Research progress in Duchenne muscular dystrophy

 

Duchenne muscular dystrophy is a muscle wasting condition that usually only affects males. However, a few exceptions have been reported where the condition has been diagnosed in females. It is a genetic condition that can be passed down from the parents but can also spontaneously appear without a previous family history.

How is Duchenne muscular dystrophy characterised?

Finding and characterising the type of mutations has brought vital insight into the underlying biology of this condition as explained below. This knowledge has been crucial for the development of therapeutic approaches and a number of these new technologies are currently being tested in clinical trial for their potential to treat Duchenne muscular dystrophy.

Duchenne muscular dystrophy is usually noticed in children when they are one to three years of age. Boys with the condition in pre-school age generally show difficulty with walking, running, jumping and climbing stairs. As they get older, they will use their hands to help them get up, looking as if they are ‘climbing up their legs’. This is called the ‘Gower’s sign’.

How does it progress?

The muscle wasting is progressive and eventually affects all the muscles involved in movement and breathing, as well as the heart. Boys will eventually lose their ability to walk, usually around the age of nine to eleven years of age. Once they are wheelchair users, the complications of Duchenne muscular dystrophy including osteoporosis (thinning of the bones), contractures (tightening of joints) and scoliosis (curvature of the spine), become more evident.

In the past, many people with the condition did not live beyond their late teens. Improvements in the management of the symptoms have meant that average life expectancy has increased to late 20s, early 30s.

How common is it?

Duchenne muscular dystrophy affects around one in 3,500 newborn boys and 100 new cases are being diagnosed each year in the UK. There are thought to be about 2,400 affected individuals in the UK.


Duchenne muscular dystrophy is caused by mutations in the gene that carries the information for a large muscle protein called dystrophin. These mutations cause complete disruption of the gene.

Dystrophin protein plays a number of vital roles in muscle. It interacts with many other muscle proteins, so that muscle fibres are strongly held together and the muscle contraction is effective. Dystrophin also acts as a shock absorber during movement thereby preventing muscle damage. By interacting with certain proteins, dystrophin has a role in increasing the blood flow to muscle during exercise. In the absence of dystrophin protein, muscle breaks down and wastes away. The muscle damage caused when dystrophin is absent cannot be repaired and muscle is eventually replaced by scar and fat tissue.

DMD is one of the most studied muscle-wasting conditions. However the function of the dystrophin protein is not yet fully understood. There are several animal models available that have been invaluable in investigating the biology of the condition. One of the most used mouse model is the mdx mouse. Much of what we know about the details of the different events associated with the loss of dystrophin in Duchenne has been derived from work done on mdx mouse.


Besides the interventions offered as the condition progresses (including supportive care, physiotherapy, ventilation for respiratory failure and medications to counter heart problems), steroid treatment is the only therapy routinely used. Steroids can stabilise the strength of DMD muscle for some time so that individuals maintain the ability to walk for one or two years longer into their mid-teens. However continual steroid treatment can cause a number of side effects including weight gain, mood changes and bone thinning.

It is thought that the presence of dystrophin protein might be essential for a treatment to be efficient and the way this can be achieved is by gene and cell therapy. Some of these approaches are mutation specific and therefore have been described as ‘personalised or precision’ medicine.

A first treatment addressing the underlying genetic mutation has received conditional marketing authorisation by the regulatory bodies in Europe. The drug is called Translarna and has been developed by the company PTC Therapeutics and has shown a moderate delay in the progression of the condition in clinical trials.

Translarna targets a specific type of mutation called nonsense mutation which causes cells to stop making the dystrophin protein. Premature stop codons in the dystrophin gene are the underlying cause of DMD in about 13 percent of cases. The strategy used by Translarna is known as stop codon read-through because it causes cells to “read through,” or “ignore,” erroneous stop signals in the dystrophin gene.

Although the development of Translarna is seen as a breakthrough, there is an urgent need to develop treatments that are more effective and which can be used for boys where the mutation is not a nonsense mutation.

A number of promising therapeutic approaches are currently developed and/or are in clinical trial and are discussed below.

Exon Skipping

Exon skipping uses small DNA fragments (molecular patches) that skip over parts of the mutated dystrophin gene so that a shortened but functional dystrophin protein can be produced. Exon skipping could theoretically be used for 83 percent of all Duchenne mutations. However it is a very personalised approach as it is mutation-specific. This means that a great number of molecular patches will have to be developed to target different mutations. It is necessary to know which mutation your son has in order to see which molecular patch would be suitable for them.

Exon skipping is not expected to be a cure; it could possibly convert the severe symptoms seen in boys with Duchenne into the milder symptoms observed in individuals with Becker muscular dystrophy (BMD).

In 2016, the first molecular patch for potentially treating Duchenne muscular dystrophy was approved in the USA. This molecular patch is called Exondys51 and could only potentially benefit boys with mutations amenable to exon 51 skipping. Exondys51 is currently being reviewed by the European regulator, the European Medicines Agency (EMA). Keep an eye on our website for future updates.

Read more about how exon skipping works.

AAV gene therapy

This approach is based on the use of a harmless virus called adeno-associated virus (AAV) which has been shown to effectively deliver genes to a range of different types of cells and tissues including muscle. The virus triggers a relatively mild immune response which could allow it to be given more than once. One of the challenges is that the dystrophin gene is too big for the virus to carry. Researchers have made mini- and micro-dystrophin genes to overcome this.

Following promising results in animal models of Duchenne muscular dystrophy, a phase I safety trial in a small number of boys was conducted in the US a few years ago. However the trial reported an immune reaction to the dystrophin protein produced in this way. Since then, researchers have been investigating ways to reduce this immune response, as well as ways to make the viral delivery system more efficient. Further clinical trials are planned to begin in 2017.

Read more about AAV gene therapy

Genome editing

Permanent correction of mutations in patient cells could potentially be achieved using genome editing. This is an exciting, rapidly moving field of research where enzymes are used that act as DNA scissors to cut the dystrophin gene at specific locations. The repair that results can be driven to completely mend the dystrophin gene to restore production of a full-length dystrophin protein. There is the potential to use these DNA scissors directly in patients, but this will require a lot of research and optimisation first. The attraction of gene editing as a therapy is that it would be a one-off permanent treatment and has the potential to provide a cure for people with Duchenne muscular dystrophy regardless of their mutation.

This approach is still in its infancy and a lot of preclinical research needs to be carried before clinical trials can be considered.

Read our feature article about genome editing.

Developing drugs to raise levels of a protein called utrophin to compensate for the missing dystrophin

Another potential therapy for DMD is to raise the levels of utrophin protein, as a functional substitute for dystrophin. The potential treatment has been developed in the laboratory of Professor Kay Davies in Oxford.

Despite excellent results in animal models, the first clinical trial in healthy volunteers of a first generation drug SMT C1100 lead to the delivery of insufficient amount of the drug to the muscles. SMT C1100 has since been improved and has recently successfully met its primary endpoint of safety and tolerability in a phase Ib clinical trial in DMD patients. On the basis of these findings, a second phase I trial tested the drug in boys with DMD when they are on a particular diet. The results showed that a balanced proportion of fats, proteins and carbohydrates increase the levels of SMT C1100 in the blood. A phase II open-label clinical trial to evaluate the safety and longer-term benefits of SMT C1100 on muscle health and function is currently underway.

There is now considerable effort ongoing in Oxford to develop second-generation drugs that have the potential to raise utrophin levels further. One such potential drug, SMT022357, has been shown to be distributed along the length of muscle fibres in the mdx mouse. Owing to its physical and chemical properties SMT022357 is likely to be more stable in the body than SMT C1100.

Developing stem cell therapies

Although first clinical trials are already taking place, this technology is still in its infancy and is thought to be far from being used in the clinic. The idea behind this approach is to use stem cells to replace the muscle tissue that is lost in Duchenne muscular dystrophy.

Considerable research is ongoing into the use of satellite cells which are muscle stem cells that are attached to the muscle fibres. The role of these cells is to repair and replace muscle fibres that are damaged as a result of injury. The hypothesis is that initially these stem cells are active in individuals with Duchenne or Becker muscular dystrophy but then lose their ability to repair and replace the damaged muscle cells. The aim of research into satellite cells is to better understand how these cells are regulated and to use them as a way to replace the damaged fibres with healthy ones.

A small scale clinical trial in Italy also tested whether mesangioblasts from healthy donors are safe to use as a treatment for children with Duchenne. Mesangioblasts are a type of stem cell found in the walls of blood vessels and have the ability to penetrate into muscle tissue. The results of trial have been inconclusive.

Stem cells could be taken from an unaffected donor in which case they have a functional dystrophin gene. However, this would trigger an immune response which would lead to the removal of the cells in the patient’s body. One way to overcome this is to use the patient’s own stem cells. However, before this can be done, the genetic defect causing Duchenne needs to be corrected.

Another approach is to take skin cells from boys with Duchenne and genetically re-programme them to become a type of stem cell called induced pluripotent stem (iPS) cells, which could then developed into any cell or tissue type, including muscle. However, this research is still in its infancy.

Even though there are several promising approaches to treat the underlying cause of Duchenne as described above, scientists believe that a combination of therapeutic approaches will be necessary to efficiently treat affected individuals. This is because the damage caused to the muscle might not be reversed by restoring dystrophin production. Therefore drugs that address complications associated with Duchenne are also necessary and are being developed. They include the following:

  • idebenone which acts on the energy state of the cell and has been shown in clinical trial to delay the respiratory decline seen in Duchenne patients
  • tadalafil, (a compound that increases the supply of oxygen to the muscles) whose effect on the decline in the walking ability of young Duchenne boys is being examined
  • eplerenone, a registered heart medication that has recently been reported to decrease the rate of heart failure in Duchenne boys when used as part of a long-term combination therapy
  • givinostat, an anti-inflammatory drug
  • PF-06252616, an antibody that blocks myostatin which is an inhibitor muscle growth.


The charity has supported high quality research into Duchenne for many years. This has made a considerable fundamental contribution to the technologies that are currently being tested in clinical trial and to recent research advances. However these are first generation treatments and therefore might only have a moderate impact. This is the reason why there is a need to continue to support high quality preclinical research to improve existing technologies.

Exon skipping research

The charity played a pioneering role in the development of exon skipping technology to treat Duchenne muscular dystrophy. We started funding research into this potential treatment in the early 1990s and orchestrated the establishment of the MDEX consortium, a group of scientists and clinicians, to advance this technology into clinical trial (2003). We provided crucial support for their successful application to the Department of Health and the Medical Research Council which lead to an award of £2.3M to carry out initial safety and efficacy studies for mutations that are amendable by skipping exon 51. The partner in the pharmaceutical industry was Sarepta Therapeutics who have continued to advance this technology further into phase II/III studies.

The charity also provided funding for the MDEX consortium to apply successfully to the EU FP7 for €5.5M to carry out a phase I trial for mutations amendable by skipping exon 53. We are actively involved in the study to represent the patient’s voice.

We are currently funding research in the laboratory of Professor Matthew Wood in Oxford to further improve the efficiency of the molecular patches to reach the muscle, diaphragm and heart.

Gene therapy

The charity played a crucial role in the development of a gene therapy approach based on the use of AAVs to deliver a functional copy of the dystrophin gene to the muscle. We funded vital work in the group of Professor George Dickson for the construction of a first generation AAV containing a micro-dystrophin gene. This AAV has been successfully tested in a dog model for Duchenne in collaboration with the French company Genethon. A first stage clinical trial to test the safety and efficiency is now planned.

Currently we fund a follow up project in Professor Dickson’s laboratory to develop a more efficient AAV that carries a mini-dystrophin gene that is thought to function more efficiently.

However it is expected that an AAV delivering a mini-dystrophin gene to the muscles will only convert the severe symptoms observed in Duchenne into the milder symptom seen in Becker. Therefore we also support research into a novel gene therapy that would allow delivery of the full-length dystrophin gene to muscle cells. In this project the researchers will use two or three viruses each carrying a different part of the dystrophin gene. In the muscle cell the different parts assemble to form the blueprint to produce a full size dystrophin protein. If successful this approach could be used to treat people with Duchenne.

Gene editing research

Professor George Dickson and his team have developed an innovative technique with the potential to repair the genetic mutation that causes Duchenne muscular dystrophy. The ground-breaking technique, described as an application of genome editing, could be the first therapy that offers permanent correction of the genetic mutation in a person’s own DNA. The technique is relevant to all boys and men with Duchenne muscular dystrophy.

We awarded a new five-year lectureship to Dr Linda Popplewell at Royal Holloway, University of London who has been working with Professor Dickson for over 10 years on gene based therapies for DMD. Dr Popplewell will use the genome editing technology to remove the mutation causing DMD from a person’s own DNA.

The charity is also funding a project in Professor Francesco Muntoni’s laboratory that uses genome editing to repair duplications in the dystrophin gene.

Utrophin up-regulation

The charity has supported the group of Dame Professor Kay Davies at the University of Oxford for more than 25 years for the development of a treatment for Duchenne based on utrophin up-regulation. Her laboratory identified a first compound, SMT C1100 that has been shown to raise the levels of utrophin in mouse models and is now in clinical trial.

We are currently supporting Professor Kay Davies and Professor Angela Russell to develop more efficient follow-up compounds and to investigate the molecular mechanism of action. A better understanding of how these drugs work will be vital for optimising existing drugs and to identify new therapeutic targets.

Stem cell repair

We currently fund three research projects at University College London investigating the use of stem cells as a therapeutic approach for Duchenne muscular dystrophy.

Professor Jenny Morgan is investigating the biological process that leads to muscle fibre death in animal models of the condition. The biological mechanisms that lead to the death of muscle fibres in Duchenne are not understood, but recent evidence has suggested that a newly discovered process of regulated cell death may play a role. Such a process that is controlled by the cells themselves could offer targets for drugs that could prevent muscle fibre death as a potential therapeutic approach for Duchenne.

In a second project Professor Morgan is looking into developing new ways to improve the efficiency of stem cell transplantation in damaged muscle using satellite cells.

Dr Saverio Tedesco is working on developing new methods that will allow the repair of a patient’s own stem cells to replace the damaged muscle.

Identification of DMD biomarkers

We fund research in the group of Professor Matthew Wood, University of Oxford, who is aiming to identify molecules which could be used as biomarkers for DMD. If successful, these biomarkers could be used to improve diagnosis, measure the progression of the condition more accurately and better assess the benefit of drugs in clinical trials without the painful procedure of muscle biopsies.

The effect of Duchenne muscular dystrophy on the brain

It is well known that the dystrophin protein acts as a shock absorber and is essential to protect muscle from damage during contraction. However dystrophin protein is also present in the brain and its function is less well understood in this organ. It is clear that boys with Duchenne have a number of psychological problems such as attention deficit and hyperactivity disorders and obsessive-compulsive disorders as well as learning difficulties and dyslexia. We are supporting Professor Volker Straub at Newcastle University who will investigate the changes that occur in the brain of boys with Duchenne. This will help understand how the lack of dystrophin affects the brain and allow scientists to develop better tests and offer more targeted help for families. The research will also enable scientist to understand whether current approaches being developed to treat Duchenne muscular dystrophy have a positive effect on the brain.

There are many ongoing clinical trials testing potential treatments for Duchenne muscular dystrophy. For the latest clinical trial updates, visit our Duchenne Research news pages.

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