05 November 2004
What is Myasthenia Gravis?
Myasthenia Gravis is a disorder in which normal communication between the nerve and muscle is interrupted at the neuromuscular junction. Normally when impulses travel down the nerve, the nerve endings release a neurotransmitter substance called acetylcholine, which travels through the short neuromuscular junction and results in the activation of muscle contraction. In myasthenia gravis, the receptors for acetylcholine at the muscle surface are destroyed or modulated by antibodies that prevent the normal reaction for occurring. The antibodies are produced by the patient's own immune system, which is believed to generate an aberrant autoimmune reaction resulting in an attack on the patient's own neuromuscular junction.
The symptoms of myasthenia gravis often consist of muscle fatigability with the patients complaining of worsening of symptoms later in the day after their muscles have fatigued or after being repetitively exercised. The symptoms range from difficulty in eye motion which results in double vision or droopy eyelids, to diffuse weakness and fatigability in the arms and legs. Other symptoms may include fatigue of throat muscles, resulting in swallowing difficulties and choking, and/or fatigue of the muscles of speech, resulting in slurred and unintelligible speech. Myasthenia gravis does not affect bowel and bladder function or the patient's mental capacity
How is Myasthenia Gravis diagnosed?
When the diagnosis of myasthenia gravis is suspected tests will be needed for confirmation of the diagnosis. A tensilon test, which is a relatively simple procedure, involves insertion of a small intravenous catheter through which tensilon is administered. Tensilon is a very short-acting drug that blocks the degradation of acetylcholine, thus increasing its levels for a very short time at the neuromuscular junction. The increased availability of acetylcholine results in improved muscle function and thus a transient improvement of the patient's symptoms. The most dramatic response is usually seen in patients with ocular difficulties. Patients with complete closure of the eyelids may open the eyes fully, but transiently, after tensilon administration. A negative tensilon test, however, does not rule out the diagnosis of myasthenia gravis. The next diagnostic step is obtaining blood for detection of acetylcholine receptor antibodies which are present in about 85-90% of patients with myasthenia gravis. The final diagnostic step is an EMG/nerve conduction study. The nerve conductions and EMG studies are usually normal in myasthenia gravis, but the repetitive stimulation of a nerve may demonstrate decrements of the muscle action potential. The muscle biopsy is usually not of diagnostic help in typical myasthenia gravis.
Once the diagnosis of myasthenia gravis is established, the patient and the treating physician will chart the appropriate therapeutic approach to the disease. Transient symptomatic control can be achieved by the initiation of Mestinon given orally. Mestinon is a medication that blocks the degradation of acetylcholine at the neuromuscular junction and provides for an increased level of acetylcholine and a better muscle response to stimulation by the nerve. Mestinon is a temporary symptomatic treatment and does not reverse the course of the illness.
In most cases, the first step in altering the course of myasthenia gravis is surgical removal of the thymus gland (thymectomy). The thymus gland is located behind the sternum (breastbone) and is considered the "training center" for the immune cells in the body. All antibody-producing cells in the body have to pass through the thymus to be properly "educated" in the production of various antibodies. In myasthenia gravis, the thymus enhances the presence and the antibody production capacity of immune cells that produce antibodies against the neuromuscular junction receptor. Although the precise role of the thymus gland in myasthenia gravis remains obscure, several studies have suggested that a thymectomy increases the chances of the patient going into remission to more than 50%. The thymectomy will also facilitate the control of the symptoms of myasthenia gravis by requiring a smaller amount of medications than prior to surgery. The benefits for the symptoms of myasthenia gravis may not be noticed until about 6-18 months after the thymectomy.
Control of myasthenia gravis is provided by the use of various immunosuppressants. The most commonly used immunosuppressant is prednisone, which is usually started at a high dose every day, and then reduced to an every other day regimen. The exact dose and mode of administration of prednisone must be tailored to the patients need. Prednisone is a type of steroid and is often associated with several side effects. In the event of intolerable side effects or failure of treatment, other immunosuppressants may be used, most commonly Imuran.
Patients with myasthenia gravis, especially untreated, may develop a "myasthenic crisis." These crises can be triggered by excessive physicial or emotional stress. A myasthenic crisis is a serious condition as the patient rapidly develops diffuse weakness, including weakness of the respiratory muscles which may temporarily require the use of mechanical ventilation. Under these conditions more aggressive treatment has to be implemented. The two most commonly used treatment regimens include several days of intravenous gamma globulin or several sessions of plasma exchange. Following resolution of the myasthenic crisis, the more conventional immune treatment is reinstuted.
Electromyography (EMG) testing is usually done on patients with symptoms of weakness and during an examination, are found to have decreased muscle strength. This testing is valuable in that it helps to differentiate between muscle weakness that is caused by neurological conditions and weakness caused by primary muscle conditions.
Electromyography is testing that is done to measure muscle response to nervous stimulation. During testing, a needle electrode is inserted through the skin into the muscle. The electrode detects electrical activity which is then displayed on an oscilloscope. Several electrodes may need to be placed at various locations to obtain an accurate study. After the electrode is in place, the muscle will need to be contracted (i.e. bending the arm or leg). A wave form can then be seen on the screen of the oscilloscope which gives information about the ability of the muscle to respond to nervous stimulation.
You may feel some discomfort with the insertion of the electrodes through the skin. It may feel like getting an injection. There is no special preparation for the testing and there are no lasting aftereffects. The exam usually takes about 20 to 60 minutes. When your exam is complete, the EMG technician will report the results to the physician who ordered the testing. Your physician will use the test results to help decide on proper management of your condition.