Discovery of a potential novel pharmacogenomic biomarker on ANK3 gene for liafensine, a triple reuptake inhibitor for treatment-resistant depression

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Authors: Wen Luo, Gang Wang, John W. Whitaker, Zafrin Dhali, Hong Sun, Haiping Lu, Xiaojun Li, Tao Shi, J Zhang
Cited by: 1
References: 34

Abstract

Liafensine is a triple reuptake inhibitor targeting transporters for serotonin, norepinephrine, and dopamine for treatment-resistant depression (TRD). It did not exhibit efficacy in non-biomarker-selected TRD patients in two Phase 2b studies. We utilized the blood samples from the patients enrolled in these two studies and extracted genomic DNA to conduct a genome‑wide association study aiming to find a biomarker which can predict liafensine response. A single single-nucleotide polymorphism (SNP), rs12217173, at ANK3 gene was identified as strongly associated with treatment response to liafensine (p = 6.61 × 10 −8 ) in the discovery set (n = 186) and was further confirmed in the replication sample set (n = 47, p = 0.05, combined p = 1.27 × 10 −8 ). In addition, this SNP was not associated with the efficacy of the duloxetine or escitalopram, suggesting it is a liafensine-specific biomarker. This finding was subsequently confirmed in a prospective clinical study. Thus, this study represents a novel approach to translating precision medicine into psychiatric diseases.

Fields of Study & Subjects

Neurotransmitter Receptor Influence on Behavior Genetic Associations and Epidemiology Nicotinic Acetylcholine Receptors Study

Publication details

Journal / source
Translational Psychiatry
Publisher
Springer Science and Business Media LLC
Volume
16
Issue
1
Publication date
19 June 2026
Language
EN