Evidence map›Paper›PMID 42466350›Full record

ArticleFrontiers in endocrinology2026

Association of the combined triglyceride glucose-body mass index and serum IQGAP3 in appraising coronary lesion severity in type 2 diabetes.

YuRong Sun, Jingsi Zhang, Yi Lu, Yeting Chang, Yanchun Ding

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Article in Frontiers in endocrinology, 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

YuRong SunDepartment of Cardiology, The Second Hospital of DaLian Medical University, Dalian, Liaoning, China.
Jingsi ZhangDepartment of Cardiology, The Second Hospital of DaLian Medical University, Dalian, Liaoning, China.
Yi LuDepartment of Cardiology, The Second Hospital of DaLian Medical University, Dalian, Liaoning, China.
Yeting ChangDepartment of Cardiology, The Second Hospital of DaLian Medical University, Dalian, Liaoning, China.
Yanchun DingDepartment of Cardiology, The Second Hospital of DaLian Medical University, Dalian, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: IQGAP3 is a novel scaffold protein involved in inflammatory and metabolic regulation and may contribute to atherosclerosis. However, its clinical significance in coronary artery disease among patients with type 2 diabetes mellitus (T2DM) remains unclear. This study investigated the association between serum IQGAP3 and coronary lesion severity and evaluated the diagnostic value of combining IQGAP3 with the triglyceride glucose-body mass index (TyG-BMI). Methods: This prospective study enrolled T2DM patients undergoing coronary angiography. Serum IQGAP3 levels were measured by enzyme-linked immunosorbent assay, and TyG-BMI was calculated using routine clinical parameters. Coronary lesion severity was assessed using the Gensini score and categorized by tertiles. Multivariable logistic regression, restricted cubic spline (RCS), subgroup, and interaction analyses were performed. ROC curves, net reclassification improvement (NRI), and integrated discrimination improvement (IDI) were used to assess model performance. Results: A total of 392 patients were included. Serum IQGAP3 levels and TyG-BMI increased significantly across Gensini score tertiles (all P< 0.05). Both IQGAP3 (OR = 3.119, 95% CI: 2.049-4.747, P< 0.001) and TyG-BMI (OR = 1.012, 95% CI: 1.003-1.021, P = 0.006) were independently associated with severe coronary stenosis. Adding TyG-BMI to the traditional risk factor model improved discrimination (AUC: 0.702 vs. 0.753; NRI = 0.180, IDI = 0.065; both P< 0.001). Further incorporation of IQGAP3 increased the AUC to 0.803 and significantly improved reclassification (NRI = 0.307, IDI = 0.138; both P< 0.001), with optimism-corrected internal validation demonstrating an AUC of 0.788 and a calibration slope of 0.926. RCS analyses demonstrated a linear positive association between IQGAP3 and disease risk, whereas TyG-BMI exhibited a nonlinear relationship. Subgroup analyses showed consistent associations across most clinical strata. Age significantly modified the association between IQGAP3 and severe coronary stenosis (Pinteraction = 0.036), with a stronger effect observed in patients younger than 65 years. Conclusion: Serum IQGAP3 and TyG-BMI are independently associated with coronary lesion severity in T2DM patients. Their combined assessment provides incremental discriminative value for coronary lesion severity and may serve as a practical, non-invasive tool for cardiovascular risk stratification.

Indexed as

Blood GlucoseBody Mass IndexCoronary Artery DiseaseDiabetes Mellitus, Type 2ras GTPase-Activating ProteinsTriglyceridesAgedBiomarkersCoronary AngiographyFemaleGTPase-Activating ProteinsHumansMaleMiddle AgedProspective StudiesROC CurveBiomarkersBlood GlucoseGTPase-Activating ProteinsIQGAP3 protein, humanras GTPase-Activating ProteinsTriglyceridescoronary artery diseaseinsulin resistanceIQGAP3TyG-BMItype 2 diabetes mellitus

Identifiers

PMID42466350
PMCPMC13372632

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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.