Defining the boundaries of atypical depression: Evidence from the HPA axis supports course of illness distinctions

被引:48
作者
Stewart, JW
Quitkin, FM
McGrath, PJ
Klein, DF
机构
[1] New York State Psychiat Inst & Hosp, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Psychiat, New York, NY 10027 USA
关键词
atypical depression; HPA axis; age of onset; chronic;
D O I
10.1016/j.jad.2005.01.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Treatment outcome and brain laterality differ between early onset (< 20 years) chronically (no well-being > 2 months) depressed patients with atypical features (early/chronic atypical) and those with either later onset or less chronic illness (late/nonchronic atypical). Because hypothalamic-pituitary-adrenal (HPA) axis abnormalities have been hypothesized to distinguish atypical depression from melancholia, we examined whether HPA measures would also differentiate these two groups of depressed patients with atypical features. Methods: Three-hour afternoon cortisol levels, stimulation of cortisol by afternoon dextroamphetamine, and suppression of cortisol by dexamethasone were investigated in 85 depressed patients with atypical features. The latter group was divided into early/chronic atypical and late/nonchronic atypical based on chart review of course of illness. Results: Patients with early/chronic atypical had significantly lower mean 3 h afternoon cortisol levels (N=21) and 4:00 p.m. post-dexamethasone cortisol levels (N=20) than did those with late/nonchronic atypical (N=43 with afternoon cortisol; N=26 with post-dexamethasone cortisol). Post-dextroamphetamine cortisol levels were numerically higher in the early/chronic atypical group (N=15 vs. 19), but this failed to reach conventional significance (0.05 < p < 0.1). Arbitrary categorical distinctions of normal and abnormal did not separate these groups on any of the tests. Limitations: Lack of demonstrated reliability of the chart review and retrospective determination of atypical features and course of illness limit the generalizability of these findings. Conclusions: These HPA data are consistent with earlier treatment and brain laterality findings that course of illness distinguishes biologically distinct groups within depressed patients with atypical features. The DSM should consider adding course of illness requirements to its criteria for atypical features. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:161 / 167
页数:7
相关论文
共 24 条
[1]  
*AM PSYCH ASS, 2000, DIAGN STAT MAN MENT, P421
[2]  
*AM PSYCH ASS, 1994, DIAGN STAT MAN MEN D
[3]   Toward validation of atypical depression in the community: results of the Zurich cohort study [J].
Angst, J ;
Gamma, A ;
Sellaro, R ;
Zhang, HP ;
Merikangas, K .
JOURNAL OF AFFECTIVE DISORDERS, 2002, 72 (02) :125-138
[4]   Endocrine and cytokine correlates of major depression and dysthymia with typical or atypical features [J].
Anisman, H ;
Ravindran, AV ;
Griffiths, J ;
Merali, Z .
MOLECULAR PSYCHIATRY, 1999, 4 (02) :182-188
[5]   CORTISOL SECRETION IN RELATION TO AGE IN MAJOR DEPRESSION [J].
ASNIS, GM ;
SACHAR, EJ ;
HALBREICH, U ;
NATHAN, RS ;
NOVACENKO, H ;
OSTROW, LC .
PSYCHOSOMATIC MEDICINE, 1981, 43 (03) :235-242
[6]   Testing early-onset chronic atypical depression subtype [J].
Benazzi, F .
NEUROPSYCHOPHARMACOLOGY, 2004, 29 (02) :440-441
[7]   Psychomotor changes in melancholic and atypical depression: unipolar and bipolar-II subtypes [J].
Benazzi, F .
PSYCHIATRY RESEARCH, 2002, 112 (03) :211-220
[8]   Depression with DSM-IV atypical features: a marker for bipolar II disorder [J].
Benazzi, F .
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, 2000, 250 (01) :53-55
[9]  
BIELSKI RJ, 1976, ARCH GEN PSYCHIAT, V33, P1479
[10]   CEREBRAL LATERALITY AND DEPRESSION - DIFFERENCES IN PERCEPTUAL ASYMMETRY AMONG DIAGNOSTIC SUBTYPES [J].
BRUDER, GE ;
QUITKIN, FM ;
STEWART, JW ;
MARTIN, C ;
VOGLMAIER, MM ;
HARRISON, WM .
JOURNAL OF ABNORMAL PSYCHOLOGY, 1989, 98 (02) :177-186