Spinal Cord Gray Matter Imaging in Spinal Muscular Atrophy

NCT ID: NCT06137612

Last Updated: 2023-11-18

Basic Information

• Recruitment Status: ENROLLING_BY_INVITATION
• Total Enrollment: 52 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2020-08-17
• Study Completion Date: 2025-09-15

Brief Summary

This study aims to measure the spinal cord gray matter in patients with spinal muscular atrophy (SMA) type II and III in comparison with age- and sex-matched healthy controls (HC) using rAMIRA (radially sampled averaged magnetization inversion recovery acquisitions) imaging, a novel MRI (Magnetic Resonance Imaging) method. Patient and HC undergo MRI examinations, clinical/neurological (handheld dynamometry) and electrophysiological investigations (MUNIX, Motor Unit Number Index). Serum markers of neuro-axonal and astrocytic injury are also assessed.

Detailed Description

Patients with the diagnosis of 5q-SMA (spinal muscular atrophy) types II or III (confirmed by genetic testing) will be recruited. Healthy age and sex-matched controls will also be investigated.

Patients will be neurologically investigated at the Neurology Policlinic, University Hospital Basel, including standard muscle force measurements on the British Medical Council (BMC) grade, and quantitative muscle force tests by hand held dynamometer of selected muscles.

All patients will also complete the SMA functional rating scale (SMA-FRS). Age and sex matched healthy controls will also undergo a standardized neurological examination to ensure that no other neurological condition is present that could potentially interfere with the test results.

All participants will be scanned on the same 3 Tesla MR-Scanner (Magnetom PRISMA, Siemens Healthineers) at the University Hospital Basel. The protocol includes axial 2D rAMIRA imaging at selected levels of cervical and thoracic spinal cord at the intervertebral disc levels perpendicular to the spinal cord, and diffusion tensor imaging (DTI) at selected positions, a standard diagnostic high-resolution T2w sequence of the spinal cord and a high-resolution T1w structural imaging of the brain for cortical/subcortical volumetry.

Serum biomarkers will also be evaluated including serum neurofilament light chain (NfL) levels .

MUNIX is an electrophysiological method that is used in clinical routine in many neuromuscular centers to quantitate the number of functioning motor units. Patients and controls will undergo MUNIX testing .

Patients will be examined by a professional physiotherapist to assess the Motor Function Measure (MFM), Revised Hammersmith Scale for SMA, Revised Upper Limb Module, time to rise from the floor, and 6 minutes walk test.

Conditions

Spinal Muscular Atrophy Type III; Spinal Muscular Atrophy Type II

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Patients with SMA

Patients with SMA type II and III

MRI

Intervention Type: DIAGNOSTIC_TEST

axial 2D rAMIRA (radially sampled averaged magnetization inversion recovery acquisitions) imaging at selected levels of cervical and thoracic spinal cord at the intervertebral disc levels perpendicular to the spinal cord.

Healthy controls

Age- and sex-matched HC

MRI

Intervention Type: DIAGNOSTIC_TEST

axial 2D rAMIRA (radially sampled averaged magnetization inversion recovery acquisitions) imaging at selected levels of cervical and thoracic spinal cord at the intervertebral disc levels perpendicular to the spinal cord.

Interventions

MRI

axial 2D rAMIRA (radially sampled averaged magnetization inversion recovery acquisitions) imaging at selected levels of cervical and thoracic spinal cord at the intervertebral disc levels perpendicular to the spinal cord.

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

1. 11 years or older

2. Informed consent by the participants or, in children below the age of legal consent, by a legally authorized representative

3. genetically confirmed diagnosis of 5q-SMA (Types II or III)

1. participants will be selected to be age-and sex-matched to the patients

2. 11 years or older

3. Informed consent by the participants or, in children below the age of legal consent, by a legally authorized representative

Exclusion Criteria

1. active other neurological or neuromuscular condition explaining the symptoms or a significant part of it

2. other neurological or neuromuscular conditions interfering with the examinations

3. other severe chronic disease

4. pregnancy

5. general contraindications against MRI scanning (e.g. pacemakers)

6. not able to understand the patient information due to language barriers

7. In the event of a participant incapable of judgment, symptoms showing that the participant is unwilling to participate in the study will result in the participant being excluded from participation

1. active neurological or neuromuscular condition

2. other neurological or neuromuscular conditions interfering with the examinations

3. other severe chronic disease

4. pregnancy

5. general contraindications against MRI scanning (e.g. pacemakers)

6. not able to understand the patient information due to language barriers

7. In the event of a participant incapable of judgment, symptoms showing that the participant is unwilling to participate in the study will result in the participant being excluded from participation

• Minimum Eligible Age: 11 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University Hospital, Basel, Switzerland

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

University Hospital Basel

Basel, Canton of Basel-City, Switzerland

Countries

Switzerland

Other Identifiers

SMA_SC_Imaging_1

Identifier Type: -

Identifier Source: org_study_id