RETRACTED: The Antidiabetic Metformin as an Adjunct to Antidepressants in Patients with Major Depressive Disorder: A Proof-of-Concept, Randomized, Double-Blind, Placebo-Controlled Trial (Retracted article. See vol. 19, pg. 1687, 2022)

被引:37
作者
Abdallah, Mahmoud S. [1 ]
Mosalam, Esraa M. [2 ]
Zidan, Abdel-Aziz A. [3 ,4 ]
Elattar, Khaled S. [5 ]
Zaki, Shimaa A. [6 ]
Ramadan, Ahmed N. [7 ]
Ebeid, Abla M. [8 ]
机构
[1] Univ Sadat City USC, Fac Pharm, Dept Clin Pharm, Menoufia 32897, Egypt
[2] Menoufia Univ, Fac Pharm, Dept Biochem, Menoufia, Egypt
[3] Damanhour Univ, Fac Sci, Zool Dept, Damanhour, Egypt
[4] Tanta Univ, Ctr Excellence Canc Res CECR, Tanta, Egypt
[5] Psychiat, 10th Of Ramadan, Egypt
[6] Menoufia Univ, Natl Liver Inst, Dept Clin Biochem & Mol Diagnost, Menoufia, Egypt
[7] Menoufia Univ, Fac Med, Dept Neuropsychiat, Menoufia, Egypt
[8] Delta Univ Sci & Technol, Fac Pharm, Dept Clin Pharm, Gamasaa, Egypt
关键词
Major depressive disorder; Metformin; Fluoxetine; Inflammatory markers; BDNF; Adjunctive therapy; INFLAMMATORY CYTOKINES; NEUROTROPHIC FACTOR; BIPOLAR DISORDER; ELDERLY-PATIENTS; GROWTH-FACTOR; FLUOXETINE; ESCITALOPRAM; PLASMA; METABOLISM; CELECOXIB;
D O I
10.1007/s13311-020-00878-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Metformin (MET) has been reported to have antidepressant effects in animal models and in diabetic patients with depression, owing to its anti-inflammatory, antioxidant, and neuroprotective activity. Accordingly, we proposed that MET would show antidepressant effects in patients with major depressive disorder (MDD) without other comorbidities. In this double-blind placebo-controlled study, 80 adult outpatients with MDD (DSM-IV criteria) and a Hamilton Depression Rating Scale (HAM-D) score >18 were randomized to receive fluoxetine 20 mg once daily plus placebo (n = 40) or fluoxetine 20 mg once daily plus MET 1000 mg once daily for 12 weeks. Patients were assessed by HAM-D score (weeks 0, 4, 8, and 12). The serum levels of TNF-alpha, IL-1 beta, IL-6, IGF-1, MDA, CRP, BDNF, and serotonin were measured before and after therapy. Mixed-effects model repeated-measures analysis of covariance was used to compare the HAM-D scores and the biological markers between the two groups. After 4, 8 and 12 weeks, patients in the MET group showed a statistically significant decline in HAM-D score relative to the placebo group (least squares mean difference [LSMD] -2.347, p = 0.000, LSMD -3.369, p = 0.000, and LSMD -3.454, p = 0.000, respectively). Response and remission rates were significantly higher in the MET group (89% and 81%, respectively) than in the placebo group (59% and 46%, respectively). Moreover, the MET group was superior in conserving the measured biological markers compared with the placebo group. Our findings suggest MET as a promising, effective, and safe short-term adjunctive approach in nondiabetic MDD patients.
引用
收藏
页码:1897 / 1906
页数:10
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