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OpenTrials
Completed

NCT Number: NCT01420328

To Study the Effect of Vytorin on Intracellular Lipid and Inflammation in Obese Subjects

This study focuses on the use of Vytorin to study inflammatory markers in subjects with normal cholesterol.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Diabetes Endocrinology Center of WNY

Buffalo, New York, 14209, United States

About this study

Following the first demonstration by our group that macronutrient (glucose, cream and a high fat high carbohydrate meal) intake results in increased ROS generation and oxidative stress at the cellular and molecular level, the investigators have now shown in our preliminary data that cream intake induces comprehensive inflammation as reflected in increased intranuclear NFkB binding, decreased IkBα expression, increased expression of IL-1β, IL-12, TNFα and other pro-inflammatory mediators. While carrying out these experiments, the investigators asked whether cream intake was associated with an uptake of lipid by peripheral blood mononuclear cells (MNC). Indeed, there was a significant increase in intracellular lipid which was visualized as intracellular lipid droplets. The increase in intracellular lipid droplets was associated with an increase in intracellular superoxide generation; the expression of CD68, a marker for macrophages; and PECAM, the adhesion molecule which mediates trans- endothelial transfer of leucocytes. The investigators also found that the lipid fractions to increase were cholesterol ester, triglyceride and fatty acids. In view of the tantalizing observation that the lipid droplet laden MNC appeared to be monocytes, looked like foam cells and the fact that CD68 expression had increased, there is a possibility that foam cells may be formed in peripheral circulation by monocytes after a lipid rich meal. This simple model of foam cell formation also lends itself for the study of the effect of various lipid lowering drugs. Our investigation will be the first to study this novel paradigm. The investigators plan to study the effect of a cholesterol lowering agent, Vytorin (simvastatin and ezetimibe), on intracellular lipid in MNC, expression of CD68 and PECAM, ROS generation and inflammation in obese subjects. This investigation may provide an additional mechanism of action by which these drugs may reduce atherosclerosis.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age 18-65years.
  • Obese BMI >30kg/m2
  • LDL cholesterol >100 mg/dl
  • Written and informed consent signed and dated 5. Not on any vitamin/antioxidants

Exclusion criteria

  • On any antilipid agents.
  • Triglyceride >500mg/dl
  • Myocardial infarction, angioplasty/stent placement or coronary artery bypass surgery in the past 6 months
  • Patient on chronic use of non-steroidal anti-inflammatory drugs or steroids
  • Hepatic disease
  • Renal impairment
  • History of drug or alcohol abuse
  • Participation in any other concurrent clinical trial
  • Use of an investigational agent or therapeutic regimen within 30 days of study.
  • Smoker
  • Pregnancy
  • Premenopausal women who are not on birth control pills and have not had a hysterectomy or tubal ligation 13. Anemia with hemoglobin <12 g/dl

Treatment and study plan

vytorin

Drug

Simvastatin 40 mg and Ezetimibe 10 mg daily combination pill (Vytorin) for 6 weeks

Other names: Ezetimibi/Simvastatin 10/40

Placebo

Drug

Placebo treatment for 6 weeks

Other names: Placebo for Vytorin

Primary outcomes

  1. Change in CD68 mRNA Expression in MNC

    Time frame: 0 weeks and 6 weeks

    Percent change from baseline (0 week) in cream challenge induced change in CD68 mRNA expression in MNC after 6 weeks of treatment with Vytorin or placebo.

    Outcome calculated as: (change at 6 weeks- change at 0 week)/ change at 0 week*100

Secondary outcomes

  1. Change in Cream-induced Expression of CD16

    Time frame: 6 weeks

    Percent change from baseline (0 week) in cream -induced change in CD16 mRNA expression in MNC after 6 weeks of treatment with Vytorin or placebo.

    Outcome calculated as: (change at 6 weeks- change at 0 week)/ change at 0 week*100

  2. Change IL-1b mRNA Expression

    Time frame: 6 weeks

    Percent change from baseline (0 week) in cream -induced change in IL-1b mRNA expression in MNC after 6 weeks of treatment with Vytorin or placebo.

    Outcome calculated as: (change at 6 weeks- change at 0 week)/ change at 0 week*100

  3. Change in Plasma Endotoxin (LPS) Concentrations

    Time frame: 6 weeks

    change from baseline (0 week) in cream -induced change in plasma endotoxin concentration after 6 weeks of treatment with Vytorin or placebo.

    Outcome calculated as: (change at 6 weeks- change at 0 week)

Sponsors and collaborators

Lead sponsor

University at Buffalo

Other

Collaborators

  • Kaleida Health

Registry information

Important dates

Study start
2011
Primary completion
2015
Study completion
2016
First posted
Aug 19, 2011
Registry last updated
Apr 17, 2024

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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