Large high-density lipoprotein particle number is independently associated with microvascular function in patients with well-controlled low-density lipoprotein concentration: A vasodilator stress magnetic resonance perfusion study
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Updated: Mar 22, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Akhil Narang1, Victor Mor-Avi1, Nicole M Bhave1
1Department of Medicine, University of Chicago, Chicago, IL, USA; Department of Electronics, Computer Science and Systems, University of Bologna, Bologna, Italy; Departments of Medicine and Radiology, University of Chicago, Chicago, IL, USA.
Insights
Lipid subfractions, specifically large HDL-P, are more strongly linked to microvascular function than standard lipid panels in patients with low LDL-C. This finding highlights the importance of detailed lipid analysis for assessing cardiovascular risk.
Area of Science:
- Cardiovascular Medicine
- Lipidology
- Diagnostic Imaging
Background:
- Abnormalities in cholesterol and triglycerides are linked to microvascular dysfunction.
- Lipid subfractions may offer better prediction of atherogenic burden than routine lipid panels.
- The association between lipid subfractions and microvascular function/atherosclerosis needs further investigation.
Purpose of the Study:
- To determine if lipid subfractions are more strongly associated with microvascular function and subclinical atherosclerosis than conventional lipid measurements.
- To utilize vasodilator stress cardiovascular magnetic resonance (CMR) for assessing these associations.
Main Methods:
- Twenty-four adults with low LDL-C (<100 mg/dL) underwent vasodilator CMR.
- Myocardial perfusion reserve index (MPRi) was calculated from stress and rest perfusion images.
- Lipid subfractions were measured using nuclear magnetic resonance testing, and associations with MPRi were analyzed via regression.
Main Results:
- MPRi showed associations with HDL-C, triglycerides, large HDL-P, and small LDL-P in univariate analysis.
- No association was found between MPRi and total cholesterol, LDL-C, total LDL-P, or total HDL-P.
- Multivariate analysis revealed large HDL-P as independently associated with MPRi.
Conclusions:
- In patients with LDL-C <100 mg/dL, large HDL-P is independently associated with CMR-derived myocardial perfusion reserve.
- Myocardial perfusion reserve serves as a surrogate for microvascular function and subclinical atherosclerosis.
- Further research into lipid subfractions is warranted to better understand cardiovascular risks.
Background:
Abnormalities in total cholesterol, high-density lipoprotein, low-density lipoprotein, and triglycerides are associated with microvascular dysfunction. Recent studies suggest that lipid subfractions better predict atherogenic burden than a routine lipid panel. We sought to determine, whether lipid subfractions are more strongly associated with microvascular function and subclinical atherosclerosis, than conventional lipid measurements using vasodilator stress cardiovascular magnetic resonance (CMR).
Methods:
Twenty-four adults referred for risk stratification from a lipid clinic with low-density lipoprotein cholesterol (LDL-C) <100 mg/dL underwent vasodilator CMR. Time-intensity curves generated from stress and rest perfusion images were used to determine the area under the curve (AUC) for the mid-ventricular slice myocardium and the left ventricular (LV) cavity. Myocardial perfusion reserve index (MPRi) was defined as stress to rest ratio of mid-ventricular myocardium AUC, normalized to LV cavity AUC. Lipid panels that included subfractions of LDL and high-density lipoprotein (HDL) were measured using nuclear magnetic resonance testing. The association between MPRi and lipid parameters was examined using univariate linear regression; lipid components statistically correlated with MPRi (P < .05) were then subjected to multivariate analysis.
Results:
Univariate regression analysis showed MPRi was associated with HDL-C, triglycerides, large HDL-P, and small LDL-P; no association was found between MPRi and total cholesterol, LDL-C, total LDL-P, or total HDL-P. Using multivariate analysis, large HDL-P was independently associated with MPRi.
Conclusions:
In patients with LDL-C <100 mg/dL, large HDL-P is independently associated with CMR-derived myocardial perfusion reserve, a surrogate for microvascular function and subclinical atherosclerosis. Further studies using lipid subfractions to better understand cardiovascular risks are warranted.
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