The Role of Curcumin Administration in Patients with Major Depressive Disorder: Mini Meta-Analysis of Clinical Trials

被引:60
作者
Al-Karawi, Dalia [1 ]
Al Mamoori, Doaa Alem [2 ]
Tayyar, Yaman [3 ]
机构
[1] Al Kadhimiya Teaching Hosp, Baghdad 10006, Iraq
[2] Baghdad Med City, Dept Emergency Med, Baghdad, Iraq
[3] Griffith Univ, Gold Coast, Qld, Australia
关键词
curcumin; major depressive disorders; QUALITY-OF-LIFE; DOUBLE-BLIND; ANTIINFLAMMATORY PROPERTIES; OXIDATIVE STRESS; ANTIOXIDANT; PREVALENCE; ANTIDEPRESSANTS; BIOAVAILABILITY; PLASTICITY; SEROTONIN;
D O I
10.1002/ptr.5524
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Major depression is a common, recurrent, and chronic disease that negatively affects the quality of life and increases the risk of mortality. Several studies have demonstrated that curcumin, the yellow-pigmented substance of the turmeric, possesses antidepressant properties. The aim of this review is to meta-analytically assess the antidepressant effect of curcumin in patients with major depressive disorders. We extensively searched the literature until August 2015. The random-effect model was used to calculate the pooled standardized difference of means (SMD). Subgroup analyses were also performed to examine the effect of different study characteristics on the overall model. Six clinical trials met the inclusion criteria. Overall, curcumin administration showed a significantly higher reduction in depression symptoms [SMD=-0.34; 95% confidence interval (CI)=-0.56, -0.13; p=0.002]. Subgroup analyses showed that curcumin had the highest effect when given to middle-aged patients (SMD=-0.36; 95% CI=-0.59; -0.13; p=0.002), for longer duration of administration (SMD=-0.40; 95% CI=-0.64, -0.16; p=0.001), and at higher doses (SMD=-0.36; 95% CI=-0.59, -0.13; p=0.002). The administration of new formulation of curcumin (BCM-95) had non-significantly higher effect on depression as compared with the conventional curcumin-piperine formula. We conclude that there is supporting evidence that curcumin administration reduces depressive symptoms in patients with major depression. Copyright (c) 2015 John Wiley & Sons, Ltd.
引用
收藏
页码:175 / 183
页数:9
相关论文
共 63 条
[1]   Curcumin: an orally bioavailable blocker of TNF and other pro-inflammatory biomarkers [J].
Aggarwal, Bharat B. ;
Gupta, Subash C. ;
Sung, Bokyung .
BRITISH JOURNAL OF PHARMACOLOGY, 2013, 169 (08) :1672-1692
[2]   Potential therapeutic effects of curcumin, the anti-inflammatory agent, against neurodegenerative, cardiovascular, pulmonary, metabolic, autoimmune and neoplastic diseases [J].
Aggarwal, Bharat B. ;
Harikumar, Kuzhuvelil B. .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2009, 41 (01) :40-59
[3]   Therapeutic Potential of Turmeric in Alzheimer's Disease: Curcumin or Curcuminoids? [J].
Ahmed, Touqeer ;
Gilani, Anwarul-Hassan .
PHYTOTHERAPY RESEARCH, 2014, 28 (04) :517-525
[4]   A Critical Examination of Studies on Curcumin for Depression [J].
Andrade, Chittaranjan .
JOURNAL OF CLINICAL PSYCHIATRY, 2014, 75 (10) :E1110-E1112
[5]  
[Anonymous], 2008, QUALITY ASSESSMENT T
[6]   A Pilot Cross-Over Study to Evaluate Human Oral Bioavailability of BCM-95® CG (Biocurcumax™), A Novel Bioenhanced Preparation of Curcumin [J].
Antony, B. ;
Merina, B. ;
Iyer, V. S. ;
Judy, N. ;
Lennertz, K. ;
Joyal, S. .
INDIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 70 (04) :445-449
[7]   Curcumin as an Add-On to Antidepressive Treatment: A Randomized, Double-Blind, Placebo-Controlled, Pilot Clinical Study [J].
Bergman, Joseph ;
Miodownik, Chanoch ;
Bersudsky, Yuly ;
Sokolik, Shmuel ;
Lerner, Paul P. ;
Kreinin, Anatoly ;
Polakiewicz, Jacob ;
Lerner, Vladimir .
CLINICAL NEUROPHARMACOLOGY, 2013, 36 (03) :73-77
[8]   Is depression associated with increased oxidative stress? A systematic review and meta-analysis [J].
Black, Catherine N. ;
Bot, Mariska ;
Scheffer, Peter G. ;
Cuijpers, Pim ;
Penninx, Brenda W. J. H. .
PSYCHONEUROENDOCRINOLOGY, 2015, 51 :164-175
[9]   Incidence of Alzheimer's disease in a rural community in India - The Indo-US Study [J].
Chandra, V ;
Pandav, R ;
Dodge, HH ;
Johnston, JM ;
Belle, SH ;
DeKosky, ST ;
Ganguli, M .
NEUROLOGY, 2001, 57 (06) :985-989
[10]  
Cheng AL, 2001, ANTICANCER RES, V21, P2895