The impact of receiving polygenic risk scores for alcohol use disorder on psychological distress, risk perception, and intentions to reduce drinking

IF 1.6 3区 医学 Q3 GENETICS & HEREDITY
Morgan N. Driver, Sally I-Chun Kuo, Jacqueline S. Dron, Jehannine Austin, Danielle M. Dick
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引用次数: 0

Abstract

For the return of polygenic risk scores to become an acceptable clinical practice in psychiatry, receipt of polygenic risk scores must be associated with minimal harm and changes in behavior that decrease one's risk for developing a psychiatric outcome. Data from a randomized controlled trial was used to assess the impact of different levels of hypothetical polygenic risk scores for alcohol use disorder on psychological distress, risk perception, and intentions to change drinking behaviors. The analytic sample consisted of 325 participants recruited from an urban, public university. Results demonstrated that there were significant increases in psychological distress as the level of genetic risk for alcohol use disorder increased. In addition, the perceived chance of developing alcohol use disorder significantly increased as the level of genetic risk increased. Promisingly, a greater proportion of participants indicated that they would intend to engage in follow-up behaviors, such as seeking additional information, talking to a healthcare provider about risk, and reducing drinking behaviors, as the level of genetic risk increased. Returning polygenic risk scores for alcohol use disorder in a clinical setting has the potential to promote risk-reducing behavior change, especially with increasing levels of genetic risk. The study was registered on ClinicalTrials.gov (Identifier: NCT05143073).

接受酒精使用障碍多基因风险评分对心理困扰、风险感知和减少饮酒意愿的影响
为了使多基因风险评分的回归成为精神病学可接受的临床实践,接受多基因风险评分必须与最小的伤害和行为改变相关联,从而降低患精神疾病的风险。来自一项随机对照试验的数据被用来评估不同水平的酒精使用障碍假设多基因风险评分对心理困扰、风险感知和改变饮酒行为意愿的影响。分析样本包括从一所城市公立大学招募的325名参与者。结果表明,随着酒精使用障碍遗传风险水平的增加,心理困扰显著增加。此外,随着遗传风险水平的增加,患酒精使用障碍的可能性也显著增加。令人鼓舞的是,更大比例的参与者表示,随着遗传风险水平的增加,他们打算采取后续行动,比如寻求额外的信息,与医疗保健提供者讨论风险,减少饮酒行为。在临床环境中返回酒精使用障碍的多基因风险评分有可能促进降低风险的行为改变,特别是在遗传风险水平增加的情况下。该研究已在ClinicalTrials.gov注册(标识符:NCT05143073)。
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来源期刊
CiteScore
5.90
自引率
7.10%
发文量
40
审稿时长
4-8 weeks
期刊介绍: Neuropsychiatric Genetics, Part B of the American Journal of Medical Genetics (AJMG) , provides a forum for experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. It is a resource for novel genetics studies of the heritable nature of psychiatric and other nervous system disorders, characterized at the molecular, cellular or behavior levels. Neuropsychiatric Genetics publishes eight times per year.
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