A Pharmacogenomic-based Antidepressant Treatment for Patients with Major Depressive Disorder: Results from an 8-week, Randomized, Single-blinded Clinical Trial.
10.9758/cpn.2018.16.4.469
- Author:
Changsu HAN
1
;
Sheng Min WANG
;
Won Myong BAHK
;
Soo Jung LEE
;
Ashwin A PATKAR
;
Prakash S MASAND
;
Laura MANDELLI
;
Chi Un PAE
;
Alessandro SERRETTI
Author Information
1. Department of Psychiatry, Korea University College of Medicine, Seoul, Korea.
- Publication Type:Clinical Trial ; Randomized Controlled Trial ; Original Article
- Keywords:
Depressive disorder;
Pharmacogenetic testing;
Antidepressants;
Precision medicine;
Effects;
Tolerance
- MeSH:
Antidepressive Agents;
Depression;
Depressive Disorder;
Depressive Disorder, Major*;
Drug Therapy;
Generalization (Psychology);
Humans;
Precision Medicine
- From:Clinical Psychopharmacology and Neuroscience
2018;16(4):469-480
- CountryRepublic of Korea
- Language:English
-
Abstract:
OBJECTIVE: Pharmacogenomic-based antidepressant treatment (PGATx) may result in more precise pharmacotherapy of major depressive disorder (MDD) with better drug therapy guidance. METHODS: An 8-week, randomized, single-blind clinical trial was conducted to evaluate the effectiveness and tolerability of PGATx in 100 patients with MDD. All recruited patients were randomly allocated either to PGATx (n=52) or treatment as usual (TAU, n=48) groups. The primary endpoint was a change of total score of the Hamilton Depression Rating Scale-17 (HAMD-17) from baseline to end of treatment. Response rate (at least 50% reduction in HAMD-17 score from baseline), remission rate (HAMD-17 score ≥7 at the end of treatment) as well as the change of total score of Frequency, Intensity, and Burden of Side Effects Ratings (FIBSER) from baseline to end of treatment were also investigated. RESULTS: The mean change of HAMD-17 score was significantly different between two groups favoring PGATx by −4.1 point of difference (p=0.010) at the end of treatment. The mean change in the FIBSER score from baseline was significantly different between two treatment groups favoring PGATx by −2.5 point of difference (p=0.028). The response rate (71.7 % vs. 43.6%, p=0.014) were also significantly higher in PGATx than in TAU at the end of treatment, while the remission rate was numerically higher in PGATx than in TAU groups without statistical difference (45.5% vs. 25.6%, p=0.071). The reason for early drop-out associated with adverse events was also numerically higher in TAU (n=9, 50.0%) than in PGATx (n=4, 30.8%). CONCLUSION: The present study clearly demonstrate that PGATx may be a better treatment option in the treatment of MDD in terms of effectiveness and tolerability; however, study shortcomings may limit a generalization. Adequately-powered, well-designed, subsequent studies should be mandatory to prove its practicability and clinical utility for routine practice.
