Evidence map›Paper›PMID 42495242›Full record

ArticleInternational journal of public health2026

Multimodal risk profiles reveal shared and disease-specific risks of major non-communicable diseases: a prospective cohort study of 42,666 individuals.

Qiaoyi Xu, Zhenqiu Liu, Renjia Zhao, Zixuan Cui, Xufei Xing, Xingdong Chen, Chen Suo

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Article in International journal of public health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Qiaoyi XuSchool of Public Health, Fudan University, Shanghai, China.
Zhenqiu LiuTaizhou Institute of Health Sciences, Fudan University, Taizhou, China.
Renjia ZhaoHuman Phenome Institute, Fudan University, Shanghai, China.
Zixuan CuiSchool of Public Health, Fudan University, Shanghai, China.
Xufei XingShanghai Institute of Infectious Disease and Biosecurity, Fudan University, Shanghai, China.
Xingdong ChenSchool of Public Health, Fudan University, Shanghai, China.
Chen SuoSchool of Public Health, Fudan University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Evaluate whether circulating blood biomarker profiles identify shared and disease-specific risks of non-communicable diseases (NCDs). Methods: We considered 42,666 participants from Taizhou, China. After exclusions, discovery (n = 14,478; recruited 2011.9-2014.1) and temporal validation (n = 25,018; recruited 2018.7-2021.11) cohorts were defined. We integrated 54 blood biomarkers and 26 questionnaire/physical indicators. Predictors were selected after Cox pre-screening based on concordant inclusion across stepwise regression, regularized regression, and Boruta random forest. Results: The final score included 15 biomarkers plus age, smoking, hypertension, and vegetable intake. In the temporal validation cohort, high-risk individuals (25.0% of participants) accounted for 53.9% of incident major NCD cases, with a 6.29-fold (4.83-8.19) higher risk than the low-risk group. Similar gradients were observed for all-cause mortality. Compared with disease-specific scores, the combined score effectively stratified both composite and individual outcomes and revealed shared risks: 56.1% of disease-specific high-risk individuals were also high risk for other NCDs. Conclusion: A score integrating blood biomarkers with epidemiological and physical measures achieved clear risk stratification in the temporal validation cohort and may support priority population identification for major NCDs.

Indexed as

BiomarkersNoncommunicable DiseasesAdultAgedChinaFemaleHumansMaleMiddle AgedProspective StudiesRisk AssessmentRisk FactorsSurveys and QuestionnairesBiomarkersblood biomarkerscohort studymulti-disease risk stratificationnon-communicable diseasesrisk stratification

Identifiers

PMID42495242
PMCPMC13391432

What Socratic holds

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LicenceCC BY
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.