Combined treatment with sertraline and liothyronine in major depression - A randomized, double-blind, placebo-controlled trial

被引:66
|
作者
Cooper-Kazaz, Rena
Apter, Jeffrey T.
Cohen, Revital
Karagichev, Leonid
Muhammed-Moussa, Said
Grupper, Daniel
Drori, Taly
Newman, Michael E.
Sackeim, Harold A.
Glaser, Benjamin
Lerer, Bernard [1 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Ctr, Dept Psychiat, Biol Psychiat Lab, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Hadassah Med Ctr, Endocrinol & Metab Serv, Dept Internal Med, IL-91120 Jerusalem, Israel
[3] Global Med Inst, Princeton, NJ USA
[4] Beer Yaakov Mental Hlth Ctr, Beer Yaagov, Israel
[5] New York State Psychiat Inst & Hosp, Dept Biol Psychiat, New York, NY 10032 USA
关键词
D O I
10.1001/archpsyc.64.6.679
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Antidepressant treatments that achieve a higher remission rate than those currently available are urgently needed. The thyroid hormone triiodothyronine may potentiate antidepressant effects. Objective: To determine the antidepressant efficacy and safety of liothyronine sodium (triiodothyronine) when administered concurrently with the selective serotonin reuptake inhibitor sertraline hydrochloride to patients with major depressive disorder. Design: Double-blind, randomized, 8-week, placebocontrolled trial. Setting: Outpatient referral centers. Patients: A total of 124 adult outpatients meeting unmodified DSM-IV criteria for major depressive disorder without psychotic features. Interventions: Patients were randomized to receive sertraline hydrochloride (50 mg/d for 1 week; 100 mg/d thereafter) plus liothyronine sodium (20-25 mu g/d for 1 week; 40-50 mu g/d thereafter) or sertraline plus placebo for 8 weeks. Main Outcome Measures: The primary outcome measure was categorical response to treatment (>= 50% decrease in scores on the 21-item Hamilton Rating Scale for Depression from baseline to study end point). Remission rate (final Hamilton Rating Scale for Depression score, >= 6) was a secondary outcome measure. Results: Intent-to-treat Hamilton Rating Scale for Depression response rates were 70% and 50% in the sertraline-liothyronine and sertraline-placebo groups, respectively (P=.02; odds ratio, 2.93; 95% confidence interval, 1.23-7.35); remission rates were 58% with sertralinehothyronine and 38% with sertraline-placebo (P=.02; odds ratio, 2.69; 95% confidence interval, 1.16-6.49). Baseline T-3 values were lower in patients treated with sertraline-liothyronine who had remissions than in those without remissions t(48)=3.36; P <.002). Among patients treated with sertraline-liothyronine, remission was associated with a significant decrease in serum thyrotropin values (F-1,(73)=4.00; P < 05). There were no significant effects of liothyronine supplementation on frequency of adverse effects. Conclusions: These results demonstrate enhancement of the antidepressant effect of sertraline by concurrent treatment with liothyronine without a significant increase in adverse effects. The antidepressant effect of liothyronine may be directly linked to thyroid function.
引用
收藏
页码:679 / 688
页数:10
相关论文
共 50 条
  • [1] A randomized, placebo-controlled, double-blind trial of sertraline for postpartum depression
    Hantsoo, Liisa
    Ward-O'Brien, Deborah
    Czarkowski, Kathryn A.
    Gueorguieva, Ralitza
    Price, Lawrence H.
    Epperson, C. Neill
    PSYCHOPHARMACOLOGY, 2014, 231 (05) : 939 - 948
  • [2] A randomized, placebo-controlled, double-blind trial of sertraline for postpartum depression
    Liisa Hantsoo
    Deborah Ward-O’Brien
    Kathryn A. Czarkowski
    Ralitza Gueorguieva
    Lawrence H. Price
    C. Neill Epperson
    Psychopharmacology, 2014, 231 : 939 - 948
  • [3] Treatment of dysthymia with sertraline: A double-blind, placebo-controlled trial in dysthymic patients without major depression
    Ravindran, AV
    Guelfi, JD
    Lane, RM
    Cassano, GB
    JOURNAL OF CLINICAL PSYCHIATRY, 2000, 61 (11) : 821 - 827
  • [4] DEXAMETHASONE FOR THE TREATMENT OF DEPRESSION - A RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND TRIAL
    ARANA, GW
    SANTOS, AB
    LARAIA, MT
    MCLEODBRYANT, S
    BEALE, MD
    RAMES, LJ
    ROBERTS, JM
    DIAS, JK
    MOLLOY, M
    AMERICAN JOURNAL OF PSYCHIATRY, 1995, 152 (02): : 265 - 267
  • [5] Sertraline for prevention of depression recurrence in diabetes mellitus - A randomized, double-blind, placebo-controlled trial
    Lustman, PJ
    Clouse, RE
    Nix, BD
    Freedland, KE
    Rubin, EH
    McGill, JB
    Williams, MM
    Gelenberg, AJ
    Ciechanowski, PS
    ARCHIVES OF GENERAL PSYCHIATRY, 2006, 63 (05) : 521 - 529
  • [6] A double-blind placebo-controlled multicentre study of sertraline in the acute and continuation treatment of major depression
    Olie, JP
    Gunn, KP
    Katz, E
    EUROPEAN PSYCHIATRY, 1997, 12 (01) : 34 - 41
  • [7] Metyrapone as additive treatment in major depression - A double-blind and placebo-controlled trial
    Jahn, H
    Schick, M
    Kiefer, F
    Kellner, M
    Yassouridis, A
    Wiedemann, K
    ARCHIVES OF GENERAL PSYCHIATRY, 2004, 61 (12) : 1235 - 1244
  • [8] A double-blind, randomized, placebo-controlled trial of escitalopram in the treatment of pediatric depression
    Wagner, KD
    Jonas, J
    Findling, RL
    Ventura, D
    Saikali, K
    JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2006, 45 (03): : 280 - 288
  • [9] SADHART: A randomized, double-blind, placebo-controlled trial of sertraline for treatment of depression in patients with acute MI and unstable angina
    Shapiro, PA
    Harrison, W
    O'Connor, CM
    van Zyl, LT
    Swenson, JR
    Glassman, AH
    PSYCHOSOMATICS, 2002, 43 (02) : 165 - 165
  • [10] A double-blind, placebo-controlled study comparing the effects of sertraline versus amitriptyline in the treatment of major depression
    Lydiard, RB
    Stahl, SM
    Hertzman, M
    Harrison, WM
    JOURNAL OF CLINICAL PSYCHIATRY, 1997, 58 (11) : 484 - 491