The Effect of Statins on Skeletal Muscle Function
Statins are a group of medications that are used to lower cholesterol levels. Although serious side effects are rare, some people taking statins experience muscle pain or weakness. This study will evaluate the number of people who experience mild muscle complaints and will determine the effect of statins on skeletal muscle strength, endurance, and aerobic exercise performance.
Description
Statins are the most effective medications for reducing high cholesterol levels. They are extremely well tolerated by the majority of people but can produce a variety of muscle-related side effects in some people. Of these side effects, the most serious is rhabdomyolysis, which involves muscle fiber damage that can begin as muscle pain and progress to a loss of muscle cells, kidney failure, and death. While rhabdomyolysis is extremely rare, some people experience the more common muscle-related side effects of statins, such as muscle pain (known as “myalgia”), cramps, and weakness. These more common side effects warrant attention because they may limit the use of statins, affect mobility, and increase the risk of injury in older individuals. Also, the term “muscle weakness,” often used by patients and their doctors, is not well defined and can refer to a wide range of complaints from simple fatigue to an actual inability to perform activities of daily living. It is important to describe and quantify in more detail the muscle-related side effects associated with statins. The purpose of this study is to determine the incidence of statin-induced mild muscle complaints and to determine the effect of statins on skeletal muscle strength, endurance, and aerobic exercise performance.
This study will enroll healthy people who have never received statin medications. First, participants will attend three study visits over a period of 2 weeks. These study visits will include blood collection, questionnaires on physical activity and pain, vital sign measurements, and body measurements, including height, weight, and head circumference. Participants will also complete two cardiopulmonary exercise stress tests on a treadmill and will undergo arm and leg strength testing. Some participants may undergo a muscle biopsy. Participants will then be randomly assigned to receive either 80 mg of atorvastatin or placebo on a daily basis for 6 months. Blood will be collected again at Month 3. At Month 6, participants will attend two study visits for repeat baseline measurements. All participants will be contacted by phone every other week during the 6-month treatment period to monitor adverse events and medication compliance.
Status: Recruiting (N/A). Started on January 1st, 2008.
Enrollment: 440 subjects
Study Type: Interventional
Study Design:
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Double Blind (Subject
- Investigator)
Conditions:
Interventions:
- Drug: Atorvastatin (Lipitor)
- Drug: Placebo
Eligibility
Inclusion Criteria:
- Statin-naive (i.e., has never taken statins before)
Exclusion Criteria:
Previous use of statins
Current treatment with cholesterol- or triglyceride-lowering drugs
Impaired liver or kidney function
Untreated hypothyroidism or hyperthyroidism
Treatment with other medications known to increase risk of myopathy in atorvastatin-treated patients (e.g., cyclosporine, azithromycin, erythromycin, azole antifungals, fusidic acid)
Existing infection requiring treatment with antibiotic therapy
Consumption of greater that 1 quart of grapefruit juice per day
Documented history of neuroleptic malignant syndrome
Inherited muscle disorders or myopathy
Known sickle cell trait
Cancer within the 5 years prior to study entry
Currently being treated for high blood pressure
Coronary artery disease
Peripheral vascular disease
Physical disability or previous injury that prevents safe exercise testing
Pregnant or breastfeeding
- Gender
Both
- Mininum Age
20 Years
- Maximum Age
N/A
- Healthy Volunteers
Accepts Healthy Volunteers
Resources
Source: National Heart, Lung, and Blood Institute (NHLBI)
Authority: United States: Federal Government
Locations
-
Hartford Hospital
Hartford
Connecticut
06102
United States
-
University of Connecticut
Storrs
Connecticut
06269
United States
-
University of Massachusetts
Amherst
Massachusetts
01003
United States
Officials
Paul D. Thompson, MD (Principal Investigator, Hartford Hospital)
Sponsors
National Heart, Lung, and Blood Institute (NHLBI) (Lead Sponsor)
References
None.
Links
None.
- Date Verified
- April 1st, 2010
- First Received
- April 7th, 2010
- Last Changed
- April 7th, 2010
Information obtained from ClinicalTrials.gov on June 09, 2011. Link to the current ClinicalTrials.gov record.
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