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The triglyceride-high-density lipoprotein-glucose-body index: a superior novel biomarker for diabetic kidney disease in type 2 diabetes

医学 2型糖尿病 内科学 胰岛素抵抗 生物标志物 2型糖尿病 体质指数 糖尿病 肿瘤科 疾病 接收机工作特性 逻辑回归 肾脏疾病 胆固醇 回顾性队列研究 发病机制 内分泌学 心脏病学 切断 代理终结点 胰岛素 胃肠病学 代谢综合征 肌酐
作者
Jian Yang,Bingsong Xie,Zhiling Deng,Zhifu Zhang,Hairong Zhou
出处
期刊:Frontiers in Endocrinology [Frontiers Media]
卷期号:16
标识
DOI:10.3389/fendo.2025.1749826
摘要

Background The triglyceride-glucose (TyG) index is a recognized surrogate marker of insulin resistance but lacks integration of high-density lipoprotein cholesterol (HDL-C) and adiposity measures, which are pivotal in the pathogenesis of diabetic kidney disease (DKD). The novel triglyceride-high-density lipoprotein-glucose-body (TyHGB) index, combining TG/HDL-C ratio, fasting blood glucose (FBG), and body mass index (BMI), may offer a more comprehensive metabolic profile. This study aimed to evaluate the associative value of TyHGB for DKD in type 2 diabetes mellitus (T2DM) patients. Methods A retrospective cross-sectional analysis of 1,382 adults with T2DM was conducted. We employed multivariable logistic regression, restricted cubic spline (RCS) analysis, and subgroup analyses to assess the independent and non-linear association of the TyHGB index with DKD. Receiver operating characteristic (ROC) curves, net reclassification improvement (NRI), and integrated discrimination improvement (IDI) were used to evaluate and compare its associative performance against the TyG index. Results Among the participants, 286 (20.7%) were diagnosed with DKD. After full adjustment for demographic, clinical, and biochemical confounders, TyHGB was independently associated with DKD (OR = 1.11, 95%CI:1.05-1.17, p<0.001). RCS analysis revealed a significant non-linear relationship, with a sharp increase in DKD risk beyond a TyHGB threshold of 8.74. The TyHGB index demonstrated superior discriminative ability (AUC = 0.775, 95% CI: 0.747-0.803) compared to the TyG index (AUC = 0.644, p<0.001). Incorporating TyHGB into a baseline clinical model significantly improved risk association (AUC increased from 0.715 to 0.788, p<0.001) and provided substantial reclassification improvement (NRI = 0.647, IDI = 0.067). Conclusion The TyHGB index exhibits a robust, independent, and non-linear association with DKD risk in T2DM patients and outperforms the established TyG index. As a readily accessible composite metric, it holds significant promise as a superior tool for early identification and risk stratification of DKD in clinical practice.

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