry 1995; 152:31-36
Copyright © 1995 by American Psychiatric Association
Atypical depression: clinical aspects and noradrenergic function
GM Asnis, LK McGinn and WC Sanderson
Department of Psychiatry, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY 10467.
OBJECTIVE: The authors assessed the frequency of atypical depression in
depressed outpatients and compared clinical and biological features of
patients with atypical and nonatypical depression. METHOD: Depressed
outpatients (N = 114) were diagnosed with the Schedule for Affective
Disorders and Schizophrenia (SADS) according to Research Diagnostic
Criteria. Patients were assessed for presence or absence of atypical
depression with the Atypical Depressive Disorder Scale. Atypical depression
was defined as the presence of mood reactivity during the depressive
episode, along with at least one of four associated features: hypersomnia,
hyperphagia, leaden paralysis, and rejection sensitivity. All patients
completed the SCL-90 and were rated with the Hamilton Depression Rating
Scale, extracted from the SADS. To assess biological functioning, the
authors examined cortisol response to 75 mg of desipramine, a relatively
selective norepinephrine reuptake inhibitor. RESULTS: Twenty-nine percent
of patients met criteria for atypical depression. Patients with atypical
depression were significantly more likely to be female. Patients with
atypical and nonatypical depression did not differ on SCL-90 subscale
scores. Although extracted Hamilton depression scale scores were
significantly higher for patients with nonatypical depression, the
difference was not clinically significant. Patients with atypical
depression exhibited a significantly different cortisol response to
desipramine injection than patients with nonatypical depression, which
suggested that nonatypical depression may be associated with a more
impaired norepinephrine system. CONCLUSIONS: In view of data in this study,
as well as earlier studies, atypical depression has a unique symptom
profile, may be widely prevalent, has a distinct treatment response, and
may indicate a less impaired biological system than nonatypical depression.
Since this is the first report to evaluate the frequency of atypical
depression as well as the norepinephrine system in atypical depression,
this study needs to be replicated. Nonetheless, the data support the
inclusion of atypical depression as a subtype of the depressive disorders
in DSM-IV.
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