Muscle CrCest Muscle Phenotyping in Primary Mitochondrial Disease
Study Details
Study Description
Brief Summary
The purpose of this study is to perform a "muscle phenotyping" magnetic resonance imaging (MRI) assessment in patients receiving clinical care at the Children's Hospital of Philadelphia (CHOP) for mitochondrial disease that is either suspected (based on clinical presentation) or has a definite genetic diagnosis. The MRI assessment quantifies skeletal muscle oxidative phosphorylation (OXPHOS) capacity.
Investigators hope that this study will contribute to our current knowledge of mitochondrial diseases and this study will help create a new diagnostic tool for use in both clinical care and in clinical trials.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
This research study visit will occur on the same day as the participants clinically scheduled MRI. The clinically indicated and study-specific scanning time will not exceed 120 minutes.
During the study visits:
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A study team member will review inclusion and exclusion criteria with the participant
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A study team member will review medical history review with the participant
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A safety assessment will occur prior to study procedures
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Study MRI scan
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During which the participant will use an MRI-safe machine to stimulate exercise, similar to pressing a gas pedal
If eligible participants return to CHOP for future clinical imaging, we will also request a study-specific MRI assessment.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Mitochondrial Disease Individuals with suspected (based on clinical presentation) or definite genetic mitochondrial disease |
Diagnostic Test: Creatine Chemical Exchange Saturation Transfer (CrCEST) Imaging Sequence
CrCEST be used to assess creatine distribution and concentrations in muscle (lower extremity), both at rest and after recovery from a brief foot-pedal depression exercise
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Outcome Measures
Primary Outcome Measures
- Post-exercise CrCEST recovery time (seconds) [During the MRI]
The time it takes after the exercise occurs to recover CrCEST
Secondary Outcome Measures
- Resting CrCEST [During the MRI]
Amount of CrCEST prior to exercise
- Muscle Lipid Content [During the MRI]
Includes both Intramyocellular lipid (IMCL) and extramyocellular lipids (EMCL) content, both expressed in arbitrary units relative to water signal and relative to creatine
- Fat-fraction [During the MRI]
n-point Dixon, expressed as a percentage of the total area
Eligibility Criteria
Criteria
Inclusion Criteria:
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Males and females, between the ages of 7 and 75, inclusive
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Suspected (based on clinical presentation) or definite genetic mitochondrial disease diagnosis (i.e., genetic mutations in the constituents of the mitochondrial respiratory chain and/or genetic mutations that are likely to affect mitochondrial function)
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Undergoing-and screened eligible for-a clinically indicated MRI of the lower leg. Investigators are conducting clinical leg MRI scans of patients with definite mitochondrial disease for indications that include muscle weakness and muscle fatigue.
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Able to perform sub-maximal ankle dorsiflexion leg exercise during the MRI study
Exclusion Criteria:
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In the investigator's opinion, inability to fully comply with research procedures
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Active alcohol and/or substance abuse, including tobacco-use
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A pacemaker; any metal-based medical or non-medical devices/implants; any non-removable metal-based object (e.g., body piercings, jewelry, etc.)
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Any history of intraocular injury or fragment in or around the orbit that cannot be cleared through radiologic evaluation
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Any history of bullet, shrapnel, or stabbing wounds that cannot be cleared through radiologic evaluation
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Past or current employment involving (or exposure to) a metal grinder (e.g., at a construction worksite)
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Claustrophobia or any known medical conditions which can be exacerbated by stress, anxiety, or panic attacks triggered by enclosed spaces
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Inability to lie flat in an MRI scanner for up to 120 minutes
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Any potentially interfering clinical MRI contrast agents, as reviewed with the radiology team
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At the discretion of the principal investigator (PI), any medical condition that will interfere with or prevent the safe completion of the study
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Any female participant with childbearing potential who is knowingly pregnant or suspects that she is pregnant will be removed from the study. (Although there are no known risks of MRI on pregnant females or fetuses, there is a possibility of yet undiscovered pregnancy-related risks. Since there is no direct benefit from participating in this protocol for pregnant females, they will be excluded to ensure their long-term safety and that of their unborn fetus.)
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To note, for this protocol, participants are instructed to lie still in the MRI scanner; there is no contrast or sedation. Participants will be asked to perform a brief (< 2 minute) foot-pedal exercise. Investigators will ensure that total MRI scanning time (i.e., clinically indicated and study-specific scanning) does not exceed 120 minutes within a single day. Participants who do not possess the cognitive and/or physical abilities to perform these procedures will not be included.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Children's Hospital of Philadelphia | Philadelphia | Pennsylvania | United States | 19104 |
Sponsors and Collaborators
- Children's Hospital of Philadelphia
Investigators
- Principal Investigator: Zarazuela Zolkipli Cunningham, MBChB MRCP, Children's Hospital of Phiadelphia
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 19-016520