Brain Structure and Clinical Endpoints in Myotonic Dystrophy Type 2 (BraCE-DM2)

Wake Forest University (WFU)

Status: Enrolling

Conditions: Myotonic Dystrophy Type 2; Myotonic Dystrophy Type 1

Treatments: Other: Non-interventional study

Study type: Observational

Funder types: Other; NIH

Identifiers

NCT05854433

IRB00065459

K23NS125110-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Nearly two-third of patients with myotonic dystrophy type 2 (DM2) report that impaired cognition is among the most disabling symptoms and deeply affects their quality of life. Yet, relatively little is known about how DM2 affects brain structure and cognitive function as brain imaging studies in DM2 are extremely limited. This is a prospective, cross-sectional study of brain structure and function on cognitive and motor performance in patients with DM2 & DM1 compared to healthy controls. All participants will undergo magnetic resonance imaging (MRI) to evaluate brain structure and white matter integrity, a comprehensive battery of cognitive and motor measures, self-reported questionnaires, and blood collection for brain-based biomarker analysis. A subset of participants will undergo lumbar puncture for cerebrospinal fluid (CSF) collection for additional biomarker analysis and validation. This work is critical to inform the development of rigorous clinical trial designs and plan for a longitudinal study to evaluate MRI measures as imaging biomarkers of disease progression and therapeutic response in DM2 & DM1.

Full description

Myotonic dystrophy type 2 (DM2), autosomal dominant muscular dystrophy, is characterized by late-onset proximal muscle weakness, myotonia, and multisystem features. Although muscle weakness is the key symptom, almost 70% of patients with DM2 report that impaired cognition is among the most disabling symptoms and affects their quality of life. This condition causes severe disability and impaired quality of life similar to those in myotonic dystrophy type 1 (DM1).Small literature describes cognitive deficits and cerebral white matter involvement in those with DM2, compared to controls. However, the mechanisms that lead to cognitive dysfunction are poorly understood.

As the momentum of therapeutic development is outpacing our understanding of the central nervous system (CNS) manifestations in myotonic dystrophy, there is an urgent need to identify measures of brain imaging, cognitive function, and biomarkers of CNS pathology that are disease-specific and clinically relevant, and establish relationships of these measures to inform future clinical trial designs in DM2. This study will carry out a comprehensive baseline characterization of 50 adults with DM2 and 50 age and gender-matched controls identified from clinical populations across the US and through the national myotonic dystrophy registry. A subset of DM1 cohort (n=20), aged over 40 years and without contraindications to MRI, will be invited to participate in the full study protocol similar to the DM2 group. All participants will undergo 3 Tesla (3T)-brain MRI to obtain voxel-based morphometry and diffusion tensor imaging (DTI) sequences, a comprehensive Clinical Assessment Battery (CAB) of cognitive and motor measures, patient-reported outcomes, and blood collection for analysis of CNS biomarkers at their baseline visits. A subset of 20 participants will undergo lumbar punctures to collect cerebrospinal fluid (CSF) specimens for additional biomarker analysis and validation. Measures of MRI, CAB, and fluid biomarkers will be compared between DM2, DM1 and controls.

Relationships between MRI measures, cognitive and motor endpoints, and biofluid (plasma and CSF) biomarkers will be analyzed within the DM2 & DM1 group. Validation of plasma and CSF biomarkers will also be determined.

Enrollment: 100 estimated patients

Sex: All

Ages: 30 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

DM 2 Inclusion Criteria:

• Age 30-65 years old
• Diagnosis of DM1 or DM2 is based on genetic testing and/or clinical criteria. If the diagnosis is based on clinical criteria, positive DM2 genetic testing is required in first-degree relatives
• Symptoms or clinical findings of proximal muscle weakness
• Ambulate independently (a cane or walking stick is permitted)
• Able to provide informed consent for participation in the study

DM1 Inclusion Criteria:

• Only individuals who are 30-65 years old will be eligible to participate for the full study protocol
• Diagnosis of adult-onset DM1 is based on genetic testing or clinical criteria. If the diagnosis is based on clinical criteria, positive DM1 genetic testing is required in first-degree relatives
• The onset of first symptoms must be between the 2nd and 4th decades of life
• Symptoms or clinical findings of distal muscle weakness and myotonia
• Ambulate independently (a cane or walking stick is permitted)
• Able to provide informed consent for participation in the study

DM 1 Exclusion Criteria:

• Congenital or juvenile-onset DM1 (onset of first symptom < 20-year-old)
• Individuals with a prior diagnosis of dementia, seizure, stroke, multiple sclerosis, Parkinson's Disease, or other neurodegenerative diseases
• Individuals with active psychiatric illness or alcohol/substance abuse.
• On medications with substantial sedative or cognitive side effects unless the doses have been stable for at least 3 months before the study visit.
• Inability or unwillingness to give written informed consent.

DM 1 and 2 and Healthy Control (HC) Exclusion Criteria:

• Individuals with a pacemaker, defibrillator, or metal implanted that is contraindicated for MRI
• Individuals who are claustrophobic
• Individuals with a prior diagnosis of dementia, seizure, stroke, multiple sclerosis, Parkinson's Disease, or other neurodegenerative diseases
• Individuals with active psychiatric illness, alcohol or substance abuse, or dependence
• Individuals with a pacemaker, defibrillator, or metal implanted that is contraindicated for MRI
• Individuals who are claustrophobic
• Major medical illness which would prevent safe testing of MRI or motor function.
• On medications with substantial sedative or cognitive side effects unless the doses have been stable over the last 3 months before the study visit
• pregnancy
• Weight > 400 pounds as the participant could not be properly positioned on the MRI table
• Inability or unwillingness to give written informed consent
• For participants who undergo lumbar puncture procedure: Use of anti-platelet medications within 7 days, use of anticoagulants such as warfarin (Coumadin), history of a bleeding disorders, evidence of platelet count < 150,000 within the last 6 months, or have hardware (i.e., pins, screws, rods, etc.) in the lower back area

Healthy Control (HC) Inclusion Criteria:

• Age 30-65 years
• Ambulate independently
• Able to provide informed consent for participation in the study

Trial design

100 participants in 2 patient groups

Myotonic dystrophy types 1 and 2

Description:

Adults with myotonic dystrophy types 1 and 2 who meet all inclusion and exclusion criteria for the study. To be assessed at the baseline visit: Medical history and a focused neurological examination, brain MRI, a comprehensive Clinical Assessment Battery (CAB) of cognitive and motor measures, self-reported questionnaires, strength and motor function evaluation, and blood drawn for biomarker analysis. A subset of the participants who agree to have cerebrospinal fluid (CSF) collection for additional biomarker analysis will undergo lumbar puncture procedure.

Treatment:

Other: Non-interventional study

Controls

Description:

Healthy individuals who meet all inclusion and exclusion criteria for healthy controls. To be assessed at the baseline visit: Medical history and a focused neurological examination, brain MRI, a comprehensive Clinical Assessment Battery (CAB) of cognitive and motor measures, self-reported questionnaires, strength and motor function evaluation, and blood drawn for biomarker analysis. A subset of the participants who agree to have cerebrospinal fluid (CSF) collection for additional biomarker analysis will undergo lumbar puncture procedure.

Treatment:

Other: Non-interventional study