Omega-3 Augmentation of Sertraline in Treatment of Depression in Patients With Coronary Heart Disease A Randomized Controlled Trial

被引:99
作者
Carney, Robert M. [1 ]
Freedland, Kenneth E.
Rubin, Eugene H.
Rich, Michael W.
Steinmeyer, Brian C.
Harris, William S. [2 ]
机构
[1] Washington Univ, Sch Med, Dept Psychiat, Behav Med Ctr, St Louis, MO 63108 USA
[2] Univ S Dakota, Cardiovasc Hlth Res Ctr, Sioux Falls, SD USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2009年 / 302卷 / 15期
关键词
POLYUNSATURATED FATTY-ACIDS; DOUBLE-BLIND; FISH-OIL; CARDIOVASCULAR-DISEASE; MAJOR DEPRESSION; RISK-FACTOR; OMEGA-3-FATTY-ACIDS; MORTALITY; ARRHYTHMIAS; CONSUMPTION;
D O I
10.1001/jama.2009.1487
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Studies of depressed psychiatric patients have shown that antidepressant efficacy can be increased by augmentation with omega-3 fatty acids. Objective To determine whether omega-3 improves the response to sertraline in patients with major depression and coronary heart disease (CHD). Design, Setting, and Participants Randomized controlled trial. Between May 2005 and December 2008, 122 patients in St Louis, Missouri, with major depression and CHD were randomized. Interventions After a 2-week run-in period, all patients were given 50 mg/d of sertraline and randomized in double-blind fashion to receive 2 g/d of omega-3 acid ethyl esters (930 mg of eicosapentaenoic acid [EPA] and 750 mg of docosahexaenoic acid [DHA]) (n=62) or to corn oil placebo capsules (n=60) for 10 weeks. Main Outcome Measures Scores on the Beck Depression Inventory (BDI-II) and the Hamilton Rating Scale for Depression (HAM-D). Results Adherence to the medication regimen was 97% or more in both groups for both medications. There were no differences in weekly BDI-II scores (treatment x time interaction=0.02; 95% confidence interval [CI], -0.33 to 0.36; t(112)=0.11; P=.91), pre-post BDI-II scores (placebo, 14.8 vs omega-3, 16.1; 95% difference-in-means CI, -4.5 to 2.0; t(116)=-0.77; P=.44), or HAM-D scores (placebo, 9.4 vs omega-3, 9.3; 95% difference-in-means CI, -2.2 to 2.4; t(115)=0.12; P=.90). The groups did not differ on predefined indicators of depression remission (BDI-II <= 8: placebo, 27.4% vs omega-3, 28.3%; odds ratio [OR], 0.96; 95% CI, 0.43-2.15; t(113)=-0.11; P=.91) or response (>50% reduction in BDI-II from baseline: placebo, 49.0% vs omega-3, 47.7%; OR, 1.06; 95% CI, 0.51-2.19; t(112)=0.15; P=.88). Conclusions Treatment of patients with CHD and major depression with sertraline and omega-3 fatty acids did not result in superior depression outcomes at 10 weeks, compared with sertraline and placebo. Whether higher doses of omega-3 or sertraline, a different ratio of EPA to DHA, longer treatment, or omega-3 monotherapy can improve depression in patients with CHD remains to be determined.
引用
收藏
页码:1651 / 1657
页数:7
相关论文
共 42 条
[1]   Omega-3 fatty acids and ventricular arrhythmias: Nothing is simple [J].
Albert, Christine M. .
AMERICAN HEART JOURNAL, 2008, 155 (06) :967-970
[2]   Blood levels of long-chain n-3 fatty acids and the risk of sudden death. [J].
Albert, CM ;
Campos, H ;
Stampfer, MJ ;
Ridker, PM ;
Manson, JE ;
Willett, WC ;
Ma, J .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (15) :1113-1118
[3]   Acute Coronary Syndrome Patients With Depression Have Low Blood Cell Membrane Omega-3 Fatty Acid Levels [J].
Amin, Alpesh A. ;
Menon, Rishi A. ;
Reid, Kimberly J. ;
Harris, William S. ;
Spertus, John A. .
PSYCHOSOMATIC MEDICINE, 2008, 70 (08) :856-862
[4]   Effects of n-3 long-chain polyunsaturated fatty acids on depressed mood: systematic review of published trials [J].
Appleton, Katherine M. ;
Hayward, Robert C. ;
Gunnell, David ;
Peters, Tim J. ;
Rogers, Peter J. ;
Kessler, David ;
Ness, Andrew R. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2006, 84 (06) :1308-1316
[5]   Small-sample degrees of freedom with multiple imputation [J].
Barnard, J ;
Rubin, DB .
BIOMETRIKA, 1999, 86 (04) :948-955
[6]   Depression as a risk factor for mortality in patients with coronary heart disease: A meta-analysis [J].
Barth, J ;
Schumacher, M ;
Herrmann-Lingen, C .
PSYCHOSOMATIC MEDICINE, 2004, 66 (06) :802-813
[7]  
Beck A.T., 1990, BAI BECK ANXIETY INV
[8]   AN INVENTORY FOR MEASURING CLINICAL ANXIETY - PSYCHOMETRIC PROPERTIES [J].
BECK, AT ;
BROWN, G ;
EPSTEIN, N ;
STEER, RA .
JOURNAL OF CONSULTING AND CLINICAL PSYCHOLOGY, 1988, 56 (06) :893-897
[9]  
Beck AT., 1996, PsycTESTS, DOI DOI 10.1037/T00742-000
[10]  
BECKER R, 1996, REV SCI INSTRUM, V67, P3