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Learning About Duchenne Muscular DystrophyWhat is Duchenne muscular dystrophy?Duchenne muscular dystrophy (DMD) is a rapidly progressive form of muscular dystrophy that occurs primarily in boys. It is caused by a mutation in a gene, called the DMD gene that can be inherited in families in an X-linked recessive fashion, but it often occurs in people from families without a known family history of the condition. Individuals who have DMD have progressive loss of muscle function and weakness, which begins in the lower limbs. The DMD gene is the largest gene to date, which encodes the muscle protein, dystrophin. Boys with Duchenne muscular dystrophy do not make the dystrophin protein in their muscles. Duchenne muscular dystrophy occurs in approximately 2 out of 10,000 males. Because this is an inherited disorder, risks include a family history of Duchenne muscular dystrophy. An estimated 1 in 3,500 boys worldwide are affected with Duchenne muscular dystrophy.
What are the symptoms of Duchenne muscular dystrophy?The symptoms usually appear before age 6 and may appear as early as infancy. Typically, the first noticeable symptom is delay of motor milestones, including sitting and standing independently. The mean age for walking in boys with Duchenne muscular dystrophy is 18 months. There is progressive muscle weakness of the legs and pelvic muscles, which is associated with a loss of muscle mass (wasting). This muscle weakness causes a waddling gait and difficulty climbing stairs. Muscle weakness also occurs in the arms, neck, and other areas, but not as severely or as early as in the lower half of the body. Calf muscles initially enlarge and the enlarged muscle tissue is eventually replaced with fat and connective tissue (pseudohypertrophy). Muscle contractures occur in the legs, making the muscles unusable because the muscle fibers shorten and fibrosis occurs in connective tissue. Occasionally, there can be pain in the calves. Symptoms usually appear in boys aged 1 to 6. There is a steady decline in muscle strength between the ages of 6 and 11 years. By age 10, braces may be required for walking, and by age 12, most boys are confined to a wheelchair. Bones develop abnormally, causing skeletal deformities of the spine and other areas. Muscular weakness and skeletal deformities frequently contribute to breathing disorders. Cardiomyopathy (enlarged heart) occurs in almost all cases, beginning in the early teens in some, and in all after the age of 18 years. Intellectual impairment may occur, but it is not inevitable and does not worsen as the disorder progresses. Few individuals with DMD live beyond their 30's. Breathing complications and cardiomyopathy are common causes of death.
How is Duchenne muscular dystrophy diagnosed?Duchenne muscular dystrophy is diagnosed in several ways. A clinical diagnosis may be made when a boys has progressive symmetrical muscle weakness, symptoms present before age 5 years, and they often have extremely elevated creatine kinase blood levels (which are described below) and, if untreated, wheelchair dependency before age 13 years. A muscle biopsy (taking a sample of muscle) for dystrophin studies can be done to look for abnormal levels of dystrophin in the muscle. The dystrophin protein can be visualized by staining the muscle sample with a special dye that allows you to visualize the dystrophin protein. A muscle which has average amounts of dystrophin will appear with the staining technique as though there is caulking around the individual muscles cells as though it is holding them together like window panes, while a boy with Duchenne will have an absence of dystrophin and appear to have absence of the caulking around the muscle cells. Some individuals can be found to have an intermediate amount of the dystrophin protein, often these boys are classified as having Becker muscular dystrophy. This is the gold standard for the diagnosis of DMD. Genetic testing (looking at the the body's instructions) on a blood sample for changes in the DMD gene can help establish the diagnosis of Duchenne muscular dystrophy without performing a muscle biopsy. Genetic testing is constantly changing, but the methods currently being used look for large changes in the gene (deletion/duplication) and another method, which looks at the letters that spell out the instructions found within the DMD gene (sequencing). Together these two methods can detect the disease causing changes in about 95 percent of patients. Those individuals without a detected change using this method, who are diagnosed with DMD by biopsy, still have a change in their gene but it is in areas of the gene that are not examined using these methods. However, the results may not be conclusive of a diagnosis of DMD, and only the muscle biopsy can tell the level of dystrophin protein for sure. For the remaining individuals, a combination of clinical findings, family history, blood creatine kinase (CK) concentration and muscle biopsy with dystrophin studies confirms the diagnosis. Creatine kinase is an enzyme that is present normally in high concentrations in the muscle cell of our body. During the process of muscle degeneration or breakdown, the muscle cells are broken open and their contents find their way to the bloodstream. Therefore elevated CK can be detected on a blood test is a measure of muscle damage. Elevated levels can be the result of multiple reasons including acute muscle injury, or chronic condition such as Duchenne.
What is the treatment for Duchenne muscular dystrophy?Treatment for Duchenne muscular dystrophy is aimed at the symptoms. Aggressive management of dilated cardiomyopathy with anti-congestive medications is used, including cardiac transplantation in severe cases. Assistive devices for respiratory complications may be needed, especially at night. The medication prednisone - a steroid - is given to improve the strength and function of individuals with DMD. Prednisone has been shown to prolong the ability to walk by 2 to 5 years. However, the possible side effects of prednisone include weight gain, high blood pressure, behavior changes, and delayed growth. A synthetic form of prednisilone, called Deflazacort, is used in Europe and believed to have fewer side effects than prednisone. A medication called cyclosporine has been used and has improved clinical function in children, but its use is controversial due to cyclosporine-induced myopathy. Oxandrolone, a medication used in a research study, has similar effects to prednisone with fewer side effects. There are several other therapies are also under investigation, including coenzyme Q10, glutamine, pentoxifylline, and PTC124 (See below: clinical research). Physical therapy is used to promote mobility and prevent contractures. Surgery may be needed for severe contractures and scoliosis.
Is Duchenne muscular dystrophy inherited?Duchenne muscular dystrophy is inherited in an X-linked recessive pattern. Males have only one copy of the X chromosome and one copy of the Y chromosome (which means boys one have one copy of the DMD gene) where as females have two copies of the X chromosomes (which means they have two copies of the DMD gene). Since females have two copies of this gene, if one copy does not work, they have a second back up copy to produce the dystrophin protein. A woman who has a genetic change in one of her two copies are said to be "a carrier" of Duchenne muscular dystrophy. Carriers do not have Duchenne and most are unaware that they even carry this change in their genetic material unless they have a family history. However, recent studies have shown that some carrier females (approximately 20 percent) will show symptoms of DMD, including muscle weakness and cardiac abnormalities. With an X-linked recessive condition, the chance of passing on the changed (non-working) copy of the gene to a child is different for males and females. Females who carry the changed copy of the gene have a 50 percent chance of passing it on with each pregnancy. Thus, there is a 25 percent chance of having a affected child with DMD ( eg. 50 percent of boys have the chance of having DMD and 50 percent of girls will be carriers). The chance of a woman who has one affected son (and no family history) of being a carrier of the changed DMD gene is approximately 2/3. However, in the remaining third of individuals with DMD, the change in the dystrophin gene is a new genetic change, or de novo change and about 10 percent of new mutations are due to gonadal mosaicism. Currently various reproductive options are available to families. The preconception options include MicroSort which is a technology that can separate sperm containing X chromosomes allowing for an increase in chances of having a female, and the second is preimplantation genetic diagnosis (PGD), which is a technique that can allow you to test cells of a fertilized egg to determine if it contains a change in the DMD gene and then implant those which do not. The post conception options include Chorionic Villus Sampling (CVS) and Amniocentesis which analyze sampled cells derived from the same cells that the pregnancy developed from early on in development. Several of the prenatal testing for pregnancies at increased risk is available when the DMD disease-causing mutation has been identified in a family member, or if informative, genetically-linked markers have been identified.
NHGRI Clinical Research on Duchenne Muscular DystrophyCurrently, NHGRI is not conducting studies on Duchenne Muscular Dystrophy
Additional Resources for Duchenne Muscular Dystrophy
Last Updated: July 28, 2008 |
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