Triglyceride-glucose index, low-density lipoprotein levels, and cardiovascular outcomes in chronic stable cardiovascular disease: results from the ONTARGET and TRANSCEND trials

Author:

Haring Bernhard12ORCID,Schumacher Helmut3,Mancia Giuseppe4ORCID,Teo Koon K5,Lonn Eva M5,Mahfoud Felix1ORCID,Schmieder Roland6,Mann Johannes F E76,Sliwa Karen8,Yusuf Salim5,Böhm Michael1ORCID

Affiliation:

1. Department of Medicine III, Saarland University, Kirrberger Strasse 100, 66421 Homburg, Germany

2. Department of Epidemiology and Population Health, Albert Einstein College of Medicine , Bronx, NY , USA

3. Ingelheim , Germany

4. Instituto Clinico Universitario Policlinico di Monza, University of Milano-Bicocca , Piazza dell'Ateneo Nuovo, 1 , Milano, Italy

5. Population Health Research Institute, McMaster University, and Hamilton Health Sciences , Hamilton , Canada

6. Department of Nephrology and Hypertension, Friedrich-Alexander University , Erlangen , Germany

7. KfH Kidney Centre , München , Germany

8. Faculty of Health Sciences, Hatter Institute for Cardiovascular Research in Africa & IIDMM, University of Cape Town , Cape Town , South Africa

Abstract

Abstract Aims The triglyceride-glucose index (TyG) has been proposed as an alternative to insulin resistance and as a predictor of cardiovascular outcomes. Little is known on its role in chronic stable cardiovascular disease and its predictive power at controlled low density lipoprotein (LDL) levels. Methods and results Our study population consisted of 29 960 participants in the ONTARGET and TRANSCEND trials that enrolled patients with known atherosclerotic disease. Triglycerides and glucose were measured at baseline. TyG was calculated as the logarithmized product of fasting triglycerides and glucose divided by 2. The primary endpoint of both trials was a composite of cardiovascular death, myocardial infarction, stroke, or hospitalization for heart failure. The secondary endpoint was all-cause death and the components of the primary endpoint. Cox proportional hazards models were used to estimate hazard ratios (HRs) and 95% confidence intervals (CI) with extensive covariate adjustment for demographic, medical history, and lifestyle factors. During a mean follow-up of 4.3 years, 4895 primary endpoints and 3571 all-cause deaths occurred. In fully adjusted models, individuals in the highest compared to the lowest quartile of the TyG index were at higher risk for the primary endpoint (HR 1.14; 95% CI 1.05–1.25) and for myocardial infarction (HR 1.30; 95% CI 1.11–1.53). A higher TyG index did not associate with the primary endpoint in individuals with LDL levels < 100 mg/dL. Conclusion A higher TyG index is associated with a modestly increased cardiovascular risk in chronic stable cardiovascular disease. This association is largely attenuated when LDL levels are controlled. Registration www.clinicaltrials.gov: NCT00153101

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Epidemiology

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