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心血管-肾脏-代谢综合征分期与癌症风险:来自蛋白质组学和代谢组学中介因子的见解

英文原题:Cardiovascular-Kidney-Metabolic Syndrome Staging and Cancer Risk: Insights From Proteomic and Metabolomic Mediators.

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Cardiovascular-Kidney-Metabolic Syndrome Staging and Cancer Risk: Insights From Proteomic and Metabolomic Mediators.

PubMed 2026/07/14(内容时间) JACC CardioOncol Q1 · IF 15.5(JCR 2025)

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研究概要

CKM 分期与递增的癌症风险及阶段特异性免疫代谢通路相关,提示了潜在的预防靶点。

研究思路结论见上方概要

心血管-肾脏-代谢(CKM)综合征是一个新兴的整合性框架,也是整体疾病风险的关键决定因素;然而,其与癌症风险的关系及潜在机制仍知之甚少。

本研究旨在探讨CKM分期与新发癌症之间的关联,并阐明该关联背后的中介因素,从而基于多组学分析揭示风险缓解的路径和潜在靶点。

UK Biobank参与者根据美国心脏协会分期框架,基于国际疾病分类第10版编码,被分为CKM 0至4期。采用Cox回归评估CKM分期与总体癌症发病率之间的关联。通过Cox回归、logistic回归和中介分析,识别连接相邻分期与癌症的蛋白质组学和代谢组学中介因子,并进行基因本体富集和相互作用网络分析。

整体癌症风险从CKM 1期至3期逐步升高,在4期略有减弱但仍持续升高。已识别出各期特异性的介质和机制:1期为白细胞/淋巴细胞激活及细胞间黏附;2期为T细胞相关免疫及新出现的免疫耐受诱导;3期为新出现的自然杀伤(NK)细胞耐受诱导及参与炎症反应的呼吸爆发;4期为占主导地位的NK细胞耐受诱导及组织驻留的慢性病理。主导性代谢组学介导从高密度脂蛋白(HDL)和富含甘油三酯的脂蛋白(TRL)演变为低密度脂蛋白(LDL)。蛋白质-代谢物相互作用网络揭示了各期不同的特征,包括早期阶段血管生成素样蛋白1/HDL和去唾液酸糖蛋白受体1/TRL相互作用,以及晚期阶段磷脂转移蛋白/HDL、载脂蛋白M/LDL和成纤维细胞生长因子结合蛋白1/中间密度脂蛋白/LDL相关性。

展开英文摘要原文

Cardiovascular-kidney-metabolic (CKM) syndrome is an emerging integrative framework and a critical determinant of overall disease risk; however, its relationship with cancer risk and underlying mechanisms remains poorly understood.

This study sought to investigate the association between CKM staging and incident cancer and elucidate mediators underlying this association, thereby uncovering pathways and potential targets for risk mitigation based on multiomics analysis.

UK Biobank participants were categorized into CKM stages 0 to 4 according to the American Heart Association staging framework based on International Classification of Diseases, 10th Revision codes. Cox regression was conducted to evaluate associations between CKM staging and overall cancer incidence. Proteomic and metabolomic mediators linking adjacent stages and cancer were identified using Cox regression, logistic regression, and mediation analysis and underwent Gene Ontology enrichment and interaction network analyses.

Overall cancer risk increased stepwise from CKM stages 1 to 3, with slight attenuation but persistent elevation in stage 4. Stage-specific mediators and mechanisms were identified: leukocyte/lymphocyte activation and cell-cell adhesion in stage 1; T cell-related immunity and emerging immune tolerance induction in stage 2; emerging natural killer (NK) cell tolerance induction and respiratory burst involved in the inflammatory response in stage 3; and dominant NK cell tolerance induction and tissue-resident chronic pathology in stage 4. Dominant metabolomic mediation evolved from high-density lipoproteins (HDLs) and triglyceride-rich lipoproteins (TRLs) to low-density lipoproteins (LDLs). Protein-metabolite interaction networks revealed distinct profiles for each stage, including angiopoietin-like protein 1/HDL and asialoglycoprotein receptor 1/TRL interactions in early stages and phospholipid transfer protein/HDL, apolipoprotein M/LDL, and fibroblast growth factor-binding protein 1/intermediate-density lipoprotein/LDL correlations in advanced stages.

CKM staging is associated with incremental cancer risk and stage-specific immune-metabolic pathways, highlighting potential prevention targets.

论文信息

作者
Xiao X、Li J、Ning Y、Yang Y、Ou Z、Dong B、Dong Y、Li Y
第一作者单位
Department of Cardiology, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, PR China.China
通讯作者单位
Department of Cardiology, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, PR China; Key NHC Key Laboratory of Assisted Circulation (Sun Yat-sen University), Guangzhou, PR China; National-Guangdong Joint Engineering Laboratory for Diagnosis and Treatment of Vascular Diseases, Guangzhou, PR China. Electronic address: xuerc3@mail.sysu.edu.cn.China
期刊
JACC. CardioOncology2026 Aug
原文标识
PubMed 42455107 · DOI 10.1016/j.jaccao.2026.05.012