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
  • [21] Safety and efficacy of sertraline for depression in patients with CHF (SADHART-CHF): A randomized, double-blind, placebo-controlled trial of sertraline for major depression with congestive heart failure
    Jiang, Wei
    O'Connor, Christopher
    Silva, Susan G.
    Kuchibhatla, Maragatha
    Cuffe, Michael S.
    Callwood, Dwayne D.
    Zakhary, Bosh
    Henke, Elizabeth
    Arias, Rebekka M.
    Krishnan, Ranga
    AMERICAN HEART JOURNAL, 2008, 156 (03) : 437 - 444
  • [22] A double-blind, placebo-controlled study of memantine in the treatment of major depression
    Singh, J
    Zarate, CA
    Quiroz, JA
    De Jesus, G
    Lukenbaugh, D
    Denicoff, KD
    Manji, HK
    Charney, DS
    BIOLOGICAL PSYCHIATRY, 2005, 57 (08) : 162S - 162S
  • [23] A double-blind, placebo-controlled study of memantine in the treatment of major depression
    Zarate, CA
    Singh, JB
    Quiroz, JA
    De Jesus, G
    Denicoff, KK
    Luckenbaugh, DA
    Manji, HK
    Charney, DS
    AMERICAN JOURNAL OF PSYCHIATRY, 2006, 163 (01): : 153 - 155
  • [24] Treatment of depression with onabotulinumtoxinA: A randomized, double-blind, placebo controlled trial
    Finzi, Eric
    Rosenthal, Norman E.
    JOURNAL OF PSYCHIATRIC RESEARCH, 2014, 52 : 1 - 6
  • [25] A double-blind, randomized, placebo-controlled study of quetiapine XR for the treatment of major depression and fibromyalgia
    McIntyre, A.
    Paisley, D.
    Kuoassi, E.
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2013, 23 : S415 - S415
  • [26] Sertraline treatment for generalized anxiety disorder: A randomized, double-blind, placebo-controlled study
    Brawman-Mintzer, Olga
    Knapp, Rebecca G.
    Rynn, Moira
    Carter, Rickey E.
    Rickels, Karl
    JOURNAL OF CLINICAL PSYCHIATRY, 2006, 67 (06) : 874 - 881
  • [27] Treatment of functional dyspepsia with sertraline:A double-blind randomized placebo-controlled pilot study
    Victoria PY Tan
    Tin K Cheung
    Wai M Wong
    Roberta Pang
    Benjamin CY Wong
    World Journal of Gastroenterology, 2012, (42) : 6127 - 6133
  • [28] Treatment of functional dyspepsia with sertraline: A double-blind randomized placebo-controlled pilot study
    Tan, Victoria P. Y.
    Cheung, Tin K.
    Wong, Wai M.
    Pang, Roberta
    Wong, Benjamin C. Y.
    WORLD JOURNAL OF GASTROENTEROLOGY, 2012, 18 (42) : 6127 - 6133
  • [29] Fish oil supplementation in the treatment of major depression: A randomised double-blind placebo-controlled trial
    Grenyer, Brin F. S.
    Crowe, Trevor
    Meyer, Barbara
    Owen, Alice J.
    Grigonis-Deane, Elizabeth M.
    Caputi, Peter
    Howe, Peter R. C.
    PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2007, 31 (07): : 1393 - 1396
  • [30] Addition of atomoxetine for depression incompletely responsive to sertraline: A randomized, double-blind, placebo-controlled study
    Michelson, David
    Adler, Lenard A.
    Amsterdam, Jay D.
    Dunner, David L.
    Nierenberg, Andrew A.
    Reimherr, Frederick W.
    Schatzberg, Alan F.
    Kelsey, Douglas K.
    Williams, David W.
    JOURNAL OF CLINICAL PSYCHIATRY, 2007, 68 (04) : 582 - 587