Evidence map›Paper›PMID 43000253›Full record

ArticleBMC cardiovascular disorders2026

Metabolic vulnerability index increased risk of all-cause mortality among individuals with stage 4 cardiovascular-renal-metabolic syndrome: a prospective cohort study in UK biobank.

Yanfang Huang, Yu Zhao, Yunpeng Cai, Chenxi Lu, Wenyu Guo, Yu Shi, Xiaoying Liu, Ke Peng, Yichong Li, Zhuguo Wu and 2 more

Abstract read
In one paragraph

Article in BMC cardiovascular disorders, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Yanfang Huang *School of Public Health, Guangdong Medical University, Dongguan, Guangdong, 523710, People's Republic of China.
Yu Zhao *Affiliated Hospital Group of Guangdong Medical University Shenzhen Baoan Central Hospital, Shenzhen, Guangdong, 518000, People's Republic of China.
Yunpeng CaiShenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, Guangdong, 518055, People's Republic of China.
Chenxi LuShenzhen Clinical Research Center for Cardiovascular Disease, Fuwai Shenzhen Hospital, Chinese Academy of Medical Sciences, Shenzhen, Guangdong, 518055, People's Republic of China.
Wenyu GuoShenzhen Clinical Research Center for Cardiovascular Disease, Fuwai Shenzhen Hospital, Chinese Academy of Medical Sciences, Shenzhen, Guangdong, 518055, People's Republic of China.
Yu ShiShenzhen Clinical Research Center for Cardiovascular Disease, Fuwai Shenzhen Hospital, Chinese Academy of Medical Sciences, Shenzhen, Guangdong, 518055, People's Republic of China.
Xiaoying LiuShenzhen Clinical Research Center for Cardiovascular Disease, Fuwai Shenzhen Hospital, Chinese Academy of Medical Sciences, Shenzhen, Guangdong, 518055, People's Republic of China.
Ke PengShenzhen Clinical Research Center for Cardiovascular Disease, Fuwai Shenzhen Hospital, Chinese Academy of Medical Sciences, Shenzhen, Guangdong, 518055, People's Republic of China.
Yichong LiShenzhen Clinical Research Center for Cardiovascular Disease, Fuwai Shenzhen Hospital, Chinese Academy of Medical Sciences, Shenzhen, Guangdong, 518055, People's Republic of China.
Zhuguo WuThe First Dongguan Affiliated Hospital of Guangdong Medical University, Dongguan, Guangdong, 523710, People's Republic of China.
Guiyuan HanShenzhen Clinical Research Center for Cardiovascular Disease, Fuwai Shenzhen Hospital, Chinese Academy of Medical Sciences, Shenzhen, Guangdong, 518055, People's Republic of China. han.guiyuan@qq.com.
Haibing YuSchool of Public Health, Guangdong Medical University, Dongguan, Guangdong, 523710, People's Republic of China. hby616688@gdmu.edu.cn.ORCID http://orcid.org/0000-0002-1877-3074

Funding

Clinical and Basic Science Innovation Program of Guangdong Medical University GDMULCJC2025183Guangdong Basic and Applied Basic Research Foundation 2023A1515010076Guangdong Basic and Applied Basic Research Foundation, Joint Fund Project 2024A1515140126Guangdong Medical University Clinical and Basic Science Innovation Special Project GDMULCJC2024142Natural Science Foundation of Guangdong Province 2022A1515012407Shenzhen Clinical Research Center for Cardiovascular Disease Fund 20220819165348002State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia Fund SKL-HIDCA-2024-GD7the National Clinical Research Center of Cardiovascular Diseases, Shenzhen NCRCSZ-2024-001the National Key Research and Development Program of China 2023ZD0503506the Program for Guangdong Introducing Innovative and Entrepreneurial Teams 2019ZT08Y481the Shenzhen High-level Hospital Construction Fund GSP-QNPY-B2025011
6 · The paper itself

Abstract

backgroundThe Metabolic Vulnerability Index (MVX), a novel composite marker of inflammation and malnutrition, has an undetermined prognostic value in stage 4 cardiovascular-kidney-metabolic (CKM) syndrome.

objectiveTo investigate the association between MVX and the risk of all-cause mortality among patients with stage 4 CKM syndrome.

methodsWe included 20,927 participants with stage 4 CKM syndrome in the UK Biobank. Sex-specific MVX scores were calculated by aggregating six biomarkers (glycoprotein acetyls (GlycA), small high-density lipoprotein particles (sHDL), valine, leucine, isoleucine, and citrate). We applied Cox proportional-hazards models to investigate the association between MVX and all-cause mortality and evaluated the performance of MVX in predicting mortality.

resultsDuring a median 13.45 years of follow-up (IQR:12.54-14.32 years), a total of 4,613 participants (22.04%) died. The fully adjusted Cox regression model indicated that a graded association between MVX quartiles and all-cause mortality, with the highest MVX quartile showing the greatest risk (HR = 1.67, 95% CI: 1.49-1.87, P < 0.001). A consistent positive association was observed between MVX score and mortality risk at 5, 10, and 15 years (P < 0.05). Subgroup analyses showed that females and individuals with cardiovascular disease (CVD) exhibited a higher mortality risk (P for interaction < 0.001). MVX significantly improved the predictive value of all-cause mortality beyond established risk factors (estimated glomerular filtration rate (eGFR), glycated hemoglobin (HbA1c), lipid accumulation Product (LAP)) (Uno's C-statistic: 0.713, 95% CI: 0.705-0.721, P < 0.001).

conclusionsElevated MVX scores were independently associated with higher all-cause mortality risk in stage 4 CKM syndrome, supporting its potential for risk stratification.

Indexed as

Cardio-Renal SyndromeEnergy MetabolismInflammation MediatorsMalnutritionMetabolic SyndromeAgedBiological Specimen BanksBiomarkersCause of DeathFemaleHumansMaleMiddle AgedNutritional StatusPredictive Value of TestsPrognosisBiomarkersInflammation MediatorsAll-cause mortalityCardiovascular-Kidney-Metabolic SyndromeMetabolic vulnerability indexUK Biobank

Identifiers

PMID43000253
PMCPMC13746416

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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.