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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01200836
Other study ID # 100165
Secondary ID 10-H-0165
Status Completed
Phase
First received
Last updated
Start date July 1, 2010
Est. completion date October 4, 2018

Study information

Verified date October 4, 2018
Source National Institutes of Health Clinical Center (CC)
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Background:

- The drug rosuvastatin (also called Crestor) is used to lower cholesterol levels in people with elevated cholesterol levels. Recent studies have suggested that rosuvastatin may affect the immune system and reduce inflammation, but the reason for this effect is unclear. Researchers are interested in testing the effect of rosuvastatin on the immune systems of healthy volunteers with good cholesterol levels.

Objectives:

- To evaluate the effect of rosuvastatin on the immune systems of healthy volunteers.

Eligibility:

- Healthy individuals at least 18 years of age who have an acceptable blood level of LDL cholesterol (below 160).

Design:

- Participants will be screened with a medical history and physical examination, as well as blood tests to check general health, cholesterol levels, liver function, and the C-reactive protein (which responds to inflammation).

- Participants will not be permitted to take most prescription and over-the-counter medications that affect the immune system, including antihistamines and certain pain relievers. For 1 week before the study, participants will have a wash-out period without any of these medications.

- Participants will take rosuvastatin daily for 4 weeks, always in the evening (to ensure consistent blood sample results).

- Participants will provide blood samples at the following time points: (1) immediately before the start of the rosuvastatin treatment, (2) after 2 weeks of treatment, (3) after 4 weeks of treatment, and (4) 2 weeks after the end of treatment.


Description:

Statins are drugs that inhibit cholesterol synthesis and are used extensively for primary and secondary prevention of heart disease. Their benefit to patients with heart diseases appears to exceed that predicted from cholesterol lowering alone. A recent study has found benefits of statin therapy in patients with normal cholesterol and high C-reactive protein, a marker of inflammation, suggesting that statins exert an anti inflammatory effect in addition to the well known cholesterol lowering activity. Studies in mice have revealed mixed observations regarding the role of statins in inflammation. Therefore the Center for Human Immunology, Autoimmunity and Inflammation is conducting this trial to study the effects of statins on the immune system and the inflammatory response in healthy volunteers with normal cholesterol levels, and normal or elevated C-reactive protein levels.

The primary objective is to characterize the immune system before and during statin therapy.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date October 4, 2018
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 99 Years
Eligibility - INCLUSION CRITERIA:

- Healthy volunteer (health status confirmed by brief History and Physical Exam and routine blood work as determined by the screening protocol)

- Age greater than or equal to18 years of age

- LDL < 160 mg/dL

- Ten subjects must have hsCRP < 2mg/L, and ten subjects must have hsCRP greater than or equal to 2 mg/L

- Subjects with psoriasis that are otherwise healthy, who have not received any systemic imunosuppression in the past 6 months

- Subjects with fasting glucose < 125 mg/dL

EXCLUSION CRITERIA:

- Female subjects may not be pregnant or lactating due to minor side effects of use of statins in a non-benefit study.

- Abnormal LFT s, i.e. AST > 34 U/L; ALT > 41 U/L; T. Bilirubin >1.0 mg/dL; Alkaline Phosphatasse > 116 U/L.

- Other contraindication to statins (i.e. inadequately treated hypothyroidism, renal impairment, liver disease, elevated transaminases, diabetes mellitus or hypersensitivity to a statin)

- Subjects unable to comprehend the investigational nature of the procedure or unable or unwilling to sign the consent.

- Statin usage within the last six months prior to enrollment.

- Diabetes mellitus

- Subjects not willing to participate in the gene expression analysis and whole genome expression and polymorphisms studies portion of this protocol.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda Maryland

Sponsors (1)

Lead Sponsor Collaborator
National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To elucidate the effects of a four week course of statins on the immune system in healthy volunteers with normal cholesterol with or without elevated C- reactive protein. An understanding of the mechanism by which statins effect the immune system may help us better define the patient population that might benefit from such therapy and potentially develop drugs that act more selectively and potently on the relevant immunologic pathway(s). We will also address the potential antithrombotic activity of statins.This study has been slow to recruit healthy subjects with elevated CRP, often because subjects with elevated CRP had mild abnormalities on a detailed history and physical exam, such as impaired fasting glucose. In addition, preliminary analysis of the cohort of normal CRP suggests a significant reduction in serum IL-17 during statin therapy. Psoriasis is an inflammatory disease that affects the skin and the joints, is assumed to be IL-17 driven17, and subjects are usually free of systemic imunosuppression.
Secondary To describe the effects of statins on platelet activity and coagulation during thrombus formation.
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