Distinguishing clinical and genetic risk factors for suicidal ideation and behavior in a diverse hospital population.

IF 6.2 1区 医学 Q1 PSYCHIATRY Translational Psychiatry Pub Date : 2025-02-20 DOI:10.1038/s41398-025-03287-6
Sarah M C Colbert, Lauren Lepow, Brian Fennessy, Nakao Iwata, Masashi Ikeda, Takeo Saito, Chikashi Terao, Michael Preuss, Jyotishman Pathak, J John Mann, Hilary Coon, Niamh Mullins
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Abstract

Suicidal ideation (SI) and behavior (SB) are major public health concerns, but risk factors for their development and progression are poorly understood. We used ICD codes and a natural language processing algorithm to identify individuals in a hospital biobank with SI-only, SB, and controls without either. We compared the profiles of SB and SI-only patients to controls, and each other, using phenome-wide association studies (PheWAS) and polygenic risk scores (PRS). PheWAS identified many risk factors for SB and SI-only, plus specific psychiatric disorders which may be involved in progression from SI-only to SB. PRS for suicide attempt were only associated with SB, and even after accounting for psychiatric disorder PRS. SI PRS were only associated with SI-only, although not after accounting for psychiatric disorder PRS. These findings advance understanding of distinct genetic and clinical risk factors for SB and SI-only, which will aid in early detection and intervention efforts.

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在不同医院人群中区分自杀意念和行为的临床和遗传风险因素。
自杀意念(SI)和自杀行为(SB)是主要的公共卫生问题,但其发展和进展的危险因素知之甚少。我们使用ICD代码和自然语言处理算法来识别医院生物库中SI-only、SB和不含两者的对照组中的个体。我们使用全现象关联研究(PheWAS)和多基因风险评分(PRS)比较了SB和si患者与对照组以及彼此的概况。PheWAS确定了SB和SI-only的许多危险因素,以及可能涉及从SI-only到SB进展的特定精神障碍。自杀企图的PRS仅与SB相关,甚至在考虑精神障碍的PRS后也是如此。SI PRS仅与SI-only相关,尽管没有考虑精神障碍PRS。这些发现促进了对SB和si的独特遗传和临床危险因素的理解,这将有助于早期发现和干预工作。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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