生命银行
疾病
多发病率
医学
癌症
构造(python库)
星团(航天器)
生物信息学
梅德林
生物沉积
组学
老年学
精密医学
流行病学转变
数据科学
基线(sea)
疾病负担
风险评估
饮食与癌症
计算生物学
系统生物学
共病
基因组学
年轻人
暴露的
肿瘤科
流行病学
前列腺癌
重症监护医学
因果关系(物理学)
疾病负担
复杂疾病
作者
Xuanwei Jiang,Guangrui Yang,Chen Meng,Nannan Feng,Lan Xu,Xihao Du,Chunlai Zeng,Victor W. Zhong
标识
DOI:10.1038/s41467-025-67510-0
摘要
Multimorbidity of cardiometabolic disease (CMD) and cancer is a growing but understudied global challenge in an aging world. Here, we perform multistate analysis in 429,555 UK Biobank participants to investigate transition patterns, identify multiomics signatures, and construct prediction models from baseline to single and multiple morbidities. During a median follow-up of 15 years, 105,903 participants develop single morbidity and 15,088 develop multimorbidity of CMD and cancer. Participants with multimorbidity have a 13%-33% higher mortality probability than those healthy or with single morbidity. In individuals living with multimorbidity, the development of CMD before cancer presents a higher mortality risk than the reverse order. Distinct and shared multiomics signatures are identified, with proteomics scores outperforming other omics in predicting disease trajectories (ΔC-statistic vs. base model: 0.03-0.14). This study reveals distinct transition patterns in CMD-cancer multimorbidity cluster and develops potentially useful prediction tools for supporting risk management if externally validated.
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