MRI and Muscle Involvement in Patients With Mutations in GMPPB

Completed

• Conditions: Limb-girdle Muscular Dystrophy

• Registration Number: NCT02635321
• Lead Sponsor: Rigshospitalet, Denmark

Brief Summary

Limb girdle muscular dystrophies (LGMD) are a very heterogeneous group of muscle disorders characterized by muscle weakness and atrophy of the proximal muscles of the shoulder and pelvic girdles. LGMD is classified based on its inheritance pattern and genetic cause into more than 31 different types.

A new type - type 2T has been found. The genetic cause of type 2T is mutations in Guanosine Diphosphate (GDP)-mannose pyrophosphorylase B (GMPPB). Mutations in GMPPB can also cause Congenital muscular dystrophies (CMD). Only 41 patients with mutations in GMPPB has been reported.

In this study, the investigators examine five new cases with the LGMD phenotype. The primary aim is to examine the muscle involvement using MRI.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-11
• Study First Submitted: 2015-12-01
• Study First Submitted QC: 2015-12-15
• Study First Posted: 2015-12-18
• Status Verified: 2016-04
• Primary Completion: 2016-04
• Study Completion: 2016-04
• Last Update Submitted: 2016-04-05
• Last Update Posted: 2016-04-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 4

Inclusion Criteria

• Persons with genetically verified mutations in GMPPB

Exclusion Criteria

• All contraindications for undergoing an MRI scan

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
MRI scan for qualitative analysis of muscle involvement	One MRI scan per subject (exam lasts approximately 60 min.)	The MRI protocol include T1-weighted brain and whole body examination. Four cross-sectional slices at shoulder, lumbar back, thigh and calf are chosen for qualitative analysis using the grading scale developed by Mercuri et al. (2007).

Secondary Outcome Measures

Name	Time	Method
Muscle biopsy for biochemical investigation	One muscle biopsy per subject (last approximately 15 min.)	Muscle biopsies from the tibialis anterior muscle and the deltoid muscle will be analyzed for glycosylated α-dystroglycan, merosin and GMPPB. (Concentration determined by standard biochemical analysis).
10 meter walk test	Exam last approximately 5 min.	Measurement of the time it takes to walk 10 meters.
Neurological examination and test of muscle strength	Exam last approximately 15 min.	Muscle strength (in arms and legs) will be examined based on the Medical Research Council (MRC) scale.
Questionnaires	Data will be collected once for patients with LGMD 2T (exam last approximately 45 min.)	Data will be collected using Minimal mental examination (MMSE) and Fatigue Severity Scale (FSS).
Heart examination	Exam last approximately 45 min	Echocardiography and Electrocardiogram (ECG).
Forced Vital Capacity (FVC)	Exam last approximately 15 min	FVC is measured as the best of three attempts using a hand-held spirometer.
Electromyography (EMG)	Exam last approximately 30 min	EMG is used for measuring nerve conducting velocity and neuromuscular activity.

Trial Locations

Locations (1)

Copenhagen Neuromuscular Center; 🇩🇰 Copenhagen, Denmark