TY - JOUR
T1 - Pioglitazone adjunctive therapy for moderate-to-severe major depressive disorder
T2 - Randomized double-blind placebo-controlled trial
AU - Sepanjnia, Khatereh
AU - Modabbernia, Amirhossein
AU - Ashrafi, Mandana
AU - Modabbernia, Mohammad Jafar
AU - Akhondzadeh, Shahin
N1 - Funding Information:
This study was Dr Khatereh Sepanjnia’s postgraduate thesis toward qualification for the Iranian Board of Psychiatry under the supervision of Prof. Shahin Akhondzadeh. This study was supported by a grant from Tehran University of Medical Sciences to Prof. Shahin Akhondzadeh (Grant No. 9476).
PY - 2012/8
Y1 - 2012/8
N2 - Thiazolidinediones have shown antidepressant effect in animal studies, as well as in some uncontrolled studies evaluating human subjects with concurrent major depressive disorder (MDD) and metabolic syndrome. Although these drugs are insulin sensitizers, they also have important anti-inflammatory, neuroprotective, and anti-excitotoxic properties. Thus, we hypothesized that they would show antidepressant effect in patients with MDD even if it was not accompanied by metabolic disturbances. In this double-blind placebo-controlled study, 40 patients with MDD (DSM-IV-TR) and Hamilton depression rating scale-17 (Ham-D) score °22 were randomized to citalopram plus pioglitazone (15 mg every 12 h) (n20) or citalopram plus placebo (n20) for 6 weeks. Patients were evaluated using Ham-D (weeks 0, 2, 4, 6). Repeated-measure analysis of variance (ANOVA) and analysis of covariance were used for comparison of scores between the two groups. Treatment response (50% reduction in Ham-D score), remission (Ham-D score7), and early improvement (20% reduction in Ham-D score within the first 2 weeks) were compared between the two groups using Fisher's exact test. Pioglitazone showed superiority over placebo during the course of the trial (F(1, 38)9.483, p0.004). Patients in the pioglitazone group had significantly lower scores at all time points than the placebo group (P0.01). Frequency of early improvement, response (week 6), and remission was significantly higher in the pioglitazone group (95%, 95%, 45%, respectively) than in the placebo (30%, 40%, 15% respectively) group (P0.001, 0.001, 0.04, respectively). Frequency of side effects was similar between the two groups. Pioglitazone is a safe and effective adjunctive short-term treatment in patients with moderate-to-severe MDD even in the absence of metabolic syndrome and diabetes (http:// clinicaltrials.gov/ct2/show/NCT01109030).
AB - Thiazolidinediones have shown antidepressant effect in animal studies, as well as in some uncontrolled studies evaluating human subjects with concurrent major depressive disorder (MDD) and metabolic syndrome. Although these drugs are insulin sensitizers, they also have important anti-inflammatory, neuroprotective, and anti-excitotoxic properties. Thus, we hypothesized that they would show antidepressant effect in patients with MDD even if it was not accompanied by metabolic disturbances. In this double-blind placebo-controlled study, 40 patients with MDD (DSM-IV-TR) and Hamilton depression rating scale-17 (Ham-D) score °22 were randomized to citalopram plus pioglitazone (15 mg every 12 h) (n20) or citalopram plus placebo (n20) for 6 weeks. Patients were evaluated using Ham-D (weeks 0, 2, 4, 6). Repeated-measure analysis of variance (ANOVA) and analysis of covariance were used for comparison of scores between the two groups. Treatment response (50% reduction in Ham-D score), remission (Ham-D score7), and early improvement (20% reduction in Ham-D score within the first 2 weeks) were compared between the two groups using Fisher's exact test. Pioglitazone showed superiority over placebo during the course of the trial (F(1, 38)9.483, p0.004). Patients in the pioglitazone group had significantly lower scores at all time points than the placebo group (P0.01). Frequency of early improvement, response (week 6), and remission was significantly higher in the pioglitazone group (95%, 95%, 45%, respectively) than in the placebo (30%, 40%, 15% respectively) group (P0.001, 0.001, 0.04, respectively). Frequency of side effects was similar between the two groups. Pioglitazone is a safe and effective adjunctive short-term treatment in patients with moderate-to-severe MDD even in the absence of metabolic syndrome and diabetes (http:// clinicaltrials.gov/ct2/show/NCT01109030).
KW - PPAR-gamma
KW - adjunctive therapy
KW - major depressive disorder
KW - pioglitazone
KW - randomized controlled trial
KW - thiazolidinedione
UR - http://www.scopus.com/inward/record.url?scp=84863987293&partnerID=8YFLogxK
U2 - 10.1038/npp.2012.58
DO - 10.1038/npp.2012.58
M3 - Article
C2 - 22549115
AN - SCOPUS:84863987293
SN - 0893-133X
VL - 37
SP - 2093
EP - 2100
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 9
ER -