Personalized medicine and opioid use disorder.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Dilek Kaya-Akyüzlü
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引用次数: 0

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.

个性化医疗与阿片类药物使用障碍。
阿片类药物使用障碍(OUD)是影响全球数百万人的一个重大公共卫生问题。虽然阿片类药物滥用症是一种慢性和复发性疾病,但目前有多种药物和非药物干预方法。药物辅助治疗 OUD 通常依赖于阿片受体与成瘾物质的竞争。这种竞争机制是阻断阿片受体或使其失活,或用间歇性或长效物质激活受体。美沙酮和丁丙诺啡是美国食品和药物管理局批准的两种药物,对阿片类药物依赖者的健康有长期的积极影响。虽然药物的临床研究一般都能证明数千人的疗效并排除毒性,但无法预测特定药物在治疗剂量下是否会对其中一名患者产生副作用。许多生物和环境因素都可以解释个体差异。编码药物代谢或细胞药物靶点的基因的变化在很大程度上解释了个体间药物反应的差异。因此,要使候选基因的作用得到认可并纳入个体治疗方案,就必须对不同种族背景的个体进行重复研究,并证明具有相似的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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