Evidence map›Paper›PMID 42405670›Full record

ArticleInvestigative ophthalmology & visual science2026

Nonlinear Associations of Estimated Glucose Disposal Rate With Incident Age-Related Eye Diseases: Implications for Metabolic Risk Stratification.

Haoyu Yuan, Xinyue Song, Shaoqing Dai, Huanhuan Li, Xiaorong Wu

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 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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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

5 authors.

Haoyu YuanThe 1st Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Xinyue SongThe 1st Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Shaoqing DaiThe 1st Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Huanhuan LiThe 1st Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Xiaorong WuThe 1st Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To investigate the associations between the estimated glucose disposal rate (eGDR), a composite indicator of insulin sensitivity, and the risks of incident age-related cataract (ARC) and AMD, with a focus on nonlinear dose-response patterns, age-specific heterogeneity, and genetic modification. Methods: This prospective cohort study included 444,137 UK Biobank participants free of ARC and AMD at baseline. eGDR was analyzed both as a continuous variable (per 1-SD increase) and by quartiles. Multivariable Cox proportional hazards models were used to estimate hazard ratios and 95% confidence intervals. Restricted cubic spline models assessed nonlinear associations and identified metabolic plateau ranges. Age-stratified analyses (<60 years vs. ≥60 years), landmark analyses, polygenic risk score-stratified analyses, and multiple sensitivity analyses were conducted to evaluate robustness. Results: A total of 29,215 incident ARC cases and 8992 incident AMD cases were documented during follow-up. A higher eGDR was consistently associated with lower risks of both ARC and AMD, corresponding with an approximately 7% to 8% risk reduction per 1-SD increase after full adjustment. Quartile-based analyses demonstrated clear dose-response relationships, with participants in the highest eGDR quartile exhibiting substantially lower risks compared with those in the lowest quartile. Restricted cubic spline analyses revealed significant nonlinear, L-shaped associations, characterized by a steep risk decline at lower eGDR levels followed by a risk-neutral metabolic plateau. The plateau range occurred at higher eGDR levels among participants aged <60 years than among those aged ≥60 years. Associations were stronger during extended follow-up periods and remained robust across landmark, competing-risk, and other sensitivity analyses. Moreover, higher eGDR levels attenuated genetic susceptibility to ARC and AMD across polygenic risk score strata. Conclusions: A higher eGDR is associated with lower risks of incident ARC and AMD in a nonlinear and age-dependent manner. These findings highlight insulin sensitivity as a modifiable metabolic factor in ocular aging and support the potential value of metabolic risk stratification for age-related eye diseases.

Indexed as

Blood GlucoseCataractInsulin ResistanceAgedFemaleGenetic Risk ScoreHumansIncidenceMaleMiddle AgedProportional Hazards ModelsProspective StudiesRisk AssessmentRisk FactorsUK BiobankUnited KingdomBlood Glucose

Identifiers

PMID42405670
PMCPMC13348928

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.