Social disconnection integrates genetic and proteomic risks in suicidal ideation and depression.

IF 7.5 1区 医学 Q1 PSYCHIATRY
Sihong Li, Zhongting Huang, Hui Chen, Xianliang Chen, Huajia Tang, Yanyue Ye, Jijun Zhu, Shenghan Wang, Pan Li, Shunjie Zhang, Haowen Zhuang, Weixin Liu, Fuqiang Cai, Zhijian Song, Yuxin Liu, Jiansong Zhou, Junfang Chen
{"title":"Social disconnection integrates genetic and proteomic risks in suicidal ideation and depression.","authors":"Sihong Li, Zhongting Huang, Hui Chen, Xianliang Chen, Huajia Tang, Yanyue Ye, Jijun Zhu, Shenghan Wang, Pan Li, Shunjie Zhang, Haowen Zhuang, Weixin Liu, Fuqiang Cai, Zhijian Song, Yuxin Liu, Jiansong Zhou, Junfang Chen","doi":"10.1038/s41398-026-04276-z","DOIUrl":null,"url":null,"abstract":"<p><p>Suicidal ideation (SI) and major depressive disorder (MDD) are complex psychiatric conditions arising from the interplay of genetic liability, molecular processes, and psychosocial factors. While these dimensions have been extensively studied in isolation, their joint contribution to SI and MDD remains unclear. This study integrates multi-modal data to elucidate these synergistic effects and develop robust models for individual-level risk stratification. Leveraging longitudinal multi-modal data from 13,085 UK Biobank participants, we integrated genomic, proteomic, and social connection profiles. We developed interpretable risk scores using a rigorous supervised machine learning framework encompassing diverse linear and ensemble classifiers. Permutation importance was employed to quantify feature contributions and derive transparent, weighted risk metrics across diverse classifiers. These scores were validated through association, interaction, and mediation analyses. Social connection-based risk scores significantly differentiated cases and controls across the two suicidal ideation phenotypes at 2017 and 2023 with cross-sectional analyses (AUCs: 0.70 - 0.73), outperforming proteomic-only models. Functional dimensions of social connection emerged as the most informative predictors. Longitudinal analyses revealed that social risk scores at baseline predicted suicidal ideation onset six years later, independent of demographic covariates. Interaction analyses demonstrated that polygenic risk for suicide attempt significantly interacted with both social and proteomic risk features in relation to depression. Structural equation models further confirmed that social disconnection acts as a key mediator linking genetic predisposition to MDD and SI. Social disconnection is a critical risk factor mediating the impact of genetic vulnerability on psychiatric outcomes. Integrating social, genetic, and molecular data supports a multilevel framework for risk stratification and highlights the potential of socially oriented interventions to mitigate biological risk.</p>","PeriodicalId":23278,"journal":{"name":"Translational Psychiatry","volume":"16 1","pages":""},"PeriodicalIF":7.5000,"publicationDate":"2026-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13549977/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41398-026-04276-z","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0

Abstract

Suicidal ideation (SI) and major depressive disorder (MDD) are complex psychiatric conditions arising from the interplay of genetic liability, molecular processes, and psychosocial factors. While these dimensions have been extensively studied in isolation, their joint contribution to SI and MDD remains unclear. This study integrates multi-modal data to elucidate these synergistic effects and develop robust models for individual-level risk stratification. Leveraging longitudinal multi-modal data from 13,085 UK Biobank participants, we integrated genomic, proteomic, and social connection profiles. We developed interpretable risk scores using a rigorous supervised machine learning framework encompassing diverse linear and ensemble classifiers. Permutation importance was employed to quantify feature contributions and derive transparent, weighted risk metrics across diverse classifiers. These scores were validated through association, interaction, and mediation analyses. Social connection-based risk scores significantly differentiated cases and controls across the two suicidal ideation phenotypes at 2017 and 2023 with cross-sectional analyses (AUCs: 0.70 - 0.73), outperforming proteomic-only models. Functional dimensions of social connection emerged as the most informative predictors. Longitudinal analyses revealed that social risk scores at baseline predicted suicidal ideation onset six years later, independent of demographic covariates. Interaction analyses demonstrated that polygenic risk for suicide attempt significantly interacted with both social and proteomic risk features in relation to depression. Structural equation models further confirmed that social disconnection acts as a key mediator linking genetic predisposition to MDD and SI. Social disconnection is a critical risk factor mediating the impact of genetic vulnerability on psychiatric outcomes. Integrating social, genetic, and molecular data supports a multilevel framework for risk stratification and highlights the potential of socially oriented interventions to mitigate biological risk.

社会脱节整合了自杀意念和抑郁的遗传和蛋白质组学风险。
自杀意念(SI)和重度抑郁症(MDD)是由遗传倾向、分子过程和社会心理因素相互作用引起的复杂精神疾病。虽然对这些方面进行了广泛的单独研究,但它们对SI和MDD的共同贡献仍不清楚。本研究整合了多模态数据来阐明这些协同效应,并为个体水平的风险分层建立了稳健的模型。利用来自13,085名英国生物银行参与者的纵向多模式数据,我们整合了基因组,蛋白质组学和社会联系概况。我们使用包含多种线性和集成分类器的严格监督机器学习框架开发了可解释的风险评分。排列重要性被用来量化特征贡献,并在不同的分类器中得出透明的、加权的风险度量。这些分数通过关联、交互和中介分析进行验证。通过横断面分析,基于社会联系的风险评分在2017年和2023年显著区分了两种自杀意念表型的病例和对照组(auc: 0.70 - 0.73),优于仅使用蛋白质组学的模型。社会联系的功能维度成为最具信息量的预测因素。纵向分析显示,基线的社会风险评分预测六年后自杀意念的发生,独立于人口统计学协变量。相互作用分析表明,自杀企图的多基因风险与抑郁相关的社会和蛋白质组学风险特征显著相互作用。结构方程模型进一步证实,社会脱节是连接MDD和SI遗传易感性的关键中介。社会脱节是介导遗传易感性对精神结果影响的关键风险因素。整合社会、遗传和分子数据支持风险分层的多层次框架,并突出了以社会为导向的干预措施减轻生物风险的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书