Neurophysiologic predictors of treatment response to fluoxetine in major depression

被引:56
|
作者
Cook, IA
Leuchter, AF
Witte, E
Abrams, M
Uijtdehaage, SHJ
Stubbeman, W
Rosenberg-Thompson, S
Anderson-Hanley, C
机构
[1] Univ Calif Los Angeles, Sch Med, Quantitat EEG Lab, Neuropsychiat Inst, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90024 USA
[3] W Los Angeles Vet Affairs Med Ctr, Los Angeles, CA 90073 USA
关键词
treatment outcomes; cordance; neurophysiology; electroencephalography; QEEG;
D O I
10.1016/S0165-1781(99)00010-4
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Treatment with antidepressants is marked by heterogeneity of response; predicting individual response to any given agent remains problematic. Neuroimaging studies suggest that response is accompanied by physiologic changes in cerebral energy utilization, but have not provided useful markers at pretreatment baseline. Using quantitative EEG (QEEG) techniques, we investigated pretreatment neurophysiologic features to identify responders and non-responders to fluoxetine. In a double-masked study, 24 adult subjects with current major depression of the unipolar type were studied over 8 weeks while receiving fluoxetine (20 mg QD) or placebo. Neurophysiology was assessed with QEEG cordance, a measure reflecting cerebral energy utilization. Response was determined with rating scales and clinical interview. Subjects were divided into discordant and concordant groups based upon the number of electrodes exhibiting discordance. The concordant group had a more robust response than the discordant group, judged by lower final Hamilton Depression (HAM-D) mean score (8.0 +/- 7.5 vs. 19.6 +/- 4.7, P = 0.01) and final Beck Depression Inventory (BDI) mean score (14.0 +/- 9.4 vs. 27.8 +/- 3.7, P = 0.015), and by faster reduction in symptoms (HAM-D: 14.0 +/- 5.0 vs. 23.8 +/- 4.1, P = 0.004 at 1 week). Groups did not differ on pretreatment clinical or historical features. Response to placebo was not predicted by this physiologic measure. We conclude that cordance distinguishes depressed adults who will respond to treatment with fluoxetine from those who will not. This measure detects a propensity to respond to fluoxetine and may indicate a more general responsiveness to antidepressants. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:263 / 273
页数:11
相关论文
共 50 条
  • [31] Predictors of response to luteal phase fluoxetine treatment of PMDD
    Cohen, L
    Davis, S
    O'Brien, PMS
    Brown, E
    Miner, C
    Jacobson, J
    [J]. EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2002, 12 : S176 - S176
  • [32] FLUOXETINE VERSUS AMITRIPTYLINE IN THE TREATMENT OF MAJOR DEPRESSION - A MULTICENTER TRIAL
    BEASLEY, CM
    SAYLER, ME
    POTVIN, JH
    [J]. INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 1993, 8 (03) : 143 - 149
  • [33] Cognitive Control and Neuronal Functioning Biomarkers as Predictors of Treatment Response in Major Depression
    Langenecker, Scott Aaron
    Dawson, Erica L.
    Mickey, Brian J.
    Ransom, Michael T.
    Walker, Sara J.
    Meyers, Kortni K.
    Haxlett, Kathleen E.
    Weldon, Anne L.
    Giordani, Bruno
    Zubieta, Jon-Kar
    [J]. BIOLOGICAL PSYCHIATRY, 2014, 75 (09) : 10S - 10S
  • [34] Fluoxetine treatment for major depression decreases the plasma levels of cytokines
    Shen, Yuedi
    Lu, Peilin
    Wei, Lili
    Cai, Liqiang
    Hu, Xingyue
    Chen, Wei
    [J]. AFRICAN JOURNAL OF BIOTECHNOLOGY, 2010, 9 (43): : 7346 - 7351
  • [35] THYROID-HORMONE SUPPLEMENTATION OF FLUOXETINE IN THE TREATMENT OF MAJOR DEPRESSION
    GUPTA, S
    MASAND, P
    TANQUARY, JF
    [J]. BRITISH JOURNAL OF PSYCHIATRY, 1991, 159 : 866 - 867
  • [36] Clinical predictors of response to olanzapine or olanzapine/fluoxetine combination for bipolar depression
    Tohen, M
    Vieta, E
    Calabrese, JR
    Ketter, TA
    Mitchell, P
    Briggs, SD
    Case, M
    [J]. EUROPEAN PSYCHIATRY, 2004, 19 : 204S - 204S
  • [37] Clinical predictors of response to olanzapine or olanzapine/fluoxetine combination for bipolar depression
    Tohen, M
    Vieta, E
    Calabrese, JR
    Ketter, TA
    Mitchell, PB
    Briggs, SD
    Case, M
    [J]. BIOLOGICAL PSYCHIATRY, 2004, 55 : 231S - 231S
  • [38] Clinical predictors of response to olanzapine or olanzapine/fluoxetine combination for bipolar depression
    Tohen, M
    Vieta, E
    Calabrese, J
    Ketter, T
    Mitchell, P
    Briggs, S
    Case, M
    [J]. INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2004, 7 : S331 - S331
  • [39] Olanzapine-fluoxetine combination for treatment of psychotic major depression
    Dubé, S
    Clemow, DB
    Andersen, SW
    Sanger, TM
    Tohen, M
    Tollefson, GD
    [J]. BIOLOGICAL PSYCHIATRY, 2002, 51 (08) : 66S - 66S
  • [40] Efficacy of treatment with trazodone in combination with pindolol or fluoxetine in major depression
    Maes, M
    Vandoolaeghe, E
    Desnyder, R
    [J]. JOURNAL OF AFFECTIVE DISORDERS, 1996, 41 (03) : 201 - 210