# The role of pharmacogenomics in the discontinuation of psychotropic medication: a scoping review protocol

**Authors:** Natalia Stollarova, Cristín Ryan, Greg Sheaf, Dolores Keating, Brian O’Donoghue, Cathal Cadogan, Malcolm Hopwood, Natalia Stollarova, Ramdas Bhat, Murari Upadhay, Natalia Stollarova

PMC · DOI: 10.12688/hrbopenres.14314.1 · HRB Open Research · 2026-01-05

## TL;DR

This paper outlines a scoping review protocol to explore how genetic factors might influence the safe discontinuation of psychiatric medications.

## Contribution

The study introduces a systematic plan to map the role of pharmacogenomics in discontinuation of psychotropic medications, an underexplored area.

## Key findings

- The review will identify studies on gene polymorphisms related to psychotropic medication discontinuation.
- It will synthesize evidence on how genetic variability influences withdrawal symptoms and tapering strategies.
- The findings will highlight current knowledge gaps in integrating pharmacogenomics into medication discontinuation practices.

## Abstract

Discontinuation of psychotropic medication is associated with considerable clinical challenges, including withdrawal symptoms and relapse. Pharmacogenomic testing is increasingly used in clinical practice to optimise pharmacotherapy by guiding drug selection and dosing, however, its role in informing medication discontinuation and tapering strategies remains underexplored. Understanding the influence of genetic variability on withdrawal symptoms could support safer, individualised discontinuation practices.

This scoping review aims to map the available evidence on the role of pharmacogenomics on the discontinuation of psychotropic medications.

The review will be conducted in accordance with the Joanna Briggs Institute (JBI) methodology for scoping reviews and reported using the PRISMA-ScR checklist. Comprehensive searches will be performed in MEDLINE, EMBASE, CINAHL, Web of Science, and PsycINFO. Studies exploring gene polymorphisms relevant to the discontinuation of psychotropic medications (antidepressants, antipsychotics, mood stabilisers, anxiolytics, hypnotics, stimulants, and opioids) will be considered. Following screening, data will be extracted, and a narrative synthesis will be undertaken to map characteristics of included studies, genes studied, medication classes involved, reported outcomes, and knowledge gaps.

This review will provide an overview of existing evidence and identify gaps regarding the role of pharmacogenomics in psychotropic medication discontinuation. The findings will help to inform future research on the integration of pharmacogenomics into individualised tapering strategies.

## Full-text entities

- **Genes:** OPRM1 (opioid receptor mu 1) [NCBI Gene 4988] {aka LMOR, M-OR-1, MOP, MOR, MOR1, OPRM}, ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 5243] {aka ABC20, CD243, CLCS, ENPAT, GP170, MDR1}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, COMT (catechol-O-methyltransferase) [NCBI Gene 1312] {aka HEL-S-98n}, HTR2A (5-hydroxytryptamine receptor 2A) [NCBI Gene 3356] {aka 5-HT2A, HTR2}, UGT1A (UDP glucuronosyltransferase family 1 member A complex locus) [NCBI Gene 7361] {aka GNT1, UGT, UGT1, UGT1A@}, SLC6A4 (solute carrier family 6 member 4) [NCBI Gene 6532] {aka 5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT}, CYP4F3 (cytochrome P450 family 4 subfamily F member 3) [NCBI Gene 4051] {aka CPF3, CYP4F, CYPIVF3, LTB4H}, CYP2D6 (cytochrome P450 family 2 subfamily D member 6 (gene/pseudogene)) [NCBI Gene 1565] {aka CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2}
- **Diseases:** concentration difficulties (MESH:C567712), memory loss (MESH:D008569), vomiting (MESH:D014839), seizures (MESH:D012640), hyperalgesia (MESH:D006930), Mood Disorders (MESH:D019964), nausea (MESH:D009325), ADRs (MESH:D064420), anxiety (MESH:D001007), dizziness (MESH:D004244), irritability (MESH:D001523), insomnia (MESH:D007319), sensory disturbances (MESH:D012678), tremors (MESH:D014202), headache (MESH:D006261), Withdrawal (MESH:D013375)
- **Chemicals:** fluoxetine (MESH:D005473), venlafaxine (MESH:D000069470), paroxetine (MESH:D017374), opiates (MESH:D053610), benzodiazepine (MESH:D001569), Bhat (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12917353/full.md

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Source: https://tomesphere.com/paper/PMC12917353