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阿片类药物使用障碍的成瘾和情感共病的表型和遗传学。

The phenomics and genetics of addictive and affective comorbidity in opioid use disorder.

机构信息

Department of Biostatistics, Epidemiology, & Informatics, The Perelman School of Medicine, University of Pennsylvania, A201 Richards Building, 3700 Hamilton Walk, Philadelphia, PA 19104, United States.

Institute for Biomedical Informatics, Division of Informatics, Department of Biostatistics, Epidemiology, & Informatics, The Perelman School of Medicine, University of Pennsylvania, D202 Richards Building, 3700 Hamilton Walk, University of Pennsylvania, Philadelphia, PA 19104-6116, United States.

出版信息

Drug Alcohol Depend. 2021 Apr 1;221:108602. doi: 10.1016/j.drugalcdep.2021.108602. Epub 2021 Feb 22.

Abstract

Opioid use disorder (OUD) creates significant public health and economic burdens worldwide. Therefore, understanding the risk factors that lead to the development of OUD is fundamental to reducing both its prevalence and its impact. Significant sources of OUD risk include co-occurring lifetime and current diagnoses of both psychiatric disorders, primarily mood disorders, and other substance use disorders, and unique and shared genetic factors. Although there appears to be pleiotropy between OUD and both mood and substance use disorders, this aspect of OUD risk is poorly understood. In this review, we describe the prevalence and clinical significance of addictive and affective comorbidities as risk factors for OUD development as a basis for rational opioid prescribing and OUD treatment and to improve efforts to prevent the disorder. We also review the genetic variants that have been associated with OUD and other addictive and affective disorders to highlight targets for future study and risk assessment protocols.

摘要

阿片类使用障碍(OUD)在全球范围内造成了重大的公共卫生和经济负担。因此,了解导致 OUD 发展的风险因素对于降低其流行率和影响至关重要。OUD 风险的主要来源包括同时存在终生和当前的精神障碍诊断,主要是心境障碍,以及其他物质使用障碍,以及独特和共同的遗传因素。尽管 OUD 似乎与心境和物质使用障碍之间存在多效性,但 OUD 风险的这一方面理解得很差。在这篇综述中,我们描述了成瘾和情感共病作为 OUD 发展的风险因素的流行率和临床意义,作为合理开阿片类药物和治疗 OUD 的基础,并改善预防该疾病的努力。我们还回顾了与 OUD 及其他成瘾和情感障碍相关的遗传变异,以突出未来研究和风险评估方案的目标。

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