Evidence map›Paper›PMID 40640722›Full record

ArticleBMC nephrology2025

Development of cardiovascular and all-cause mortality risk prediction models for maintenance hemodialysis patients based on metabolomics.

Lian-Lian You, Cui Dong, Zhi-Hong Wang, Shuang Zhang, Yu Zhang, Ting-Ting Kuai, Jia Xiao, Shu-Xin Liu, Qing-Cheng Zeng

Abstract read
In one paragraph

Article in BMC nephrology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Lian-Lian You *School of Maritime Economics and Management, Dalian Maritime University, No.1, Linghai Road, Dalian, Liaoning, 116026, P. R. China.
Cui DongDepartment of Nephrology, Central Hospital of Dalian University of Technology, No.826, Xinan Road, Dalian, Liaoning, 116033, P. R. China.
Zhi-Hong WangDepartment of Nephrology, Central Hospital of Dalian University of Technology, No.826, Xinan Road, Dalian, Liaoning, 116033, P. R. China.
Shuang ZhangDepartment of Nephrology, Central Hospital of Dalian University of Technology, No.826, Xinan Road, Dalian, Liaoning, 116033, P. R. China.
Yu ZhangDepartment of Nephrology, Central Hospital of Dalian University of Technology, No.826, Xinan Road, Dalian, Liaoning, 116033, P. R. China.
Ting-Ting KuaiDepartment of Nephrology, Central Hospital of Dalian University of Technology, No.826, Xinan Road, Dalian, Liaoning, 116033, P. R. China.
Jia XiaoDepartment of Nephrology, Central Hospital of Dalian University of Technology, No.826, Xinan Road, Dalian, Liaoning, 116033, P. R. China.
Shu-Xin LiuDepartment of Nephrology, Central Hospital of Dalian University of Technology, No.826, Xinan Road, Dalian, Liaoning, 116033, P. R. China. root8848@sina.com.
Qing-Cheng ZengSchool of Maritime Economics and Management, Dalian Maritime University, No.1, Linghai Road, Dalian, Liaoning, 116026, P. R. China. qzeng@dlmu.edu.cn.

Funding

the Applied Basic Research Project of Liaoning Province, China 2023JH2/101300091the Dalian Key Medical Specialty Dengfeng Project, China 2021ZZ242the Medical Science Research Project of Dalian Heart Association, China DHA2217
6 · The paper itself

Abstract

introductionThe outcome of maintenance hemodialysis (MHD) remains poor, with cardiovascular death accounting for more than half of all-cause death cases. In this study, cardiovascular mortality and all-cause mortality prediction models were developed to investigate the predictive role of metabolites in MHD patients.

methodsClinical and metabolomics data of 135 hemodialysis patients from a single center were collected with a 6-year follow-up. Univariate Cox regression and random forest were respectively applied to preliminarily screen clinical and metabolomics characteristics, followed by multivariate Cox regression for identifying features predicting cardiovascular or all-cause mortality. Multivariate Cox proportional regression risk models were constructed using clinical, metabolomics, and combined features. Subgroup survival differences were compared via risk score stratification.

resultsThe combined model showed significant superiority in predicting cardiovascular mortality (3-year AUC = 0.901, 5-year AUC = 0.876), surpassing the clinical-only model (0.868/0.826) and metabolomics-only model (0.659/0.641). For all-cause mortality, the combined model demonstrated modest improvement (0.859/0.834) but still outperformed the metabolomics model (0.534/0.653). Thirty 5-fold cross-validations confirmed stable performance. High-risk groups had significantly higher cumulative mortality than low-risk groups (p < 0.0001).

conclusionThe metabolomics-alone model showed limited predictive performance, but its synergistic integration with clinical indicators further improved the predictive performance of mortality risk models, particularly for cardiovascular mortality.

Indexed as

Cardiovascular DiseasesKidney Failure, ChronicMetabolomicsRenal DialysisAgedCause of DeathFemaleHumansMaleMiddle AgedMortalityProportional Hazards ModelsRisk AssessmentAll-cause mortalityCardiovascular mortalityMaintenance hemodialysisMetabolomicsPrediction model

Identifiers

PMID40640722
PMCPMC12243235

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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 OpenQuestion graph.