Plasma proteomic signatures of social support and their association with cardiovascular disease and mortality: exploratory analyses in a national cohort study.

IF 6 2区 医学 Q1 GERIATRICS & GERONTOLOGY
GeroScience Pub Date : 2026-12-01 Epub Date: 2025-12-29 DOI:10.1007/s11357-025-02031-8
Pei Qin, Jessica Gong, Andrew Steptoe, Daisy Fancourt
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引用次数: 0

Abstract

Social support has been related to cardiovascular disease (CVD) incidence and mortality in longitudinal cohort analyses, but the biological pathways underpinning this remain underexplored. This exploratory study examined the associations between social support and a wide range of proteomic biomarkers and performed the mediating effect of proteomic biomarkers in the association between social support and CVD and mortality to identify potential biological pathways linking social support to health outcomes. Data from 3141 adults over the age of 50 in the English Longitudinal Study of Ageing who had plasma proteome data were analyzed, with CVD and mortality outcomes followed up for 16 years following through Hospital Episode Statistics and the National Health Service's Central Registry. Linear and Cox regression analyses were used to identify proteins associated with social support, CVD, and mortality. Mediation analysis was then performed on the identified proteins to explore their role as a potential mediator between social support and CVD and mortality risk. Over a median of 15.8-year follow-up, 889 participants have died, and 627 developed CVD. Of 276 plasma proteins measured, greater social support was associated with lower levels of 13 proteins and higher TN-R levels, after adjusting for baseline socioeconomic confounders. We also identified 49 protein-CVD and 70 protein-mortality associations after minimal adjustments, including 11 and 14 proteins simultaneously associated with social support. All the significant proteins together mediated about 20.9% and 26.4% of the associations for CVD and mortality, respectively. The main enriched biological pathways involved death receptor activity and carbohydrate binding. Social support was related to a cluster of proteomic biomarkers, which may be linked to inflammation, apoptosis, and atherosclerosis/vascular pathways. The identified plasma proteins partly mediated the association between social support and CVD and mortality risk, independently and cumulatively. These findings deepen our understanding of the intricate connections between relationship quality, proteomic signatures, and CVD and mortality development.

社会支持的血浆蛋白质组学特征及其与心血管疾病和死亡率的关联:一项国家队列研究的探索性分析
在纵向队列分析中,社会支持与心血管疾病(CVD)发病率和死亡率有关,但支撑这一观点的生物学途径仍未得到充分探索。本探索性研究考察了社会支持与广泛的蛋白质组生物标志物之间的关联,并在社会支持与心血管疾病和死亡率之间的关联中执行了蛋白质组生物标志物的中介作用,以确定将社会支持与健康结果联系起来的潜在生物学途径。在英国老龄化纵向研究中,研究人员分析了3141名50岁以上的成年人的血浆蛋白质组数据,并通过医院事件统计和国家卫生服务中心登记处对心血管疾病和死亡率结果进行了16年的随访。线性和Cox回归分析用于鉴定与社会支持、心血管疾病和死亡率相关的蛋白质。然后对鉴定的蛋白质进行中介分析,以探索它们在社会支持与心血管疾病和死亡风险之间的潜在中介作用。在中位15.8年的随访中,889名参与者死亡,627人发展为心血管疾病。在测量的276种血浆蛋白中,在调整基线社会经济混杂因素后,社会支持程度越高,13种蛋白水平越低,TN-R水平越高。经过最小调整后,我们还确定了49种蛋白质与心血管疾病和70种蛋白质与死亡率相关,包括11种和14种同时与社会支持相关的蛋白质。所有重要蛋白共同介导的CVD和死亡率的相关性分别为20.9%和26.4%。主要富集的生物学途径包括死亡受体活性和碳水化合物结合。社会支持与一系列蛋白质组学生物标志物相关,这些生物标志物可能与炎症、细胞凋亡和动脉粥样硬化/血管通路有关。鉴定的血浆蛋白部分介导了社会支持与心血管疾病和死亡风险之间的关联,独立和累积。这些发现加深了我们对关系质量、蛋白质组学特征、心血管疾病和死亡率发展之间复杂联系的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
GeroScience
GeroScience Medicine-Complementary and Alternative Medicine
CiteScore
10.50
自引率
5.40%
发文量
182
期刊介绍: GeroScience is a bi-monthly, international, peer-reviewed journal that publishes articles related to research in the biology of aging and research on biomedical applications that impact aging. The scope of articles to be considered include evolutionary biology, biophysics, genetics, genomics, proteomics, molecular biology, cell biology, biochemistry, endocrinology, immunology, physiology, pharmacology, neuroscience, and psychology.
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