酒精使用障碍患者终生自杀企图的临床、基因组和神经生理学相关性

Complex psychiatry Pub Date : 2025-02-13 eCollection Date: 2025-01-01 DOI:10.1159/000543222
Peter B Barr, Zoe Neale, Chris Chatzinakos, Jessica Schulman, Niamh Mullins, Jian Zhang, David B Chorlian, Chella Kamarajan, Sivan Kinreich, Ashwini K Pandey, Gayathri Pandey, Stacey Saenz de Viteri, Laura Acion, Lance Bauer, Kathleen K Bucholz, Grace Chan, Danielle M Dick, Howard J Edenberg, Tatiana Foroud, Alison Goate, Victor Hesselbrock, Emma C Johnson, John R Kramer, Dongbing Lai, Martin H Plawecki, Jessica Salvatore, Leah Wetherill, Arpana Agrawal, Bernice Porjesz, Jacquelyn L Meyers
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引用次数: 0

摘要

研究已经确定了与精神疾病患者自杀企图(SA)相关的多种危险因素。然而,对酒精使用障碍(AUD)患者的研究有限,尽管他们的SA发病率不成比例地高。方法:我们检查了来自酒精中毒遗传学合作研究的4,068例AUD患者的终生SA(23%终生SA;53%的女性;平均年龄:38岁。我们通过临床访谈、共病精神问题的多基因评分和神经认知功能,探讨了其他临床条件下终生SA的风险。结果:患有AUD的参与者有更高的创伤暴露率、重度抑郁症、创伤后应激障碍、其他物质使用障碍(sud)和自杀意念。SA、抑郁和创伤后应激障碍的多基因评分与SA报告的几率增加相关(or = 1.22-1.44)。与未报告SA的参与者相比,报告SA的参与者的右半球额-顶叶θ和半球间颞-顶叶α脑电图静息状态一致性也有所下降,但差异很小。结论:总体而言,报告终生SA的AUD患者经历了更大程度的创伤,有更严重的合并症,并且具有更高的其他精神问题的多基因风险。我们的结果表明,有必要在sud存在的情况下进一步研究sa。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical, Genomic, and Neurophysiological Correlates of Lifetime Suicide Attempts among Individuals with an Alcohol Use Disorder.

Introduction: Research has identified multiple risk factors associated with suicide attempt (SA) among individuals with psychiatric illness. However, there is limited research among those with an alcohol use disorder (AUD), despite their disproportionately higher rates of SA.

Methods: We examined lifetime SA in 4,068 individuals with an AUD from the Collaborative Study on the Genetics of Alcoholism (23% lifetime SA; 53% female; mean age: 38). We explored risk for lifetime SA across other clinical conditions ascertained from a clinical interview, polygenic scores for comorbid psychiatric problems, and neurocognitive functioning.

Results: Participants with an AUD who attempted suicide had greater rates of trauma exposure, major depressive disorder, post-traumatic stress disorder, other substance use disorders (SUDs), and suicidal ideation. Polygenic scores for SA, depression, and PTSD were associated with increased odds of reporting an SA (ORs = 1.22-1.44). Participants who reported an SA also had decreased right hemispheric frontal-parietal theta and decreased interhemispheric temporal-parietal alpha electroencephalogram resting-state coherences relative to those who did not, but differences were small.

Conclusions: Overall, individuals with an AUD who report lifetime SA experience greater levels of trauma, have more severe comorbidities, and carry increased polygenic risk for other psychiatric problems. Our results demonstrate the need to further investigate SAs in the presence of SUDs.

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