Muscle Relaxation in Myopathies With Positive Muscle Phenomena

McArdle Disease Clinical Trial

Official title:

Muscle Relaxation Properties in Myopathies With Positive Muscle Phenomena: a Study Using Transcranial Magnetic Stimulation

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT03211923
• Other study ID #: NL57301.091.16
• Status: Enrolling by invitation
• Start date: January 5, 2017
• Est. completion date: December 31, 2019

Study information

• Verified date: September 2018
• Source: Radboud University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The aim of this study is to quantify muscle relaxation properties of the finger flexor muscles in patients with different myopathies. The inhibiting effects of transcranial magnetic stimulation (TMS) on the cortical motor hand area are used to induce relaxation, which in turn will be monitored with handgrip dynamometry and EMG. The investigators will evaluate if this technique can be implemented as a diagnostic tool in clinical practice.

Muscle relaxation is an often overlooked property of the muscle as compared to muscle strength or activation. Muscle relaxation is affected in different myopathies, such as myotonic dystrophy, non-dystrophic myotonias, and Brody myopathy. Therefore, a diagnostic tool to quantify muscle relaxation is of clinical and scientific importance. In this study, transcranial magnetic stimulation (TMS) is used, in combination with a dynamometer to quantify muscle relaxation properties.

Transcranial magnetic stimulation (TMS) is a non-invasive technique that is commonly used to stimulate the brain. In practice, a circular coil is held directly above the scalp, upon which a strong current pulse induces a magnetic field that stimulates the underlying superficial brain areas. This stimulation can have both activating and inhibiting effects.

When the motor cortex (i.e. the area of the brain that controls muscle contractions) is strongly stimulated with TMS during a voluntary muscle contraction, both excitatory and inhibitory effects can be observed in the muscle the targeted cortical area controls. The inhibitory effect entails a transient interruption of neural drive to the muscle. This interruption, called the "silent period", lasts for less than half a second and results in the relaxation of the muscle. Muscle activity and control quickly return to normal after the silent period.

The elegance and main advantage of TMS-induced muscle relaxation lies in the fact that it excludes all voluntary influences on the relaxation process. Furthermore, the TMS pulse causes all muscle fibres involved in the contraction just prior to the onset of the silent period to relax simultaneously. This allows us to study muscle relaxation as only a property of the muscle, i.e. without voluntary influences.

In this study, the investigators will measure muscle relaxation in several myopathies (McArdle disease, Nemaline myopathy type 6 and myotonic dystrophy type 2) and compare this to healthy controls and to controls with no myopathy but with similar complaints (myalgia, stiffness, cramps). The data from these two control groups has been gathered previously in a different study. The investigators will also compare this to patients suffering from Brody disease who were previously measured in a different study.

Muscle relaxation will be evaluated in fresh and fatigued finger flexor muscles. The main outcome of this study is the peak relaxation rate normalized to the peak force preceding relaxation.

The final outlook of this research is to evaluate whether muscle relaxation studied with TMS, can be used for different myopathies as a diagnostic tool, to monitor disease progression, and to study the effects of different interventions (e.g. medication, exercise).

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 30
• Est. completion date: December 31, 2019
• Est. primary completion date: December 31, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Diagnosis of one of the following myopathies: Nemaline myopathy type 6 (NEM6), Myotonic dystrophy type 2 (DM2), McArdle disease.

Exclusion Criteria:

• Pregnancy

• Serious head trauma or brain surgery

• Large or ferromagnetic metal parts in the head

• Implanted cardiac pacemaker or neurostimulator

• Epilepsy, convulsion or seizure

• Use of medication that can influence muscle relaxation or cortical excitability

Related Conditions & MeSH terms

• Glycogen Storage Disease Type V
• McArdle Disease
• Muscular Diseases
• Myotonic Dystrophy
• Myotonic Dystrophy Type 2
• Nemaline Myopathy Type 6

Intervention

Diagnostic Test:
• Transcranial magnetic stimulation (TMS)
Single pulse, monophasic transcranial magnetic stimulation

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Radboud University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Normalized peak relaxation rate	Maximal rate at which the muscle relaxes after the TMS pulse, defined as the steepest point on the force curve.; This value is normalised to the force that preceded relaxation, i.e. top of the superimposed twitch.	1 hour
Secondary	Force decline at 150ms	The force decline (percentage of peak force) at 150ms after TMS stimulation.	1 hour
Secondary	Relaxation times (RT)	The time needed for force to decline to a certain percentage of peak force. E.g. the 75% relaxation time, is defined as the time needed for force to decline from 100% (i.e. force before relaxation onset) to 75%.; Different relaxation times will be evaluated, e.g. 90% RT, 75% RT, and 50% RT	1 hour
Secondary	Maximal muscle strength	The highest point on the force curve prior to TMS stimulus	1 hour