Evidence map›Paper›PMID 42511623›Full record

ArticleInternational journal of molecular sciences2026

Stage-Dependent Genetic Association of the TyG Index with Cardiovascular-Kidney-Metabolic Syndrome Severity: A Genome-Wide Association and Mendelian Randomization Study.

Yu-Lin Ko, Lung-An Hsu, Ngoc Yen Tran, Semon Wu

Abstract read
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Article in International journal of molecular sciences, 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

4 authors.

Yu-Lin KoDivision of Cardiology, Department of Internal Medicine, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan.ORCID 0000-0002-8218-6827
Lung-An HsuCardiovascular Division, Department of Internal Medicine, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan 33305, Taiwan.ORCID 0000-0002-0012-2804
Ngoc Yen TranDivision of Cardiology, Department of Internal Medicine, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan.ORCID 0009-0002-1861-7239
Semon WuDepartment of Life Science, Chinese Culture University, Taipei 11114, Taiwan.

Funding

National Science and Technology Council NSTC 112-2314-B-303-023-MY3National Science and Technology Council NSTC 114-2314-B-303-003Taipei Tzu Chi Hospital TCRD-TPE-115-RT-1
6 · The paper itself

Abstract

We aimed to determine whether the genetically predicted triglyceride-glucose (TyG) index, a surrogate marker of insulin resistance, is associated with cardiovascular-kidney-metabolic (CKM) stage severity and whether these associations are consistent with a potential causal role of insulin resistance within the CKM staging framework. The associations between the TyG index and CKM stages were assessed among 107,161 Taiwan Biobank participants using multivariable regression. CKM stages 3 and 4 were combined as the advanced CKM stage group. A genome-wide association study (GWAS) in 104,778 participants identified genetic determinants of the TyG index, followed by Mendelian randomization (MR), weighted genetic risk score (wGRS) analyses, and sample-split MR analyses. CKM stage severity was evaluated using ordinal regression analysis, a sensitivity analysis (CKM stages ≥ 1 vs. stage 0), and a later-stage comparison analysis (CKM stages ≥ 2 vs. stages 0-1). The TyG index increased progressively across CKM stages. GWAS identified 61 genome-wide significant loci associated with the TyG index. MR analyses demonstrated that genetically predicted TyG index was associated with greater CKM stage severity across all models, with consistent findings in the sample-split analyses. Genetic associations were modest for CKM stage 1 versus stage 0 but became substantially stronger for CKM stage 2 and the advanced CKM stages. Genetically predicted TyG index was associated with higher CKM stage severity in a stage-dependent manner, with substantially stronger genetic associations from CKM stage 2 onward. These findings are consistent with a potential causal role of insulin resistance in CKM stage severity and highlight the TyG index as a complementary biomarker for metabolic risk stratification.

Indexed as

Blood GlucoseCardiovascular DiseasesGenome-Wide Association StudyKidney DiseasesMetabolic SyndromeTriglyceridesFemaleGenetic Predisposition to DiseaseGenetic Risk ScoreHumansInsulin ResistanceMaleMendelian Randomization AnalysisMiddle AgedPolymorphism, Single NucleotideSeverity of Illness IndexBlood GlucoseTriglyceridescardiovascular–kidney–metabolic syndromeinsulin resistancemendelian randomizationtriglyceride–glucose index

Identifiers

PMID42511623
PMCPMC13411448

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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.