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Muscular DystrophyNCT05715957

Follow-up Study on Female Carriers With DMD Gene Variants

An observational study of Muscular Dystrophy and Duchenne Muscular Dystrophy, run by Copenhagen University Hospital, Rigshospitalet at 1 site in Denmark.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

Background Duchenne and Becker muscular dystrophies are X-linked recessive allelic disorders caused by mutations of the dystrophin gene on chromosome Xp21. Female carriers may pass on the pathogenic variant to their daughters, resulting in a significant number of female carriers of pathogenic DMD variants. Read more about this study

Who is it for?
Ages 18 years and older
How many people
103 participants
Where
1 siteDenmark
Study dates
18 May 2023to 1 Dec 2025
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: All patients are identified from the Department of Clinical Genetics and Copenhagen Neuromuscular Center, Rigshospitalet. We aim at including the 53 carriers of DMD variants that we investigated 6 years ago for Part 1. These patients will be asked to participate in Part 2 as well (optional). If we cannot recruit 20 patients for Part 2 from Part 1 (see Power Calculation), we will recruit new patients identified from the Department of Clinical Genetics or Copenhagen Neuromuscular Center, Rigshospitalet. We need 32 patients with BMD for Part 3 (see Power Calculation), which will be recruited from Copenhagen Neuromuscular Center, Rigshospitalet.

Part 1:

Criteria of inclusion:

  • Female gender
  • Verified carrier of DMD gene mutations through genetic testing.
  • Age of 18 years or more
  • Participation in the study 6 years ago

Criteria of exclusion from MRI:

  • Contraindications to MRI (pacemaker or other internal metal or magnetic devices)
  • Claustrophobia.
  • Pregnant or nursing women.
  • Competing disorders and other muscle disorders, which may alter measurements of i.e., muscle strength. The investigator will decide whether or not the competing disorder can significantly influence the results.

Patients will be investigated with all other measurements than MRI if not eligible for MRI.

Part 2:

Criteria of inclusion:

  • Female gender
  • Verified carrier of DMD gene mutations through genetic testing.
  • Age of 18 years or more

Criteria of exclusion:

  • Anticoagulating medicine that cannot be paused due to health reasons

Part 3:

Criteria of inclusion:

  • Genetically verified patient with BMD
  • Age of 18 years or more

Criteria of exclusion:

  • Contraindications to MRI (pacemaker or other internal metal or magnetic devices)
  • Claustrophobia.
  • Atrial fibrillation
  • Competing disorders and other muscle disorders, which may alter measurements of i.e., muscle strength. The investigator will decide whether or not the competing disorder can significantly influence the results.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Denmark1 site
  • Copenhagen neuromuscular center

    Copenhagen, 2100

Other trials in Denmark

About this study

Official title: Influence of X- Chromosome Activation Pattern in Muscles on Symptoms and Progression of Cardiac and Muscle Symptoms Signs in Women With Pathogenic Dystrophin Gene Variants: A 6-year Follow-up of 53 Patients

Background Duchenne and Becker muscular dystrophies are X-linked recessive allelic disorders caused by mutations of the dystrophin gene on chromosome Xp21. Female carriers may pass on the pathogenic variant to their daughters, resulting in a significant number of female carriers of pathogenic DMD variants. There was a large variability in the severity of symptoms with some being asymptomatic and some having severe symptoms. Skewed X-Chromosome Inactivation (XCI) might explain some of this variability. But now, the underlying cause of the large variability in phenotype is therefore uncertain.

Aim

Read more
  1. To describe the change over a 6-year follow-up period in the structure and function of the heart and in function and muscle fat fraction in skeletal muscle of DMD/BMD carriers.
  2. To explain the relationship between the XCI and the severity of the disease (phenotype).
  3. To compare cardiac affection of female carriers of DMD/BMD to patients with BMD using new cardiac MRI techniques (spectroscopy and Dixon sequences).

Methods

This study contains three parts:

Part 1 is a 6-year follow-up on 53 genetically verified female carriers of pathogenic DMD variants initially investigated in 2016-2018 at Copenhagen Neuromuscular Center, Rigshospitalet (Ethical journal no. H-16035677). In this part, the same 53 females will be investigated with the same measurements as 6 years ago to describe the progression of symptoms. All the follow-up results from this study will be compared to the results from 6 years ago.

In Part 2 a muscle biopsy will be taken from 1-3 muscles (see "3.3.3 Description of outcomes) to investigate the XCI. To correlate the XCI to the phenotype, these patients will also undergo a muscle MRI and a Medical Research Council scale score for muscle strength (MRC).

In Part 3 The cardiac structure and function in patients with BMD will be investigated using a cardiac MRI to compare the findings with that of female carriers. An MRC will carried out to investigate if the heart affection correlates to the muscle affection.

Female carriers can decide whether to participate in Part 1, Part 2, or both. Patient with BMD can only participate in Part 3.

Read the detailed description

Duchenne and Becker muscular dystrophies are X-linked recessive allelic disorders caused by mutations of the dystrophin gene on chromosome Xp21. The gene mutation causes the absence or very severe reduction of dystrophin protein in the muscle cells, triggering chronic myofiber damage, inflammation, and loss of muscle fibers. Muscle tissue is replaced by fibrous and adipose tissue which further leads to necrosis, progressive muscle weakness, and loss of independent ambulation [1].

Duchenne muscular dystrophy (DMD) is one of the commonest inherited disorders of muscle. Based on a systematic review of worldwide population-based studies the pooled prevalence of DMD and BMD was 4.78 (95% CI 1.94-11.81) and 1.53 (95% CI 0.26-8.94) per 100,000 males respectively [2].

The disorders preferentially affect males due to the X-linked inheritance. Female carriers may pass on the pathogenic variant to their daughters, resulting in a significant number of female carriers of pathogenic DMD variants. A third of all new cases are caused by de novo pathogenic variants [3].

Even though female carriers have one healthy X-chromosome, they are not necessarily asymptomatic as both muscular and cardiac involvement has been reported in carriers [4-12]. These females are classified as "manifesting carriers" [13,14]. The incidence of skeletal muscle involvement among female carriers of DMD was 2.5%-19%, and of dilated cardiomyopathy (DCM) 7.3%-16.7% for DMD carriers and 0%-13.3% for BMD carriers [2], but in one of the latest cross-sectional studies with some of the most sensitive outcome measures to date 81 % showed muscle affection [4] and 62 % cardiac dysfunction [15]. Since then, cardiac MRI techniques have been further developed, why the numbers might be even higher. Patients with BMD have not even been investigated with these techniques. Cardiomyopathy in female DMD and BMD carriers can be clinically significant. Therefore, adult unaffected dystrophinopathy carriers are recommended to undergo echocardiography every 5 years according to the clinical guidelines in Europe and the United States [16,17]. Carriers with cardiac affection are often examined even more frequently. However, no one has yet investigated the rate of progression, which can make it difficult to determine the frequency of clinical visits.

In the above-mentioned studies, there was a large variability in the severity of symptoms with some being asymptomatic and some having severe symptoms. Skewed X-Chromosome Inactivation (XCI) might explain some of this variability. When the X chromosome carrying the normal DMD gene is preferentially inactivated this will in theory lead to moderate-severe muscle involvement.

Some studies have observed that DMD carriers with moderate/severe muscle involvement, exhibit a moderate or extremely skewed XCI, in particular, if presenting with an early onset of symptoms, while DMD carriers with mild muscle involvement present a random XCI [4, 18]. However, former studies have generally had a low power, investigated the XCI in blood and not muscle, and have often not investigated asymptomatic vs symptomatic patients. Some studies are inconclusive and some even contradictory and therefore no conclusions can be made [18]. Thus, the underlying cause of the large variability in phenotype is therefore uncertain.

2.2 Aim

The aims of this study are thus:

  1. To describe the change over a 6-year follow-up period in the structure and function of the heart and in function and muscle fat fraction in skeletal muscle of DMD/BMD carriers.
  2. To explain the relationship between the XCI and the severity of the disease (phenotype).
  3. To compare cardiac affection of female carriers of DMD/BMD to patients with BMD using new cardiac MRI techniques (spectroscopy and Dixon sequences).
  4. Methods 3.1 Study methods

This study contains three parts:

Part 1 is a 6-year follow-up on 53 genetically verified female carriers of pathogenic DMD variants initially investigated in 2016-2018 at Copenhagen Neuromuscular Center, Rigshospitalet (Ethical journal no. H-16035677). In this part, the same 53 females will be investigated with the same measurements as 6 years ago to describe the progression of symptoms. All the follow-up results from this study will be compared to the results from 6 years ago.

In Part 2 a muscle biopsy will be taken from 1-3 muscles (see "3.3.3 Description of outcomes) to investigate the XCI. To correlate the XCI to the phenotype, these patients will also undergo a muscle MRI and a Medical Research Council scale score for muscle strength (MRC).

In Part 3 The cardiac structure and function in patients with BMD will be investigated using a cardiac MRI to compare the findings with that of female carriers. An MRC will carried out to investigate if the heart affection correlates to the muscle affection.

Female carriers can decide whether to participate in Part 1, Part 2, or both. Patient with BMD can only participate in Part 3.

Being tested
No intervention
Keywords
XCI, follow up, MRI, spectroscopy
Medical subject headings
Muscular Dystrophies, Muscular Dystrophy, Duchenne

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • No interventionOther

    No intervention

Study groups in NCT05715957
Study groupRoleWhat they receive
female carriers of DMD gene variantsNot described
Receives: Other: No intervention
patients with BMDNot described
Receives: Other: No intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in fat fraction

    Change in fat fraction (in %) in leg muscles from baseline to 6-year follow-up

    Measured: 30 minutes

  2. Change in fibrosis in the heart

    Change in fibrosis (in %) in the heart from baseline to 6-year follow-up

    Measured: 1 hour

  3. Change in LVEF/GLS-score

    Change in LVEF/GLS-score (in %) in the heart from baseline to 6-year follow-up

    Measured: 1 hour

  4. Correlation between XCI and phenotype

    Correlation between XCI (ratio of healthy vs mutant X chromosome) and phenotype (from fat fraction and clinical symptoms). Correlation measured using linear regression.

    Measured: 1 hour

  5. Cardiac status in patients with BMD vs carriers of variants in the DMD gene

    Correlation between cardiac structure and function (measured through Dixon and spectroscopy from cardiac MRI) between patients with BMD and carriers of genetic variants of the DMD gene.

    Measured: 1 hour

Secondary outcomes (10)
  1. Change in contractility

    Change in contractility (measured as the peak torque divided by the contractile cross sectional area of the muscle) in leg muscles from baseline to 6-year follow-up

    Measured: 1 hour

  2. Change in blood concentrations

    Change in blood concentrations of myoglobin(ng/ML)

    Measured: 1 hour

  3. Change in blood concentrations

    Change in blood concentrations of Creatine kinase(U/L)

    Measured: 1 hour

  4. Change in blood concentrations

    Change in blood concentrations of Creatine kinase MB(U/L)

    Measured: 1 hour

  5. Change in blood concentrations

    Change in blood concentrations of troponin T (TnT) (ng/ML)

    Measured: 1 hour

  6. Change in blood concentrations

    Change in blood concentrations of pro-brain natriuretic peptide (proBNP)(pg/ML)

    Measured: 1 hour

  7. Change in lower extremity strength

    Change in lower extremity strength(measured by biodex 4 in Nm) from baseline to 6-year follow-up.

    Measured: 1 hour

  8. Change in questionnaires on fatigue

    Change in questionnaires on fatigue (using the fatigue severity scale score) from baseline to 6-year follow-up.

    Measured: 5 minutes

  9. Progression of electrocardiographic findings

    Progression of electrocardiographic findings from baseline to 6 year follow-up (measured by electrocardiographic as number of new incidents)

    Measured: 10 minutes

  10. Correlation between cardiac structure and function

    Correlation between cardiac structure (Dixon and spectroscopy from cardiac MRI) and muscle function (measured through the medical research council score from 1-5) in patients with BMD

    Measured: 1 hour

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Feb 2023
  2. Study start18 May 2023
  3. Primary completion1 Aug 2025 (estimated)
  4. Study completion1 Dec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
103 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05715957
Sponsor's protocol ID
98434
Status last verified
Jun 2025
First submitted
27 Jan 2023
Last updated
6 Jun 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Muscular Dystrophy and Duchenne Muscular Dystrophy, run by Copenhagen University Hospital, Rigshospitalet at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 6 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in fat fraction (time frame: 30 minutes). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Jun 2025.

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