NCT01200836

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jul 2010

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2010

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

September 10, 2010

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 14, 2010

Completed
8.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

October 4, 2018

Completed
Last Updated

October 9, 2018

Status Verified

October 4, 2018

First QC Date

September 10, 2010

Last Update Submit

October 5, 2018

Conditions

Keywords

StatinsImmune ModulationHealthy Volunteer

Outcome Measures

Primary Outcomes (1)

  • 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 Outcomes (1)

  • To describe the effects of statins on platelet activity and coagulation during thrombus formation.

Eligibility Criteria

Age18 Years - 99 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, Maryland, 20892, United States

Location

Related Publications (1)

  • Karmaus PW, Shi M, Perl S, Biancotto A, Candia J, Cheung F, Kotliarov Y, Young N, Fessler MB; CHI Consortium. Effects of rosuvastatin on the immune system in healthy volunteers with normal serum cholesterol. JCI Insight. 2019 Nov 1;4(21):e131530. doi: 10.1172/jci.insight.131530.

Study Officials

  • Angelique Biancotto, Ph.D.

    National Institute of Allergy and Infectious Diseases (NIAID)

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
NIH
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 10, 2010

First Posted

September 14, 2010

Study Start

July 1, 2010

Study Completion

October 4, 2018

Last Updated

October 9, 2018

Record last verified: 2018-10-04

Locations