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OpenTrials
Completed

NCT Number: NCT00988364

Effects of Ezetimibe, Simvastatin, and Vytorin on Reducing L5 a Subfraction of LDL in Patients With Metabolic Syndrome.

The purpose of this study is:

* To identify the common factor for L5 prevalence in patients with Metabolic Syndrome. * To determine whether Ezetimibe, Simvastatin, and Vytorin can correct the L5- promoting factor and reduce L5 in Metabolic Syndrome patients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Baylor College of Medicine

Houston, Texas, 77030, United States

About this study

Epidemiological evidence indicates that metabolic syndrome (MS) is a strong predisposing condition for atherosclerosis. Elevation of plasma low-density lipoprotein (LDL) cholesterol(LDL-C) concentration is the most important risk factor for atherosclerosis; however, LDL-C elevation is not a criterion for metabolic syndrome, raising the question of LDL's role in the syndrome's association with atherosclerosis. L5, a highly electronegative and mildly oxidized LDL subfraction that we recently isolated from hypercholesterolemic human plasma, may provide a key to answering this question. In cultured vascular endothelial cells (EC), L5 inhibits proliferation and induces apoptosis and monocyte-EC adhesion. In our preliminary studies, L5 could also be detected in patients with MS without elevated LDL-C. Because other LDL subfractions were harmless to EC, the presence of MS-L5 prompted us to hypothesize that the atherogenic role of LDL is not solely determined by plasma LDL-C concentration, but more importantly, by its composition. The proposed study is designed to test this hypothesis. The first question we will address is what lipid factor determines the prevalence of L5 in MS.

Subsequently, we will examine whether treatment with selected medicines can effectively reduce L5 in MS patients by correcting the factor favorable for L5 formation.

We are in the process of identifying the active components of L5 to fully characterize the atherogenic role of L5 in MS,. In the current proposal, we focus our interest on the efficacy of Ezetimibe, Simvastatin, and Vytorin in reducing L5 from the plasma of MS patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants who meet 3 or more of the 5 criteria specified in the ATPIII guidelines will be recruited.
  • The 5 criteria are:
  • abdominal obesity (men>40 inches, women >35 inches);
  • TG> 150mg/dL;
  • low HDL-C (men < 40mg/dL, women < 50 mg/dL);
  • high blood pressure (>or=130/>or=85 mmHg);
  • fasting glucose > or = 110mg/dL.
  • People with different ethnic backgrounds will be included.

Exclusion criteria

  • symptomatic coronary artery disease
  • peripheral vascular disease
  • cerebral ischemia (stroke)
  • smoking
  • hypothyroidism
  • kidney diseases
  • consumption of antioxidation supplements/drugs or use of lipid-lowering drugs in the last 3 months
  • women who are pregnant, nursing, or planning to become pregnant

Treatment and study plan

simvastatin

Drug

Simvastatin 20mg daily for 3 months.

Other names: Zocor

vytorin

Drug

Vytorin 20/10mg daily for 3 months.

Other names: Ezetimibe/Simvastatin

Placebo

Drug

Placebo one tablet daily times 3 months.

Other names: Control

ezetimibe

Drug

Ezetimibe 10mg daily for 3 months.

Other names: Zetia

Primary outcomes

  1. L5 Concentration in Metabolic Syndrome Patients

    Time frame: 0 months, at the start

    Patient's blood samples were collected before treatment. L5 were purified by ultracentrifugation then FPLC. Quantification analysis will indicate the L5 concentration (mg/dL) per group.

Secondary outcomes

  1. L5 Concentration After Treatment of Ezetimibe, Simvastatin, or Vytorin in Metabolic Syndrome Patients

    Time frame: 3 months

    Patient's blood samples were collected at the corresponding time point for L5 purification. L5 quantification and characterization were investigated with chemical analysis, proteomics and in-vitro cell signaling analysis. Final data analysis will determine total L5 concentration (mg/dL).

Sponsors and collaborators

Lead sponsor

Baylor College of Medicine

Other

Collaborators

  • Merck Sharp & Dohme LLC

Registry information

Official study title

Effects of Ezetimibe, Simvastatin, and Vytorin on Reducing L5 in Patients With Metabolic Syndrome

Acronym: Merck-123

Important dates

Study start
2007
Primary completion
2008
Study completion
2008
First posted
Oct 2, 2009
Registry last updated
Nov 30, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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