# Investigating the prediction potential of cholesterol, high-density lipoprotein, and glucose index surpasses TyG, AIP, and METS-IR for type 2 diabetes: a longitudinal cohort study

**Authors:** Si-Yuan Chen, Xiang-Xiang Li, Feng Lu, Hao Shen

PMC · DOI: 10.3389/fendo.2026.1665074 · Frontiers in Endocrinology · 2026-02-05

## TL;DR

A new index combining cholesterol, HDL-C, and glucose better predicts type 2 diabetes than existing indices, offering a practical tool for early risk detection.

## Contribution

The CHG index is introduced as a novel and superior predictor of type 2 diabetes compared to TyG, AIP, and METS-IR.

## Key findings

- The CHG index had the highest hazard ratio (6.18) for predicting T2DM compared to other indices.
- The CHG index showed a dose-response relationship and linear association with T2DM risk over 12 years.
- The CHG index achieved high discriminative accuracy (AUC: 0.783) and remained robust in various subgroups.

## Abstract

To compare the predictive performance of the novel Cholesterol, High-Density Lipoprotein, and Glucose (CHG) index for the incident type 2 diabetes mellitus (T2DM) versus the established indices—triglyceride-glucose (TyG), atherogenic index of plasma (AIP), and metabolic score for insulin resistance (METS-IR).

A longitudinal cohort study was performed on 15, 453 participants from the NAGALA cohort (2004–2015) without baseline T2DM. The CHG index was calculated from total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), and fasting blood glucose (FBG). Several additional indices were established, including the TyG, AIP, and METS-IR. Cox regression, Kaplan-Meier analysis, restricted cubic spline (RCS) analysis, and time-dependent receiver operating characteristic (ROC) curves were performed to determine the predictive performance, after adjusting for various confounders (e.g., obesity, liver function). Robustness was assessed through sensitivity analyses.

During a 6.13-year follow-up, 373 T2DM cases were recorded. In the fully adjusted models, we found that the CHG index had the highest hazard ratio (HR): 6.18 per unit (95% CI: 3.38–11.27), outperforming the TyG index (HR: 1.39), AIP (HR: 1.80), and METS-IR (HR: 1.07). Quartile analysis revealed a dose-response relationship for CHG (Q4 HR: 4.36 vs. Q1, P < 0.001). Further, the RCS analysis revealed a linear association between CHG and T2DM risk (P for overall trend < 0.001; P for nonlinearity = 0.712). Moreover, the CHG index achieved a satisfactory discriminative accuracy (based on the area under the curve [AUC]: 0.783 vs. TyG: 0.751, AIP: 0.745, METS-IR: 0.780) and its predictive power was consisted over the 12 years (peak AUC: 0.798 at 7 years). Sensitivity analyses for various subgroups (e.g., non-obese, non-fatty liver) confirmed that the obtained results were robust.

The CHG index that integrates cholesterol, HDL-C, and glucose metabolism, showed superior predictive performance for the incidence of T2DM. Suggesting that it effectively captures the multifactorial pathophysiology of the disease. It is based on routine biomarkers making it easily applicable in risk stratification, offering a cost-effective tool for early intervention and precise prevention in clinical and public health settings.

## Linked entities

- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), T2DM (MONDO:0005148)

## Full-text entities

- **Genes:** ETV3 (ETS variant transcription factor 3) [NCBI Gene 2117] {aka METS, PE-1, PE1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, AIP (AHR interacting HSP90 co-chaperone) [NCBI Gene 9049] {aka ARA9, FKBP16, FKBP37, PITA1, SMTPHN, XAP-2}, GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, GGTLC5P (gamma-glutamyltransferase light chain 5 pseudogene) [NCBI Gene 653590] {aka GGT}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** HbA1c (MESH:D006445), lipid metabolic dysfunction (MESH:D052439), hyperinsulinemic-euglycemic (MESH:D044903), atherogenic (MESH:D050197), microvascular injury (MESH:D017566), IR (MESH:D007333), cardiovascular disease (MESH:D002318), diabetic retinopathy (MESH:D003930), hepatic comorbidities (MESH:D056486), non-diabetic hypothyroidism (MESH:C565705), T2DM (MESH:D003924), adiposity (MESH:D018205), nephropathy (MESH:D007674), chronic (MESH:D002908), glucose dysregulation (MESH:D018149), gallstone disease (MESH:D002769), lipid abnormalities (MESH:D011017), Dyslipidemia (MESH:D050171), hepatic dysfunction (MESH:D008107), adipose inflammation (MESH:D007249), Hyperglycemia (MESH:D006943), metabolic disturbances (MESH:D024821), fibrosis (MESH:D005355), glucose metabolic disorders (MESH:D044882), NAFLD (MESH:D065626), Diabetes (MESH:D003920), Fatty liver (MESH:D005234), CHG (MESH:D052456), obese (MESH:D009765), TG (MESH:C566031), metabolic dysfunction (MESH:D008659), metabolic dysregulation (MESH:D021081)
- **Chemicals:** FPG (-), lipid (MESH:D008055), Glucose (MESH:D005947), Alcohol (MESH:D000438), TG (MESH:D014280), Cholesterol (MESH:D002784), blood glucose (MESH:D001786)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]

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## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916360/full.md

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Source: https://tomesphere.com/paper/PMC12916360