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Related Experiment Video

Updated: Jun 8, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
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High-density lipoprotein therapy: is there hope?

Kunal N Bhatt1, Bryan J Wells, Laurence S Sperling

  • 1Department of Medicine, Division of Cardiology (Section of Preventive Cardiology), Emory University School of Medicine, 1364 Clifton Road, Atlanta, GA, 30322, USA.

Current Treatment Options in Cardiovascular Medicine
|September 16, 2010
PubMed
Summary

Low high-density lipoprotein cholesterol (HDL-C) is linked to increased cardiovascular disease risk. Niacin and emerging therapies show promise for raising HDL-C when LDL-C reduction is insufficient.

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Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation
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Published on: January 28, 2021

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Last Updated: Jun 8, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
07:29

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein

Published on: October 12, 2017

Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation
06:47

Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation

Published on: January 28, 2021

Area of Science:

  • Cardiology
  • Metabolic Disorders
  • Pharmacology

Background:

  • Traditional lipid management focuses on LDL-C reduction, yet many patients still experience cardiovascular events.
  • Low HDL-C levels (<40 mg/dL) are independently associated with increased cardiovascular disease (CVD) risk.
  • Low HDL-C is a component of the metabolic syndrome and often observed in insulin resistance states.

Purpose of the Study:

  • To review the role of high-density lipoprotein cholesterol (HDL-C) in cardiovascular disease (CVD).
  • To discuss current and emerging therapeutic strategies for managing low HDL-C levels.
  • To evaluate the efficacy of various agents in raising HDL-C and reducing CVD risk.

Main Methods:

  • Review of epidemiological studies and clinical trial data on lipid abnormalities and CVD.
  • Analysis of current guidelines and treatment approaches for low HDL-C.
  • Discussion of pharmacologic options, including statins, fibrates, niacin, and CETP inhibitors.

Main Results:

  • Low HDL-C is prevalent in patients with CVD and associated with higher cardiovascular risk.
  • Lifestyle modifications are the first-line approach for increasing HDL-C.
  • Niacin is the most potent available HDL-C-raising therapy; CETP inhibitors are under investigation.

Conclusions:

  • Despite LDL-C control, low HDL-C remains a significant CVD risk factor.
  • Pharmacologic intervention to raise HDL-C, particularly with niacin, should be considered in select patients.
  • Novel therapies like CETP inhibitors may offer future options for managing dyslipidemia and reducing CVD events.