Official Title
Genomic Profiling of Mitochondrial Disease - Imaging Analysis for Precise Mitochondrial
Brief Title
Genomic Profiling of Mitochondrial Disease - Imaging Analysis for Precise Mitochondrial Medicine
Protocol ID
NCT05012358
Lead Sponsor
Mayo Clinic
Brief Summary
This study is an observational longitudinal study involving the use of MRIs and video
recordings taken at home of patients completing basic tasks. Once consent is obtained,
subjects will be asked to schedule an appointment with radiology to undergo the listed
MRIs of the heart and/or muscle. Subjects will also be given instructions on how to use
the video recording app on their personal devices, or study provided device. The subjects
will be followed regularly over the course of two years, submitting video recordings of
their movements and reporting to Mayo Clinic for MRIs as scheduled.
Detailed Description
Mitochondrial myopathy follows a slowly progressive disease course of gradual worsening
of muscle weakness and fatigability. Progressive mitochondrial dysfunction is thought to
result in structural muscle deterioration (eventually muscle fiber atrophy/necrosis) and
underlie these symptoms. Therefore, the study hypothesis is that longitudinal imaging of
muscle will capture mitochondrial (using muscle MRS) and structural (using muscle MRI)
abnormalities to inform objectively disease progression by capturing structural and
biochemical changes in muscle over time.
Conventional multivariate analysis tools such as partial least squares-discriminant
analysis (PLS-DA) and principal component analysis (PCA) will be used to assess variables
of importance in discrimination of 3 subgroups based on underlying molecular defect
(mitochondrial DNA (mtDNA) mutations and deletions, and nuclear gene mutations (nDNA)).
This will be followed by implementation of Collaborative Laboratory Integrated Reports
(CLIR) software, a multivariate pattern recognition software that generates
post-analytical interpretive tools. This study proposes to quantitatively measure MRS
analytes (i.e. lactate, adenosine triphosphate (ATP), etc.) and structural muscle changes
by MRI (edema, fat content, etc.). The capability for interactive data analysis would be
necessary because of the nature of mitochondrial myopathy (MM) progression. One of the
functionalities of CLIR is the creation of post-analytical tools applicable to either
diagnosis of one condition - single condition tool; or differential diagnosis between two
conditions with overlapping phenotypes (mtDNA deletions, mtDNA mutations, nDNA mutations)
- dual scatter plots. The advantages of CLIR are (1) integration of primary markers with
all informative permutations of ratios/biomarkers. Ratios calculated between markers not
directly related at the biochemical level are particularly helpful to correct for
pre-analytical factors and potential analytical bias (2) adjusted for multiple covariates
(age, sex) (3) generating individual plots of disease progression.
This study is an observational longitudinal study involving the use of MRIs and video
recordings taken at home of patients completing basic tasks. Subjects will be approached
at outpatient appointments, or via phone/mail. Once consent is obtained, subjects will be
asked to schedule an appointment with radiology to undergo the listed MRIs of the heart
and/or muscle. Subjects will also be given instructions on how to use the video recording
app on their personal devices, or study provided device. The subjects will be followed
regularly over the course of two years, submitting video recordings of their movements
and reporting to Mayo Clinic for MRIs as scheduled. Patients may withdraw from the study
at any time without repercussion.
Study Period
-
Enrollment Count
9 participants
Eligibility Criteria
Inclusion Criteria:
- Confirmed or suspected primary mitochondrial disorder *Suspected mitochondrial
disorder would mean that the patient meets clinical criteria and has either biopsy
or biochemical testing that supports the diagnosis.
Exclusion Criteria:
- Pregnant, breastfeeding
- Severe cardiac disease who are unable to undergo all the required testing
- Requiring anesthesia for MRIs
- Has severe claustrophobia
- Has implanted devices
Filters
Mitochondrial Myopathies
Mitochondrial DNA Mutation
Mitochondrial Diseases
Chronic Progressive External Ophthalmoplegia With Myopathy
Kearns-Sayre Syndrome
COMPLETED
CHILD
ADULT
OLDER_ADULT