Editorial
Copyright ©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Psychiatry. Sep 19, 2024; 14(9): 1285-1288
Published online Sep 19, 2024. doi: 10.5498/wjp.v14.i9.1285
Personalized medicine and opioid use disorder
Dilek Kaya-Akyüzlü
Dilek Kaya-Akyüzlü, Institute of Forensic Sciences, Ankara University, Ankara 06590, Türkiye
Author contributions: Kaya-Akyüzlü D designed the overall concept and outline of the manuscript, reviewed the literature, and wrote and edited the manuscript.
Conflict-of-interest statement: The author has no conflicts of interest to declare.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Dilek Kaya-Akyüzlü, PhD, Associate Professor, Institute of Forensic Sciences, Ankara University, Balkiraz Mah. Mamak Cad. No. 27, Dikimevi, Ankara 06590, Türkiye. akyuzludilek@gmail.com
Received: April 27, 2024
Revised: July 30, 2024
Accepted: August 7, 2024
Published online: September 19, 2024
Processing time: 136 Days and 12.7 Hours
Abstract

Opioid use disorder (OUD) is a major public health problem affecting millions of people worldwide. Although OUD is a chronic and relapsing disorder, a variety of pharmacological and non-pharmacological interventions are available. Medication-assisted treatment of OUD generally relies on competition for opioid receptors against the addictive substance. The mechanisms of this competition are to block or inactivate the opioid receptor or activate the receptor with a substance that is intermittent or long acting. Methadone and buprenorphine are two United States Food and Drug Administration-approved medications that have long-term positive effects on the health of opioid-dependent individuals. Although clinical studies of drugs generally demonstrate efficacy in thousands of people and toxicity is excluded, it cannot be predicted whether the given drug will cause side effects in one of the patients at the treatment dose. Individual differences can be explained by many biological and environmental factors. Variations in genes encoding drug metabolism or cellular drug targets significantly explain the variability in drug response between individuals. Therefore, for the effects of candidate genes to be accepted and included in individual treatment protocols, it is important to repeat studies on individuals of different ethnic backgrounds and prove a similar effect.

Keywords: Opioid use disorder; Genetic vulnerability; Treatment failures; Personalized medicine; Pharmacogenetics

Core Tip: Although maintenance treatment with methadone or buprenorphine is effective for treating opioid use disorder, the rate of treatment failure is high among patients, which leads to significant costs to society in terms of healthcare and justice. Thus, it is important to understand the genetic information of patients to increase treatment effectiveness. There has been evidence showing the interaction between genetic variants and the rate of metabolism, the mechanism of action and transport of drugs. Therefore, patient-tailored treatment would be a good approach to facilitate longer periods of abstinence in addicts who are at high risk of treatment failure.