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Exercise And Rosuvastatin Treatment: Is There an Anti-Inflammatory Synergy?

Primary Purpose

Nonfamilial Hypercholesterolemia, Physical Inactivity

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Rosuvastatin
Exercise Training
Sponsored by
Purdue University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nonfamilial Hypercholesterolemia focused on measuring Hypercholesterolemia, Exercise, Statin, Rosuvastatin, TLR4, Inflammation

Eligibility Criteria

40 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Nonfamilial hypercholesterolemia Total cholesterol >200 mg/dl, LDL >130 mg/dL Physical inactivity Moderate to low alcohol intake Exclusion Criteria: Liver or kidney disease Acute illness or infection Use of corticosteroids, ACE inhibitors, platelet aggregating inhibitors, thiazolidinediones, and bis-phosphonates. Use of cyclosporine, warfarin, gemfibrozil or other lipid lowering agents Regular antacid or aspirin use Type I & II diabetes with insulin treatment hypothyroidism, and/or renal insufficiency Chronic/debilitating osteoarthritis Rheumatoid arthritis Central or peripheral nervous system disorders Anti-depressant medications Major affective disorder HIV infection or auto-immune disorders Use of tobacco products unexplained or intended weight loss of > 2 kg during the previous six months Surgery within the previous three months

Sites / Locations

  • Purdue University

Outcomes

Primary Outcome Measures

The following measures will be made at 0, 10 and 20 weeks:
Monocyte cell-surface expression of TLR4, CD14, and CD16
LPS-stimulated whole blood production of IL-6 and TNF-α
Serum levels of hsCRP and TNF-α
Serum levels of Endotoxin LDL, OxLDL, HDL, sCD14, and
Lipopolysaccharide Binding Protein.

Secondary Outcome Measures

Creatine kinase & ALT (0, 5, 10 weeks; rosuvastatin group)
Creatine kinase & ALT (48hrs after 1st and 5th exercise
bout; rosuvastatin + exercise group)

Full Information

First Posted
February 21, 2006
Last Updated
April 19, 2007
Sponsor
Purdue University
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1. Study Identification

Unique Protocol Identification Number
NCT00295373
Brief Title
Exercise And Rosuvastatin Treatment: Is There an Anti-Inflammatory Synergy?
Official Title
Phase 4 Clinical Trial to Examine the Role of Rosuvastatin and Exercise Treatment in Modulating Inflammatory Response in Hypercholesterolemic Subjects
Study Type
Interventional

2. Study Status

Record Verification Date
April 2007
Overall Recruitment Status
Unknown status
Study Start Date
February 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2007 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Purdue University

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine whether the effects of rosuvastatin treatment and exercise training can be synergistic, with respect to the innate immune receptor TLR4, markers of systemic inflammation, and stimulated production of inflammatory cytokines, in hypercholesterolemic subjects. It is hypothesized that a rosuvastatin and exercise intervention will synergistically lower measured variables, so as to be anti-inflammatory.
Detailed Description
Both statin drugs and exercise training are known to exert anti-inflammatory effects. We found that both high levels of physical activity and an exercise training program reduced markers of inflammation and lowered monocyte Toll-like receptor 4 (TLR4) expression. It has not been determined whether statins exert their anti-inflammatory effects through the toll-like receptors or whether combined statin/exercise treatment will exert synergistic anti-inflammatory effects. Thus, the primary purposes of this study are two-fold: 1) Determine whether rosuvastatin treatment downregulates LPS-induced inflammatory responses, serum hsCRP, and monocyte TLR4 expression in hypercholesterolemic patients; and 2) Determine whether adding exercise training to rosuvastatin treatment induces an anti-inflammatory synergy and further lowers LPS-induced inflammatory response, hsCRP, and TLR4 expression. Thirty two hypercholesterolemic (total cholesterol > 200 mg/dL, LDL > 130 mg/dL) will be randomly divided into two groups: statin (ST) and statin and exercise (ST+E). Sixteen physically active, no-statin subjects will also be recruited as a control group(CON). After baseline blood sampling, ST and ST+E groups will begin a 10-week course of rosuvastatin calcium treatment (10 mg/d) after which a second blood sample will be obtained. The ST+E group will then begin a 10 week (three days per week) combined endurance (20 min at 70% of heart rate reserve) and resistive training (2 sets of 10 upper- and lower-body exercises) program. The ST group will not exercise and both ST+E and ST groups will continue taking their medication, as prescribed. A final blood sample will be taken at the end of this 10-week segment. Blood samples will also be taken from the CON group at 0, 10 and 20 weeks. Monocyte expression of TLR4, CD14 (LPS receptor) and CD16 (monocyte maturation marker) will be assessed using flow cytometry. LPS-stimulated inflammatory cytokine production and serum levels of hsCRP, TNF-a, oxLDL, LDL, HDL, endotoxin, LPS binding protein, and sCD14 will also be measured at each time point (baseline, 10 weeks, 20 weeks). These experiments will allow us to determine whether rosuvastatin downregulates TLR4, an important mediator of inflammation, and whether exercise, known to lower TLR4 expression, can augment the rosuvastatin effects. Regular exercise and statin treatment are known to reduce disease risk, but the benefits of these treatments is infrequently attributed to their anti-inflammatory effects. It is important to document mechanisms of anti-inflammatory action for exercise training and statin treatment and to determining whether these treatments have combined beneficial effects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nonfamilial Hypercholesterolemia, Physical Inactivity
Keywords
Hypercholesterolemia, Exercise, Statin, Rosuvastatin, TLR4, Inflammation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
48 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Rosuvastatin
Intervention Type
Behavioral
Intervention Name(s)
Exercise Training
Primary Outcome Measure Information:
Title
The following measures will be made at 0, 10 and 20 weeks:
Title
Monocyte cell-surface expression of TLR4, CD14, and CD16
Title
LPS-stimulated whole blood production of IL-6 and TNF-α
Title
Serum levels of hsCRP and TNF-α
Title
Serum levels of Endotoxin LDL, OxLDL, HDL, sCD14, and
Title
Lipopolysaccharide Binding Protein.
Secondary Outcome Measure Information:
Title
Creatine kinase & ALT (0, 5, 10 weeks; rosuvastatin group)
Title
Creatine kinase & ALT (48hrs after 1st and 5th exercise
Title
bout; rosuvastatin + exercise group)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Nonfamilial hypercholesterolemia Total cholesterol >200 mg/dl, LDL >130 mg/dL Physical inactivity Moderate to low alcohol intake Exclusion Criteria: Liver or kidney disease Acute illness or infection Use of corticosteroids, ACE inhibitors, platelet aggregating inhibitors, thiazolidinediones, and bis-phosphonates. Use of cyclosporine, warfarin, gemfibrozil or other lipid lowering agents Regular antacid or aspirin use Type I & II diabetes with insulin treatment hypothyroidism, and/or renal insufficiency Chronic/debilitating osteoarthritis Rheumatoid arthritis Central or peripheral nervous system disorders Anti-depressant medications Major affective disorder HIV infection or auto-immune disorders Use of tobacco products unexplained or intended weight loss of > 2 kg during the previous six months Surgery within the previous three months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert E Hannemann, MD
Organizational Affiliation
Purdue University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michael G Flynn, PhD
Organizational Affiliation
Purdue University
Official's Role
Study Director
Facility Information:
Facility Name
Purdue University
City
West Lafayette
State/Province
Indiana
ZIP/Postal Code
47906
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
15963685
Citation
Stewart LK, Flynn MG, Campbell WW, Craig BA, Robinson JP, McFarlin BK, Timmerman KL, Coen PM, Felker J, Talbert E. Influence of exercise training and age on CD14+ cell-surface expression of toll-like receptor 2 and 4. Brain Behav Immun. 2005 Sep;19(5):389-97. doi: 10.1016/j.bbi.2005.04.003.
Results Reference
background
PubMed Identifier
15514501
Citation
McFarlin BK, Flynn MG, Campbell WW, Stewart LK, Timmerman KL. TLR4 is lower in resistance-trained older women and related to inflammatory cytokines. Med Sci Sports Exerc. 2004 Nov;36(11):1876-83. doi: 10.1249/01.mss.0000145465.71269.10. Erratum In: Med Sci Sports Exerc. 2005 Feb;37(2):345.
Results Reference
background
PubMed Identifier
15860745
Citation
Methe H, Kim JO, Kofler S, Nabauer M, Weis M. Statins decrease Toll-like receptor 4 expression and downstream signaling in human CD14+ monocytes. Arterioscler Thromb Vasc Biol. 2005 Jul;25(7):1439-45. doi: 10.1161/01.ATV.0000168410.44722.86. Epub 2005 Apr 28.
Results Reference
background
Links:
URL
http://www.irb.purdue.edu/
Description
Committee on the use of Human Research Subjects at Purdue University

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Exercise And Rosuvastatin Treatment: Is There an Anti-Inflammatory Synergy?

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