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7 Tesla MRI Study in Patients With Statin Related Muscle Complaints

7 Tesla MRI Study in Patients With Statin Related Muscle Complaints

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04575090
Enrollment
8
Registered
2020-10-05
Start date
2016-03-05
Completion date
2021-06-23
Last updated
2022-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscle Aches, Muscle Cramp, Muscle Stiffness, Muscle Weakness, Statin-related Muscle Pain

Brief summary

Roughly 5-10% of statin-treated patients report muscle pain, aches, weakness, cramps, stiffness, or heaviness - typically occurring symmetrically in the legs. For healthcare providers, the major diagnostic challenge is to unambiguously link these symptoms to statin use, especially since some patients can have normal serum creatine kinase (CK) levels despite demonstrable weakness and muscle biopsy proven statin-induced myopathy . No well accepted, standardized, or Food and Drug Administration (FDA)-endorsed diagnostic method exists for statin-induced muscle injury. This lack of an objective diagnostic methodology blocks vertical advancement of the field. The successful completion of this project will develop in vivo techniques that will provide insight into how statins affect muscle metabolism and help establish a methodology to objectively diagnose muscle injury due to statins. The development of an MRS technique will allow for in-vivo analyses and the data accumulated here will serve as preliminary data for futher extramural funding of studies with much larger sample sizes. Ultimately, this focus of research will lead to improved diagnosis and treatment of patients with statin-related muscle complaints, which is central to obtaining the cardiovascular risk reduction from lipid-lowering drugs.

Detailed description

The goal of the first study will be to generate hypothesis regarding the long-term effects of statin in muscles by studying 7T MRS findings in patients who are currently experiencing statin-related muscle complaints or who have a history of severe reactions to statins (i.e. rhabdomyolysis, anti-HMGCR-associated autoimmune myopathy, or CK elevation \> 10 times the upper limit of normal). We anticipate enrolling roughly 5 such patients. The protocol involves a single visit for a blood draw and MRS of calf muscle. The data will be compared to historical controls provided by the Advanced Imaging Research Center. Second, we will study the effect of short-term statin administration in 5 patients with a history of statin related muscle complaints and 5 controls with no statin related muscle complaints . Controls will be matched for age, weight, and body mass index. Patients will undergo a wash-out of lipid lowering drugs followed by a challenge with simvastatin 40 mg daily (similar to a statin withdrawal and rechallenge). We chose simvastatin since it is the most common statin that caused myopathy according to our preliminary data (as well as most other published reports). Each patient will have 5 visits. The screening visit will involve a review of inclusion/exclusion criteria, blood draw, questionnaire, and instructions to withhold all lipid lowering drugs until visit 1. Any patient with known antibodies to HMGCR will be excluded from the remainder of the study. Visit 1 will occur 2 weeks after stopping all lipid lowering drugs. A minimum 2 week period off lipid lowering drugs is required to allow clearance of any medication from the systemic circulation. Patients will undergo MRS of the calf muscle and a blood draw. Patients will then start simvastatin 40 mg daily.

Interventions

DRUGSimvastatin

Simvastatin 40 mg daily.

Sponsors

Garg, Abhimanya, M.D.
CollaboratorINDIV
Prishant Mishra
CollaboratorUNKNOWN
Jimin Ren
CollaboratorUNKNOWN
University of Texas Southwestern Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

Adults age \>18 yrs or \<80 yrs Patients reporting complaints of statin-associated muscle symptoms, aches, weakness, cramps, or stiffness of legs.

Exclusion criteria

Patients who drink large quantities of grapefruit juice (\>1 quart daily)

Design outcomes

Primary

MeasureTime frameDescription
Change in Pre- and Post-phosphocreatine Relaxation TimeBaseline, 10 WeeksMeasure differences in pre- and post-phosphocreatine relaxation time in SAMS (Statin Associated Muscle Symptoms) patients on simvastatin compared to placebo.

Countries

United States

Participant flow

Pre-assignment details

Arm 1 is an observational study. No intervention involved. No data was collected for arm 1

Participants by arm

ArmCount
No Intervention: Arm 1 (Observational Arm)
Patients in arm 1 will be identified by the PI from the clinic as individuals who are currently experiencing statin related muscle complaints or who have had severe reactions to statins in the past. There is going to be only one visit which will last for apprximately 3.5 hrs. Subjects will have height, weight and vitals measured. They will be asked pain and and demographic questionnaire. They will have their blood draw and will undergo MRS.
0
Experimental: Arm 2 (Interventional Experimental Arm)
Subjects with statin related muscle complaints were enrolled in this arm and will have 3 visits. First visit is screening visit which will last for about 2 hrs and the next 2 visits will last for about 3.5 hrs. The screening visit will occur 2 weeks prior to visit 1. Subjects will have height, weight and vitals measured. They will be asked pain and and demographic questionnaire. They will have their blood draw and will undergo MRS. Some volunteers who do/do not regularly exercise or are/are not active in sports may be asked to exercise prior to the MRS. This exercise may be in the form of hand grasps, toe-raises, bicycling on a stationary bike or walking on a treadmill. Exercise will be limited to up to one hour, during which time the subject's vital signs and blood oxygenation will be monitored. During the scan, the subject's heart rate and respiratory rate may be monitored
7
Experimental: Arm 3 (Interventional Control Arm)
Subjects with no statin related muscle complaints were enrolled in this arm and will have 3 visits. First visit is screening visit which will last for about 2 hrs and the next 2 visits will last for about 3.5 hrs. The screening visit will occur 2 weeks prior to visit 1. Subjects will have height, weight and vitals measured. They will be asked pain and and demographic questionnaire. They will have their blood draw and will undergo MRS. Some volunteers who do/do not regularly exercise or are/are not active in sports may be asked to exercise prior to the MRS. This exercise may be in the form of hand grasps, toe-raises, bicycling on a stationary bike or walking on a treadmill. Exercise will be limited to up to one hour, during which time the subject's vital signs and blood oxygenation will be monitored. During the scan, the subject's heart rate and respiratory rate may be monitored
1
Total8

Baseline characteristics

CharacteristicNo Intervention: Arm 1 (Observational Arm)Experimental: Arm 2 (Interventional Experimental Arm)Experimental: Arm 3 (Interventional Control Arm)Total
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants5 Participants0 Participants5 Participants
Age, Categorical
Between 18 and 65 years
0 Participants2 Participants1 Participants3 Participants
BMI31.2 kg/m^2
STANDARD_DEVIATION 6
22 kg/m^2
STANDARD_DEVIATION 0
26.6 kg/m^2
STANDARD_DEVIATION 6
Phospho Creatnine/ Adenosine Triphosphate (PCr/gATP)4.765 ratio
STANDARD_DEVIATION 0.459
4.344 ratio
STANDARD_DEVIATION 0
12.85 ratio
STANDARD_DEVIATION 0.29
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants3 Participants1 Participants4 Participants
Race (NIH/OMB)
Black or African American
0 Participants2 Participants0 Participants2 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
0 Participants2 Participants0 Participants2 Participants
Sex: Female, Male
Female
0 Participants4 Participants0 Participants4 Participants
Sex: Female, Male
Male
0 Participants3 Participants1 Participants4 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 00 / 70 / 1
other
Total, other adverse events
0 / 00 / 70 / 1
serious
Total, serious adverse events
0 / 00 / 70 / 1

Outcome results

Primary

Change in Pre- and Post-phosphocreatine Relaxation Time

Measure differences in pre- and post-phosphocreatine relaxation time in SAMS (Statin Associated Muscle Symptoms) patients on simvastatin compared to placebo.

Time frame: Baseline, 10 Weeks

Population: Arm 1 is an observational study. No intervention involved. No data was collected for arm 1 Arm 2: Data of 5 subjects were analyzed. For the remaining 2 - data was not analyzable.

ArmMeasureValue (MEAN)Dispersion
Experimental: Arm 2 (Interventional Experimental Arm)Change in Pre- and Post-phosphocreatine Relaxation Time5.58 millisecondsStandard Deviation 1.6
Experimental: Arm 3 (Interventional Control Arm)Change in Pre- and Post-phosphocreatine Relaxation Time5.083 millisecondsStandard Deviation 0

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026