Abstract
Despite the common use of antidepressant drugs for the treatment of various psychiatric illnesses, selection of initial antidepressant therapy and subsequent drug modification strategies continue to be largely based on trial and error. There are no biomarkers that can objectively guide dose and treatment selection or alteration. The approach for antidepressant therapy management is even more concerning when we consider that the effectiveness of antidepressants tend to be delayed with low response rates. Therefore, strategies aimed at improving the current standard for selecting antidepressant treatment and doses may have significant economic and clinical benefit. A promising approach towards this effort is the use of pharmacogenomics to better identify patients that are likely to have an efficacious or adverse response from antidepressant treatment. Candidate gene approaches as well as genome-wide association studies have been conducted to identify genes or loci that influence antidepressant response. In this report, we highlighted key antidepressant pharmacogenomic findings and identified candidate pharmacokinetic and pharmacodynamic genes for downstream analyses and further validation. We also provided future directions regarding study methodologies and experimental design that are aimed to move antidepressant pharmacogenomics research forward.
Keywords: Antidepressants, biomarkers, depression, genes, genetics, pharmacogenomics, and pharmacogenetics.
Current Pharmacogenomics and Personalized Medicine
Title:Pharmacogenomics of Antidepressant Drugs: Focus on Key Findings and Future Directions
Volume: 12
Author(s): Cristina S. Benton and Tim Wiltshire
Affiliation:
Keywords: Antidepressants, biomarkers, depression, genes, genetics, pharmacogenomics, and pharmacogenetics.
Abstract: Despite the common use of antidepressant drugs for the treatment of various psychiatric illnesses, selection of initial antidepressant therapy and subsequent drug modification strategies continue to be largely based on trial and error. There are no biomarkers that can objectively guide dose and treatment selection or alteration. The approach for antidepressant therapy management is even more concerning when we consider that the effectiveness of antidepressants tend to be delayed with low response rates. Therefore, strategies aimed at improving the current standard for selecting antidepressant treatment and doses may have significant economic and clinical benefit. A promising approach towards this effort is the use of pharmacogenomics to better identify patients that are likely to have an efficacious or adverse response from antidepressant treatment. Candidate gene approaches as well as genome-wide association studies have been conducted to identify genes or loci that influence antidepressant response. In this report, we highlighted key antidepressant pharmacogenomic findings and identified candidate pharmacokinetic and pharmacodynamic genes for downstream analyses and further validation. We also provided future directions regarding study methodologies and experimental design that are aimed to move antidepressant pharmacogenomics research forward.
Export Options
About this article
Cite this article as:
S. Benton Cristina and Wiltshire Tim, Pharmacogenomics of Antidepressant Drugs: Focus on Key Findings and Future Directions, Current Pharmacogenomics and Personalized Medicine 2014; 12 (3) . https://dx.doi.org/10.2174/1875692113666150115222819
DOI https://dx.doi.org/10.2174/1875692113666150115222819 |
Print ISSN 1875-6921 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6913 |

- Author Guidelines
- Bentham Author Support Services (BASS)
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
- Announcements
Related Articles
-
Integrating Pathophysiology in Migraine: Role of the Gut Microbiome and Melatonin
Current Pharmaceutical Design Sympathetic Activation in Hypertension and in Hypertension-Related Metabolic Disease
Current Hypertension Reviews Concepts for Biologically Active Peptides
Current Pharmaceutical Design Effects of Psychoactive Substances in Schizophrenia – Findings of Structural and Functional Neuroimaging
Current Topics in Medicinal Chemistry Modafinil: A Useful Medication for Cocaine Addiction? Review of the Evidence from Neuropharmacological, Experimental and Clinical Studies
Current Drug Abuse Reviews Prevalence of Thyroid Dysfunction in Thai HIV-Infected Patients
Current HIV Research The Use of Bifunctional NOP/Mu and NOP Receptor Selective Compounds for the Treatment of Pain, Drug Abuse, and Psychiatric Disorders
Current Pharmaceutical Design The Role of Cytokine Network in the Pathophysiology of Schizophrenia
Current Psychiatry Reviews Recent Advances in Use of Topoisomerase Inhibitors in Combination Cancer Therapy
Current Topics in Medicinal Chemistry Affective Disorder and Hyperandrogenism
Recent Patents on Endocrine, Metabolic & Immune Drug Discovery (Discontinued) GABA<sub>B</sub> Agonists for the Treatment of Alcohol Use Disorder
Current Pharmaceutical Design Uteroplacental Circulation and Fetal Vascular Function and Development
Current Vascular Pharmacology Urinary Steroids Measured by Modern Separation Techniques and Applied as Biomarkers in Stress Studies
Current Pharmaceutical Analysis Suicide and the Polyamine System
CNS & Neurological Disorders - Drug Targets Obesity Pharmacotherapy: Current Perspectives and Future Directions
Current Cardiology Reviews Proteomics Approaches to Understand Linkage Between Alzheimer’s Disease and Type 2 Diabetes Mellitus
CNS & Neurological Disorders - Drug Targets Genetics of Anxiety Disorders - Status Quo and Quo Vadis
Current Pharmaceutical Design Mitochondrial Dysfunction in Depression
Current Neuropharmacology 8-Azapurine Nucleus: A Versatile Scaffold for Different Targets
Mini-Reviews in Medicinal Chemistry Classical and New Renin-Angiotensin Signalling in Atherosclerosis
Current Signal Transduction Therapy