Evidence map›Paper›PMID 42701202›Full record

ArticleBMC cancer2026

eGDR and gastrointestinal cancer mortality in the UK Biobank: a prospective cohort study.

Chuang Yang, Patrick S Plum, Thomas Ebert, Jeanette Köppe, Ines Gockel, René Thieme

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Article in BMC cancer, 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

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

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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

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Chuang YangDepartment of Visceral, Transplant, Thoracic and Vascular Surgery, University Hospital Leipzig, Liebigstr. 19, Leipzig, D-04103, Germany.
Patrick S PlumDepartment of Visceral, Transplant, Thoracic and Vascular Surgery, University Hospital Leipzig, Liebigstr. 19, Leipzig, D-04103, Germany.
Thomas EbertMedical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, Germany.
Jeanette KöppeDepartment of Epidemiology and Biostatistics, Public and Global Health, Medical University Lausitz - Carl Thiem, Cottbus, Germany.
Ines GockelDepartment of Visceral Surgery, Clarunis - Universitäres Bauchzentrum Basel, Basel, Switzerland.
René ThiemeDepartment of Visceral, Transplant, Thoracic and Vascular Surgery, University Hospital Leipzig, Liebigstr. 19, Leipzig, D-04103, Germany. rene.thieme@medizin.uni-leipzig.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study examined the associations of estimated glucose disposal rate (eGDR), a surrogate of insulin sensitivity, and the insulin resistance indices TG/HDL-C and TyG with gastrointestinal (GI) cancer mortality in the UK Biobank.

methodsWe included 369,447 participants without cancer at baseline and recorded 4,305 GI cancer-related deaths over a mean follow-up of 13.5 years. Fine-Gray models assessed associations of eGDR, TG/HDL-C, and TyG with GI cancer mortality.

resultsHigher eGDR was associated with lower pooled GI cancer mortality (sHR, 0.67; 95% CI, 0.61-0.74; P < 0.001); associations with EC, ESCC, CRC, LC, and PC mortality remained significant after false discovery rate (FDR) correction. TyG, but not TG/HDL-C, remained associated with pooled GI cancer mortality, and both markers remained associated with LC mortality. Subgroup analyses were exploratory.

conclusionsHigher eGDR was associated with lower pooled and several site-specific GI cancer mortality outcomes, whereas TG/HDL-C and TyG associations were modest and site-specific. These findings do not establish clinical utility.

Indexed as

Blood GlucoseGastrointestinal NeoplasmsGlucoseInsulin ResistanceAgedBiological Specimen BanksFemaleHumansMaleMiddle AgedProspective StudiesUK BiobankUnited KingdomBlood GlucoseGlucoseEstimated Glucose Disposal RateGastrointestinal cancer mortalityInsulin ResistanceInsulin SensitivityReal-world evidence

Identifiers

PMID42701202
PMCPMC13545786

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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.