Effects of Rosuvastatin on the Immune System in Healthy Volunteers With Normal Cholesterol

NCT ID: NCT01200836

Last Updated: 2018-10-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-07-01

Study Completion Date

2018-10-04

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Healthy Volunteers Statins Immune Modulation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Heart, Lung, and Blood Institute (NHLBI)

NIH

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Angelique Biancotto, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

National Institute of Allergy and Infectious Diseases (NIAID)

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, Maryland, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

References

Explore related publications, articles, or registry entries linked to this study.

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.

Reference Type DERIVED
PMID: 31573980 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

10-H-0165

Identifier Type: -

Identifier Source: secondary_id

100165

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Drug Interaction Study With Rosuvastatin
NCT02101125 COMPLETED PHASE1
Investigation of the Gut Microbiome and Statin Response
NCT04098003 ACTIVE_NOT_RECRUITING PHASE4