Abstract

BackgroundTriglyceride/high-density lipoprotein-cholesterol (TG/HDL-C) ratio was a surrogate marker of IR; however, the relationship of TG/HDL-C with IR might vary by ethnicity. This study aims to investigate whether lipid ratios-TG/HDL-C, cholesterol/high-density lipoprotein-cholesterol (TC/HDL-C) ratio, low-density lipoprotein-cholesterol/high-density lipoprotein-cholesterol (LDL-C/HDL-C)) could be potential clinical markers of insulin resistance (IR) and β cell function and further to explore the optimal cut-offs in a Chinese population with different levels of glucose tolerance.MethodsFour hundred seventy-nine subjects without a history of diabetes underwent a 75 g 2 h Oral Glucose Tolerance Test (OGTT). New-onset diabetes (n = 101), pre-diabetes (n = 186), and normal glucose tolerance (n = 192) were screened. IR was defined by HOMA-IR > 2.69. Based on indices (HOMA-β, early-phase disposition index [DI30], (ΔIns30/ΔGlu30)/HOMA-IR and total-phase index [DI120]) that indicated different phases of insulin secretion, the subjects were divided into two groups, and the lower group was defined as having inadequate β cell compensation. Logistic regression models and accurate estimates of the areas under receiver operating characteristic curves (AUROC) were obtained.ResultsIn all of the subjects, TG/HDL, TC/HDL-C, LDL-C/HDL-C, and TG were significantly associated with IR. The AUROCs of TG/HDL-C and TG were 0.71 (95 % CI: 0.66–0.75) and 0.71 (95 % CI: 0.65–0.75), respectively. The optimal cut-offs of TG/HDL-C and TG for IR diagnosis were 1.11 and 1.33 mmol/L, respectively. The AUROCs of TC/HDL-C and LDL-C/HDL-C were 0.66 and 0.65, respectively, but they were not acceptable for IR diagnosis. TG/HDL-C,LDL-C/HDL-C and TG were significantly associated with HOMA-β, but AUROCs were less than 0.50; therefore, the lipid ratios could not be predictors of basal β cell dysfunction. None of the lipid ratios was associated with early-phase insulin secretion. Only TG/HDL-C and TG were significantly correlated with total-phase insulin secretion, but they also were not acceptable predictors of total-phase insulin secretion (0.60 < AUROC < 0.70).ConclusionsIn a Chinese population with different levels of glucose tolerance, TG/HDL-C and TG could be the predictors of IR. The lipid ratios could not be reliable makers of β cell function in the population.

Highlights

  • Triglyceride/high-density lipoprotein-cholesterol (TG/HDL-C) ratio was a surrogate marker of Insulin resistance (IR); the relationship of TG/HDL-C with IR might vary by ethnicity

  • Previous studies have reported that the triglyceride/high-density lipoproteincholesterol (TG/HDL-C) ratio was a surrogate marker of IR [4,5,6]; the relationship of TG/HDL-C with IR might vary by ethnicity [5, 7, 8]

  • IR exists throughout all the glucose tolerance status, and whether TG/HDL-C could be a surrogate marker for IR and β cell function in populations with different levels of glucose tolerance remains unknown

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Summary

Introduction

Triglyceride/high-density lipoprotein-cholesterol (TG/HDL-C) ratio was a surrogate marker of IR; the relationship of TG/HDL-C with IR might vary by ethnicity. Previous studies have reported that the triglyceride/high-density lipoproteincholesterol (TG/HDL-C) ratio was a surrogate marker of IR [4,5,6]; the relationship of TG/HDL-C with IR might vary by ethnicity [5, 7, 8]. In normoglycemic African American women, TG/HDL-C was inversely associated with β cell function, suggesting that the TG/HDL-C ratio could be a simple tool for effectively identifying African Americans at risk for diabetes [16]. IR exists throughout all the glucose tolerance status, and whether TG/HDL-C could be a surrogate marker for IR and β cell function in populations with different levels of glucose tolerance remains unknown

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