Effects of fenofibrate on high-density lipoprotein particle size in patients with hyperlipidemia: a randomized,

Jun Sasaki1, Kyosuke Yamamoto, Masato Ageta

  • 1Graduate School of Public Health Medicine, International University of Health and Welfare, Fukuoka, Japan. jsas@nifty.com

Clinical Therapeutics
|December 5, 2002
PubMed

Insights

Fenofibrate treatment significantly reduced cholesterol and triglyceride levels while increasing high-density lipoprotein cholesterol (HDL-C). This study found fenofibrate therapy increased HDL3 particles, crucial for cholesterol removal.

Area of Science:

  • Lipid metabolism and cardiovascular health.
  • Pharmacological interventions for dyslipidemia.

Background:

  • Fenofibrate is known to decrease total cholesterol and triglycerides, and increase high-density lipoprotein cholesterol (HDL-C).
  • The specific impact of fenofibrate on the particle size distribution of HDL has not been fully elucidated.

Purpose of the Study:

  • To investigate the effects of fenofibrate on the particle size of high-density lipoprotein (HDL).

Main Methods:

  • A randomized, double-blind, placebo-controlled, crossover study involving 50 hyperlipidemic patients.
  • Patients received fenofibrate 300 mg or placebo daily for 8 weeks, followed by crossover for another 8 weeks.

Main Results:

  • Fenofibrate significantly reduced serum total cholesterol and triglycerides by 9.4% and 34.4%, respectively.
  • HDL-C levels increased by 25.8% with fenofibrate. Lipoprotein lipase activity and hepatic triglyceride lipase activity also increased.
  • Fenofibrate significantly increased the amount of HDL3 particles (smallest diameter), with P < 0.001.

Conclusions:

  • Fenofibrate therapy increases the HDL3 subfraction, which plays a key role in reverse cholesterol transport.
  • These findings suggest fenofibrate favorably alters HDL composition, potentially contributing to its cardioprotective effects.
Abstract

Related Concept Videos

Lipid-Lowering Drugs: Statins and Miscellaneous Agents01:20

Lipid-Lowering Drugs: Statins and Miscellaneous Agents

Hyperlipidemia, a medical condition often referred to as high cholesterol, is characterized by abnormally elevated levels of lipids in the bloodstream. When present in excess, these lipids, specifically cholesterol and triglycerides, can lead to serious health complications, often involving cardiovascular diseases. Illnesses like atherosclerosis, heart attacks, and pancreatitis have all been linked to untreated hyperlipidemia. This means controlling and regulating cholesterol and triglyceride...
Pharmacokinetics in Obese Patients: Drug Absorption and Distribution01:25

Pharmacokinetics in Obese Patients: Drug Absorption and Distribution

Obesity significantly alters the pharmacokinetic processes of drug absorption and distribution, presenting unique challenges in medical treatment. The increased fat tissue and decreased lean muscle in obese individuals can significantly affect how drugs are absorbed into the body and distributed across different tissues. This alteration can lead to variances in the effectiveness and safety of medications, necessitating adjustments in dosing or drug selection for obese patients.One notable...
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment01:08

Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment

Hepatic impairment, characterized by decreased liver function, does not uniformly mandate adjustments in drug dosage. Whether dosage modifications are necessary depends on various factors related to the drug's metabolism and elimination pathways. If a drug is primarily excreted via the kidneys and bypasses significant hepatic processing, if it undergoes minimal metabolic transformation in the liver, or if it is volatile and primarily expelled through the lungs, dose adjustments may not be...
Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion01:20

Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion

Drug metabolism, a critical process in the liver, involves two primary phases: Phase I reactions and Phase II conjugation. Obesity introduces significant alterations in this metabolic process, primarily due to fatty infiltration of the liver, leading to conditions such as nonalcoholic fatty liver disease (NAFLD). This condition can modify the activities of both Phase I and II enzymes, impacting how drugs are metabolized in obese patients.Phase I metabolism sees variable effects across...
Modified-Release Drug Delivery Systems: Bioavailability01:30

Modified-Release Drug Delivery Systems: Bioavailability

Modified-release (MR) dosage forms are designed to extend drug release over time, thereby maintaining stable plasma concentrations and reducing dosing frequency. However, their bioavailability is typically below 100% due to incomplete drug release and presystemic metabolism, and limitations in drug permeability across the gastrointestinal epithelium, all of which can restrict the fraction of the drug reaching systemic circulation. Consequently, studying the in vivo bioavailability of MR...
Bioavailability Study Design: Healthy Subjects Versus Patients01:15

Bioavailability Study Design: Healthy Subjects Versus Patients

Bioavailability studies are essential for evaluating a drug's therapeutic efficacy and understanding its absorption patterns under various physiological conditions. Conducting such studies on target patient populations provides more relevant data by simulating real-world disease states. However, practical challenges often necessitate the use of young, healthy adult volunteers as study subjects.Patients may exhibit altered drug absorption patterns due to the effects of the disease itself,...