Abstract

BackgroundThe presence of smaller low-density lipoproteins (LDL) has been associated with atherosclerosis risk, and the insulin resistance (IR) underlying the metabolic syndrome (MetS). In addition, some research has supported the association of very low-, low- and high-density lipoprotein (VLDL HDL) particle diameters with components of the metabolic syndrome (MetS), although this has been the focus of less research. We aimed to explore the relationship of VLDL, LDL and HDL diameters to MetS and its features, and by clustering individuals by their diameters of VLDL, LDL and HDL particles, to capture information across all three fractions of lipoprotein into a unified phenotype.MethodsWe used nuclear magnetic resonance spectroscopy measurements on fasting plasma samples from a general population sample of 1,036 adults (mean ± SD, 48.8 ± 16.2 y of age). Using latent class analysis, the sample was grouped by the diameter of their fasting lipoproteins, and mixed effects models tested whether the distribution of MetS components varied across the groups.ResultsEight discrete groups were identified. Two groups (N = 251) were enriched with individuals meeting criteria for the MetS, and were characterized by the smallest LDL/HDL diameters. One of those two groups, one was additionally distinguished by large VLDL, and had significantly higher blood pressure, fasting glucose, triglycerides, and waist circumference (WC; P < .001). However, large VLDL, in the absence of small LDL and HDL particles, did not associate with MetS features. These associations held after additionally controlling for VLDL, LDL and HDL particle concentrations.ConclusionsWhile small LDL diameters remain associated with IR and the MetS, the occurrence of these in conjunction with a shift to overall larger VLDL diameter may identify those with the highest fasting glucose, TG and WC within the MetS. If replicated, the association of this phenotype with more severe IR-features indicated that it may contribute to identifying of those most at risk for incident type II diabetes and cardiometabolic disease.

Highlights

  • insulin resistance (IR) is defined as cellular resistance to insulin stimulated glucose uptake

  • We further aimed to examine the distribution of the metabolic syndrome (MetS), and its individual components across these groupings, and assess whether any association between group and IR help when controlling for overall lipoprotein concentrations

  • Within the sample as a whole, low-density lipoproteins (LDL) diameter was highly correlated with High-density lipoprotein (HDL) diameter (r = .78; P < 0.0001), but Very-low density lipoprotein (VLDL) diameter was not significantly correlated with LDL diameter (r = -.02; P = 0.51) nor HDL diameter (r = .02; P = .54)

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Summary

Introduction

IR is defined as cellular resistance to insulin stimulated glucose uptake. The compensatory hyperinsulinemia associates with a set of metabolic features that characterize the metabolic syndrome. In addition to the smaller LDL particles seen in MetS, some preliminary evidence suggest associations between IR and larger VLDL particles, and between IR and smaller HDL particles [3,4,12,13,14] Despite these associations, how the diameters covary across the three fractions is poorly understood, and, as yet, information on all three fractions of lipoprotein diameter has not been captured into a single phenotype and examined for its relationship to disease. We aimed to explore the relationship of VLDL, LDL and HDL diameters to MetS and its features, and by clustering individuals by their diameters of VLDL, LDL and HDL particles, to capture information across all three fractions of lipoprotein into a unified phenotype

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