Triglyceride Glucose-Body Mass Index Is a Simple and Clinically Useful Surrogate Marker for Insulin Resistance in Nondiabetic Individuals

PLoS One. 2016 Mar 1;11(3):e0149731. doi: 10.1371/journal.pone.0149731. eCollection 2016.

Abstract

Background: Insulin resistance (IR) and the consequences of compensatory hyperinsulinemia are pathogenic factors for a set of metabolic abnormalities, which contribute to the development of diabetes mellitus and cardiovascular diseases. We compared traditional lipid levels and ratios and combined them with fasting plasma glucose (FPG) levels or adiposity status for determining their efficiency as independent risk factors for IR.

Methods: We enrolled 511 Taiwanese individuals for the analysis. The clinical usefulness of various parameters--such as traditional lipid levels and ratios; visceral adiposity indicators, visceral adiposity index (VAI), and lipid accumulation product (LAP); the product of triglyceride (TG) and FPG (the TyG index); TyG with adiposity status (TyG-body mass index [BMI]) and TyG-waist circumference index [WC]); and adipokine levels and ratios--was analyzed to identify IR.

Results: For all lipid ratios, the TG/high-density lipoprotein cholesterol (HDL-C) ratio had the highest additional percentage of variation in the homeostasis model assessment of insulin resistance (HOMA-IR; 7.0% in total); for all variables of interest, TyG-BMI and leptin-adiponectin ratio (LAR) were strongly associated with HOMA-IR, with 16.6% and 23.2% of variability, respectively. A logistic regression analysis revealed similar patterns. A receiver operating characteristic (ROC) curve analysis indicated that TG/HDL-C was a more efficient IR discriminator than other lipid variables or ratios. The area under the ROC curve (AUC) for VAI (0.734) and TyG (0.708) was larger than that for TG/HDL-C (0.707). TyG-BMI and LAR had the largest AUC (0.801 and 0.801, respectively).

Conclusion: TyG-BMI is a simple, powerful, and clinically useful surrogate marker for early identification of IR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiposity
  • Adult
  • Biomarkers / blood*
  • Blood Glucose / metabolism*
  • Body Mass Index*
  • Cholesterol, HDL / blood
  • Fasting / blood
  • Female
  • Humans
  • Insulin Resistance*
  • Intra-Abdominal Fat / metabolism
  • Linear Models
  • Male
  • Middle Aged
  • Risk Factors
  • Triglycerides / blood*
  • Waist Circumference

Substances

  • Biomarkers
  • Blood Glucose
  • Cholesterol, HDL
  • Triglycerides

Grants and funding

This study was supported by a grant from the National Science Council, Taiwan (No. NSC101-2314-B-303-023-MY3), grants from the Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation (No. TCRD-TPE-99-07, TCRD-TPE-NSC-102-01, TCRD-TPE-MOST-103-01 and No. TCRD-TPE-103-R-2), and Tzu Chi University (No. TCIRP102001-02Y1 TCIRP99001-04Y1) to YL Ko. The authors greatly appreciate the technical support from the Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation Core Laboratory. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.