将多基因评分应用于药物使用障碍患者临床治疗的考虑因素。

Rachel L Kember,Christal N Davis,Kyra L Feuer,Henry R Kranzler
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摘要

药物使用失调症(SUDs)的发病率很高,并且与过高的发病率、死亡率和经济成本有关。因此,人们非常关注如何及早发现更容易患上药物滥用症的人群,以及如何改进针对药物滥用症患者的个性化治疗决策。众所周知,SDD 受遗传和环境因素的双重影响。多基因评分(PGSs)提供了一种单一的遗传责任测量方法,可用作预测疾病发展、进展和治疗反应的生物标志物。虽然 PGSs 正在迅速融入临床实践,但指导临床医生负责任地使用和解释 PGSs 的信息却很少。在本综述中,我们将讨论在 SUD 临床治疗中使用 PGS 的潜在益处和陷阱,并重点介绍当前的研究。我们还就临床使用 PGS 之前的重要注意事项提出了建议,并推荐了未来的研究方向。
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Considerations for the application of polygenic scores to clinical care of individuals with substance use disorders.
Substance use disorders (SUDs) are highly prevalent and associated with excess morbidity, mortality, and economic costs. Thus, there is considerable interest in the early identification of individuals who may be more susceptible to developing SUDs and in improving personalized treatment decisions for those who have SUDs. SUDs are known to be influenced by both genetic and environmental factors. Polygenic scores (PGSs) provide a single measure of genetic liability that could be used as a biomarker in predicting disease development, progression, and treatment response. Although PGSs are rapidly being integrated into clinical practice, there is little information to guide clinicians in their responsible use and interpretation. In this Review, we discuss the potential benefits and pitfalls of the use of PGSs in the clinical care of SUDs, highlighting current research. We also provide suggestions for important considerations prior to implementing the clinical use of PGSs and recommend future directions for research.
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